Celon Pharma（8RP）株式概要セロン・ファルマS.A.は総合製薬会社で、医薬品および製剤の研究、製造、販売に従事している。 詳細8RP ファンダメンタル分析スノーフレーク・スコア評価3/6将来の成長1/6過去の実績0/6財務の健全性5/6配当金0/6報酬当社が推定した公正価値より74.1%で取引されている 収益は年間8.03%増加すると予測されています リスク分析German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現在は利益が出ておらず、今後3年間で利益が出る見込みはない キャッシュランウェイが1年未満である すべてのリスクチェックを見る8RP Community Fair Values Create NarrativeSee what others think this stock is worth. Follow their fair value or set your own to get alerts.Your Fair Value€Current Price€4.7037.8% 割高 内在価値ディスカウントGrowth estimate overAnnual revenue growth rate5 Yearstime period%/yrDecreaseIncreasePastFuture-122m332m2016201920222025202620282031Revenue zł332.0mEarnings zł48.8mAdvancedSet Fair ValueView all narrativesCelon Pharma S.A. 競合他社PEPTONIC medicalSymbol: DB:28LMarket cap: €560.2mCantourage GroupSymbol: XTRA:HIGHMarket cap: €75.6mDermapharm HoldingSymbol: XTRA:DMPMarket cap: €2.4bBiofronteraSymbol: XTRA:B8FKMarket cap: €14.7m価格と性能株価の高値、安値、推移の概要Celon Pharma過去の株価現在の株価zł4.7052週高値zł5.7752週安値zł4.27ベータ0.721ヶ月の変化-7.84%3ヶ月変化-9.27%1年変化-7.48%3年間の変化41.14%5年間の変化-53.19%IPOからの変化-52.24%最新ニュースお知らせ • Jan 27+ 3 more updatesCelon Pharma S.A. to Report Fiscal Year 2025 Results on Apr 22, 2026Celon Pharma S.A. announced that they will report fiscal year 2025 results at 8:30 AM, Central European Standard Time on Apr 22, 2026お知らせ • Nov 15Celon Pharma S.A. to Report Q3, 2025 Results on Nov 19, 2025Celon Pharma S.A. announced that they will report Q3, 2025 results on Nov 19, 2025お知らせ • Oct 10FDA Clears Celon Pharma's Schizophrenia Drug for Phase 3 TrialCelon Pharma S.A. announced it has secured a key regulatory milestone for its lead neuroscience program. The U.S. Food and Drug Administration (FDA) provided positive feedback clearing the path for Phase 3 testing of CPL'36, the company's novel second-generation PDE10A inhibitor for schizophrenia. The FDA confirmed that Celon Pharma's existing preclinical data are sufficient to begin pivotal studies and approved the proposed Phase 3 program, which includes two 28-day randomized, double-blind trials in patients with acute schizophrenia episodes and a 12-month open-label extension to establish long-term safety. The FDA also agreed that "treatment of schizophrenia" is the appropriate indication for CPL'36, confirming the compound's potential for broad labeling at registration. The Agency supported Celon Pharma's plan to conduct required supportive studies--including drug-drug interaction (DDI), QTc, and mass balance--concurrently with the pivotal trials, provided key safety measures are in place. This parallel development plan is expected to streamline timelines and maintain strategic flexibility. Strong Efficacy in Phase 2 Sets the Stage: CPL'36 previously demonstrated robust and clinically meaningful efficacy in a 189-patient Phase 2 trial, with both the 20 mg and 40 mg doses producing statistically significant improvements versus placebo across positive and total PANSS scores. The 40 mg dose also showed early signs of cognitive benefit. At Week 4, the positive PANSS subscale improved by 3.7 points for the 20 mg dose.お知らせ • Aug 21Celon Pharma S.A. to Report First Half, 2025 Results on Sep 17, 2025Celon Pharma S.A. announced that they will report first half, 2025 results on Sep 17, 2025お知らせ • Mar 05Celon Pharma S.A. Announces Strong Proof-of-Concept Data from Phase 2 Trial of PDE10A Inhibitor (CPL’36), a Novel Once-Daily Treatment of Levodopa-Induced Dyskinesia in Parkinson’s DiseaseCelon Pharma S.A. announced robust and positive Phase 2 clinical trial results for its PDE10A inhibitor (CPL’36), a novel, oral, once-daily medication for the treatment of Levodopa-Induced Dyskinesia (LID) in Parkinson’s disease. The study met its primary endpoint and many of its secondary endpoints. CPL’36 demonstrated robust and consistent efficacy across all utilized scales measuring improvement in treatment of LID in Parkinson’s disease. The effect size was large and clinically meaningful. CPL’36 was previously investigated as a potential treatment for schizophrenia and demonstrated positive Phase 2 results that were reported in July 2024. Trial description The CPL’36 Phase 2 study was multinational, multicenter, randomized, placebo-controlled trial conducted in a group 105 adult patients with LID dyskinesia in Parkinson’s disease. CPL’36 was administered orally in one of two doses of 20 mg or 40 mg, once daily and placebo controlled at a ratio (1:1:1) for a period of 4 weeks. Patient baseline severity was moderate-severe to severe, as characterized by a UDysRS (Unified Dyskinesia Rating Scale) total score of approximately 45. At Week 4, the improvement in UDysRS total score (primary endpoint) for the 20 mg dose was 12.30 units (LS Mean difference from placebo, p<0.001, Cohen’s d: 0.90) and improvement for the 40 mg dose was 13.58 units (LS Mean difference from placebo, p<0.001, Cohen’s d: 1.00). CPL’36 treatment was associated with improvement in most secondary endpoints, including the UDysRS objective subscale, in which the improvement in both active groups was statistically significant from Day 7 of the treatment phase. Drug tolerability was favorable with most severe adverse events occurring in the placebo-treated patients (8.8% in placebo group, 0% in 20 mg dose and 5.7% in 40 mg dose). Treatment related emergent adverse events leading to discontinuation of study medication were recorded in 2.9% of the placebo group, 11.1% of the 20 mg dosing arm, and 8.6% in the 40 mg dosing arm. The most common adverse event reported in both active groups was somnolence with mild to moderate intensity. No deaths were reported in the trial, and one Serious Adverse Event of atrial fibrillation with moderate intensity was reported in the 40 mg dosing arm.