View Financial HealthGemina Laboratories 配当と自社株買い配当金 基準チェック /06Gemina Laboratories配当金を支払った記録がありません。主要情報n/a配当利回り-0.4%バイバック利回り総株主利回り-0.4%将来の配当利回りn/a配当成長n/a次回配当支払日n/a配当落ち日n/a一株当たり配当金n/a配当性向n/a最近の配当と自社株買いの更新更新なしすべての更新を表示Recent updatesお知らせ • Mar 27Gemina Laboratories Ltd. Announces Delisting from the Canadian Securities ExchangeGemina Laboratories Ltd. ("Gemina" or the "Company") announced that the Canadian Securities Exchange (the "CSE") has approved is application to voluntarily delist its common shares from trading on the CSE. The Company obtained the approval of its disinterested shareholders at its annual general and special meeting held on March 13, 2026. The Company expects the delisting to become effective at the close of trading on 27th March, 2026. Following the delisting, the Company will remain a reporting issuer in the provinces of Alberta, British Columbia and Ontario and will continue to comply with its continuous disclosure obligations under applicable securities laws in those jurisdictions. The decision to delist from the CSE was made after careful consideration of the Company's current operational needs, trading volumes, and the costs associated with maintaining a listing. The Company believes that the delisting is in the best interests of the Company and its shareholders.お知らせ • Dec 31Gemina Laboratories Ltd. announced that it expects to receive $3 million in fundingGemina Laboratories Ltd. announced a private placement of secured, non-convertible debentures for gross proceeds of a minimum of $1,000,000 and maximum of $3,000,000 on December 30, 2025. Each debenture will consist of a $1,000 principal amount and the payment of the principal and premium, if any, of and interest on, the debentures will be secured by a first priority security interest against the company's intellectual property. The Debentures will mature on the date that is twelve months from the date of closing of the offering and accrue interest at a rate of 18% per annum, which will be compounded monthly, and payable at the maturity date. The company may prepay the principal amount of the Debentures at any time prior to the Maturity Date at a price equal to 105% of the principal amount of the debentures, plus accrued and unpaid interest thereon. The company may close the offering in one or more tranches, up until January 15, 2026 or on such other date as determined by the Company. The Offering is also subject to other customary conditions, including but not limited to, the receipt of all necessary approvals of applicable securities regulatory authorities.お知らせ • Dec 24Gemina Laboratories Ltd., Annual General Meeting, Feb 13, 2026Gemina Laboratories Ltd., Annual General Meeting, Feb 13, 2026. Location: british columbia, vancouver Canadaお知らせ • Nov 14Gemina Laboratories Ltd. announced that it expects to receive CAD 7 million in fundingGemina Laboratories Ltd. announced a non-brokered private placement that it will issue up to 9,333,333 common shares in the capital of the company at a price of CAD 0.75 per share for the gross proceeds of up to CAD 7,000,000 on November 13, 2024. The securities issued under the offering will be subject to a statutory hold period in Canada expiring four months and one day from the date of issuance.お知らせ • Mar 19Gemina Laboratories Ltd. announced that it has received CAD 0.91 million in fundingOn March 18, 2024, Gemina Laboratories Ltd closed the transaction. The company has raised gross proceeds of CAD 910,000 of unsecured convertible notes. All securities issued pursuant to the Private Placement are and will be subject to a four month hold period from the date of issue, expiring July 19, 2024, in addition to such other restrictions as may apply under applicable securities laws of jurisdictions outside Canada.お知らせ • Mar 16Gemina Laboratories Ltd., Annual General Meeting, May 13, 2024Gemina Laboratories Ltd., Annual General Meeting, May 13, 2024.