SanBio（4592）株式概要サンバイオ株式会社は、中枢神経系再生細胞医薬品の開発・製造・販売を行っています。 詳細4592 ファンダメンタル分析スノーフレーク・スコア評価1/6将来の成長5/6過去の実績0/6財務の健全性6/6配当金0/6報酬収益は年間40.07%増加すると予測されています 過去5年間の収益は年間0.8%増加しました。 リスク分析収益が 100 万ドル未満 ( ¥0 )JP市場と比較して、過去 3 か月間の株価の変動が非常に大きいすべてのリスクチェックを見る4592 Community Fair Values Create NarrativeSee what others think this stock is worth. Follow their fair value or set your own to get alerts.Analyst Price TargetsAN40.1% undervaluedAnalystConsensusTarget•4d agoRegenerative Medicine Tailwinds Will Support Long Term Brain Disease Treatment Potential2701AN65.7% undervaluedAnalystHighTarget•3mo agoBrain Regeneration Platform Will Transform Chronic Injury Treatment And Open Multiple Future Indications500Top Analyst NarrativesAN40.1% undervaluedAnalystConsensusTarget•4d agoRegenerative Medicine Tailwinds Will Support Long Term Brain Disease Treatment Potential2701AN65.7% undervaluedAnalystHighTarget•3mo agoBrain Regeneration Platform Will Transform Chronic Injury Treatment And Open Multiple Future Indications500View all narrativesSanBio Company Limited 競合他社Oncolys BioPharmaSymbol: TSE:4588Market cap: JP¥85.7b3-D MatrixSymbol: TSE:7777Market cap: JP¥46.1bPeptiDreamSymbol: TSE:4587Market cap: JP¥137.0bGNI GroupSymbol: TSE:2160Market cap: JP¥155.6b価格と性能株価の高値、安値、推移の概要SanBio過去の株価現在の株価JP¥994.0052週高値JP¥3,990.0052週安値JP¥914.00ベータ0.281ヶ月の変化-30.39%3ヶ月変化-48.68%1年変化-57.38%3年間の変化61.36%5年間の変化-27.55%IPOからの変化-43.94%最新ニュースナラティブの更新 • Jun 264592: Conditional Approval And Reimbursement Will Support Future Regenerative Therapy UpsideAnalysts have reduced their price target on SanBio from ¥2,100 to ¥1,660, citing updated assumptions around the discount rate, revenue growth, profit margin, and a higher future P/E multiple. What’s in the News for SanBio SanBio received marketing approval in Japan on July 31, 2024 for AKUUGO Suspension for Intracranial Implantation, indicated for improving chronic motor paralysis associated with traumatic brain injury.Major Estimate Revision • Jun 16Consensus revenue estimates increase by 16%The consensus outlook for revenues in fiscal year 2027 has improved. 2027 revenue forecast increased from JP¥400.0m to JP¥464.4m. Forecast losses expected to reduce from -JP¥66.90 to -JP¥60.48 per share. Biotechs industry in Japan expected to see average net income decline 20% next year. Consensus price target down from JP¥1,800 to JP¥1,660. Share price fell 5.1% to JP¥1,182 over the past week.Price Target Changed • Jun 05Price target decreased by 14% to JP¥1,800Down from JP¥2,100, the current price target is an average from 5 analysts. New target price is 43% above last closing price of JP¥1,263. Stock is down 63% over the past year. The company is forecast to post a net loss per share of JP¥66.90 next year compared to a net loss per share of JP¥52.55 last year.Major Estimate Revision • Apr 17Consensus revenue estimates increase by 22%The consensus outlook for revenues in fiscal year 2027 has improved. 2027 revenue forecast increased from JP¥3.47b to JP¥4.23b. Forecast losses expected to reduce from -JP¥68.53 to -JP¥62.44 per share. Biotechs industry in Japan expected to see average net income decline 32% next year. Consensus price target broadly unchanged at JP¥2,100. Share price rose 5.7% to JP¥2,099 over the past week.Major Estimate Revision • Apr 07Consensus EPS estimates fall by 55%The consensus outlook for fiscal year 2027 has been updated. 2027 expected loss increased from -JP¥44.09 to -JP¥68.53 per share. Revenue forecast of JP¥3.47b unchanged since last update. Biotechs industry in Japan expected to see average net income decline 51% next year. Consensus price target broadly unchanged at JP¥2,060. Share price rose 9.8% to JP¥1,955 over the past week.Major Estimate Revision • Mar 27Consensus EPS estimates fall by 21%The consensus outlook for fiscal year 2027 has been updated. 2027 expected loss increased from -JP¥39.72 to -JP¥47.91 per share. Revenue forecast of JP¥3.42b unchanged since last update. Biotechs industry in Japan expected to see average net income decline 41% next year. Consensus price target of JP¥2,100 unchanged from last update. Share price fell 2.0% to JP¥1,880 over the past week.最新情報をもっと見るRecent updatesナラティブの更新 • Jun 264592: Conditional Approval And Reimbursement Will Support Future Regenerative Therapy UpsideAnalysts have reduced their price target on SanBio from ¥2,100 to ¥1,660, citing updated assumptions around the discount rate, revenue growth, profit margin, and a higher future P/E multiple. What’s in the News for SanBio SanBio received marketing approval in Japan on July 31, 2024 for AKUUGO Suspension for Intracranial Implantation, indicated for improving chronic motor paralysis associated with traumatic brain injury.Major Estimate Revision • Jun 16Consensus revenue estimates increase by 16%The consensus outlook for revenues in fiscal year 2027 has improved. 2027 revenue forecast increased from JP¥400.0m to JP¥464.4m. Forecast losses expected to reduce from -JP¥66.90 to -JP¥60.48 per share. Biotechs industry in Japan expected to see average net income decline 20% next year. Consensus price target down from JP¥1,800 to JP¥1,660. Share price fell 5.1% to JP¥1,182 over the past week.Price Target Changed • Jun 05Price target decreased by 14% to JP¥1,800Down from JP¥2,100, the current price target is an average from 5 analysts. New target price is 43% above last closing price of JP¥1,263. Stock is down 63% over the past year. The company is forecast to post a net loss per share of JP¥66.90 next year compared to a net loss per share of JP¥52.55 last year.Major Estimate Revision • Apr 17Consensus revenue estimates increase by 22%The consensus outlook for revenues in fiscal year 2027 has improved. 2027 revenue forecast increased from JP¥3.47b to JP¥4.23b. Forecast losses expected to reduce from -JP¥68.53 to -JP¥62.44 per share. Biotechs industry in Japan expected to see average net income decline 32% next year. Consensus price target broadly unchanged at JP¥2,100. Share price rose 5.7% to JP¥2,099 over the past week.Major Estimate Revision • Apr 07Consensus EPS estimates fall by 55%The consensus outlook for fiscal year 2027 has been updated. 2027 expected loss increased from -JP¥44.09 to -JP¥68.53 per share. Revenue forecast of JP¥3.47b unchanged since last update. Biotechs industry in Japan expected to see average net income decline 51% next year. Consensus price target broadly unchanged at JP¥2,060. Share price rose 9.8% to JP¥1,955 over the past week.Major Estimate Revision • Mar 27Consensus EPS estimates fall by 21%The consensus outlook for fiscal year 2027 has been updated. 2027 expected loss increased from -JP¥39.72 to -JP¥47.91 per share. Revenue forecast of JP¥3.42b unchanged since last update. Biotechs industry in Japan expected to see average net income decline 41% next year. Consensus price target of JP¥2,100 unchanged from last update. Share price fell 2.0% to JP¥1,880 over the past week.Major Estimate Revision • Mar 24Consensus EPS estimates fall by 81%The consensus outlook for fiscal year 2027 has been updated. 2027 expected loss increased from -JP¥21.95 to -JP¥39.72 per share. Revenue forecast of JP¥3.42b unchanged since last update. Biotechs industry in Japan expected to see average net income decline 41% next year. Consensus price target up from JP¥2,050 to JP¥2,100. Share price fell 7.0% to JP¥1,847 over the past week.新しいナラティブ • Mar 19Regenerative Medicine Tailwinds Will Support Long Term Brain Disease Treatment PotentialCatalysts About SanBio SanBio is a regenerative medicine company focused on cell therapies for brain diseases such as traumatic brain injury. What are the underlying business or industry changes driving this perspective?お知らせ • Mar 17SanBio Company Limited, Annual General Meeting, Apr 22, 2026SanBio Company Limited, Annual General Meeting, Apr 22, 2026.Breakeven Date Change • Mar 17No longer forecast to breakevenThe 4 analysts covering SanBio no longer expect the company to break even during the foreseeable future. The company was expected to make a profit of JP¥3.82b in 2028. New consensus forecast suggests the company will make a loss of JP¥2.41b in 2029.新しいナラティブ • Mar 05Brain Regeneration Platform Will Transform Chronic Injury Treatment And Open Multiple Future IndicationsCatalysts About SanBio SanBio is a regenerative medicine company focused on cell therapies for brain diseases such as traumatic brain injury and ischemic stroke. What are the underlying business or industry changes driving this perspective?Major Estimate Revision • Jan 06Consensus revenue estimates fall by 41%The consensus outlook for revenues in fiscal year 2026 has deteriorated. 2026 revenue forecast decreased from JP¥50.0m to JP¥29.3m. Forecast losses increased from -JP¥50.74 to -JP¥54.39 per share. Biotechs industry in Japan expected to see average net income growth of 10% next year. Consensus price target broadly unchanged at JP¥2,050. Share price rose 3.6% to JP¥1,750 over the past week.Price Target Changed • Jan 06Price target increased by 8.7% to JP¥2,250Up from JP¥2,070, the current price target is an average from 5 analysts. New target price is 29% above last closing price of JP¥1,750. Stock is up 133% over the past year. The company is forecast to post a net loss per share of JP¥49.86 next year compared to a net loss per share of JP¥41.85 last year.お知らせ • Nov 07SanBio Company Limited has filed a Follow-on Equity Offering in the amount of ¥14.922 billion.SanBio Company Limited has filed a Follow-on Equity Offering in the amount of ¥14.922 billion. Security Name: Shares Security Type: Common Stock Securities Offered: 6,000,000 Price\Range: ¥2487 Discount Per Security: ¥109.36お知らせ • Oct 28SanBio Company Limited to Report Q3, 2026 Results on Dec 15, 2025SanBio Company Limited announced that they will report Q3, 2026 results on Dec 15, 2025Price Target Changed • Oct 10Price target increased by 17% to JP¥2,028Up from JP¥1,735, the current price target is an average from 4 analysts. New target price is 47% below last closing price of JP¥3,850. Stock is up 260% over the past year. The company is forecast to post a net loss per share of JP¥46.21 next year compared to a net loss per share of JP¥41.85 last year.お知らせ • Sep 14SanBio Company Limited to Report Q2, 2026 Results on Sep 12, 2025SanBio Company Limited announced that they will report Q2, 2026 results on Sep 12, 2025Major Estimate Revision • Jul 04Consensus revenue estimates increase by 291%, EPS downgradedThe consensus outlook for fiscal year 2026 has been updated. 2026 revenue forecast increased from JP¥44.0m to JP¥172.0m. EPS estimate fell from -JP¥41.26 to -JP¥48.65 per share. Biotechs industry in Japan expected to see average net income decline 21% next year. Consensus price target up from JP¥1,560 to JP¥1,735. Share price was steady at JP¥2,173 over the past week.Price Target Changed • Jul 02Price target increased by 19% to JP¥1,735Up from JP¥1,460, the current price target is an average from 4 analysts. New target price is 20% below last closing price of JP¥2,174. Stock is up 111% over the past year. The company is forecast to post a net loss per share of JP¥48.65 next year compared to a net loss per share of JP¥41.85 last year.New Risk • Jun 15New major risk - Financial positionThe company has less than a year of cash runway based on its current free cash flow trend. Free cash flow: -JP¥3.6b This is considered a major risk. With less than a year's worth of cash, the company will need to raise capital or take on debt unless its cash flows improve. This would dilute existing shareholders or increase balance sheet risk. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-JP¥3.6b free cash flow). Share price has been highly volatile over the past 3 months (16% average weekly change). Earnings are forecast to decline by an average of 3.5% per year for the foreseeable future. Revenue is less than US$1m. Minor Risk Currently unprofitable and not forecast to become profitable over next 3 years (JP¥2.7b net loss in 3 years).お知らせ • May 29SanBio Co., Ltd. Announces Results of the Third Commercial Production Run to Meet the Approval Conditions for the Shipment of AKUUGO Suspension for Intracranial ImplantationSanBio Co. Ltd. announced on April 18, 2025, that the expected yield from the third manufacturing of AKUUGO® Suspension for Intracranial Implantation was successfully secured, regarding the three production runs required for the release of shipments. The Company has completed specification testing and characteristic analysis for the third manufacturing run and has confirmed its results. The third manufacturing run cleared all specification requirements and was deemed compliant as well. With the fulfilment of the shipment conditions for AKUUGO, the company plans to promptly file a partial change application and proceed with obtaining full product approval.お知らせ • May 03SanBio Company Limited to Report Q1, 2026 Results on Jun 13, 2025SanBio Company Limited announced that they will report Q1, 2026 results on Jun 13, 2025Price Target Changed • Mar 22Price target increased by 10% to JP¥1,320Up from JP¥1,195, the current price target is an average from 4 analysts. New target price is approximately in line with last closing price of JP¥1,360. Stock is up 134% over the past year. The company is forecast to post a net loss per share of JP¥29.41 next year compared to a net loss per share of JP¥41.86 last year.Price Target Changed • Mar 18Price target increased by 33% to JP¥1,500Up from JP¥1,130, the current price target is an average from 3 analysts. New target price is 16% above last closing price of JP¥1,297. Stock is up 120% over the past year. The company is forecast to post a net loss per share of JP¥40.86 next year compared to a net loss per share of JP¥41.85 last year.お知らせ • Mar 17+ 1 more updateSanBio Company Limited, Annual General Meeting, Apr 23, 2025SanBio Company Limited, Annual General Meeting, Apr 23, 2025.New Risk • Feb 27New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 0.1% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Share price has been highly volatile over the past 3 months (9.6% average weekly change). Earnings are forecast to decline by an average of 0.1% per year for the foreseeable future. Revenue is less than US$1m. Minor Risk Currently unprofitable and not forecast to become profitable over next 3 years (JP¥4.0b net loss in 3 years).New Risk • Feb 07New major risk - Share price stabilityThe company's share price has been highly volatile over the past 3 months. It is more volatile than 90% of Japanese stocks, typically moving 8.8% a week. This is considered a major risk. Share price volatility increases the risk of potential losses in the short-term as the stock tends to have larger drops in price more frequently than other stocks. It may also indicate the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. Currently, the following risks have been identified for the company: Major Risks Share price has been highly volatile over the past 3 months (8.8% average weekly change). Revenue is less than US$1m. Minor Risk Currently unprofitable and not forecast to become profitable over next 3 years (JP¥3.9b net loss in 3 years).