お知らせ • Jan 15Celon Pharma S.A. to Report Fiscal Year 2024 Results on Apr 16, 2025Celon Pharma S.A. announced that they will report fiscal year 2024 results at 8:30 AM, Central European Standard Time on Apr 16, 2025最新情報をもっと見るRecent updatesお知らせ • Jan 27+ 3 more updatesCelon Pharma S.A. to Report Fiscal Year 2025 Results on Apr 22, 2026Celon Pharma S.A. announced that they will report fiscal year 2025 results at 8:30 AM, Central European Standard Time on Apr 22, 2026お知らせ • Nov 15Celon Pharma S.A. to Report Q3, 2025 Results on Nov 19, 2025Celon Pharma S.A. announced that they will report Q3, 2025 results on Nov 19, 2025お知らせ • Oct 10FDA Clears Celon Pharma's Schizophrenia Drug for Phase 3 TrialCelon Pharma S.A. announced it has secured a key regulatory milestone for its lead neuroscience program. The U.S. Food and Drug Administration (FDA) provided positive feedback clearing the path for Phase 3 testing of CPL'36, the company's novel second-generation PDE10A inhibitor for schizophrenia. The FDA confirmed that Celon Pharma's existing preclinical data are sufficient to begin pivotal studies and approved the proposed Phase 3 program, which includes two 28-day randomized, double-blind trials in patients with acute schizophrenia episodes and a 12-month open-label extension to establish long-term safety. The FDA also agreed that "treatment of schizophrenia" is the appropriate indication for CPL'36, confirming the compound's potential for broad labeling at registration. The Agency supported Celon Pharma's plan to conduct required supportive studies--including drug-drug interaction (DDI), QTc, and mass balance--concurrently with the pivotal trials, provided key safety measures are in place. This parallel development plan is expected to streamline timelines and maintain strategic flexibility. Strong Efficacy in Phase 2 Sets the Stage: CPL'36 previously demonstrated robust and clinically meaningful efficacy in a 189-patient Phase 2 trial, with both the 20 mg and 40 mg doses producing statistically significant improvements versus placebo across positive and total PANSS scores. The 40 mg dose also showed early signs of cognitive benefit. At Week 4, the positive PANSS subscale improved by 3.7 points for the 20 mg dose.お知らせ • Aug 21Celon Pharma S.A. to Report First Half, 2025 Results on Sep 17, 2025Celon Pharma S.A. announced that they will report first half, 2025 results on Sep 17, 2025お知らせ • Mar 05Celon Pharma S.A. Announces Strong Proof-of-Concept Data from Phase 2 Trial of PDE10A Inhibitor (CPL’36), a Novel Once-Daily Treatment of Levodopa-Induced Dyskinesia in Parkinson’s DiseaseCelon Pharma S.A. announced robust and positive Phase 2 clinical trial results for its PDE10A inhibitor (CPL’36), a novel, oral, once-daily medication for the treatment of Levodopa-Induced Dyskinesia (LID) in Parkinson’s disease. The study met its primary endpoint and many of its secondary endpoints. CPL’36 demonstrated robust and consistent efficacy across all utilized scales measuring improvement in treatment of LID in Parkinson’s disease. The effect size was large and clinically meaningful. CPL’36 was previously investigated as a potential treatment for schizophrenia and demonstrated positive Phase 2 results that were reported in July 2024. Trial description The CPL’36 Phase 2 study was multinational, multicenter, randomized, placebo-controlled trial conducted in a group 105 adult patients with LID dyskinesia in Parkinson’s disease. CPL’36 was administered orally in one of two doses of 20 mg or 40 mg, once daily and placebo controlled at a ratio (1:1:1) for a period of 4 weeks. Patient baseline severity was moderate-severe to severe, as characterized by a UDysRS (Unified Dyskinesia Rating Scale) total score of approximately 45. At Week 4, the improvement in UDysRS total score (primary endpoint) for the 20 mg dose was 12.30 units (LS Mean difference from placebo, p<0.001, Cohen’s d: 0.90) and improvement for the 40 mg dose was 13.58 units (LS Mean difference from placebo, p<0.001, Cohen’s d: 1.00). CPL’36 treatment was associated with improvement in most secondary endpoints, including the UDysRS objective subscale, in which the improvement in both active groups was statistically significant from Day 7 of the treatment phase. Drug tolerability was favorable with most severe adverse events occurring in the placebo-treated patients (8.8% in placebo group, 0% in 20 mg dose and 5.7% in 40 mg dose). Treatment related emergent adverse events leading to discontinuation of study medication were recorded in 2.9% of the placebo group, 11.1% of the 20 mg dosing arm, and 8.6% in the 40 mg dosing arm. The most common adverse event reported in both active groups was somnolence with mild to moderate intensity. No deaths were reported in the trial, and one Serious Adverse Event of atrial fibrillation with moderate intensity was reported in the 40 mg dosing arm.お知らせ • Jan 15Celon Pharma S.A. to Report Fiscal Year 2024 Results on Apr 16, 2025Celon Pharma S.A. announced that they will report fiscal year 2024 results at 8:30 AM, Central European Standard Time on Apr 16, 2025Reported Earnings • Sep 20Second quarter 2024 earnings released: zł0.15 loss per share (vs zł0.18 profit in 2Q 2023)Second quarter 2024 results: zł0.15 loss per share (down from zł0.18 profit in 2Q 2023). Revenue: zł65.6m (down 3.5% from 2Q 2023). Net loss: zł8.03m (down 188% from profit in 2Q 2023). Revenue is forecast to grow 7.3% p.a. on average during the next 3 years, compared to a 3.7% growth forecast for the Pharmaceuticals industry in Germany. Over the last 3 years on average, earnings per share has fallen by 39% per year but the company’s share price has only fallen by 11% per year, which means it has not declined as severely as earnings.New Risk • Aug 12New minor risk - Shareholder dilutionThe company's shareholders have been diluted in the past year. Increase in shares outstanding: 5.3% This is considered a minor risk. Shareholder dilution occurs when there is an increase in the number of shares on issue that is not proportionally distributed between all shareholders. Often due to the company raising equity capital or some options being converted into stock. All else being equal, if there are more shares outstanding then each existing share will be entitled to a lower proportion of the company's total earnings, thus reducing earnings per share (EPS). While dilution might not always result in lower EPS (like if the company is using the capital to fund an EPS accretive acquisition) in a lot cases it does, along with lower dividends per share and less voting power at shareholder meetings. Currently, the following risks have been identified for the company: Major Risk Share price has been highly volatile over the past 3 months (16% average weekly change). Minor Risk Shareholders have been diluted in the past year (5.3% increase in shares outstanding).