お知らせ • Feb 24Gemina Laboratories Ltd. announced that it expects to receive CAD 1 million in fundingGemina Laboratories Ltd announced a non brokered private placement to issue 10% unsecured convertible notes for the gross proceeds of CAD 1,000,000 on February 22, 2024. The Notes will be unsecured and have a maturity date of 12 months from the date of issuance, unless earlier converted in accordance with the terms of the Note. At the option may be converted into common shares at a price per Common Share equal to of the Note holder, any principal amount of CAD 0.50 or in the event the Company completes an equity financing prior to the Maturity Date the Late Conversion Price. The Note holder may elect to convert the outstanding Principal into Common Shares at any time prior to the Maturity Date. Interest on the Notes will accrue at a rate of 10% per annum, payable in cash on the Maturity Date or in the case of conversion of the entire Principal, at the time of conversion. The Note holder may elect to have the Interest repaid in cash or converted into Common Shares at the applicable Conversion Price, in accordance with the terms of the Note and by providing the Company with written notice of such election. All securities issued in connection with the Private Placement will be subject to a four-month hold period from the date of issue under applicable Canadian securities laws, in addition to such other restrictions as may apply under applicable securities laws of jurisdictions outside Canada.お知らせ • Dec 31Gemina Laboratories Ltd. Announces the Resignation of Rob Porter as Director and PresidentGemina Laboratories Ltd. announced the Dr. Rob Porter has stepped down from the board and resigned as President. Dr. Porter will continue as Managing Director of RAPIvD and will focus on its continued growth.お知らせ • Jun 07Gemina Laboratories Ltd. Laboratories and ReadyGo Diagnostics Limited Diagnostics Achieve Mycobacterium Tuberculosis Diagnosis in SalivaGemina Laboratories Ltd. announced significant technical results from its collaboration with ReadyGo Diagnostics Ltd. This represents the first step of Gemina's move into molecular diagnostics adding further diagnostic capability to compliment their lateral flow programme. Results from a collaboration which began in January 2023, Gemina and ReadyGo are proud to announce the successful feasibility of detecting Mycobacterium Tuberculosis ("MTB") in a saliva matrix using the ReadyGo GEO platform. This breakthrough in MTB detection paves the way for affordable testing which will have the potential to significantly impact MTB eradication efforts in countries such as India, Indonesia, and other affected regions worldwide. The feasibility of utilizing saliva as a sample for the detection of Mycobacterium tuberculosis through a molecular diagnostic test has been successfully demonstrated. MTB, commonly referred to as "Tuberculosis", is a highly infectious airborne disease caused by bacteria that affects the lungs, and was responsible for more than 10 million global infections in 2021, causing 1.6 million deaths. Alarmingly, an estimated 4 million infections (2 out of every 5 cases) remain undiagnosed and untreated, enhancing disease control efforts. Diagnosis in low- to middle-income countries, where MTB is most prevalent, typically relies on sm microscopy using sputum samples. However, these tests have significant limitations, particularly in remote areas and when diagnosing certain patient populations such as children and the elderly, who struggle to produce sputum. This innovative solution will provide results within 30 minutes, anywhere, at an affordable cost. Following the successful feasibility stage, the team anticipates introducing a compact laboratory instrument retailing for less than $1000, with a per-test cost of $5, enabling field testing near patients.お知らせ • May 18Gemina Laboratories Ltd. Antibody Immobilization Chemistry Platform Demonstrates Major Lateral Flow Assay Performance ImprovementGemina Laboratories Ltd. announced that its patented chemistry for Antibody Immobilization allows for a massive reduction in antibody usage when used in lateral flow assay (LFA) diagnostic tests. This represents the confirmation of a major technical milestone on the LFA format for Gemina. The Antibody Immobilization Platform allows for the reduction of test line antibody requirements by 75% vs. standard physisorption, without impacting limit-of-detection. Gemina's Antibody Immobilization Platform creates a bridge (the Gemina Bridge) between a sensor surface and the antibodies stuck on that surface for target capture. Use of the Gemina Bridge results in optimized antibody usage and increased target capture activity per unit area of sensor surface. Therefore, use of the Gemina Bridge imparts both significant performance advantages and significant manufacturing advantages with LFA tests. The industry