お知らせ • Feb 06SanBio Company Limited Announces Results of the Second Commercial Production Run of AKUUGOSanBio Company Limited announced on December 6, 2024, that it had secured the planned production yield for the second commercial production run of AKUUGO® Suspension for Intracranial Implantation (INN: vandefitemcel), conducted to meet the shipment conditions required for obtaining product approval. The Company has completed specification testing and characteristic analysis for the second manufacturing run and has confirmed its results. The second manufacturing run cleared all specification requirements and was deemed compliant. The third manufacturing run has already commenced. With the compliance of this manufacturing run, the company will run one more manufacturing compliant with necessary specifications and plans to file a partial change application and subsequently obtain approval for the partial change to meet the shipment conditions. As a result, the anticipated timing for AKUUGO® to become eligible for shipment remains unchanged, with shipment expected to begin in the second quarter of the fiscal year ending January 31, 2026 (May-July 2025). AKUUGO suspension for intracranial implantation (INN: vandefitemcel) is a human (allogeneic) bone marrow-derived modified mesenchymal stem cell that is produced by modifying and culturing mesenchymal stem cells derived from the bone marrow aspirate of healthy adults. The transplantation of AKUUGO into damaged nerve tissues in the brain is expected to trigger the release of FGF-2 (a type of protein) and other substances, which in turn will promote the natural regenerative ability of damaged nerve cells and induce proliferation and differentiation of nerve cells.お知らせ • Jan 28SanBio Company Limited to Report Fiscal Year 2025 Results on Mar 17, 2025SanBio Company Limited announced that they will report fiscal year 2025 results on Mar 17, 2025New Risk • Dec 16New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 7.6% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Share price has been highly volatile over the past 3 months (11% average weekly change). Earnings are forecast to decline by an average of 7.6% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (JP¥3.2b net loss in 3 years). Shareholders have been diluted in the past year (4.8% increase in shares outstanding).お知らせ • Dec 04SanBio Company Limited announced that it expects to receive ¥1.99992672 billion in funding from Athos Capital LimitedSanBio Company Limited announced a private placement to issue 2,295,600 common shares at issue price of ¥871.2 per share for gross proceeds of ¥1,999,926,720 on December 2, 2024. The transaction includes participation from new investor,Athos Asia Event Driven Master Fund. The transaction will happen through third party allocation. The issue date will be December 18, 2024. The transaction has been approved at board of director meeting of the company. The company will incur issuance cost of ¥98,996,000 and the net proceeds will be ¥1,900,930,720.お知らせ • Nov 17SanBio Company Limited Announces the Results of the First Commercial Production Run of AKUUGOSanBio Co. Ltd. announced on July 31, 2024, that it had obtained conditional and time-limited approval for AKUUGO suspension for intracranial implantation from the Ministry of Health, Labour and Welfare and that it planned to conduct about two commercial production runs to meet the shipment conditions required under this approval. They hereby provide the results of the first production run. The first production run did not meet the specification standards. However, only one specification value was non-compliant, while all other specification values, including the yield--a key issue identified during the approval review process--were compliant. Moreover, the results of the characterization analysis were equivalent to those of the clinical trials product. They anticipated some non-conforming products due to batch-to-batch variability arising from the heterogeneity of cells, a critical raw material for AKUUGO®, and they consider the non-conformity of the first manufacturing lot to be within expectations. Regarding the outlook, since the manufacturing process has already been established and approved, they have commenced the second production run. After obtaining manufacturing results that conform to the specifications for the second time, they will file an application for a partial change and aim to obtain approval for the subsequent partial change. As a result, the expected timeline for completing the two commercial production runs required to begin shipments of AKUUGO® has been delayed by a quarter, from the first quarter of the fiscal year ending January 2026 (February-April 2025) to the second quarter of the same fiscal year (May-July 2025). This matter will have only a minimal impact on the financial performance of the current fiscal year.お知らせ • Oct 29SanBio Company Limited to Report Q3, 2025 Results on Dec 16, 2024SanBio Company Limited announced that they will report Q3, 2025 results on Dec 16, 2024New Risk • Sep 18New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 1.8% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Share price has been highly volatile over the past 3 months (19% average weekly change). Earnings are forecast to decline by an average of 1.8% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Less than 1 year of cash runway based on current free cash flow (-JP¥4.8b). Currently unprofitable and not forecast to become profitable over next 3 years (JP¥1.7b net loss in 3 years). Shareholders have been diluted in the past year (5.7% increase in shares outstanding).お知らせ • Jul 31Sanbio Co., Ltd. Obtains Marketing Approval for AKUUGO Suspension for Intracranial ImplantationSanBio Co. Ltd. announced that on July 31, 2024, it obtained conditional and time-limited marketing approval for the human somatic stem cell-processed product "AKUUGO suspension for intracranial implantation" in Japan, for the indication of improving chronic motor paralysis resulting from traumatic brain injury. Details of product overview and conditional and time-limited marketing approved for AKUUGO are provided in the attached reference material. The company expects shipment and sales to begin in the first quarter of the fiscal year ending January 31, 2026. Moreover, to satisfy the conditions for full approval, the company plan to conduct post-marketing clinical trials and other necessary studies within the seven-year marketing authorization period with the aim of obtaining full approval. Based on track record of having obtained conditional and time- limited marketing approval for AKUUGO, the company plan to reallocate resources concentrated on the SB623 program for TBI to expanding indications and regions for the product. Through AKUUGO, company hope to bring hope to the lives of as many TBI patients as possible. The approval of AKUUGO was based on the results of the global Phase 2 clinical trial SanBio conducted in Japan and the United States. Dr. Nobuhito Saito, Professor of Neurology at the University of Tokyo led the clinical trial, commented as follows. Thaw the cell suspension for intracranial implants, wash it with the dedicated preparation solution, and adjust the concentration of the cell suspension to 1.67 x 106 cells/100uL using the dedicated preparation solution. Cleanse the micro-syringe fixed with the cannula from the dedicated delivery device set with the dedicated preparation solution before filling it with the prepared cell suspension. Date of marketing approval, July 31, 2024, Product image, Vial containing cell suspension for intracraial implantation, Dry shipper, Hard case and dry shipper for transportation, Dedicated preparation solution, Dedicated preparation solution, dedicated preparation solution, Dedicated delivery device set, Outer package for dedicated delivery device set. Condition of approval. Considering the limited manufacturing record for the Product, the Company shall promptly collect information on the Product's quality based on a pre-determined plan, and evaluate and report on the equivalence/homogeneity, in terms of quality, of the investigational product (clinical trials product) and the Product intended for commercial distribution. Based on the evaluation results, the Company shall apply for a partial change of approved matters. It shall not ship the Product until the partial change application has been approved. The Company must ensure that the Product is used in medical facilities fully equipped to handle emergencies, by physicians who possess sufficient knowledge and experience in the diagnosis and treatment of traumatic brain injury and stereotactic treatment.お知らせ • Jul 27SanBio Company Limited to Report Q2, 2025 Results on Sep 17, 2024SanBio Company Limited announced that they will report Q2, 2025 results on Sep 17, 2024Price Target Changed • Jul 01Price target increased by 20% to JP¥960Up from JP¥800, the current price target is an average from 5 analysts. New target price is 21% below last closing price of JP¥1,218. Stock is up 98% over the past year. The company is forecast to post a net loss per share of JP¥41.16 next year compared to a net loss per share of JP¥40.48 last year.Price Target Changed • Jun 20Price target increased by 23% to JP¥983Up from JP¥800, the current price target is an average from 5 analysts. New target price is 16% above last closing price of JP¥848. Stock is up 27% over the past year. The company is forecast to post a net loss per share of JP¥38.58 next year compared to a net loss per share of JP¥40.48 last year.New Risk • Jun 13New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 1.0% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-JP¥4.8b free cash flow). Share price has been highly volatile over the past 3 months (13% average weekly change). Earnings are forecast to decline by an average of 1.0% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (JP¥2.4b net loss in 3 years). Shareholders have been diluted in the past year (5.8% increase in shares outstanding).お知らせ • Jun 13SanBio Company Limited Announces Update on Status of Manufacturing and Marketing Approval for Sb623 Chronic Traumatic Brain Injury Program in JapanOn March 26, 2024, SanBio Co. Ltd. (the "Company") provided an update on the progress toward obtaining marketing approval of SB623 to treat chronic traumatic brain injury (TBI) in Japan, stating it was concluded to continue the deliberation at a later date by the Pharmaceutical Affairs and Food Sanitation Council's Subcommittee on Regenerative Medicine Products (the "Subcommittee") and company planned to engage in further consultations with the regulatory authorities and to submit additional information such as additional data addressing quality. the Ministry of Health, Labour and Welfare announced that the Pharmaceutical Affairs and the Subcommittee will hold a meeting on June 19, and company learned that the Subcommittee will deliberate, among others, on whether to grant marketing approval for the regenerative medicine "AKUUGO suspension for intracranial implantation", whether to stipulate conditions and a time limit for the approval, and whether to designate a reexamination period. Accordingly, the Subcommittee will determine whether to grant the Company's development product SB623 marketing approval in the meeting. SB623 (INN: vandefitemcel) is a human (allogeneic) bone marrow-derived modified mesenchymal stem cell that is produced by modifying and culturing mesenchymal stem cells derived from the bone marrow aspirate of healthy adults. Implantation of SB623 cells into injured nerve tissues in the brain is expected to trigger the brain's natural regenerative ability to restore lost functions. SB623 is currently being investigated for the treatment of several conditions including chronic neurological motor deficit resulting from traumatic brain injury and ischemic stroke.お知らせ • May 05SanBio Company Limited to Report Q1, 2025 Results on Jun 13, 2024SanBio Company Limited announced that they will report Q1, 2025 results on Jun 13, 2024New Risk • Apr 02New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 3.6% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-JP¥4.8b free cash flow). Share price has been highly volatile over the past 3 months (15% average weekly change). Earnings are forecast to decline by an average of 3.6% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (JP¥2.9b net loss in 3 years). Shareholders have been diluted in the past year (6.4% increase in shares outstanding).Price Target Changed • Mar 28Price target decreased by 30% to JP¥1,214Down from JP¥1,742, the current price target is an average from 5 analysts. New target price is 188% above last closing price of JP¥421. Stock is down 38% over the past year. The company is forecast to post a net loss per share of JP¥68.35 next year compared to a net loss per share of JP¥40.48 last year.お知らせ • Mar 19SanBio Company Limited, Annual General Meeting, Apr 24, 2024SanBio Company Limited, Annual General Meeting, Apr 24, 2024. Agenda: To consider to reduce the amounts of stated capital and capital reserves and to make an appropriation of other capital surplus.Price Target Changed • Mar 18Price target increased by 18% to JP¥2,100Up from JP¥1,782, the current price target is an average from 5 analysts. New target price is 184% above last closing price of JP¥740. Stock is up 5.4% over the past year. The company is forecast to post a net loss per share of JP¥63.15 next year compared to a net loss per share of JP¥95.98 last year.Breakeven Date Change • Jan 31Forecast to breakeven in 2027The 4 analysts covering SanBio expect the company to break even for the first time. New consensus forecast suggests the company will make a profit of JP¥712.0m in 2027. Average annual earnings growth of 62% is required to achieve expected profit on schedule.お知らせ • Jan 28SanBio Company Limited to Report Fiscal Year 2024 Results on Mar 18, 2024SanBio Company Limited announced that they will report fiscal year 2024 results on Mar 18, 2024お知らせ • Jan 25Sanbio Co., Ltd. Provides Update on Status of Manufacturing and Marketing Approval for Sb623 Chronic Traumatic Brain Injury Program in JapanSanBio Co. Ltd. provided an update on the progress toward obtaining marketing approval of SB623 to treat chronic traumatic brain injury (TBI) in Japan, stating it aims to achieve approval by March 2024 and is actively engaged in the review process. Amidst this situation, the Ministry of Health, Labour and Welfare announced on January 22 that the Pharmaceutical Affairs and Food Sanitation Council's Subcommittee on Regenerative Medicine Products (the "Sub committee") would hold a meeting on February 5. However, developmental product SB623, which is undergoing approval review as a treatment for TBI under the framework of the Sakigake Designation System, was not included in the agenda for this meeting.New Risk • Dec 15New major risk - Financial positionThe company has less than a year of cash runway based on its current free cash flow trend. Free cash flow: -JP¥6.1b This is considered a major risk. With less than a year's worth of cash, the company will need to raise capital or take on debt unless its cash flows improve. This would dilute existing shareholders or increase balance sheet risk. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-JP¥6.1b free cash flow). Share price has been highly volatile over the past 3 months (8.8% average weekly change). Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (JP¥280m net loss in 3 years). Shareholders have been diluted in the past year (6.5% increase in shares outstanding).お知らせ • Dec 14SanBio Company Limited Provides Update on Status of Manufacturing and Marketing Approval for SB623 Chronic Traumatic Brain Injury (TBI) Program in JapanSanBio Company Limited provided an update on the progress toward obtaining marketing approval of SB623 to treat chronic traumatic brain injury (TBI) in Japan, stating that the Company was focused on resolving the issue related to the production yield and responding to production-related review by regulatory authorities, with the goal of obtaining approval by the end of the current fiscal year. The Company hereby provides another progress update, to ensure timely disclosure to concerned patients and their families, as well as shareholders and investors who await the approval of SB623. SB623 is undergoing approval review under the framework of the Sakigake Designation System as a treatment for chronic effects associated with TBI. The production yield-related issue has been resolved, and the review process is proceeding to a conclusion. However, given the status of the review process, it will take some more time until approval is granted, and for this reason, the Company now expects to obtain approval in March 2024. Although the timing of approval is outside of the Company's control, SanBio will continue to work as one and do utmost to obtain approval.お知らせ • Oct 14SanBio Company Limited to Report Q3, 2024 Results on Dec 14, 2023SanBio Company Limited announced that they will report Q3, 2024 results on Dec 14, 2023お知らせ • Jul 29SanBio Company Limited to Report Q2, 2024 Results on Sep 15, 2023SanBio Company Limited announced that they will report Q2, 2024 results on Sep 15, 2023Major Estimate Revision • Jul 28Consensus revenue estimates fall by 15%The consensus outlook for revenues in fiscal year 2024 has deteriorated. 2024 revenue forecast decreased from JP¥459.0m to JP¥389.0m. Forecast losses increased from -JP¥74.33 to -JP¥80.94 per share. Biotechs industry in Japan expected to see average net income growth of 39% next year. Consensus price target broadly unchanged at JP¥1,824. Share price was steady at JP¥596 over the past week.お知らせ • Jun 15+ 1 more updateSanBio Co., Ltd. Updates on Status of Manufacturing and Marketing Approval for SB623 Chronic Traumatic Brain Injury Program in JapanSanBio Co. Ltd. announced that it was working to resolve the issue of production yield, to bring yield back to the level at the time of application filing toward obtaining marketing approval of SB623 to treat chronic traumatic brain injury (TBI) in Japan during the current fiscal year ending January 2024. The Company announced that whether the issue is resolved should be known by June 2023 and will be reported at the result briefing for the first quarter of the fiscal year ending January 2024. The Company hereby provides a progress update, to ensure timely disclosure to concerned patients, their families, as well as shareholders and investors who await the approval of SB623. SB623 is under review in the Sakigake Designation System for approval as a treatment for chronic effects associated with TBI. Toward obtaining approval, the Company is currently focused on resolving the issue related to the production yield and responding to production-related review. Although the company have yet to fully recover the production yield obtained at the time of application filing, additional data from the latest production run has led to measures that could resolve the yield-related issue. A production run with implemented measures is currently underway, and results are expected in August. Although the timing of approval is outside of the Company's control, by resolving the yield-related issue and responding to production-related review in a timely manner, presently the Company's goal remains to obtain approval during the current fiscal year. SB623 (INN: vandefitemcel) is a human (allogeneic) bone marrow-derived modified mesenchymal stem cell that is produced by modifying and culturing mesenchymal stem cells derived from the bone marrow aspirate of healthy adults. Implantation of SB623 cells into injured nerve tissues in the brain is expected to trigger the brain's natural regenerative ability to restore lost functions. SB623 is currently being investigated for the treatment of several conditions including chronic neurological motor deficit resulting from traumatic brain injury and ischemic stroke. Traumatic brain injury (TBI) is one of the leading causes of death and disability worldwide. The estimated global incidence of acute TBI during 2016 was 27 million cases, and the estimated global prevalence of chronic impairment secondary to TBI was 55.5 million cases. Overall, TBI and long-term motor deficits secondary to TBI significantly impair a person's self-care, employability, and quality of life, and are major burdens on healthcare systems worldwide. In the United States, approximately 43% of surviving hospitalized persons with TBI experience long-term disabilities, and it is estimated that 3.17 million people are living with long-term disabilities secondary to TBI.Price Target Changed • Jun 15Price target increased by 13% to JP¥2,290Up from JP¥2,022, the current price target is an average from 4 analysts. New target price is 276% above last closing price of JP¥609. Stock is down 44% over the past year. The company is forecast to post a net loss per share of JP¥72.57 next year compared to a net loss per share of JP¥95.98 last year.Breakeven Date Change • Jun 01No longer forecast to breakevenThe 4 analysts covering SanBio no longer expect the company to break even during the foreseeable future. The company was expected to make a profit of JP¥1.27b in 2026. New consensus forecast suggests the company will make a loss of JP¥1.44b in 2026.お知らせ • May 13SanBio Company Limited to Report Q1, 2024 Results on Jun 14, 2023SanBio Company Limited announced that they will report Q1, 2024 results on Jun 14, 2023Price Target Changed • Mar 20Price target increased by 12% to JP¥2,465Up from JP¥2,192, the current price target is an average from 4 analysts. New target price is 251% above last closing price of JP¥702. Stock is down 50% over the past year. The company is forecast to post a net loss per share of JP¥59.64 next year compared to a net loss per share of JP¥95.98 last year.Breakeven Date Change • Mar 16No longer forecast to breakevenThe 5 analysts covering SanBio no longer expect the company to break even during the foreseeable future. The company was expected to make a profit of JP¥1.27b in 2026. New consensus forecast suggests the company will make a loss of JP¥203.3m in 2026.Price Target Changed • Feb 20Price target increased by 12% to JP¥2,465Up from JP¥2,192, the current price target is an average from 4 analysts. New target price is 265% above last closing price of JP¥675. Stock is down 57% over the past year. The company is forecast to post a net loss per share of JP¥99.89 next year compared to a net loss per share of JP¥90.31 last year.お知らせ • Feb 03SanBio Company Limited to Report Fiscal Year 2023 Results on Mar 16, 2023SanBio Company Limited announced that they will report fiscal year 2023 results on Mar 16, 2023Breakeven Date Change • Jan 31Forecast to breakeven in 2026The 4 analysts covering SanBio expect the company to break even for the first time. New consensus forecast suggests the company will make a profit of JP¥954.5m in 2026. Average annual earnings growth of 47% is required to achieve expected profit on schedule.お知らせ • Jan 20SanBio Co., Ltd. Announces Board ChangesSanBio Co. Ltd. announced that at a meeting held on January 20, 2023, its Board of Directors resolved to make the following changes to senior management (representative director and corporate officer). Representative Director, Executive Vice President, and COO Akihiro Tsujimura has submitted his resignation for personal reasons and the Company has accepted it. Due to the resignation of Mr. Tsujimura, Corporate Officer and Business Head (Japan/Asia) Naoki Tsukahara will be appointed executive corporate officer responsible for HR, Japan Regulatory Affairs & Quality Compliance Japan, and Japan/Asia business, and will take over some of the responsibilities of Mr. Tsujimura. Effective date of change is January 20, 2023.お知らせ • Dec 16SanBio Company Limited Provides Earnings Guidance for the Fiscal Year Ending January 31, 2023SanBio Company Limited provided earnings guidance for the Fiscal Year Ending January 31, 2023. For the full year, the company expected Operating loss of JPY 8,131 million; Net loss attributable to owners of parent to be JPY 5,684 million and net loss per share of JPY 95.36.Board Change • Nov 16Less than half of directors are independentNo new directors have joined the board in the last 3 years. The company's board is composed of: No new directors. 3 experienced directors. 4 highly experienced directors. 1 independent director (3 non-independent directors). Independent External Director Noboru Kotani was the last independent director to join the board, commencing their role in 2013. The following issues are considered to be risks according to the Simply Wall St Risk Model: Minority of independent directors. Insufficient board refreshment.お知らせ • Oct 01SanBio Company Limited to Report Q3, 2023 Results on Dec 15, 2022SanBio Company Limited announced that they will report Q3, 2023 results on Dec 15, 2022お知らせ • Sep 14Sanbio Company Limited Provides Earnings Guidance for the Fiscal Year Ending January 31, 2023SanBio Company Limited provided earnings guidance for the Fiscal Year Ending January 31, 2023. For the full year, the company expected Operating loss of JPY 8,131 million; Net loss attributable to owners of parent to be JPY 5,684 million and net loss per share of JPY 95.36.Price Target Changed • Jul 23Price target decreased to JP¥2,233Down from JP¥2,567, the current price target is an average from 7 analysts. New target price is 70% above last closing price of JP¥1,312. Stock is up 7.5% over the past year. The company is forecast to post a net loss per share of JP¥85.62 next year compared to a net loss per share of JP¥90.31 last year.お知らせ • Jul 22SanBio Company Announces Update on Status of Manufacturing and Marketing Approval for SB623 Chronic Traumatic Brain Injury (TBI) Program in JapanJapan's Ministry of Health, Labour, and Welfare (MHLW) on July 20 announced that the Regenerative Medicine Subcommittee (lower panel of Pharmaceutical Affairs and Food Sanitation Council) meeting will be held on August 3. SanBio's SB623, currently undergoing review in the Sakigake Designation System for the treatment of traumatic brain injury, is not included in the topic of deliberations. SanBio's corporate policy is to refrain from setting or disclosing a target timing for approval, as there are many factors outside of the company's control. Do recognize that, based on public perceptions regarding the Sakigake Designation System, there may be expectations for a September approval among patients and family members as well as shareholders and investors. Had SB623 been included in the meeting agenda, a September approval was a possibility. Now believe that a September approval is unlikely. Pledge to work diligently as one team to facilitate the review of this truly innovative product to ensure the swiftest possible regulatory approval and achieve SanBio's first to market. Take this opportunity to reassure all stakeholders that work continues steadily to ensure that not a day is wasted in bringing approval to reality. SB623 (INN: vandefitemcel) is a human (allogeneic) bone marrow-derived modified mesenchymal stem cell that is produced by modifying and culturing mesenchymal stem cells derived from the bone marrow aspirate of healthy adults. Implantation of SB623 cells into injured nerve tissues in the brain is expected to trigger the brain's natural regenerative ability to restore lost functions. SB623 is currently being investigated for the treatment of several conditions including chronic neurological motor deficit resulting from traumatic brain injury and ischemic stroke.お知らせ • Jul 02Keizo Nakada to Join Sanbio as Corporate Officer and Head of ProductionThe SanBio Group announced that Mr. Keizo Nakada joined the Group as a new Corporate Officer and Head of Production on July 1, 2022. Previously, at Santen Pharmaceutical Co. Ltd., Mr. Nakada gained experience setting up overseas plants and serving as the head of a domestic plant. Afterward, as an executive officer and head of Product Supply Department, he established a stable global product supply system while successfully reducing costs. Later, as an executive officer in charge of production departments at Bushu Pharmaceuticals Ltd. and Taiko Pharmaceutical Co. Ltd., Mr. Nakada assumed responsibility for domestic production plants, supply chain management, quality control, and technological development. At the same time, he fully optimized the supply chains of these companies, achieving dramatic increases in production capacity.Price Target Changed • Jun 24Price target decreased to JP¥2,200Down from JP¥2,467, the current price target is an average from 5 analysts. New target price is 91% above last closing price of JP¥1,154. Stock is down 20% over the past year. The company is forecast to post a net loss per share of JP¥100 next year compared to a net loss per share of JP¥90.31 last year.お知らせ • Jun 14SanBio Company Limited Provides Consolidated Earnings Guidance for the First Half and Full Year Ending January 31, 2023SanBio Company Limited provided consolidated earnings guidance for the first half and full year ending January 31, 2023. For the first half, the company expects operating loss of JPY 3,067 million, net loss attributable to owners of parent of JPY 3,169 million and net loss per share of JPY 61.19.For the full year, the company expects operating loss of JPY 5,858 million, net loss attributable to owners of parent of JPY 5,997 million and net loss per share of JPY 115.79.お知らせ • Jun 01SanBio Company Limited Appoints Andrew Liu as Chief Strategy OfficerSanBio Company Limited announced as follows the appointment of Andrew Liu as Chief Strategy Officer of the SanBio Group, effective May 16, 2022.Board Change • Apr 27Less than half of directors are independentFollowing the recent departure of a director, there is only 1 independent director on the board. The company's board is composed of: 1 independent director. 3 non-independent directors. Independent External Director Noboru Kotani was the last independent director to join the board, commencing their role in 2013. The company's minority of independent directors is a risk according to the Simply Wall St Risk Model.