お知らせ • Jul 09Celon Pharma S.A. Announces Strong Proof-Of-Concept Data from Phase 2 Trial of PDE10A Inhibitor (CPL'36), a Novel Oral AntipsychoticCelon Pharma S.A. announces robust and positive Phase 2 clinical trial results for its PDE10A inhibitor (CPL’36), a novel, oral, once-daily antipsychotic. Statistically significant and clinically meaningful improvements in the primary endpoint of positive subscale of the PANSS were seen in both tested doses of CPL’36, with a dose-response effect. Management plans to discuss these highly encouraging results with regulatory agencies to advance CPL’36 towards registrational trials and global marketing approvals. Additionally, CPL’36 is being investigated as a potential treatment for levodopa-induced dyskinesia in Parkinson’s disease, with Phase 2 results expected to be reported in Fourth Quarter 2024. The CPL’36 Phase 2 study was an international, multicenter, randomized, placebo-controlled clinical trial conducted on a group of 189 adult patients hospitalized due to acute schizophrenia. CPL’36 was administered for 4 weeks in two doses of 20 and 40 mg once daily and was placebo-controlled at a ratio of 1:1:1. Patient baseline severity was moderate-severe to severe, as characterized by a PANSS total score of approximately 106. Patients were screened for up to 10 days and then randomized and treated over a four-week period, at which time the primary endpoint assessment was conducted at Day 28. At Week 4 of treatment, the reduction in positive PANSS subscale score which was the primary endpoint in the trial was 3.7 units from baseline in the 20 mg dose (LS mean difference from placebo, p<0.001, Cohen’s d: 0.73), and 6.3 units in the 40 mg dose (LS Mean difference from placebo, p<0.001, Cohen’s d: 1.38). For total PANSS score at week 4 of treatment (a key secondary endpoint), the 20 mg dose of CPL’36 demonstrated a 9.7 unit reduction from baseline compared to placebo (LS mean difference from placebo, p<0.001, Cohen’s d: 0.77), and 16.4 units in the 40 mg dose (LS mean difference from placebo, p<0.001, Cohen’s d: 1.47). Other secondary endpoints in the trial included the effects of CPL’36 on overall clinical improvement cognitive performance and functioning such as Clinical Global Impression Scale Improvement (CGI-I), Brief Assessment of Cognition in Schizophrenia (BACS), and number of participants who withdraw due to adverse events (AEs). Results across all of these endpoints were also positive. Drug tolerability was favorable with most treatment emergent adverse events characterized as mild. Exacerbations of schizophrenia represented the most common severe adverse events that were potentially related to the drug (1.5% in the placebo group, 1.8% in the 20 mg group and 3.1% in the 40 mg group). Treatment discontinuation due to adverse events likely related to the drug occurred in 3.1% patients in the placebo group, 0% patients in the 20 mg group and 7.7% patients in the 40 mg group.Upcoming Dividend • Jun 20Upcoming dividend of zł0.08 per shareEligible shareholders must have bought the stock before 27 June 2024. Payment date: 04 July 2024. The company is not currently making a profit and is not cash flow positive. Trailing yield: 0.5%. Lower than top quartile of German dividend payers (4.8%). Lower than average of industry peers (2.2%).お知らせ • Jun 18Celon Pharma Announces Results of Phase Ii Clinical Trial for Cpl’ 116, A Jak/Rock Dual Inhibitor in the Treatment of Rheumatoid Arthritis (Ra)Celon Pharma S.A. announced the successful completion of a Phase 2 trial a JAK/ROCK dual inhibitor in the treatment of Rheumatoid Arthritis (RA). The primary endpoint results are statistically significant, the primary endpoint is met. The study was a multicentre, randomised, double-blind clinical trial conducted on over 100 patients who have had inadequate therapeutic response to methotrexate. The compound was administered over the course of 12 weeks in 3 doses of 60, 120 and 240 mg BID as an add-on to methotrexate therapy. The trial was placebo-controlled. The objective of the trial was to determine the dose-dependent response to treatment. The primary endpoint was efficacy determined based on the change (compared to baseline) at week 12, measured as the Disease Activity Score-28 for RA with CRP. (DAS 28-CRP). Other, secondary endpoints included efficacy assessment measured using other scales, remission and safety of use. Findings: CPL’116 improved the patients’ condition measured with DAS28-CRP in a dose-dependent manner. Change in the DAS28-CRP score in week 12 compared to baseline was 1.702; 2.032; 2.361 and 1.668 for doses of 60, 120, 240 mg and placebo, respectively. Change in the DAS28-CRP score compared to placebo (LS MD) was 0.145 (p=0.67); 0.564 (p=0.10), and 0.887 (p=0.01) for doses of 60, 120 and 240 mg, respectively. Hence the primary endpoint results are statistically significant, the primary endpoint is met. The response to treatment in the 240 mg dose was fast – a statistically significant benefit over placebo with regard to the DAS28-CRP score was already observed at week 4 of treatment. The difference of the 240 mg dose compared to placebo was statistically significant in most of the secondary endpoints. The high remission rate observed at this dose throughout the trial (defined as DAS28-CRP<2.6) – which exceeded 45% – is particularly noteworthy. The 120 mg dose was partially efficacious. Statistically significant differences compared to placebo were observed is some measurements and scales. The overall tolerability of the compound was good and no unexpected adverse effects previously unknown for these drug classes have been observed. In the upcoming weeks, the Company will present results of pharmacokinetic and pharmacodynamic analyses for this trial, as well as detailed safety parameter analyses. The positive outcomes of this trial validate clinical development of CPL’116 as the world's first dual JAK/ROCK inhibitor in a broad spectrum of autoimmune diseases, in particular conditions with an inflammatory and fibrotic component, such as idiopathic pulmonary fibrosis (IPF) or rheumatoid arthritis-associated interstitial lung disease (RA-ILD).Reported Earnings • Apr 26Full year 2023 earnings released: zł0.55 loss per share (vs zł0.77 loss in FY 2022)Full year 2023 results: zł0.55 loss per share (improved from zł0.77 loss in FY 2022). Revenue: zł216.6m (up 12% from FY 2022). Net loss: zł28.1m (loss narrowed 28% from FY 2022). Revenue is forecast to grow 6.4% p.a. on average during the next 3 years, compared to a 3.4% growth forecast for the Pharmaceuticals industry in Germany. Over the last 3 years on average, earnings per share has fallen by 59% per year but the company’s share price has only fallen by 32% per year, which means it has not declined as severely as earnings.