standard antibody immobilization technique on nitrocellulose used in LFAs - non-specific physisorption, results in only 5-20% of the antibodies deposited on a sensor being "active" or capable of target capture. The Gemina Bridge rescues this lost antibody activity, meaning much less antibody is required to deliver the same test performance. Laboratory Study: This massive reduction in antibody requirements was thoroughly demonstrated on the lateral flow assay test line with a COVID-19 rapid antigen test developed by Gemina Labs at the RAPIvD laboratories in Sharnbrook, UK. Instead of striping the antibodies directly onto the nitrocellulose (NC) strip, the Gemina Bridge is first stripped down to form a closely-packed monolayer, onto which the antibodies form a dense secondary layer with four times higher target capture activity than standard antibody-only test lines. Modeling Study: Dr. Robert Davies, an independent surface chemist expert, specializing in lateral flow assay development, was engaged by Gemina Laboratories to model the adsorption of the Gemina Antibody Immobilization Bridge to nitrocellulose, in comparison to optimal close packing of non-specifically adsorbed IgG antibodies. Calculations support the creation of four times more antibody immobilization sites per unit of surface area with the Gemina Bridge, as highlighted in the above-linked white paper. In summary, the Gemina Antibody Immobilization Platform acts as a bridge between a sensor surface, in this instance the nitrocellulose test strip in a lateral flow assay, and the antibody used for target capture. Modeling data and internal experimental results indicate that use of the Gemina Bridge increases the density of active antibodies on the test strip by four times versus standard immobilization methods, meaning 75% less antibody is needed with the Gemina Bridge to achieve the same performance as a standard test. This represents a massive savings in antibody consumption during test fabrication.お知らせ • Jan 26Gemina Laboratories Ltd. Announces Board ChangesGemina Laboratories Ltd. announced the appointment of Dr. Bola Grace to the Board of Directors. Dr. Grace brings extensive leadership experience in the biotech/healthcare industry to the Board, having provided strategic, commercial and technical direction on many complex programmes, delivering numerous diagnostic products to the consumer marketplace. With a career that started in research and development at Unipath, she went on to hold a Lead Scientist role at Alere before becoming Head of R&D for the global leader in reproductive health testing, Swiss Precision Diagnostics (SPD), a company jointly owned by Abbott Laboratories and Proctor and Gamble. Dr. Grace is a passionate believer in inclusive, user-centric design, not least because of its impact on healthcare equity. She holds a prestigious visiting professorship in this field with the UK's Royal Academy of Engineering. Dr. Grace has always succeeded in balancing her private sector career with her academic interests. Beyond her current visiting professorship with the Royal Academy of Engineering, she previously held a 3-year visiting faculty position at Kings College London and a 9-year engagement with University College London (UCL), initially with the Elizabeth Garrett Anderson Institute for Women's Health, which became a visiting faculty position with UCL's Global Business School for Health. She has Bachelor and Master's degrees in biomedical sciences and molecular biology, and a Ph.D from UCL in population health and epidemiology. She also holds an executive MBA from Cambridge University. She is a fellow of the Royal Society of Public Health and a Fellow of the Chartered Management Institute. With Dr. Grace's appointment to the Board, the Company also announced that Dr. James Tansey has resigned his directorship of Gemina. James will continue to serve the Company as an advisor.