お知らせ • Apr 06Sanbio Group Provides an Update on One-Year Analysis of the Phase 2 STEMTRA TrialSanBio Company Limited announced that SB623 met the primary endpoint and demonstrated a trend toward maintaining the improvement of function and activities of daily living in the final, one-year analysis of the Phase 2 STEMTRA trial, which evaluated the efficacy and safety of SB623 compared to sham surgery in patients with chronic motor deficit from traumatic brain injury (TBI). These results will be presented in an oral plenary session at theAmerican Academy of Neurology (AAN) Annual Meeting, taking place on April 5, 2022, in Seattle, Washington, USA. SB623 is an investigational, regenerative cell medicine comprised of bone-marrow-derived, mesenchymal stem cells that are implanted intracranially around the area of the injury. SanBio is preparing to initiate a Phase 3 trial for SB623 in the United States, where many traumatic brain injury patients currently live.お知らせ • Mar 07Sanbio Company Limited Announces Filing with Japan’S Ministry of Health, Labour, and Welfare for Manufacture and Marketing Approval as A Regenerative Medicine Product for the Investigational Product Sb623The SanBio Group announced the completion of an application filing with Japan’s Ministry of Health, Labour, and Welfare (MHLW) for manufacture and marketing approval as a regenerative medicine product for the investigational product SB623, as a treatment for chronic motor deficit from traumatic brain injury (TBI). This application for approval is based on efficacy and safety results from the US-Japan global Phase 2 clinical trial (Study of Modified Stem Cells in Traumatic Brain Injury, or STEMTRA). STEMTRA is a randomized, double-blind, surgical sham-controlled trial evaluating the efficacy and safety of SB623 in patients with chronic motor deficits secondary to traumatic brain injury. In this study, SB623 met its primary endpoint, with patients treated with SB623 achieving statistically significant improvement in motor function compared with sham surgery. The trial also demonstrated that SB623 was generally safe and well tolerated.Price Target Changed • Feb 14Price target increased to JP¥2,900Up from JP¥2,660, the current price target is an average from 3 analysts. New target price is 109% above last closing price of JP¥1,385. Stock is down 19% over the past year. The company is forecast to post a net loss per share of JP¥89.16 next year compared to a net loss per share of JP¥65.37 last year.お知らせ • Feb 11+ 1 more updateSanBio Company Limited announced that it expects to receive ¥33.75 million in funding from Nomura Securities Co., Ltd.SanBio Company Limited (TSE:4592) announced a private placement of 75,000 32nd series warrants at a price of ¥450 per warrant for gross proceeds of ¥33,750,000 on February 10, 2022. The transaction will include participation from existing investor Nomura Securities Co., Ltd. The securities are issued through a third party allotment method. The transaction has been approved by the board of directors of the company. The company will receive proceeds of ¥8,258,750,000 if the warrants are exercised fully. The transaction is expected to close any day between March 4, 2022 and March 11, 2022. The exercise period will start from the trading day following date of allocation to March 7, 2025.お知らせ • Dec 17SanBio Company Limited Provides Consolidated Earnings Guidance for the Fiscal Year Ending January 31, 2022SanBio Company Limited provided consolidated earnings guidance for the fiscal year ending January 31, 2022. For the period, the company expects Operating loss of JPY 5,786 million; Ordinary loss of JPY 5,876 million; Net loss attributable to owners of parent of JPY 5,877 million and Net loss per share of JPY 113.49.お知らせ • Sep 15+ 1 more updateSanBio Company Limited Provides Consolidated Earnings Guidance for the Fiscal Year Ending January 31, 2022SanBio Company Limited provided consolidated earnings guidance for the fiscal year ending January 31, 2022. For the period, the company expects operating loss of JPY 5,786 million, ordinary loss of JPY 5,876 million and net loss attributable to owners of parent of JPY 5,877 million or JPY 113.49 per share.Executive Departure • Jul 13Corporate Officer & Business Head of Japan/Asia Hiroshi Yamamoto has left the companyOn the 1st of July, Hiroshi Yamamoto's tenure as Corporate Officer & Business Head of Japan/Asia ended after 2.4 years in the role. We don't have any record of a personal shareholding under Hiroshi's name. Hiroshi is the only executive to leave the company over the last 12 months. The current median tenure of the management team is 1.50 years, which is considered inexperienced in the Simply Wall St Risk Model.Price Target Changed • Jul 07Price target increased to JP¥2,660Up from JP¥2,417, the current price target is an average from 3 analysts. New target price is 99% above last closing price of JP¥1,337. Stock is down 17% over the past year.お知らせ • Jun 15SanBio Company Limited Provides Consolidated Earnings Guidance for the First Half and Full Year of the Fiscal Year Ending January 31, 2022SanBio Company Limited provided consolidated earnings guidance for the first half and full year of the fiscal year ending January 31, 2022. For the first half, the company expected operating loss of JPY 3,492 million, ordinary loss of JPY 3,550 million and net loss attributable to owners of parent of JPY 3,551 million or JPY 68.57 per share. For the full year, the company expected operating loss of JPY 5,786 million, ordinary loss of JPY 5,876 million and net loss attributable to owners of parent of JPY 5,877 million or JPY 113.49 per share.お知らせ • Mar 17+ 1 more updateSanBio Company Limited Provides Earnings Guidance for the First Half and Full Year of the Fiscal Year Ending January 31, 2022SanBio Company Limited provided earnings guidance for the first half and full year of the fiscal year ending January 31, 2022. For the first half, the company expected operating loss of JPY 3,492 million, ordinary loss of JPY 3,550 million and net loss attributable to owners of parent of JPY 3,551 million or JPY 68.57 per share. For the full year, the company expected operating loss of JPY 5,786 million, ordinary loss of JPY 5,876 million and net loss attributable to owners of parent of JPY 5,877 million or JPY 113.49 per share.お知らせ • Mar 01Sanbio Company Limited Presents STEMTRA Phase 2 Trial Results At the 44Th Annual Meeting of the Japan Society of NeurotraumatologyThe SanBio Group announcde that Masahito Kawabori, Specially Appointed Associate Professor of the Department of Neurosurgery and Neuronal Cell Therapy, Hokkaido University Hospital presented the results of the global Phase 2 clinical trial of SB623 targeting chronic effects associated with traumatic brain injury (STEMTRA study) during Symposium 3, Brain Protection and Regenerative Medicine, of the 44th Annual Meeting of the Japan Society of Neurotraumatology in Takamatsu, Kagawa Prefecture. The STEMTRA study was a randomized, double-blind, surgical sham-controlled, global Phase 2 trial to evaluate the efficacy and safety of SB623 in patients with chronic motor deficit resulting from traumatic brain injury. The primary endpoint of the study was met, with patients who received SB623 demonstrating statistically significant improvement in motor functions compared to the control group patients who received sham surgery. Further, interim analysis based on data obtained six months after the administration of SB623 or sham surgery indicated that SB623 was well-tolerated. The SanBio Group, based on the study results, aims to apply for manufacture and marketing approval for SB623 as a regenerative medicine product by utilizing Japan's conditional and time-limited approval system for regenerative medicine products.お知らせ • Jan 28SanBio Company Limited to Report Fiscal Year 2021 Results on Mar 17, 2021SanBio Company Limited announced that they will report fiscal year 2021 results on Mar 17, 2021お知らせ • Jan 06SanBio Company Limited Announces Publication of STEMTRA Phase 2 Interim Analysis for SB623 in NeurologyThe SanBio Group announced that the interim analysis from the Company's SB623 Phase 2 clinical "STEM cell therapy for TRAumatic brain injury" (STEMTRA) trial was published in the January 4, 2021 online issue of Neurology®, the medical journal of the American Academy of Neurology. The full manuscript, entitled "Cell Therapy for Chronic TBI: Interim Analysis of the Randomized Controlled STEMTRA Trial" can be accessed here. STEMTRA was a Phase 2, randomized, double-blind, surgical sham-controlled, global trial evaluating the efficacy and safety of SB623 compared to sham surgery in patients with stable chronic neurological motor deficits secondary to traumatic brain injury (TBI). The study achieved its primary efficacy endpoint of significant improvement from baseline of Fugl-Meyer Motor Scale (FMMS) score at six months for SB623-treated patients. Secondary efficacy endpoints improved from baseline but were not statistically significant versus control. In the six-month, pre-specified interim analysis, treatment with SB623 cells appeared to be safe and well-tolerated. In the trial, patients were followed for efficacy and safety for up to twelve months. STEMTRA was a 12-month, Phase 2, randomized, double-blind, surgical sham-controlled, global trial evaluating the efficacy and safety of SB623 compared to sham surgery in patients with stable chronic neurological motor deficits secondary to TBI (https://clinicaltrials.gov identifier: NCT02416492). In this study, SB623 cells were implanted directly around the site of brain injury. The primary endpoint was mean change from baseline in FMMS score at six months to measure changes in motor impairment. To be eligible for this trial, patients (ages 18-75) must have been at least 12 months post-TBI and had a Glasgow Outcome Scale extended (GOS-E) score of 3-6 (e.g., moderate or severe disability). Patients must also have been able to undergo all planned neurological assessments and had no seizures in the prior three months. The STEMTRA trial treated 61 patients from 27 sites in the U.S., Japan and Ukraine. In this study, SB623 met its primary endpoint, with patients treated with SB623 achieving an average 8.3-point improvement from baseline in the FMMS, versus 2.3-points in the control group, at 6 months (p=0.040). Of patients treated with SB623, 18 (39.1%) reached a 10 or more point improvement of FMMS compared to one control patient (6.7%; p=0.039). No new safety signals were identified, and the most commonly reported adverse event was headaches. SB623 is a proprietary, cell-based investigational product made from allogeneic modified and cultured adult bone marrow-derived mesenchymal stem cells (MSCs) that undergo temporary genetic modification. Implantation of SB623 cells into injured nerve tissue in the brain is expected to trigger the brain's natural regenerative ability to recover lost motor functions. SanBio is preparing to file a Biologics License Application with the Pharmaceuticals and Medical Devices Agency in Japan for SB623 for the treatment of chronic motor deficits resulting from traumatic brain injury, while also making progress in its global development program. Further, the Company is working toward commencing clinical trials of SB623 for stroke in Japan. SB623 has been granted Sakigake designation for innovative medical products from the Ministry of Health, Labour, and Welfare of Japan, Regenerative Medicine Advanced Therapy (RMAT) designation from the U.S. Food and Drug Association, and the Advanced Therapy Medicinal Product classification from the European Medicines Agency.Price Target Changed • Dec 16Price target lowered to JP¥2,683Down from JP¥3,114, the current price target is an average from 5 analysts. The new target price is 93% above the current share price of JP¥1,388. As of last close, the stock is down 47% over the past year.Is New 90 Day High Low • Dec 16New 90-day low: JP¥1,388The company is down 34% from its price of JP¥2,100 on 17 September 2020. The Japanese market is up 8.0% over the last 90 days, indicating the company underperformed over that time. It also underperformed the Biotechs industry, which is down 2.0% over the same period. According to the Simply Wall St valuation model, the estimated intrinsic value of the company is JP¥3.04 per share.Price Target Changed • Dec 10Price target lowered to JP¥2,683Down from JP¥3,114, the current price target is an average from 5 analysts. The new target price is 45% above the current share price of JP¥1,852. As of last close, the stock is down 56% over the past year.お知らせ • Dec 05SanBio Company Limited to Report Q3, 2021 Results on Dec 15, 2020SanBio Company Limited announced that they will report Q3, 2021 results on Dec 15, 2020株主還元4592JP BiotechsJP 市場7D2.1%6.7%-3.0%1Y-57.4%-27.5%40.2%株主還元を見る業界別リターン: 4592過去 1 年間で-27.5 % の収益を上げたJP Biotechs業界を下回りました。リターン対市場: 4592は、過去 1 年間で40.2 % のリターンを上げたJP市場を下回りました。価格変動Is 4592's price volatile compared to industry and market?4592 volatility4592 Average Weekly Movement10.2%Biotechs Industry Average Movement7.9%Market Average Movement4.4%10% most volatile stocks in JP Market9.3%10% least volatile stocks in JP Market2.3%安定した株価: 4592の株価は、 JP市場と比較して過去 3 か月間で変動しています。時間の経過による変動: 4592の weekly volatility ( 10% ) は過去 1 年間安定していますが、依然としてJPの株式の 75% よりも高くなっています。会社概要設立従業員CEO（最高経営責任者ウェブサイト200133Keita Moriwww.sanbio.comサンバイオ株式会社は中枢神経系の再生細胞医薬品の開発、製造、販売を行っている。米国と日本で外傷性脳損傷を対象とした第2相臨床試験を完了したSB623を開発している。また、慢性脳梗塞、慢性外傷性脳梗塞、慢性脳出血、加齢黄斑変性症、網膜色素変性症、脊髄損傷、パーキンソン病、アルツハイマー病などを適応症とするSB623、末梢神経障害を適応症とするSB618、筋ジストロフィー疾患を適応症とするSB308、がんを適応症とするMSC1、炎症性疾患や視神経炎を適応症とするMSC2からなる研究パイプラインを有している。同社は2001年に設立され、東京に本社を置いている。もっと見るSanBio Company Limited 基礎のまとめSanBio の収益と売上を時価総額と比較するとどうか。4592 基礎統計学時価総額JP¥78.68b収益（TTM）-JP¥3.15b売上高(TTM)n/a0.0xP/Sレシオ-24.7xPER（株価収益率4592 は割高か？公正価値と評価分析を参照収益と収入最新の決算報告書（TTM）に基づく主な収益性統計4592 損益計算書（TTM）収益JP¥0売上原価JP¥0売上総利益JP¥0その他の費用JP¥3.15b収益-JP¥3.15b直近の収益報告Apr 30, 2026次回決算日該当なし一株当たり利益（EPS）-40.31グロス・マージン0.00%純利益率0.00%有利子負債／自己資本比率9.3%4592 の長期的なパフォーマンスは？過去の実績と比較を見るView Valuation企業分析と財務データの現状データ最終更新日（UTC時間）企業分析2026/06/30 12:39終値2026/06/30 00:00収益2026/04/30年間収益2026/01/31データソース企業分析に使用したデータはS&P Global Market Intelligence LLC のものです。本レポートを作成するための分析モデルでは、以下のデータを使用しています。データは正規化されているため、ソースが利用可能になるまでに時間がかかる場合があります。パッケージデータタイムフレーム米国ソース例会社財務10年損益計算書キャッシュ・フロー計算書貸借対照表SECフォーム10-KSECフォーム10-Qアナリストのコンセンサス予想+プラス3年予想財務アナリストの目標株価アナリストリサーチレポートBlue Matrix市場価格30年株価配当、分割、措置ICEマーケットデータSECフォームS-1所有権10年トップ株主インサイダー取引SECフォーム4SECフォーム13Dマネジメント10年リーダーシップ・チーム取締役会SECフォーム10-KSECフォームDEF 14A主な進展10年会社からのお知らせSECフォーム8-K* 米国証券を対象とした例であり、非米国証券については、同等の規制書式および情報源を使用。特に断りのない限り、すべての財務データは1年ごとの期間に基づいていますが、四半期ごとに更新されます。これは、TTM（Trailing Twelve Month）またはLTM（Last Twelve Month）データとして知られています。詳細はこちら。分析モデルとスノーフレークこのレポートを生成するために使用した分析モデルの詳細は、当社の Github ページ でご覧いただけます。また、レポートの使い方に関する ガイド や YouTube の チュートリアル もご用意しています。シンプリー・ウォールストリート分析モデルを設計・構築した世界トップクラスのチームについてご紹介します。業界およびセクターの指標私たちの業界とセクションの指標は、Simply Wall Stによって6時間ごとに計算されます。アナリスト筋SanBio Company Limited 5 これらのアナリストのうち、弊社レポートのインプットとして使用した売上高または利益の予想を提出したのは、 。アナリストの投稿は一日中更新されます。10 アナリスト機関Hidemaru YamaguchiCitigroup IncStephen BarkerJefferies LLCMiyabi YamakitaJefferies LLC7 その他のアナリストを表示
ナラティブの更新 • Jun 264592: Conditional Approval And Reimbursement Will Support Future Regenerative Therapy UpsideAnalysts have reduced their price target on SanBio from ¥2,100 to ¥1,660, citing updated assumptions around the discount rate, revenue growth, profit margin, and a higher future P/E multiple. What’s in the News for SanBio SanBio received marketing approval in Japan on July 31, 2024 for AKUUGO Suspension for Intracranial Implantation, indicated for improving chronic motor paralysis associated with traumatic brain injury.