お知らせ • Jan 19+ 3 more updatesCelon Pharma S.A. to Report Fiscal Year 2023 Results on Apr 24, 2024Celon Pharma S.A. announced that they will report fiscal year 2023 results on Apr 24, 2024Reported Earnings • Nov 25Third quarter 2023 earnings releasedThird quarter 2023 results: Revenue: zł48.8m (up 8.8% from 3Q 2022). Net loss: zł6.82m (loss narrowed 42% from 3Q 2022). Revenue is forecast to grow 5.5% p.a. on average during the next 3 years, compared to a 3.7% growth forecast for the Pharmaceuticals industry in Germany.New Risk • Sep 22New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 13% 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 Risk Earnings are forecast to decline by an average of 13% per year for the foreseeable future. Minor Risk Share price has been volatile over the past 3 months (6.5% average weekly change).Reported Earnings • Sep 21Second quarter 2023 earnings releasedSecond quarter 2023 results: Revenue: zł69.0m (up 31% from 2Q 2022). Net income: zł9.14m (up zł17.3m from 2Q 2022). Profit margin: 13% (up from net loss in 2Q 2022). The move to profitability was primarily driven by higher revenue. Revenue is forecast to grow 6.1% p.a. on average during the next 3 years, compared to a 3.4% growth forecast for the Pharmaceuticals industry in Germany.Upcoming Dividend • Jun 22Upcoming dividend of zł0.09 per share at 0.6% yieldEligible shareholders must have bought the stock before 29 June 2023. Payment date: 06 July 2023. The company is not currently making a profit and is not cash flow positive. Trailing yield: 0.6%. Lower than top quartile of German dividend payers (4.7%). Lower than average of industry peers (2.6%).Reported Earnings • May 01Full year 2022 earnings releasedFull year 2022 results: Revenue: zł194.6m (flat on FY 2021). Net loss: zł39.3m (loss widened 238% from FY 2021). Revenue is forecast to grow 6.0% p.a. on average during the next 3 years, compared to a 3.3% growth forecast for the Pharmaceuticals industry in Germany.お知らせ • Jan 31+ 2 more updatesCelon Pharma S.A. to Report Q3, 2023 Results on Nov 22, 2023Celon Pharma S.A. announced that they will report Q3, 2023 results on Nov 22, 2023Reported Earnings • Nov 25Third quarter 2022 earnings releasedThird quarter 2022 results: Revenue: zł45.0m (up 13% from 3Q 2021). Net loss: zł11.7m (loss widened 49% from 3Q 2021). Revenue is forecast to grow 5.2% p.a. on average during the next 3 years, compared to a 3.8% growth forecast for the Pharmaceuticals industry in Germany.Reported Earnings • Sep 30Second quarter 2022 earnings releasedSecond quarter 2022 results: Revenue: zł52.8m (down 8.2% from 2Q 2021). Net loss: zł8.11m (down zł10.1m from profit in 2Q 2021). Revenue is forecast to grow 5.4% p.a. on average during the next 3 years, compared to a 4.2% growth forecast for the Pharmaceuticals industry in Germany.Upcoming Dividend • Jun 23Upcoming dividend of zł0.29 per shareEligible shareholders must have bought the stock before 30 June 2022. Payment date: 11 July 2022. The company is not currently making a profit and is not cash flow positive. Trailing yield: 1.9%. Lower than top quartile of German dividend payers (4.6%). Lower than average of industry peers (2.7%).お知らせ • May 31Celon Pharma S.A., Annual General Meeting, Jun 22, 2022Celon Pharma S.A., Annual General Meeting, Jun 22, 2022, at 10:00 Central European Standard Time.Reported Earnings • Dec 03Third quarter 2021 earnings: EPS in line with analyst expectations despite revenue beatThird quarter 2021 results: zł0.17 loss per share (down from zł0.04 profit in 3Q 2020). Revenue: zł39.9m (up 4.8% from 3Q 2020). Net loss: zł7.83m (down zł9.64m from profit in 3Q 2020). Revenue exceeded analyst estimates by 9.5%. Over the next year, revenue is forecast to grow 39%, compared to a 6.9% growth forecast for the industry in Germany.Reported Earnings • Oct 03Second quarter 2021 earnings released: EPS zł0.01 (vs zł0.25 in 2Q 2020)The company reported a mediocre second quarter result with weaker earnings and profit margins, although revenues improved. Second quarter 2021 results: Revenue: zł57.7m (up 48% from 2Q 2020). Net income: zł2.02m (down 82% from 2Q 2020). Profit margin: 3.5% (down from 29% in 2Q 2020).Reported Earnings • Oct 03Second quarter 2021 earnings released: EPS zł0.01 (vs zł0.25 in 2Q 2020)The company reported a mediocre second quarter result with weaker earnings and profit margins, although revenues improved. Second quarter 2021 results: Revenue: zł57.7m (up 48% from 2Q 2020). Net income: zł2.02m (down 82% from 2Q 2020). Profit margin: 3.5% (down from 29% in 2Q 2020).お知らせ • Jun 23Celon Pharma Files for Approval of Phase II Trial of CPL’280, a Second Generation GPR40 Agonist, in Type 2 DiabetesCelon Pharma announced filing for approval to start a Phase II clinical study of CPL’280, its second generation GPR40 agonist in type 2 diabetes. This double-blind, randomized, placebo-controlled, multiple dose Phase II study will evaluate the ability of orally administered CPL’280 to control blood glucose in patients with diagnosed type 2 diabetes. Both naive and metformin-inadequate responders will be administered once-daily CPL’280 for two weeks. Safety and pharmacokinetics will be secondary endpoints. The trial plans to include 80 patients. Celon Pharma expects to dose the first patient in Fourth Quarter 2021 and top-line results are anticipated in first half of 2022. CPL’280 was designed to improve on the drawbacks of the first generation GPR40 agonists. The molecule, which is structurally different from the first generation agonists, is free from known risk factors associated with liver injury, i.e. bile acid transporter inhibition and the formation of reactive metabolites. The molecule showed strong evidence of safety both in preclinical and Phase I clinical studies including liver safety. Liver injury was a known risk factor identified for fasiglifam, which was the most advanced first generation GPR40 agonist which was terminated in late-stage clinical development.