お知らせ • Jan 07Gemina Laboratories Ltd. Completes Influenza A/B Diagnostic Test PrototypeGemina Laboratories Ltd. announced the completion of its influenza A/B rapid test prototype. The company announced its intention to develop an influenza diagnostic in second quarter of 2022, using the company's unique chemistry platform. Influenza A/B: Demand for tests for influenza and other common illnesses has been growing significantly as health care providers seek to distinguish between diseases with common symptoms. In the post-pandemic era, consumers are also demanding greater control over their health status, creating substantial global demand for low-cost diagnostic tools that can be self-administered. After an extensive antibody screening program, Gemina Laboratories, in partnership with RAPIvD, has completed the development of an influenza A/B rapid test prototype (the Gemina Benchmark Test) for internal benchmarking studies to further demonstrate the performance improvements imparted by the Gemina chemistry platform. The Gemina Benchmark Test is designed using the traditional Lateral Flow Assay ("LFA") format commonly found in the rapid COVID tests used throughout the pandemic. The Gemina Benchmark Test has been shown to reliably detect multiple strains of whole influenza A and influenza B viruses in artificial nasal fluid-spiked samples on a single test strip with no cross-reactivity between flu A and B. The Benchmark will now enter the optimization phase, followed by pre-clinical performance evaluation with patient samples. Once performance evaluation is complete, the Gemina Benchmark Test will be put through a series of head-to-head performance evaluation studies against the same test built using Gemina's proprietary immobilization chemistry. This will be a true direct comparison between its proprietary LFA design and the industry standard LFA design. The resultant data will provide a direct measure of the improvements imparted by the Gemina technology in comparison to standard LFAs. Indeed, preliminary comparative studies utilizing the Gemina immobilization chemistry indicate the potential to reduce antibody usage by 6-8 times, while maintaining equivalent sensitivity to the traditional design. Since the majority of LFA tests use expensive antibodies to capture the virus and allow for detection on the test strip, this potential large reduction in antibody use represents a substantial benefit in terms of both cost reduction and improved supply chain security. The next steps for the further integration of the Gemina chemistry platform into its panel of upcoming diagnostic products will be provided in the CEO's strategy update to be released in January 2023.お知らせ • Nov 12Gemina Laboratories Ltd., Annual General Meeting, Jan 12, 2023Gemina Laboratories Ltd., Annual General Meeting, Jan 12, 2023.決済の安定と成長配当データの取得安定した配当: GLAB.Fの 1 株当たり配当が過去に安定していたかどうかを判断するにはデータが不十分です。増加する配当: GLAB.Fの配当金が増加しているかどうかを判断するにはデータが不十分です。配当利回り対市場Gemina Laboratories 配当利回り対市場GLAB.F 配当利回りは市場と比べてどうか？セグメント配当利回り会社 (GLAB.F)n/a市場下位25% (US)1.4%市場トップ25% (US)4.3%業界平均 (Biotechs)2.5%アナリスト予想 (GLAB.F) (最長3年)n/a注目すべき配当: GLAB.Fは最近配当金を報告していないため、配当金支払者の下位 25% に対して同社の配当利回りを評価することはできません。高配当: GLAB.Fは最近配当金を報告していないため、配当金支払者の上位 25% に対して同社の配当利回りを評価することはできません。株主への利益配当収益カバレッジ: GLAB.Fの 配当性向 を計算して配当金の支払いが利益で賄われているかどうかを判断するにはデータが不十分です。株主配当金キャッシュフローカバレッジ: GLAB.Fが配当金を報告していないため、配当金の持続可能性を計算できません。高配当企業の発掘7D1Y7D1Y7D1YUS 市場の強力な配当支払い企業。View Management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2026/03/29 18:33終値2025/12/31 00:00収益2025/10/31年間収益2025/01/31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本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、レポートの使用方法に関するガイドやYoutubeのチュートリアルも掲載しています。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Gemina Laboratories Ltd. 0 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。0
お知らせ • Mar 27Gemina Laboratories Ltd. Announces Delisting from the Canadian Securities ExchangeGemina Laboratories Ltd. ("Gemina" or the "Company") announced that the Canadian Securities Exchange (the "CSE") has approved is application to voluntarily delist its common shares from trading on the CSE. The Company obtained the approval of its disinterested shareholders at its annual general and special meeting held on March 13, 2026. The Company expects the delisting to become effective at the close of trading on 27th March, 2026. Following the delisting, the Company will remain a reporting issuer in the provinces of Alberta, British Columbia and Ontario and will continue to comply with its continuous disclosure obligations under applicable securities laws in those jurisdictions. The decision to delist from the CSE was made after careful consideration of the Company's current operational needs, trading volumes, and the costs associated with maintaining a listing. The Company believes that the delisting is in the best interests of the Company and its shareholders.