Major Estimate Revision • Jun 16Consensus revenue estimates increase by 16%The consensus outlook for revenues in fiscal year 2027 has improved. 2027 revenue forecast increased from JP¥400.0m to JP¥464.4m. Forecast losses expected to reduce from -JP¥66.90 to -JP¥60.48 per share. Biotechs industry in Japan expected to see average net income decline 20% next year. Consensus price target down from JP¥1,800 to JP¥1,660. Share price fell 5.1% to JP¥1,182 over the past week.
Price Target Changed • Jun 05Price target decreased by 14% to JP¥1,800Down from JP¥2,100, the current price target is an average from 5 analysts. New target price is 43% above last closing price of JP¥1,263. Stock is down 63% over the past year. The company is forecast to post a net loss per share of JP¥66.90 next year compared to a net loss per share of JP¥52.55 last year.
Major Estimate Revision • Apr 17Consensus revenue estimates increase by 22%The consensus outlook for revenues in fiscal year 2027 has improved. 2027 revenue forecast increased from JP¥3.47b to JP¥4.23b. Forecast losses expected to reduce from -JP¥68.53 to -JP¥62.44 per share. Biotechs industry in Japan expected to see average net income decline 32% next year. Consensus price target broadly unchanged at JP¥2,100. Share price rose 5.7% to JP¥2,099 over the past week.
Major Estimate Revision • Apr 07Consensus EPS estimates fall by 55%The consensus outlook for fiscal year 2027 has been updated. 2027 expected loss increased from -JP¥44.09 to -JP¥68.53 per share. Revenue forecast of JP¥3.47b unchanged since last update. Biotechs industry in Japan expected to see average net income decline 51% next year. Consensus price target broadly unchanged at JP¥2,060. Share price rose 9.8% to JP¥1,955 over the past week.
Major Estimate Revision • Mar 27Consensus EPS estimates fall by 21%The consensus outlook for fiscal year 2027 has been updated. 2027 expected loss increased from -JP¥39.72 to -JP¥47.91 per share. Revenue forecast of JP¥3.42b unchanged since last update. Biotechs industry in Japan expected to see average net income decline 41% next year. Consensus price target of JP¥2,100 unchanged from last update. Share price fell 2.0% to JP¥1,880 over the past week.
ナラティブの更新 • Jun 264592: Conditional Approval And Reimbursement Will Support Future Regenerative Therapy UpsideAnalysts have reduced their price target on SanBio from ¥2,100 to ¥1,660, citing updated assumptions around the discount rate, revenue growth, profit margin, and a higher future P/E multiple. What’s in the News for SanBio SanBio received marketing approval in Japan on July 31, 2024 for AKUUGO Suspension for Intracranial Implantation, indicated for improving chronic motor paralysis associated with traumatic brain injury.
Major Estimate Revision • Jun 16Consensus revenue estimates increase by 16%The consensus outlook for revenues in fiscal year 2027 has improved. 2027 revenue forecast increased from JP¥400.0m to JP¥464.4m. Forecast losses expected to reduce from -JP¥66.90 to -JP¥60.48 per share. Biotechs industry in Japan expected to see average net income decline 20% next year. Consensus price target down from JP¥1,800 to JP¥1,660. Share price fell 5.1% to JP¥1,182 over the past week.
Price Target Changed • Jun 05Price target decreased by 14% to JP¥1,800Down from JP¥2,100, the current price target is an average from 5 analysts. New target price is 43% above last closing price of JP¥1,263. Stock is down 63% over the past year. The company is forecast to post a net loss per share of JP¥66.90 next year compared to a net loss per share of JP¥52.55 last year.
Major Estimate Revision • Apr 17Consensus revenue estimates increase by 22%The consensus outlook for revenues in fiscal year 2027 has improved. 2027 revenue forecast increased from JP¥3.47b to JP¥4.23b. Forecast losses expected to reduce from -JP¥68.53 to -JP¥62.44 per share. Biotechs industry in Japan expected to see average net income decline 32% next year. Consensus price target broadly unchanged at JP¥2,100. Share price rose 5.7% to JP¥2,099 over the past week.
Major Estimate Revision • Apr 07Consensus EPS estimates fall by 55%The consensus outlook for fiscal year 2027 has been updated. 2027 expected loss increased from -JP¥44.09 to -JP¥68.53 per share. Revenue forecast of JP¥3.47b unchanged since last update. Biotechs industry in Japan expected to see average net income decline 51% next year. Consensus price target broadly unchanged at JP¥2,060. Share price rose 9.8% to JP¥1,955 over the past week.
Major Estimate Revision • Mar 27Consensus EPS estimates fall by 21%The consensus outlook for fiscal year 2027 has been updated. 2027 expected loss increased from -JP¥39.72 to -JP¥47.91 per share. Revenue forecast of JP¥3.42b unchanged since last update. Biotechs industry in Japan expected to see average net income decline 41% next year. Consensus price target of JP¥2,100 unchanged from last update. Share price fell 2.0% to JP¥1,880 over the past week.
Major Estimate Revision • Mar 24Consensus EPS estimates fall by 81%The consensus outlook for fiscal year 2027 has been updated. 2027 expected loss increased from -JP¥21.95 to -JP¥39.72 per share. Revenue forecast of JP¥3.42b unchanged since last update. Biotechs industry in Japan expected to see average net income decline 41% next year. Consensus price target up from JP¥2,050 to JP¥2,100. Share price fell 7.0% to JP¥1,847 over the past week.
新しいナラティブ • Mar 19Regenerative Medicine Tailwinds Will Support Long Term Brain Disease Treatment PotentialCatalysts About SanBio SanBio is a regenerative medicine company focused on cell therapies for brain diseases such as traumatic brain injury. What are the underlying business or industry changes driving this perspective?
お知らせ • Mar 17SanBio Company Limited, Annual General Meeting, Apr 22, 2026SanBio Company Limited, Annual General Meeting, Apr 22, 2026.
Breakeven Date Change • Mar 17No longer forecast to breakevenThe 4 analysts covering SanBio no longer expect the company to break even during the foreseeable future. The company was expected to make a profit of JP¥3.82b in 2028. New consensus forecast suggests the company will make a loss of JP¥2.41b in 2029.
新しいナラティブ • Mar 05Brain Regeneration Platform Will Transform Chronic Injury Treatment And Open Multiple Future IndicationsCatalysts About SanBio SanBio is a regenerative medicine company focused on cell therapies for brain diseases such as traumatic brain injury and ischemic stroke. What are the underlying business or industry changes driving this perspective?
Major Estimate Revision • Jan 06Consensus revenue estimates fall by 41%The consensus outlook for revenues in fiscal year 2026 has deteriorated. 2026 revenue forecast decreased from JP¥50.0m to JP¥29.3m. Forecast losses increased from -JP¥50.74 to -JP¥54.39 per share. Biotechs industry in Japan expected to see average net income growth of 10% next year. Consensus price target broadly unchanged at JP¥2,050. Share price rose 3.6% to JP¥1,750 over the past week.
Price Target Changed • Jan 06Price target increased by 8.7% to JP¥2,250Up from JP¥2,070, the current price target is an average from 5 analysts. New target price is 29% above last closing price of JP¥1,750. Stock is up 133% over the past year. The company is forecast to post a net loss per share of JP¥49.86 next year compared to a net loss per share of JP¥41.85 last year.
お知らせ • Nov 07SanBio Company Limited has filed a Follow-on Equity Offering in the amount of ¥14.922 billion.SanBio Company Limited has filed a Follow-on Equity Offering in the amount of ¥14.922 billion. Security Name: Shares Security Type: Common Stock Securities Offered: 6,000,000 Price\Range: ¥2487 Discount Per Security: ¥109.36
お知らせ • Oct 28SanBio Company Limited to Report Q3, 2026 Results on Dec 15, 2025SanBio Company Limited announced that they will report Q3, 2026 results on Dec 15, 2025
Price Target Changed • Oct 10Price target increased by 17% to JP¥2,028Up from JP¥1,735, the current price target is an average from 4 analysts. New target price is 47% below last closing price of JP¥3,850. Stock is up 260% over the past year. The company is forecast to post a net loss per share of JP¥46.21 next year compared to a net loss per share of JP¥41.85 last year.
お知らせ • Sep 14SanBio Company Limited to Report Q2, 2026 Results on Sep 12, 2025SanBio Company Limited announced that they will report Q2, 2026 results on Sep 12, 2025
Major Estimate Revision • Jul 04Consensus revenue estimates increase by 291%, EPS downgradedThe consensus outlook for fiscal year 2026 has been updated. 2026 revenue forecast increased from JP¥44.0m to JP¥172.0m. EPS estimate fell from -JP¥41.26 to -JP¥48.65 per share. Biotechs industry in Japan expected to see average net income decline 21% next year. Consensus price target up from JP¥1,560 to JP¥1,735. Share price was steady at JP¥2,173 over the past week.
Price Target Changed • Jul 02Price target increased by 19% to JP¥1,735Up from JP¥1,460, the current price target is an average from 4 analysts. New target price is 20% below last closing price of JP¥2,174. Stock is up 111% over the past year. The company is forecast to post a net loss per share of JP¥48.65 next year compared to a net loss per share of JP¥41.85 last year.
New Risk • Jun 15New major risk - Financial positionThe company has less than a year of cash runway based on its current free cash flow trend. Free cash flow: -JP¥3.6b This is considered a major risk. With less than a year's worth of cash, the company will need to raise capital or take on debt unless its cash flows improve. This would dilute existing shareholders or increase balance sheet risk. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-JP¥3.6b free cash flow). Share price has been highly volatile over the past 3 months (16% average weekly change). Earnings are forecast to decline by an average of 3.5% per year for the foreseeable future. Revenue is less than US$1m. Minor Risk Currently unprofitable and not forecast to become profitable over next 3 years (JP¥2.7b net loss in 3 years).