株主還元8RPDE PharmaceuticalsDE 市場7D0.4%5.7%2.4%1Y-7.5%25.9%1.2%株主還元を見る業界別リターン: 8RP過去 1 年間で25.9 % の収益を上げたGerman Pharmaceuticals業界を下回りました。リターン対市場: 8RPは、過去 1 年間で1.2 % のリターンを上げたGerman市場を下回りました。価格変動Is 8RP's price volatile compared to industry and market?8RP volatility8RP Average Weekly Movement15.1%Pharmaceuticals Industry Average Movement6.4%Market Average Movement6.1%10% most volatile stocks in DE Market13.4%10% least volatile stocks in DE Market2.7%安定した株価: 8RPの株価は、 German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: 8RPの 週次ボラティリティ は、過去 1 年間で10%から15%に増加しました。会社概要設立従業員CEO（最高経営責任者ウェブサイト2002566Maciej Wieczorekwww.celonpharma.comCelon Pharma S.A.は総合製薬企業で、医薬品および製剤の研究、製造、販売に従事している。がん、神経疾患、糖尿病、その他代謝異常の治療薬を提供している。同社は2002年に設立され、ポーランドのロミアンキに拠点を置く。Celon Pharma S.A.はGlatton Sp.もっと見るCelon Pharma S.A. 基礎のまとめCelon Pharma の収益と売上を時価総額と比較するとどうか。8RP 基礎統計学時価総額€266.21m収益（TTM）-€28.88m売上高(TTM)€53.23m5.0xP/Sレシオ-9.2xPER（株価収益率8RP 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8RP 損益計算書（TTM）収益zł225.60m売上原価zł71.47m売上総利益zł154.13mその他の費用zł276.52m収益-zł122.39m直近の収益報告Sep 30, 2025次回決算日Sep 16, 2026一株当たり利益（EPS）-2.27グロス・マージン68.32%純利益率-54.25%有利子負債／自己資本比率0.1%8RP 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2026/05/25 18:51終値2026/05/22 00:00収益2025/09/30年間収益2024/12/31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Celon Pharma S.A. 3 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。7 アナリスト機関Beata Szparaga-WasniewskaBiuro maklerskie mBankuTomasz SokolowskiErste Bank Polska S.A.Piotr ZielonkaErste Bank Polska S.A.4 その他のアナリストを表示
お知らせ • Jan 27+ 3 more updatesCelon Pharma S.A. to Report Fiscal Year 2025 Results on Apr 22, 2026Celon Pharma S.A. announced that they will report fiscal year 2025 results at 8:30 AM, Central European Standard Time on Apr 22, 2026
お知らせ • Nov 15Celon Pharma S.A. to Report Q3, 2025 Results on Nov 19, 2025Celon Pharma S.A. announced that they will report Q3, 2025 results on Nov 19, 2025
お知らせ • Oct 10FDA Clears Celon Pharma's Schizophrenia Drug for Phase 3 TrialCelon Pharma S.A. announced it has secured a key regulatory milestone for its lead neuroscience program. The U.S. Food and Drug Administration (FDA) provided positive feedback clearing the path for Phase 3 testing of CPL'36, the company's novel second-generation PDE10A inhibitor for schizophrenia. The FDA confirmed that Celon Pharma's existing preclinical data are sufficient to begin pivotal studies and approved the proposed Phase 3 program, which includes two 28-day randomized, double-blind trials in patients with acute schizophrenia episodes and a 12-month open-label extension to establish long-term safety. The FDA also agreed that "treatment of schizophrenia" is the appropriate indication for CPL'36, confirming the compound's potential for broad labeling at registration. The Agency supported Celon Pharma's plan to conduct required supportive studies--including drug-drug interaction (DDI), QTc, and mass balance--concurrently with the pivotal trials, provided key safety measures are in place. This parallel development plan is expected to streamline timelines and maintain strategic flexibility. Strong Efficacy in Phase 2 Sets the Stage: CPL'36 previously demonstrated robust and clinically meaningful efficacy in a 189-patient Phase 2 trial, with both the 20 mg and 40 mg doses producing statistically significant improvements versus placebo across positive and total PANSS scores. The 40 mg dose also showed early signs of cognitive benefit. At Week 4, the positive PANSS subscale improved by 3.7 points for the 20 mg dose.
お知らせ • Aug 21Celon Pharma S.A. to Report First Half, 2025 Results on Sep 17, 2025Celon Pharma S.A. announced that they will report first half, 2025 results on Sep 17, 2025
お知らせ • Mar 05Celon Pharma S.A. Announces Strong Proof-of-Concept Data from Phase 2 Trial of PDE10A Inhibitor (CPL’36), a Novel Once-Daily Treatment of Levodopa-Induced Dyskinesia in Parkinson’s DiseaseCelon Pharma S.A. announced robust and positive Phase 2 clinical trial results for its PDE10A inhibitor (CPL’36), a novel, oral, once-daily medication for the treatment of Levodopa-Induced Dyskinesia (LID) in Parkinson’s disease. The study met its primary endpoint and many of its secondary endpoints. CPL’36 demonstrated robust and consistent efficacy across all utilized scales measuring improvement in treatment of LID in Parkinson’s disease. The effect size was large and clinically meaningful. CPL’36 was previously investigated as a potential treatment for schizophrenia and demonstrated positive Phase 2 results that were reported in July 2024. Trial description The CPL’36 Phase 2 study was multinational, multicenter, randomized, placebo-controlled trial conducted in a group 105 adult patients with LID dyskinesia in Parkinson’s disease. CPL’36 was administered orally in one of two doses of 20 mg or 40 mg, once daily and placebo controlled at a ratio (1:1:1) for a period of 4 weeks. Patient baseline severity was moderate-severe to severe, as characterized by a UDysRS (Unified Dyskinesia Rating Scale) total score of approximately 45. At Week 4, the improvement in UDysRS total score (primary endpoint) for the 20 mg dose was 12.30 units (LS Mean difference from placebo, p<0.001, Cohen’s d: 0.90) and improvement for the 40 mg dose was 13.58 units (LS Mean difference from placebo, p<0.001, Cohen’s d: 1.00). CPL’36 treatment was associated with improvement in most secondary endpoints, including the UDysRS objective subscale, in which the improvement in both active groups was statistically significant from Day 7 of the treatment phase. Drug tolerability was favorable with most severe adverse events occurring in the placebo-treated patients (8.8% in placebo group, 0% in 20 mg dose and 5.7% in 40 mg dose). Treatment related emergent adverse events leading to discontinuation of study medication were recorded in 2.9% of the placebo group, 11.1% of the 20 mg dosing arm, and 8.6% in the 40 mg dosing arm. The most common adverse event reported in both active groups was somnolence with mild to moderate intensity. No deaths were reported in the trial, and one Serious Adverse Event of atrial fibrillation with moderate intensity was reported in the 40 mg dosing arm.