お知らせ • Dec 31Gemina Laboratories Ltd. announced that it expects to receive $3 million in fundingGemina Laboratories Ltd. announced a private placement of secured, non-convertible debentures for gross proceeds of a minimum of $1,000,000 and maximum of $3,000,000 on December 30, 2025. Each debenture will consist of a $1,000 principal amount and the payment of the principal and premium, if any, of and interest on, the debentures will be secured by a first priority security interest against the company's intellectual property. The Debentures will mature on the date that is twelve months from the date of closing of the offering and accrue interest at a rate of 18% per annum, which will be compounded monthly, and payable at the maturity date. The company may prepay the principal amount of the Debentures at any time prior to the Maturity Date at a price equal to 105% of the principal amount of the debentures, plus accrued and unpaid interest thereon. The company may close the offering in one or more tranches, up until January 15, 2026 or on such other date as determined by the Company. The Offering is also subject to other customary conditions, including but not limited to, the receipt of all necessary approvals of applicable securities regulatory authorities.
お知らせ • Dec 24Gemina Laboratories Ltd., Annual General Meeting, Feb 13, 2026Gemina Laboratories Ltd., Annual General Meeting, Feb 13, 2026. Location: british columbia, vancouver Canada
お知らせ • Nov 14Gemina Laboratories Ltd. announced that it expects to receive CAD 7 million in fundingGemina Laboratories Ltd. announced a non-brokered private placement that it will issue up to 9,333,333 common shares in the capital of the company at a price of CAD 0.75 per share for the gross proceeds of up to CAD 7,000,000 on November 13, 2024. The securities issued under the offering will be subject to a statutory hold period in Canada expiring four months and one day from the date of issuance.
お知らせ • Mar 19Gemina Laboratories Ltd. announced that it has received CAD 0.91 million in fundingOn March 18, 2024, Gemina Laboratories Ltd closed the transaction. The company has raised gross proceeds of CAD 910,000 of unsecured convertible notes. All securities issued pursuant to the Private Placement are and will be subject to a four month hold period from the date of issue, expiring July 19, 2024, in addition to such other restrictions as may apply under applicable securities laws of jurisdictions outside Canada.
お知らせ • Mar 16Gemina Laboratories Ltd., Annual General Meeting, May 13, 2024Gemina Laboratories Ltd., Annual General Meeting, May 13, 2024.
お知らせ • Feb 24Gemina Laboratories Ltd. announced that it expects to receive CAD 1 million in fundingGemina Laboratories Ltd announced a non brokered private placement to issue 10% unsecured convertible notes for the gross proceeds of CAD 1,000,000 on February 22, 2024. The Notes will be unsecured and have a maturity date of 12 months from the date of issuance, unless earlier converted in accordance with the terms of the Note. At the option may be converted into common shares at a price per Common Share equal to of the Note holder, any principal amount of CAD 0.50 or in the event the Company completes an equity financing prior to the Maturity Date the Late Conversion Price. The Note holder may elect to convert the outstanding Principal into Common Shares at any time prior to the Maturity Date. Interest on the Notes will accrue at a rate of 10% per annum, payable in cash on the Maturity Date or in the case of conversion of the entire Principal, at the time of conversion. The Note holder may elect to have the Interest repaid in cash or converted into Common Shares at the applicable Conversion Price, in accordance with the terms of the Note and by providing the Company with written notice of such election. All securities issued in connection with the Private Placement will be subject to a four-month hold period from the date of issue under applicable Canadian securities laws, in addition to such other restrictions as may apply under applicable securities laws of jurisdictions outside Canada.
お知らせ • Dec 31Gemina Laboratories Ltd. Announces the Resignation of Rob Porter as Director and PresidentGemina Laboratories Ltd. announced the Dr. Rob Porter has stepped down from the board and resigned as President. Dr. Porter will continue as Managing Director of RAPIvD and will focus on its continued growth.