お知らせ • May 29SanBio Co., Ltd. Announces Results of the Third Commercial Production Run to Meet the Approval Conditions for the Shipment of AKUUGO Suspension for Intracranial ImplantationSanBio Co. Ltd. announced on April 18, 2025, that the expected yield from the third manufacturing of AKUUGO® Suspension for Intracranial Implantation was successfully secured, regarding the three production runs required for the release of shipments. The Company has completed specification testing and characteristic analysis for the third manufacturing run and has confirmed its results. The third manufacturing run cleared all specification requirements and was deemed compliant as well. With the fulfilment of the shipment conditions for AKUUGO, the company plans to promptly file a partial change application and proceed with obtaining full product approval.
お知らせ • May 03SanBio Company Limited to Report Q1, 2026 Results on Jun 13, 2025SanBio Company Limited announced that they will report Q1, 2026 results on Jun 13, 2025
Price Target Changed • Mar 22Price target increased by 10% to JP¥1,320Up from JP¥1,195, the current price target is an average from 4 analysts. New target price is approximately in line with last closing price of JP¥1,360. Stock is up 134% over the past year. The company is forecast to post a net loss per share of JP¥29.41 next year compared to a net loss per share of JP¥41.86 last year.
Price Target Changed • Mar 18Price target increased by 33% to JP¥1,500Up from JP¥1,130, the current price target is an average from 3 analysts. New target price is 16% above last closing price of JP¥1,297. Stock is up 120% over the past year. The company is forecast to post a net loss per share of JP¥40.86 next year compared to a net loss per share of JP¥41.85 last year.
お知らせ • Mar 17+ 1 more updateSanBio Company Limited, Annual General Meeting, Apr 23, 2025SanBio Company Limited, Annual General Meeting, Apr 23, 2025.
New Risk • Feb 27New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 0.1% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Share price has been highly volatile over the past 3 months (9.6% average weekly change). Earnings are forecast to decline by an average of 0.1% per year for the foreseeable future. Revenue is less than US$1m. Minor Risk Currently unprofitable and not forecast to become profitable over next 3 years (JP¥4.0b net loss in 3 years).
New Risk • Feb 07New major risk - Share price stabilityThe company's share price has been highly volatile over the past 3 months. It is more volatile than 90% of Japanese stocks, typically moving 8.8% a week. This is considered a major risk. Share price volatility increases the risk of potential losses in the short-term as the stock tends to have larger drops in price more frequently than other stocks. It may also indicate the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. Currently, the following risks have been identified for the company: Major Risks Share price has been highly volatile over the past 3 months (8.8% average weekly change). Revenue is less than US$1m. Minor Risk Currently unprofitable and not forecast to become profitable over next 3 years (JP¥3.9b net loss in 3 years).
お知らせ • Feb 06SanBio Company Limited Announces Results of the Second Commercial Production Run of AKUUGOSanBio Company Limited announced on December 6, 2024, that it had secured the planned production yield for the second commercial production run of AKUUGO® Suspension for Intracranial Implantation (INN: vandefitemcel), conducted to meet the shipment conditions required for obtaining product approval. The Company has completed specification testing and characteristic analysis for the second manufacturing run and has confirmed its results. The second manufacturing run cleared all specification requirements and was deemed compliant. The third manufacturing run has already commenced. With the compliance of this manufacturing run, the company will run one more manufacturing compliant with necessary specifications and plans to file a partial change application and subsequently obtain approval for the partial change to meet the shipment conditions. As a result, the anticipated timing for AKUUGO® to become eligible for shipment remains unchanged, with shipment expected to begin in the second quarter of the fiscal year ending January 31, 2026 (May-July 2025). AKUUGO suspension for intracranial implantation (INN: vandefitemcel) is a human (allogeneic) bone marrow-derived modified mesenchymal stem cell that is produced by modifying and culturing mesenchymal stem cells derived from the bone marrow aspirate of healthy adults. The transplantation of AKUUGO into damaged nerve tissues in the brain is expected to trigger the release of FGF-2 (a type of protein) and other substances, which in turn will promote the natural regenerative ability of damaged nerve cells and induce proliferation and differentiation of nerve cells.
お知らせ • Jan 28SanBio Company Limited to Report Fiscal Year 2025 Results on Mar 17, 2025SanBio Company Limited announced that they will report fiscal year 2025 results on Mar 17, 2025
New Risk • Dec 16New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 7.6% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Share price has been highly volatile over the past 3 months (11% average weekly change). Earnings are forecast to decline by an average of 7.6% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (JP¥3.2b net loss in 3 years). Shareholders have been diluted in the past year (4.8% increase in shares outstanding).
お知らせ • Dec 04SanBio Company Limited announced that it expects to receive ¥1.99992672 billion in funding from Athos Capital LimitedSanBio Company Limited announced a private placement to issue 2,295,600 common shares at issue price of ¥871.2 per share for gross proceeds of ¥1,999,926,720 on December 2, 2024. The transaction includes participation from new investor,Athos Asia Event Driven Master Fund. The transaction will happen through third party allocation. The issue date will be December 18, 2024. The transaction has been approved at board of director meeting of the company. The company will incur issuance cost of ¥98,996,000 and the net proceeds will be ¥1,900,930,720.
お知らせ • Nov 17SanBio Company Limited Announces the Results of the First Commercial Production Run of AKUUGOSanBio Co. Ltd. announced on July 31, 2024, that it had obtained conditional and time-limited approval for AKUUGO suspension for intracranial implantation from the Ministry of Health, Labour and Welfare and that it planned to conduct about two commercial production runs to meet the shipment conditions required under this approval. They hereby provide the results of the first production run. The first production run did not meet the specification standards. However, only one specification value was non-compliant, while all other specification values, including the yield--a key issue identified during the approval review process--were compliant. Moreover, the results of the characterization analysis were equivalent to those of the clinical trials product. They anticipated some non-conforming products due to batch-to-batch variability arising from the heterogeneity of cells, a critical raw material for AKUUGO®, and they consider the non-conformity of the first manufacturing lot to be within expectations. Regarding the outlook, since the manufacturing process has already been established and approved, they have commenced the second production run. After obtaining manufacturing results that conform to the specifications for the second time, they will file an application for a partial change and aim to obtain approval for the subsequent partial change. As a result, the expected timeline for completing the two commercial production runs required to begin shipments of AKUUGO® has been delayed by a quarter, from the first quarter of the fiscal year ending January 2026 (February-April 2025) to the second quarter of the same fiscal year (May-July 2025). This matter will have only a minimal impact on the financial performance of the current fiscal year.
お知らせ • Oct 29SanBio Company Limited to Report Q3, 2025 Results on Dec 16, 2024SanBio Company Limited announced that they will report Q3, 2025 results on Dec 16, 2024
New Risk • Sep 18New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 1.8% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Share price has been highly volatile over the past 3 months (19% average weekly change). Earnings are forecast to decline by an average of 1.8% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Less than 1 year of cash runway based on current free cash flow (-JP¥4.8b). Currently unprofitable and not forecast to become profitable over next 3 years (JP¥1.7b net loss in 3 years). Shareholders have been diluted in the past year (5.7% increase in shares outstanding).
お知らせ • Jul 31Sanbio Co., Ltd. Obtains Marketing Approval for AKUUGO Suspension for Intracranial ImplantationSanBio Co. Ltd. announced that on July 31, 2024, it obtained conditional and time-limited marketing approval for the human somatic stem cell-processed product "AKUUGO suspension for intracranial implantation" in Japan, for the indication of improving chronic motor paralysis resulting from traumatic brain injury. Details of product overview and conditional and time-limited marketing approved for AKUUGO are provided in the attached reference material. The company expects shipment and sales to begin in the first quarter of the fiscal year ending January 31, 2026. Moreover, to satisfy the conditions for full approval, the company plan to conduct post-marketing clinical trials and other necessary studies within the seven-year marketing authorization period with the aim of obtaining full approval. Based on track record of having obtained conditional and time- limited marketing approval for AKUUGO, the company plan to reallocate resources concentrated on the SB623 program for TBI to expanding indications and regions for the product. Through AKUUGO, company hope to bring hope to the lives of as many TBI patients as possible. The approval of AKUUGO was based on the results of the global Phase 2 clinical trial SanBio conducted in Japan and the United States. Dr. Nobuhito Saito, Professor of Neurology at the University of Tokyo led the clinical trial, commented as follows. Thaw the cell suspension for intracranial implants, wash it with the dedicated preparation solution, and adjust the concentration of the cell suspension to 1.67 x 106 cells/100uL using the dedicated preparation solution. Cleanse the micro-syringe fixed with the cannula from the dedicated delivery device set with the dedicated preparation solution before filling it with the prepared cell suspension. Date of marketing approval, July 31, 2024, Product image, Vial containing cell suspension for intracraial implantation, Dry shipper, Hard case and dry shipper for transportation, Dedicated preparation solution, Dedicated preparation solution, dedicated preparation solution, Dedicated delivery device set, Outer package for dedicated delivery device set. Condition of approval. Considering the limited manufacturing record for the Product, the Company shall promptly collect information on the Product's quality based on a pre-determined plan, and evaluate and report on the equivalence/homogeneity, in terms of quality, of the investigational product (clinical trials product) and the Product intended for commercial distribution. Based on the evaluation results, the Company shall apply for a partial change of approved matters. It shall not ship the Product until the partial change application has been approved. The Company must ensure that the Product is used in medical facilities fully equipped to handle emergencies, by physicians who possess sufficient knowledge and experience in the diagnosis and treatment of traumatic brain injury and stereotactic treatment.
お知らせ • Jul 27SanBio Company Limited to Report Q2, 2025 Results on Sep 17, 2024SanBio Company Limited announced that they will report Q2, 2025 results on Sep 17, 2024
Price Target Changed • Jul 01Price target increased by 20% to JP¥960Up from JP¥800, the current price target is an average from 5 analysts. New target price is 21% below last closing price of JP¥1,218. Stock is up 98% over the past year. The company is forecast to post a net loss per share of JP¥41.16 next year compared to a net loss per share of JP¥40.48 last year.
Price Target Changed • Jun 20Price target increased by 23% to JP¥983Up from JP¥800, the current price target is an average from 5 analysts. New target price is 16% above last closing price of JP¥848. Stock is up 27% over the past year. The company is forecast to post a net loss per share of JP¥38.58 next year compared to a net loss per share of JP¥40.48 last year.
New Risk • Jun 13New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 1.0% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-JP¥4.8b free cash flow). Share price has been highly volatile over the past 3 months (13% average weekly change). Earnings are forecast to decline by an average of 1.0% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (JP¥2.4b net loss in 3 years). Shareholders have been diluted in the past year (5.8% increase in shares outstanding).
お知らせ • Jun 13SanBio Company Limited Announces Update on Status of Manufacturing and Marketing Approval for Sb623 Chronic Traumatic Brain Injury Program in JapanOn March 26, 2024, SanBio Co. Ltd. (the "Company") provided an update on the progress toward obtaining marketing approval of SB623 to treat chronic traumatic brain injury (TBI) in Japan, stating it was concluded to continue the deliberation at a later date by the Pharmaceutical Affairs and Food Sanitation Council's Subcommittee on Regenerative Medicine Products (the "Subcommittee") and company planned to engage in further consultations with the regulatory authorities and to submit additional information such as additional data addressing quality. the Ministry of Health, Labour and Welfare announced that the Pharmaceutical Affairs and the Subcommittee will hold a meeting on June 19, and company learned that the Subcommittee will deliberate, among others, on whether to grant marketing approval for the regenerative medicine "AKUUGO suspension for intracranial implantation", whether to stipulate conditions and a time limit for the approval, and whether to designate a reexamination period. Accordingly, the Subcommittee will determine whether to grant the Company's development product SB623 marketing approval in the meeting. SB623 (INN: vandefitemcel) is a human (allogeneic) bone marrow-derived modified mesenchymal stem cell that is produced by modifying and culturing mesenchymal stem cells derived from the bone marrow aspirate of healthy adults. Implantation of SB623 cells into injured nerve tissues in the brain is expected to trigger the brain's natural regenerative ability to restore lost functions. SB623 is currently being investigated for the treatment of several conditions including chronic neurological motor deficit resulting from traumatic brain injury and ischemic stroke.
お知らせ • May 05SanBio Company Limited to Report Q1, 2025 Results on Jun 13, 2024SanBio Company Limited announced that they will report Q1, 2025 results on Jun 13, 2024
New Risk • Apr 02New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 3.6% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-JP¥4.8b free cash flow). Share price has been highly volatile over the past 3 months (15% average weekly change). Earnings are forecast to decline by an average of 3.6% per year for the foreseeable future. Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (JP¥2.9b net loss in 3 years). Shareholders have been diluted in the past year (6.4% increase in shares outstanding).
Price Target Changed • Mar 28Price target decreased by 30% to JP¥1,214Down from JP¥1,742, the current price target is an average from 5 analysts. New target price is 188% above last closing price of JP¥421. Stock is down 38% over the past year. The company is forecast to post a net loss per share of JP¥68.35 next year compared to a net loss per share of JP¥40.48 last year.