お知らせ • Jan 15Celon Pharma S.A. to Report Fiscal Year 2024 Results on Apr 16, 2025Celon Pharma S.A. announced that they will report fiscal year 2024 results at 8:30 AM, Central European Standard Time on Apr 16, 2025
お知らせ • Jan 27+ 3 more updatesCelon Pharma S.A. to Report Fiscal Year 2025 Results on Apr 22, 2026Celon Pharma S.A. announced that they will report fiscal year 2025 results at 8:30 AM, Central European Standard Time on Apr 22, 2026
お知らせ • Nov 15Celon Pharma S.A. to Report Q3, 2025 Results on Nov 19, 2025Celon Pharma S.A. announced that they will report Q3, 2025 results on Nov 19, 2025
お知らせ • Oct 10FDA Clears Celon Pharma's Schizophrenia Drug for Phase 3 TrialCelon Pharma S.A. announced it has secured a key regulatory milestone for its lead neuroscience program. The U.S. Food and Drug Administration (FDA) provided positive feedback clearing the path for Phase 3 testing of CPL'36, the company's novel second-generation PDE10A inhibitor for schizophrenia. The FDA confirmed that Celon Pharma's existing preclinical data are sufficient to begin pivotal studies and approved the proposed Phase 3 program, which includes two 28-day randomized, double-blind trials in patients with acute schizophrenia episodes and a 12-month open-label extension to establish long-term safety. The FDA also agreed that "treatment of schizophrenia" is the appropriate indication for CPL'36, confirming the compound's potential for broad labeling at registration. The Agency supported Celon Pharma's plan to conduct required supportive studies--including drug-drug interaction (DDI), QTc, and mass balance--concurrently with the pivotal trials, provided key safety measures are in place. This parallel development plan is expected to streamline timelines and maintain strategic flexibility. Strong Efficacy in Phase 2 Sets the Stage: CPL'36 previously demonstrated robust and clinically meaningful efficacy in a 189-patient Phase 2 trial, with both the 20 mg and 40 mg doses producing statistically significant improvements versus placebo across positive and total PANSS scores. The 40 mg dose also showed early signs of cognitive benefit. At Week 4, the positive PANSS subscale improved by 3.7 points for the 20 mg dose.
お知らせ • Aug 21Celon Pharma S.A. to Report First Half, 2025 Results on Sep 17, 2025Celon Pharma S.A. announced that they will report first half, 2025 results on Sep 17, 2025
お知らせ • Mar 05Celon Pharma S.A. Announces Strong Proof-of-Concept Data from Phase 2 Trial of PDE10A Inhibitor (CPL’36), a Novel Once-Daily Treatment of Levodopa-Induced Dyskinesia in Parkinson’s DiseaseCelon Pharma S.A. announced robust and positive Phase 2 clinical trial results for its PDE10A inhibitor (CPL’36), a novel, oral, once-daily medication for the treatment of Levodopa-Induced Dyskinesia (LID) in Parkinson’s disease. The study met its primary endpoint and many of its secondary endpoints. CPL’36 demonstrated robust and consistent efficacy across all utilized scales measuring improvement in treatment of LID in Parkinson’s disease. The effect size was large and clinically meaningful. CPL’36 was previously investigated as a potential treatment for schizophrenia and demonstrated positive Phase 2 results that were reported in July 2024. Trial description The CPL’36 Phase 2 study was multinational, multicenter, randomized, placebo-controlled trial conducted in a group 105 adult patients with LID dyskinesia in Parkinson’s disease. CPL’36 was administered orally in one of two doses of 20 mg or 40 mg, once daily and placebo controlled at a ratio (1:1:1) for a period of 4 weeks. Patient baseline severity was moderate-severe to severe, as characterized by a UDysRS (Unified Dyskinesia Rating Scale) total score of approximately 45. At Week 4, the improvement in UDysRS total score (primary endpoint) for the 20 mg dose was 12.30 units (LS Mean difference from placebo, p<0.001, Cohen’s d: 0.90) and improvement for the 40 mg dose was 13.58 units (LS Mean difference from placebo, p<0.001, Cohen’s d: 1.00). CPL’36 treatment was associated with improvement in most secondary endpoints, including the UDysRS objective subscale, in which the improvement in both active groups was statistically significant from Day 7 of the treatment phase. Drug tolerability was favorable with most severe adverse events occurring in the placebo-treated patients (8.8% in placebo group, 0% in 20 mg dose and 5.7% in 40 mg dose). Treatment related emergent adverse events leading to discontinuation of study medication were recorded in 2.9% of the placebo group, 11.1% of the 20 mg dosing arm, and 8.6% in the 40 mg dosing arm. The most common adverse event reported in both active groups was somnolence with mild to moderate intensity. No deaths were reported in the trial, and one Serious Adverse Event of atrial fibrillation with moderate intensity was reported in the 40 mg dosing arm.
お知らせ • Jan 15Celon Pharma S.A. to Report Fiscal Year 2024 Results on Apr 16, 2025Celon Pharma S.A. announced that they will report fiscal year 2024 results at 8:30 AM, Central European Standard Time on Apr 16, 2025
Reported Earnings • Sep 20Second quarter 2024 earnings released: zł0.15 loss per share (vs zł0.18 profit in 2Q 2023)Second quarter 2024 results: zł0.15 loss per share (down from zł0.18 profit in 2Q 2023). Revenue: zł65.6m (down 3.5% from 2Q 2023). Net loss: zł8.03m (down 188% from profit in 2Q 2023). Revenue is forecast to grow 7.3% p.a. on average during the next 3 years, compared to a 3.7% growth forecast for the Pharmaceuticals industry in Germany. Over the last 3 years on average, earnings per share has fallen by 39% per year but the company’s share price has only fallen by 11% per year, which means it has not declined as severely as earnings.
New Risk • Aug 12New minor risk - Shareholder dilutionThe company's shareholders have been diluted in the past year. Increase in shares outstanding: 5.3% This is considered a minor risk. Shareholder dilution occurs when there is an increase in the number of shares on issue that is not proportionally distributed between all shareholders. Often due to the company raising equity capital or some options being converted into stock. All else being equal, if there are more shares outstanding then each existing share will be entitled to a lower proportion of the company's total earnings, thus reducing earnings per share (EPS). While dilution might not always result in lower EPS (like if the company is using the capital to fund an EPS accretive acquisition) in a lot cases it does, along with lower dividends per share and less voting power at shareholder meetings. Currently, the following risks have been identified for the company: Major Risk Share price has been highly volatile over the past 3 months (16% average weekly change). Minor Risk Shareholders have been diluted in the past year (5.3% increase in shares outstanding).