お知らせ • Jun 07Gemina Laboratories Ltd. Laboratories and ReadyGo Diagnostics Limited Diagnostics Achieve Mycobacterium Tuberculosis Diagnosis in SalivaGemina Laboratories Ltd. announced significant technical results from its collaboration with ReadyGo Diagnostics Ltd. This represents the first step of Gemina's move into molecular diagnostics adding further diagnostic capability to compliment their lateral flow programme. Results from a collaboration which began in January 2023, Gemina and ReadyGo are proud to announce the successful feasibility of detecting Mycobacterium Tuberculosis ("MTB") in a saliva matrix using the ReadyGo GEO platform. This breakthrough in MTB detection paves the way for affordable testing which will have the potential to significantly impact MTB eradication efforts in countries such as India, Indonesia, and other affected regions worldwide. The feasibility of utilizing saliva as a sample for the detection of Mycobacterium tuberculosis through a molecular diagnostic test has been successfully demonstrated. MTB, commonly referred to as "Tuberculosis", is a highly infectious airborne disease caused by bacteria that affects the lungs, and was responsible for more than 10 million global infections in 2021, causing 1.6 million deaths. Alarmingly, an estimated 4 million infections (2 out of every 5 cases) remain undiagnosed and untreated, enhancing disease control efforts. Diagnosis in low- to middle-income countries, where MTB is most prevalent, typically relies on sm microscopy using sputum samples. However, these tests have significant limitations, particularly in remote areas and when diagnosing certain patient populations such as children and the elderly, who struggle to produce sputum. This innovative solution will provide results within 30 minutes, anywhere, at an affordable cost. Following the successful feasibility stage, the team anticipates introducing a compact laboratory instrument retailing for less than $1000, with a per-test cost of $5, enabling field testing near patients.
お知らせ • May 18Gemina Laboratories Ltd. Antibody Immobilization Chemistry Platform Demonstrates Major Lateral Flow Assay Performance ImprovementGemina Laboratories Ltd. announced that its patented chemistry for Antibody Immobilization allows for a massive reduction in antibody usage when used in lateral flow assay (LFA) diagnostic tests. This represents the confirmation of a major technical milestone on the LFA format for Gemina. The Antibody Immobilization Platform allows for the reduction of test line antibody requirements by 75% vs. standard physisorption, without impacting limit-of-detection. Gemina's Antibody Immobilization Platform creates a bridge (the Gemina Bridge) between a sensor surface and the antibodies stuck on that surface for target capture. Use of the Gemina Bridge results in optimized antibody usage and increased target capture activity per unit area of sensor surface. Therefore, use of the Gemina Bridge imparts both significant performance advantages and significant manufacturing advantages with LFA tests. The industry standard antibody immobilization technique on nitrocellulose used in LFAs - non-specific physisorption, results in only 5-20% of the antibodies deposited on a sensor being "active" or capable of target capture. The Gemina Bridge rescues this lost antibody activity, meaning much less antibody is required to deliver the same test performance. Laboratory Study: This massive reduction in antibody requirements was thoroughly demonstrated on the lateral flow assay test line with a COVID-19 rapid antigen test developed by Gemina Labs at the RAPIvD laboratories in Sharnbrook, UK. Instead of striping the antibodies directly onto the nitrocellulose (NC) strip, the Gemina Bridge is first stripped down to form a closely-packed monolayer, onto which the antibodies form a dense secondary layer with four times higher target capture activity than standard antibody-only test lines. Modeling Study: Dr. Robert Davies, an independent surface chemist expert, specializing in lateral flow assay development, was engaged by Gemina Laboratories to model the adsorption of the Gemina Antibody Immobilization Bridge to nitrocellulose, in comparison to optimal close packing of non-specifically adsorbed IgG antibodies. Calculations support the creation of four times more antibody immobilization sites per unit of surface area with the Gemina Bridge, as highlighted in the above-linked white paper. In summary, the Gemina Antibody Immobilization Platform acts as a bridge between a sensor surface, in this instance the nitrocellulose test strip in a lateral flow assay, and the antibody used for target capture. Modeling data and internal experimental results indicate that use of the Gemina Bridge increases the density of active antibodies on the test strip by four times versus standard immobilization methods, meaning 75% less antibody is needed with the Gemina Bridge to achieve the same performance as a standard test. This represents a massive savings in antibody consumption during test fabrication.