お知らせ • Mar 19SanBio Company Limited, Annual General Meeting, Apr 24, 2024SanBio Company Limited, Annual General Meeting, Apr 24, 2024. Agenda: To consider to reduce the amounts of stated capital and capital reserves and to make an appropriation of other capital surplus.
Price Target Changed • Mar 18Price target increased by 18% to JP¥2,100Up from JP¥1,782, the current price target is an average from 5 analysts. New target price is 184% above last closing price of JP¥740. Stock is up 5.4% over the past year. The company is forecast to post a net loss per share of JP¥63.15 next year compared to a net loss per share of JP¥95.98 last year.
Breakeven Date Change • Jan 31Forecast to breakeven in 2027The 4 analysts covering SanBio expect the company to break even for the first time. New consensus forecast suggests the company will make a profit of JP¥712.0m in 2027. Average annual earnings growth of 62% is required to achieve expected profit on schedule.
お知らせ • Jan 28SanBio Company Limited to Report Fiscal Year 2024 Results on Mar 18, 2024SanBio Company Limited announced that they will report fiscal year 2024 results on Mar 18, 2024
お知らせ • Jan 25Sanbio Co., Ltd. Provides Update on Status of Manufacturing and Marketing Approval for Sb623 Chronic Traumatic Brain Injury Program in JapanSanBio Co. Ltd. provided an update on the progress toward obtaining marketing approval of SB623 to treat chronic traumatic brain injury (TBI) in Japan, stating it aims to achieve approval by March 2024 and is actively engaged in the review process. Amidst this situation, the Ministry of Health, Labour and Welfare announced on January 22 that the Pharmaceutical Affairs and Food Sanitation Council's Subcommittee on Regenerative Medicine Products (the "Sub committee") would hold a meeting on February 5. However, developmental product SB623, which is undergoing approval review as a treatment for TBI under the framework of the Sakigake Designation System, was not included in the agenda for this meeting.
New Risk • Dec 15New major risk - Financial positionThe company has less than a year of cash runway based on its current free cash flow trend. Free cash flow: -JP¥6.1b This is considered a major risk. With less than a year's worth of cash, the company will need to raise capital or take on debt unless its cash flows improve. This would dilute existing shareholders or increase balance sheet risk. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-JP¥6.1b free cash flow). Share price has been highly volatile over the past 3 months (8.8% average weekly change). Revenue is less than US$1m. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (JP¥280m net loss in 3 years). Shareholders have been diluted in the past year (6.5% increase in shares outstanding).
お知らせ • Dec 14SanBio Company Limited Provides Update on Status of Manufacturing and Marketing Approval for SB623 Chronic Traumatic Brain Injury (TBI) Program in JapanSanBio Company Limited provided an update on the progress toward obtaining marketing approval of SB623 to treat chronic traumatic brain injury (TBI) in Japan, stating that the Company was focused on resolving the issue related to the production yield and responding to production-related review by regulatory authorities, with the goal of obtaining approval by the end of the current fiscal year. The Company hereby provides another progress update, to ensure timely disclosure to concerned patients and their families, as well as shareholders and investors who await the approval of SB623. SB623 is undergoing approval review under the framework of the Sakigake Designation System as a treatment for chronic effects associated with TBI. The production yield-related issue has been resolved, and the review process is proceeding to a conclusion. However, given the status of the review process, it will take some more time until approval is granted, and for this reason, the Company now expects to obtain approval in March 2024. Although the timing of approval is outside of the Company's control, SanBio will continue to work as one and do utmost to obtain approval.
お知らせ • Oct 14SanBio Company Limited to Report Q3, 2024 Results on Dec 14, 2023SanBio Company Limited announced that they will report Q3, 2024 results on Dec 14, 2023
お知らせ • Jul 29SanBio Company Limited to Report Q2, 2024 Results on Sep 15, 2023SanBio Company Limited announced that they will report Q2, 2024 results on Sep 15, 2023
Major Estimate Revision • Jul 28Consensus revenue estimates fall by 15%The consensus outlook for revenues in fiscal year 2024 has deteriorated. 2024 revenue forecast decreased from JP¥459.0m to JP¥389.0m. Forecast losses increased from -JP¥74.33 to -JP¥80.94 per share. Biotechs industry in Japan expected to see average net income growth of 39% next year. Consensus price target broadly unchanged at JP¥1,824. Share price was steady at JP¥596 over the past week.
お知らせ • Jun 15+ 1 more updateSanBio Co., Ltd. Updates on Status of Manufacturing and Marketing Approval for SB623 Chronic Traumatic Brain Injury Program in JapanSanBio Co. Ltd. announced that it was working to resolve the issue of production yield, to bring yield back to the level at the time of application filing toward obtaining marketing approval of SB623 to treat chronic traumatic brain injury (TBI) in Japan during the current fiscal year ending January 2024. The Company announced that whether the issue is resolved should be known by June 2023 and will be reported at the result briefing for the first quarter of the fiscal year ending January 2024. The Company hereby provides a progress update, to ensure timely disclosure to concerned patients, their families, as well as shareholders and investors who await the approval of SB623. SB623 is under review in the Sakigake Designation System for approval as a treatment for chronic effects associated with TBI. Toward obtaining approval, the Company is currently focused on resolving the issue related to the production yield and responding to production-related review. Although the company have yet to fully recover the production yield obtained at the time of application filing, additional data from the latest production run has led to measures that could resolve the yield-related issue. A production run with implemented measures is currently underway, and results are expected in August. Although the timing of approval is outside of the Company's control, by resolving the yield-related issue and responding to production-related review in a timely manner, presently the Company's goal remains to obtain approval during the current fiscal year. SB623 (INN: vandefitemcel) is a human (allogeneic) bone marrow-derived modified mesenchymal stem cell that is produced by modifying and culturing mesenchymal stem cells derived from the bone marrow aspirate of healthy adults. Implantation of SB623 cells into injured nerve tissues in the brain is expected to trigger the brain's natural regenerative ability to restore lost functions. SB623 is currently being investigated for the treatment of several conditions including chronic neurological motor deficit resulting from traumatic brain injury and ischemic stroke. Traumatic brain injury (TBI) is one of the leading causes of death and disability worldwide. The estimated global incidence of acute TBI during 2016 was 27 million cases, and the estimated global prevalence of chronic impairment secondary to TBI was 55.5 million cases. Overall, TBI and long-term motor deficits secondary to TBI significantly impair a person's self-care, employability, and quality of life, and are major burdens on healthcare systems worldwide. In the United States, approximately 43% of surviving hospitalized persons with TBI experience long-term disabilities, and it is estimated that 3.17 million people are living with long-term disabilities secondary to TBI.
Price Target Changed • Jun 15Price target increased by 13% to JP¥2,290Up from JP¥2,022, the current price target is an average from 4 analysts. New target price is 276% above last closing price of JP¥609. Stock is down 44% over the past year. The company is forecast to post a net loss per share of JP¥72.57 next year compared to a net loss per share of JP¥95.98 last year.
Breakeven Date Change • Jun 01No longer forecast to breakevenThe 4 analysts covering SanBio no longer expect the company to break even during the foreseeable future. The company was expected to make a profit of JP¥1.27b in 2026. New consensus forecast suggests the company will make a loss of JP¥1.44b in 2026.
お知らせ • May 13SanBio Company Limited to Report Q1, 2024 Results on Jun 14, 2023SanBio Company Limited announced that they will report Q1, 2024 results on Jun 14, 2023
Price Target Changed • Mar 20Price target increased by 12% to JP¥2,465Up from JP¥2,192, the current price target is an average from 4 analysts. New target price is 251% above last closing price of JP¥702. Stock is down 50% over the past year. The company is forecast to post a net loss per share of JP¥59.64 next year compared to a net loss per share of JP¥95.98 last year.
Breakeven Date Change • Mar 16No longer forecast to breakevenThe 5 analysts covering SanBio no longer expect the company to break even during the foreseeable future. The company was expected to make a profit of JP¥1.27b in 2026. New consensus forecast suggests the company will make a loss of JP¥203.3m in 2026.
Price Target Changed • Feb 20Price target increased by 12% to JP¥2,465Up from JP¥2,192, the current price target is an average from 4 analysts. New target price is 265% above last closing price of JP¥675. Stock is down 57% over the past year. The company is forecast to post a net loss per share of JP¥99.89 next year compared to a net loss per share of JP¥90.31 last year.
お知らせ • Feb 03SanBio Company Limited to Report Fiscal Year 2023 Results on Mar 16, 2023SanBio Company Limited announced that they will report fiscal year 2023 results on Mar 16, 2023
Breakeven Date Change • Jan 31Forecast to breakeven in 2026The 4 analysts covering SanBio expect the company to break even for the first time. New consensus forecast suggests the company will make a profit of JP¥954.5m in 2026. Average annual earnings growth of 47% is required to achieve expected profit on schedule.
お知らせ • Jan 20SanBio Co., Ltd. Announces Board ChangesSanBio Co. Ltd. announced that at a meeting held on January 20, 2023, its Board of Directors resolved to make the following changes to senior management (representative director and corporate officer). Representative Director, Executive Vice President, and COO Akihiro Tsujimura has submitted his resignation for personal reasons and the Company has accepted it. Due to the resignation of Mr. Tsujimura, Corporate Officer and Business Head (Japan/Asia) Naoki Tsukahara will be appointed executive corporate officer responsible for HR, Japan Regulatory Affairs & Quality Compliance Japan, and Japan/Asia business, and will take over some of the responsibilities of Mr. Tsujimura. Effective date of change is January 20, 2023.
お知らせ • Dec 16SanBio Company Limited Provides Earnings Guidance for the Fiscal Year Ending January 31, 2023SanBio Company Limited provided earnings guidance for the Fiscal Year Ending January 31, 2023. For the full year, the company expected Operating loss of JPY 8,131 million; Net loss attributable to owners of parent to be JPY 5,684 million and net loss per share of JPY 95.36.
Board Change • Nov 16Less than half of directors are independentNo new directors have joined the board in the last 3 years. The company's board is composed of: No new directors. 3 experienced directors. 4 highly experienced directors. 1 independent director (3 non-independent directors). Independent External Director Noboru Kotani was the last independent director to join the board, commencing their role in 2013. The following issues are considered to be risks according to the Simply Wall St Risk Model: Minority of independent directors. Insufficient board refreshment.
お知らせ • Oct 01SanBio Company Limited to Report Q3, 2023 Results on Dec 15, 2022SanBio Company Limited announced that they will report Q3, 2023 results on Dec 15, 2022
お知らせ • Sep 14Sanbio Company Limited Provides Earnings Guidance for the Fiscal Year Ending January 31, 2023SanBio Company Limited provided earnings guidance for the Fiscal Year Ending January 31, 2023. For the full year, the company expected Operating loss of JPY 8,131 million; Net loss attributable to owners of parent to be JPY 5,684 million and net loss per share of JPY 95.36.
Price Target Changed • Jul 23Price target decreased to JP¥2,233Down from JP¥2,567, the current price target is an average from 7 analysts. New target price is 70% above last closing price of JP¥1,312. Stock is up 7.5% over the past year. The company is forecast to post a net loss per share of JP¥85.62 next year compared to a net loss per share of JP¥90.31 last year.
お知らせ • Jul 22SanBio Company Announces Update on Status of Manufacturing and Marketing Approval for SB623 Chronic Traumatic Brain Injury (TBI) Program in JapanJapan's Ministry of Health, Labour, and Welfare (MHLW) on July 20 announced that the Regenerative Medicine Subcommittee (lower panel of Pharmaceutical Affairs and Food Sanitation Council) meeting will be held on August 3. SanBio's SB623, currently undergoing review in the Sakigake Designation System for the treatment of traumatic brain injury, is not included in the topic of deliberations. SanBio's corporate policy is to refrain from setting or disclosing a target timing for approval, as there are many factors outside of the company's control. Do recognize that, based on public perceptions regarding the Sakigake Designation System, there may be expectations for a September approval among patients and family members as well as shareholders and investors. Had SB623 been included in the meeting agenda, a September approval was a possibility. Now believe that a September approval is unlikely. Pledge to work diligently as one team to facilitate the review of this truly innovative product to ensure the swiftest possible regulatory approval and achieve SanBio's first to market. Take this opportunity to reassure all stakeholders that work continues steadily to ensure that not a day is wasted in bringing approval to reality. SB623 (INN: vandefitemcel) is a human (allogeneic) bone marrow-derived modified mesenchymal stem cell that is produced by modifying and culturing mesenchymal stem cells derived from the bone marrow aspirate of healthy adults. Implantation of SB623 cells into injured nerve tissues in the brain is expected to trigger the brain's natural regenerative ability to restore lost functions. SB623 is currently being investigated for the treatment of several conditions including chronic neurological motor deficit resulting from traumatic brain injury and ischemic stroke.
お知らせ • Jul 02Keizo Nakada to Join Sanbio as Corporate Officer and Head of ProductionThe SanBio Group announced that Mr. Keizo Nakada joined the Group as a new Corporate Officer and Head of Production on July 1, 2022. Previously, at Santen Pharmaceutical Co. Ltd., Mr. Nakada gained experience setting up overseas plants and serving as the head of a domestic plant. Afterward, as an executive officer and head of Product Supply Department, he established a stable global product supply system while successfully reducing costs. Later, as an executive officer in charge of production departments at Bushu Pharmaceuticals Ltd. and Taiko Pharmaceutical Co. Ltd., Mr. Nakada assumed responsibility for domestic production plants, supply chain management, quality control, and technological development. At the same time, he fully optimized the supply chains of these companies, achieving dramatic increases in production capacity.