お知らせ • Jul 09Celon Pharma S.A. Announces Strong Proof-Of-Concept Data from Phase 2 Trial of PDE10A Inhibitor (CPL'36), a Novel Oral AntipsychoticCelon Pharma S.A. announces robust and positive Phase 2 clinical trial results for its PDE10A inhibitor (CPL’36), a novel, oral, once-daily antipsychotic. Statistically significant and clinically meaningful improvements in the primary endpoint of positive subscale of the PANSS were seen in both tested doses of CPL’36, with a dose-response effect. Management plans to discuss these highly encouraging results with regulatory agencies to advance CPL’36 towards registrational trials and global marketing approvals. Additionally, CPL’36 is being investigated as a potential treatment for levodopa-induced dyskinesia in Parkinson’s disease, with Phase 2 results expected to be reported in Fourth Quarter 2024. The CPL’36 Phase 2 study was an international, multicenter, randomized, placebo-controlled clinical trial conducted on a group of 189 adult patients hospitalized due to acute schizophrenia. CPL’36 was administered for 4 weeks in two doses of 20 and 40 mg once daily and was placebo-controlled at a ratio of 1:1:1. Patient baseline severity was moderate-severe to severe, as characterized by a PANSS total score of approximately 106. Patients were screened for up to 10 days and then randomized and treated over a four-week period, at which time the primary endpoint assessment was conducted at Day 28. At Week 4 of treatment, the reduction in positive PANSS subscale score which was the primary endpoint in the trial was 3.7 units from baseline in the 20 mg dose (LS mean difference from placebo, p<0.001, Cohen’s d: 0.73), and 6.3 units in the 40 mg dose (LS Mean difference from placebo, p<0.001, Cohen’s d: 1.38). For total PANSS score at week 4 of treatment (a key secondary endpoint), the 20 mg dose of CPL’36 demonstrated a 9.7 unit reduction from baseline compared to placebo (LS mean difference from placebo, p<0.001, Cohen’s d: 0.77), and 16.4 units in the 40 mg dose (LS mean difference from placebo, p<0.001, Cohen’s d: 1.47). Other secondary endpoints in the trial included the effects of CPL’36 on overall clinical improvement cognitive performance and functioning such as Clinical Global Impression Scale Improvement (CGI-I), Brief Assessment of Cognition in Schizophrenia (BACS), and number of participants who withdraw due to adverse events (AEs). Results across all of these endpoints were also positive. Drug tolerability was favorable with most treatment emergent adverse events characterized as mild. Exacerbations of schizophrenia represented the most common severe adverse events that were potentially related to the drug (1.5% in the placebo group, 1.8% in the 20 mg group and 3.1% in the 40 mg group). Treatment discontinuation due to adverse events likely related to the drug occurred in 3.1% patients in the placebo group, 0% patients in the 20 mg group and 7.7% patients in the 40 mg group.
Upcoming Dividend • Jun 20Upcoming dividend of zł0.08 per shareEligible shareholders must have bought the stock before 27 June 2024. Payment date: 04 July 2024. The company is not currently making a profit and is not cash flow positive. Trailing yield: 0.5%. Lower than top quartile of German dividend payers (4.8%). Lower than average of industry peers (2.2%).
お知らせ • Jun 18Celon Pharma Announces Results of Phase Ii Clinical Trial for Cpl’ 116, A Jak/Rock Dual Inhibitor in the Treatment of Rheumatoid Arthritis (Ra)Celon Pharma S.A. announced the successful completion of a Phase 2 trial a JAK/ROCK dual inhibitor in the treatment of Rheumatoid Arthritis (RA). The primary endpoint results are statistically significant, the primary endpoint is met. The study was a multicentre, randomised, double-blind clinical trial conducted on over 100 patients who have had inadequate therapeutic response to methotrexate. The compound was administered over the course of 12 weeks in 3 doses of 60, 120 and 240 mg BID as an add-on to methotrexate therapy. The trial was placebo-controlled. The objective of the trial was to determine the dose-dependent response to treatment. The primary endpoint was efficacy determined based on the change (compared to baseline) at week 12, measured as the Disease Activity Score-28 for RA with CRP. (DAS 28-CRP). Other, secondary endpoints included efficacy assessment measured using other scales, remission and safety of use. Findings: CPL’116 improved the patients’ condition measured with DAS28-CRP in a dose-dependent manner. Change in the DAS28-CRP score in week 12 compared to baseline was 1.702; 2.032; 2.361 and 1.668 for doses of 60, 120, 240 mg and placebo, respectively. Change in the DAS28-CRP score compared to placebo (LS MD) was 0.145 (p=0.67); 0.564 (p=0.10), and 0.887 (p=0.01) for doses of 60, 120 and 240 mg, respectively. Hence the primary endpoint results are statistically significant, the primary endpoint is met. The response to treatment in the 240 mg dose was fast – a statistically significant benefit over placebo with regard to the DAS28-CRP score was already observed at week 4 of treatment. The difference of the 240 mg dose compared to placebo was statistically significant in most of the secondary endpoints. The high remission rate observed at this dose throughout the trial (defined as DAS28-CRP<2.6) – which exceeded 45% – is particularly noteworthy. The 120 mg dose was partially efficacious. Statistically significant differences compared to placebo were observed is some measurements and scales. The overall tolerability of the compound was good and no unexpected adverse effects previously unknown for these drug classes have been observed. In the upcoming weeks, the Company will present results of pharmacokinetic and pharmacodynamic analyses for this trial, as well as detailed safety parameter analyses. The positive outcomes of this trial validate clinical development of CPL’116 as the world's first dual JAK/ROCK inhibitor in a broad spectrum of autoimmune diseases, in particular conditions with an inflammatory and fibrotic component, such as idiopathic pulmonary fibrosis (IPF) or rheumatoid arthritis-associated interstitial lung disease (RA-ILD).
Reported Earnings • Apr 26Full year 2023 earnings released: zł0.55 loss per share (vs zł0.77 loss in FY 2022)Full year 2023 results: zł0.55 loss per share (improved from zł0.77 loss in FY 2022). Revenue: zł216.6m (up 12% from FY 2022). Net loss: zł28.1m (loss narrowed 28% from FY 2022). Revenue is forecast to grow 6.4% p.a. on average during the next 3 years, compared to a 3.4% growth forecast for the Pharmaceuticals industry in Germany. Over the last 3 years on average, earnings per share has fallen by 59% per year but the company’s share price has only fallen by 32% per year, which means it has not declined as severely as earnings.