お知らせ • Jan 26Gemina Laboratories Ltd. Announces Board ChangesGemina Laboratories Ltd. announced the appointment of Dr. Bola Grace to the Board of Directors. Dr. Grace brings extensive leadership experience in the biotech/healthcare industry to the Board, having provided strategic, commercial and technical direction on many complex programmes, delivering numerous diagnostic products to the consumer marketplace. With a career that started in research and development at Unipath, she went on to hold a Lead Scientist role at Alere before becoming Head of R&D for the global leader in reproductive health testing, Swiss Precision Diagnostics (SPD), a company jointly owned by Abbott Laboratories and Proctor and Gamble. Dr. Grace is a passionate believer in inclusive, user-centric design, not least because of its impact on healthcare equity. She holds a prestigious visiting professorship in this field with the UK's Royal Academy of Engineering. Dr. Grace has always succeeded in balancing her private sector career with her academic interests. Beyond her current visiting professorship with the Royal Academy of Engineering, she previously held a 3-year visiting faculty position at Kings College London and a 9-year engagement with University College London (UCL), initially with the Elizabeth Garrett Anderson Institute for Women's Health, which became a visiting faculty position with UCL's Global Business School for Health. She has Bachelor and Master's degrees in biomedical sciences and molecular biology, and a Ph.D from UCL in population health and epidemiology. She also holds an executive MBA from Cambridge University. She is a fellow of the Royal Society of Public Health and a Fellow of the Chartered Management Institute. With Dr. Grace's appointment to the Board, the Company also announced that Dr. James Tansey has resigned his directorship of Gemina. James will continue to serve the Company as an advisor.
お知らせ • Jan 07Gemina Laboratories Ltd. Completes Influenza A/B Diagnostic Test PrototypeGemina Laboratories Ltd. announced the completion of its influenza A/B rapid test prototype. The company announced its intention to develop an influenza diagnostic in second quarter of 2022, using the company's unique chemistry platform. Influenza A/B: Demand for tests for influenza and other common illnesses has been growing significantly as health care providers seek to distinguish between diseases with common symptoms. In the post-pandemic era, consumers are also demanding greater control over their health status, creating substantial global demand for low-cost diagnostic tools that can be self-administered. After an extensive antibody screening program, Gemina Laboratories, in partnership with RAPIvD, has completed the development of an influenza A/B rapid test prototype (the Gemina Benchmark Test) for internal benchmarking studies to further demonstrate the performance improvements imparted by the Gemina chemistry platform. The Gemina Benchmark Test is designed using the traditional Lateral Flow Assay ("LFA") format commonly found in the rapid COVID tests used throughout the pandemic. The Gemina Benchmark Test has been shown to reliably detect multiple strains of whole influenza A and influenza B viruses in artificial nasal fluid-spiked samples on a single test strip with no cross-reactivity between flu A and B. The Benchmark will now enter the optimization phase, followed by pre-clinical performance evaluation with patient samples. Once performance evaluation is complete, the Gemina Benchmark Test will be put through a series of head-to-head performance evaluation studies against the same test built using Gemina's proprietary immobilization chemistry. This will be a true direct comparison between its proprietary LFA design and the industry standard LFA design. The resultant data will provide a direct measure of the improvements imparted by the Gemina technology in comparison to standard LFAs. Indeed, preliminary comparative studies utilizing the Gemina immobilization chemistry indicate the potential to reduce antibody usage by 6-8 times, while maintaining equivalent sensitivity to the traditional design. Since the majority of LFA tests use expensive antibodies to capture the virus and allow for detection on the test strip, this potential large reduction in antibody use represents a substantial benefit in terms of both cost reduction and improved supply chain security. The next steps for the further integration of the Gemina chemistry platform into its panel of upcoming diagnostic products will be provided in the CEO's strategy update to be released in January 2023.
お知らせ • Nov 12Gemina Laboratories Ltd., Annual General Meeting, Jan 12, 2023Gemina Laboratories Ltd., Annual General Meeting, Jan 12, 2023.