Price Target Changed • Jun 24Price target decreased to JP¥2,200Down from JP¥2,467, the current price target is an average from 5 analysts. New target price is 91% above last closing price of JP¥1,154. Stock is down 20% over the past year. The company is forecast to post a net loss per share of JP¥100 next year compared to a net loss per share of JP¥90.31 last year.
お知らせ • Jun 14SanBio Company Limited Provides Consolidated Earnings Guidance for the First Half and Full Year Ending January 31, 2023SanBio Company Limited provided consolidated earnings guidance for the first half and full year ending January 31, 2023. For the first half, the company expects operating loss of JPY 3,067 million, net loss attributable to owners of parent of JPY 3,169 million and net loss per share of JPY 61.19.For the full year, the company expects operating loss of JPY 5,858 million, net loss attributable to owners of parent of JPY 5,997 million and net loss per share of JPY 115.79.
お知らせ • Jun 01SanBio Company Limited Appoints Andrew Liu as Chief Strategy OfficerSanBio Company Limited announced as follows the appointment of Andrew Liu as Chief Strategy Officer of the SanBio Group, effective May 16, 2022.
Board Change • Apr 27Less than half of directors are independentFollowing the recent departure of a director, there is only 1 independent director on the board. The company's board is composed of: 1 independent director. 3 non-independent directors. Independent External Director Noboru Kotani was the last independent director to join the board, commencing their role in 2013. The company's minority of independent directors is a risk according to the Simply Wall St Risk Model.
お知らせ • Apr 06Sanbio Group Provides an Update on One-Year Analysis of the Phase 2 STEMTRA TrialSanBio Company Limited announced that SB623 met the primary endpoint and demonstrated a trend toward maintaining the improvement of function and activities of daily living in the final, one-year analysis of the Phase 2 STEMTRA trial, which evaluated the efficacy and safety of SB623 compared to sham surgery in patients with chronic motor deficit from traumatic brain injury (TBI). These results will be presented in an oral plenary session at theAmerican Academy of Neurology (AAN) Annual Meeting, taking place on April 5, 2022, in Seattle, Washington, USA. SB623 is an investigational, regenerative cell medicine comprised of bone-marrow-derived, mesenchymal stem cells that are implanted intracranially around the area of the injury. SanBio is preparing to initiate a Phase 3 trial for SB623 in the United States, where many traumatic brain injury patients currently live.
お知らせ • Mar 07Sanbio Company Limited Announces Filing with Japan’S Ministry of Health, Labour, and Welfare for Manufacture and Marketing Approval as A Regenerative Medicine Product for the Investigational Product Sb623The SanBio Group announced the completion of an application filing with Japan’s Ministry of Health, Labour, and Welfare (MHLW) for manufacture and marketing approval as a regenerative medicine product for the investigational product SB623, as a treatment for chronic motor deficit from traumatic brain injury (TBI). This application for approval is based on efficacy and safety results from the US-Japan global Phase 2 clinical trial (Study of Modified Stem Cells in Traumatic Brain Injury, or STEMTRA). STEMTRA is a randomized, double-blind, surgical sham-controlled trial evaluating the efficacy and safety of SB623 in patients with chronic motor deficits secondary to traumatic brain injury. In this study, SB623 met its primary endpoint, with patients treated with SB623 achieving statistically significant improvement in motor function compared with sham surgery. The trial also demonstrated that SB623 was generally safe and well tolerated.
Price Target Changed • Feb 14Price target increased to JP¥2,900Up from JP¥2,660, the current price target is an average from 3 analysts. New target price is 109% above last closing price of JP¥1,385. Stock is down 19% over the past year. The company is forecast to post a net loss per share of JP¥89.16 next year compared to a net loss per share of JP¥65.37 last year.
お知らせ • Feb 11+ 1 more updateSanBio Company Limited announced that it expects to receive ¥33.75 million in funding from Nomura Securities Co., Ltd.SanBio Company Limited (TSE:4592) announced a private placement of 75,000 32nd series warrants at a price of ¥450 per warrant for gross proceeds of ¥33,750,000 on February 10, 2022. The transaction will include participation from existing investor Nomura Securities Co., Ltd. The securities are issued through a third party allotment method. The transaction has been approved by the board of directors of the company. The company will receive proceeds of ¥8,258,750,000 if the warrants are exercised fully. The transaction is expected to close any day between March 4, 2022 and March 11, 2022. The exercise period will start from the trading day following date of allocation to March 7, 2025.
お知らせ • Dec 17SanBio Company Limited Provides Consolidated Earnings Guidance for the Fiscal Year Ending January 31, 2022SanBio Company Limited provided consolidated earnings guidance for the fiscal year ending January 31, 2022. For the period, the company expects Operating loss of JPY 5,786 million; Ordinary loss of JPY 5,876 million; Net loss attributable to owners of parent of JPY 5,877 million and Net loss per share of JPY 113.49.
お知らせ • Sep 15+ 1 more updateSanBio Company Limited Provides Consolidated Earnings Guidance for the Fiscal Year Ending January 31, 2022SanBio Company Limited provided consolidated earnings guidance for the fiscal year ending January 31, 2022. For the period, the company expects operating loss of JPY 5,786 million, ordinary loss of JPY 5,876 million and net loss attributable to owners of parent of JPY 5,877 million or JPY 113.49 per share.
Executive Departure • Jul 13Corporate Officer & Business Head of Japan/Asia Hiroshi Yamamoto has left the companyOn the 1st of July, Hiroshi Yamamoto's tenure as Corporate Officer & Business Head of Japan/Asia ended after 2.4 years in the role. We don't have any record of a personal shareholding under Hiroshi's name. Hiroshi is the only executive to leave the company over the last 12 months. The current median tenure of the management team is 1.50 years, which is considered inexperienced in the Simply Wall St Risk Model.
Price Target Changed • Jul 07Price target increased to JP¥2,660Up from JP¥2,417, the current price target is an average from 3 analysts. New target price is 99% above last closing price of JP¥1,337. Stock is down 17% over the past year.
お知らせ • Jun 15SanBio Company Limited Provides Consolidated Earnings Guidance for the First Half and Full Year of the Fiscal Year Ending January 31, 2022SanBio Company Limited provided consolidated earnings guidance for the first half and full year of the fiscal year ending January 31, 2022. For the first half, the company expected operating loss of JPY 3,492 million, ordinary loss of JPY 3,550 million and net loss attributable to owners of parent of JPY 3,551 million or JPY 68.57 per share. For the full year, the company expected operating loss of JPY 5,786 million, ordinary loss of JPY 5,876 million and net loss attributable to owners of parent of JPY 5,877 million or JPY 113.49 per share.
お知らせ • Mar 17+ 1 more updateSanBio Company Limited Provides Earnings Guidance for the First Half and Full Year of the Fiscal Year Ending January 31, 2022SanBio Company Limited provided earnings guidance for the first half and full year of the fiscal year ending January 31, 2022. For the first half, the company expected operating loss of JPY 3,492 million, ordinary loss of JPY 3,550 million and net loss attributable to owners of parent of JPY 3,551 million or JPY 68.57 per share. For the full year, the company expected operating loss of JPY 5,786 million, ordinary loss of JPY 5,876 million and net loss attributable to owners of parent of JPY 5,877 million or JPY 113.49 per share.
お知らせ • Mar 01Sanbio Company Limited Presents STEMTRA Phase 2 Trial Results At the 44Th Annual Meeting of the Japan Society of NeurotraumatologyThe SanBio Group announcde that Masahito Kawabori, Specially Appointed Associate Professor of the Department of Neurosurgery and Neuronal Cell Therapy, Hokkaido University Hospital presented the results of the global Phase 2 clinical trial of SB623 targeting chronic effects associated with traumatic brain injury (STEMTRA study) during Symposium 3, Brain Protection and Regenerative Medicine, of the 44th Annual Meeting of the Japan Society of Neurotraumatology in Takamatsu, Kagawa Prefecture. The STEMTRA study was a randomized, double-blind, surgical sham-controlled, global Phase 2 trial to evaluate the efficacy and safety of SB623 in patients with chronic motor deficit resulting from traumatic brain injury. The primary endpoint of the study was met, with patients who received SB623 demonstrating statistically significant improvement in motor functions compared to the control group patients who received sham surgery. Further, interim analysis based on data obtained six months after the administration of SB623 or sham surgery indicated that SB623 was well-tolerated. The SanBio Group, based on the study results, aims to apply for manufacture and marketing approval for SB623 as a regenerative medicine product by utilizing Japan's conditional and time-limited approval system for regenerative medicine products.
お知らせ • Jan 28SanBio Company Limited to Report Fiscal Year 2021 Results on Mar 17, 2021SanBio Company Limited announced that they will report fiscal year 2021 results on Mar 17, 2021
お知らせ • Jan 06SanBio Company Limited Announces Publication of STEMTRA Phase 2 Interim Analysis for SB623 in NeurologyThe SanBio Group announced that the interim analysis from the Company's SB623 Phase 2 clinical "STEM cell therapy for TRAumatic brain injury" (STEMTRA) trial was published in the January 4, 2021 online issue of Neurology®, the medical journal of the American Academy of Neurology. The full manuscript, entitled "Cell Therapy for Chronic TBI: Interim Analysis of the Randomized Controlled STEMTRA Trial" can be accessed here. STEMTRA was a Phase 2, randomized, double-blind, surgical sham-controlled, global trial evaluating the efficacy and safety of SB623 compared to sham surgery in patients with stable chronic neurological motor deficits secondary to traumatic brain injury (TBI). The study achieved its primary efficacy endpoint of significant improvement from baseline of Fugl-Meyer Motor Scale (FMMS) score at six months for SB623-treated patients. Secondary efficacy endpoints improved from baseline but were not statistically significant versus control. In the six-month, pre-specified interim analysis, treatment with SB623 cells appeared to be safe and well-tolerated. In the trial, patients were followed for efficacy and safety for up to twelve months. STEMTRA was a 12-month, Phase 2, randomized, double-blind, surgical sham-controlled, global trial evaluating the efficacy and safety of SB623 compared to sham surgery in patients with stable chronic neurological motor deficits secondary to TBI (https://clinicaltrials.gov identifier: NCT02416492). In this study, SB623 cells were implanted directly around the site of brain injury. The primary endpoint was mean change from baseline in FMMS score at six months to measure changes in motor impairment. To be eligible for this trial, patients (ages 18-75) must have been at least 12 months post-TBI and had a Glasgow Outcome Scale extended (GOS-E) score of 3-6 (e.g., moderate or severe disability). Patients must also have been able to undergo all planned neurological assessments and had no seizures in the prior three months. The STEMTRA trial treated 61 patients from 27 sites in the U.S., Japan and Ukraine. In this study, SB623 met its primary endpoint, with patients treated with SB623 achieving an average 8.3-point improvement from baseline in the FMMS, versus 2.3-points in the control group, at 6 months (p=0.040). Of patients treated with SB623, 18 (39.1%) reached a 10 or more point improvement of FMMS compared to one control patient (6.7%; p=0.039). No new safety signals were identified, and the most commonly reported adverse event was headaches. SB623 is a proprietary, cell-based investigational product made from allogeneic modified and cultured adult bone marrow-derived mesenchymal stem cells (MSCs) that undergo temporary genetic modification. Implantation of SB623 cells into injured nerve tissue in the brain is expected to trigger the brain's natural regenerative ability to recover lost motor functions. SanBio is preparing to file a Biologics License Application with the Pharmaceuticals and Medical Devices Agency in Japan for SB623 for the treatment of chronic motor deficits resulting from traumatic brain injury, while also making progress in its global development program. Further, the Company is working toward commencing clinical trials of SB623 for stroke in Japan. SB623 has been granted Sakigake designation for innovative medical products from the Ministry of Health, Labour, and Welfare of Japan, Regenerative Medicine Advanced Therapy (RMAT) designation from the U.S. Food and Drug Association, and the Advanced Therapy Medicinal Product classification from the European Medicines Agency.
Price Target Changed • Dec 16Price target lowered to JP¥2,683Down from JP¥3,114, the current price target is an average from 5 analysts. The new target price is 93% above the current share price of JP¥1,388. As of last close, the stock is down 47% over the past year.
Is New 90 Day High Low • Dec 16New 90-day low: JP¥1,388The company is down 34% from its price of JP¥2,100 on 17 September 2020. The Japanese market is up 8.0% over the last 90 days, indicating the company underperformed over that time. It also underperformed the Biotechs industry, which is down 2.0% over the same period. According to the Simply Wall St valuation model, the estimated intrinsic value of the company is JP¥3.04 per share.
Price Target Changed • Dec 10Price target lowered to JP¥2,683Down from JP¥3,114, the current price target is an average from 5 analysts. The new target price is 45% above the current share price of JP¥1,852. As of last close, the stock is down 56% over the past year.
お知らせ • Dec 05SanBio Company Limited to Report Q3, 2021 Results on Dec 15, 2020SanBio Company Limited announced that they will report Q3, 2021 results on Dec 15, 2020