お知らせ • Jan 19+ 3 more updatesCelon Pharma S.A. to Report Fiscal Year 2023 Results on Apr 24, 2024Celon Pharma S.A. announced that they will report fiscal year 2023 results on Apr 24, 2024
Reported Earnings • Nov 25Third quarter 2023 earnings releasedThird quarter 2023 results: Revenue: zł48.8m (up 8.8% from 3Q 2022). Net loss: zł6.82m (loss narrowed 42% from 3Q 2022). Revenue is forecast to grow 5.5% p.a. on average during the next 3 years, compared to a 3.7% growth forecast for the Pharmaceuticals industry in Germany.
New Risk • Sep 22New major risk - Revenue and earnings growthEarnings are forecast to decline by an average of 13% 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 Risk Earnings are forecast to decline by an average of 13% per year for the foreseeable future. Minor Risk Share price has been volatile over the past 3 months (6.5% average weekly change).
Reported Earnings • Sep 21Second quarter 2023 earnings releasedSecond quarter 2023 results: Revenue: zł69.0m (up 31% from 2Q 2022). Net income: zł9.14m (up zł17.3m from 2Q 2022). Profit margin: 13% (up from net loss in 2Q 2022). The move to profitability was primarily driven by higher revenue. Revenue is forecast to grow 6.1% p.a. on average during the next 3 years, compared to a 3.4% growth forecast for the Pharmaceuticals industry in Germany.
Upcoming Dividend • Jun 22Upcoming dividend of zł0.09 per share at 0.6% yieldEligible shareholders must have bought the stock before 29 June 2023. Payment date: 06 July 2023. The company is not currently making a profit and is not cash flow positive. Trailing yield: 0.6%. Lower than top quartile of German dividend payers (4.7%). Lower than average of industry peers (2.6%).
Reported Earnings • May 01Full year 2022 earnings releasedFull year 2022 results: Revenue: zł194.6m (flat on FY 2021). Net loss: zł39.3m (loss widened 238% from FY 2021). Revenue is forecast to grow 6.0% p.a. on average during the next 3 years, compared to a 3.3% growth forecast for the Pharmaceuticals industry in Germany.
お知らせ • Jan 31+ 2 more updatesCelon Pharma S.A. to Report Q3, 2023 Results on Nov 22, 2023Celon Pharma S.A. announced that they will report Q3, 2023 results on Nov 22, 2023
Reported Earnings • Nov 25Third quarter 2022 earnings releasedThird quarter 2022 results: Revenue: zł45.0m (up 13% from 3Q 2021). Net loss: zł11.7m (loss widened 49% from 3Q 2021). Revenue is forecast to grow 5.2% p.a. on average during the next 3 years, compared to a 3.8% growth forecast for the Pharmaceuticals industry in Germany.
Reported Earnings • Sep 30Second quarter 2022 earnings releasedSecond quarter 2022 results: Revenue: zł52.8m (down 8.2% from 2Q 2021). Net loss: zł8.11m (down zł10.1m from profit in 2Q 2021). Revenue is forecast to grow 5.4% p.a. on average during the next 3 years, compared to a 4.2% growth forecast for the Pharmaceuticals industry in Germany.
Upcoming Dividend • Jun 23Upcoming dividend of zł0.29 per shareEligible shareholders must have bought the stock before 30 June 2022. Payment date: 11 July 2022. The company is not currently making a profit and is not cash flow positive. Trailing yield: 1.9%. Lower than top quartile of German dividend payers (4.6%). Lower than average of industry peers (2.7%).
お知らせ • May 31Celon Pharma S.A., Annual General Meeting, Jun 22, 2022Celon Pharma S.A., Annual General Meeting, Jun 22, 2022, at 10:00 Central European Standard Time.
Reported Earnings • Dec 03Third quarter 2021 earnings: EPS in line with analyst expectations despite revenue beatThird quarter 2021 results: zł0.17 loss per share (down from zł0.04 profit in 3Q 2020). Revenue: zł39.9m (up 4.8% from 3Q 2020). Net loss: zł7.83m (down zł9.64m from profit in 3Q 2020). Revenue exceeded analyst estimates by 9.5%. Over the next year, revenue is forecast to grow 39%, compared to a 6.9% growth forecast for the industry in Germany.
Reported Earnings • Oct 03Second quarter 2021 earnings released: EPS zł0.01 (vs zł0.25 in 2Q 2020)The company reported a mediocre second quarter result with weaker earnings and profit margins, although revenues improved. Second quarter 2021 results: Revenue: zł57.7m (up 48% from 2Q 2020). Net income: zł2.02m (down 82% from 2Q 2020). Profit margin: 3.5% (down from 29% in 2Q 2020).
Reported Earnings • Oct 03Second quarter 2021 earnings released: EPS zł0.01 (vs zł0.25 in 2Q 2020)The company reported a mediocre second quarter result with weaker earnings and profit margins, although revenues improved. Second quarter 2021 results: Revenue: zł57.7m (up 48% from 2Q 2020). Net income: zł2.02m (down 82% from 2Q 2020). Profit margin: 3.5% (down from 29% in 2Q 2020).
お知らせ • Jun 23Celon Pharma Files for Approval of Phase II Trial of CPL’280, a Second Generation GPR40 Agonist, in Type 2 DiabetesCelon Pharma announced filing for approval to start a Phase II clinical study of CPL’280, its second generation GPR40 agonist in type 2 diabetes. This double-blind, randomized, placebo-controlled, multiple dose Phase II study will evaluate the ability of orally administered CPL’280 to control blood glucose in patients with diagnosed type 2 diabetes. Both naive and metformin-inadequate responders will be administered once-daily CPL’280 for two weeks. Safety and pharmacokinetics will be secondary endpoints. The trial plans to include 80 patients. Celon Pharma expects to dose the first patient in Fourth Quarter 2021 and top-line results are anticipated in first half of 2022. CPL’280 was designed to improve on the drawbacks of the first generation GPR40 agonists. The molecule, which is structurally different from the first generation agonists, is free from known risk factors associated with liver injury, i.e. bile acid transporter inhibition and the formation of reactive metabolites. The molecule showed strong evidence of safety both in preclinical and Phase I clinical studies including liver safety. Liver injury was a known risk factor identified for fasiglifam, which was the most advanced first generation GPR40 agonist which was terminated in late-stage clinical development.
