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Übersicht Suchergebnisse zum Thema BILIA

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DiGilead's investigational seladelpar shows promise in primary biliary cholangitis3
09.05.Merck' Keytruda Receives Approval From Health Canada For Biliary Tract Carcinoma In Adults219KENILWORTH (NJ) (dpa-AFX) - Thursday, Merck & Co., Inc. (MRK) announced that Health Canada has approved Keytruda, also known as pembrolizumab, for the treatment of adult patients with locally...
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09.05.Health Canada Approves KEYTRUDA for adult patients with locally advanced unresectable or metastatic biliary tract carcinoma, in combination with gemcitabine-based chemotherapy1
25.04.Compass gains FDA Fast Track status for biliary tract cancer candidate1
24.04.Bilia AB: Bulletin from Bilia's annual general meeting 20241.636Bilia AB's AGM took place on Wednesday, 24 April 2024. Adoption of the profit and loss statement and balance sheet The profit and loss statements and the balance sheets of the parent company and the...
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16.04.AstraZeneca's Imfinzi/Chemo Combo Doubles Overall Survival In Biliary Tract Cancer Patients At 3 Years, Data Shows264
16.04.AstraZeneca shares positive three-year results for Imfinzi combination in biliary tract cancer284
03.04.Ascletis pulls FXR agonist from pipeline over phase 2 primary biliary cholangitis data1
02.04.Jazz Pharmaceuticals plc: Jazz Pharmaceuticals Completes Zanidatamab Biologics License Application for Previously Treated HER2-Positive Metastatic Biliary Tract Cancer122Submission based on data from Phase 2b HERIZON-BTC-01 trial, which met its primary endpoint in patients receiving zanidatamab for previously treated HER2-positive biliary tract cancer (BTC) Confirmatory...
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20.03.Biliary Tumor drugs in development, 20231
12.02.CymaBay Therapeutics: CymaBay Announces FDA Acceptance of NDA and Priority Review for Seladelpar for the Treatment of Primary Biliary Cholangitis241- FDA has granted Priority Review with a target PDUFA date of August 14 - NEWARK, Calif., Feb. 12, 2024 /PRNewswire/ -- CymaBay Therapeutics, Inc. (NASDAQ: CBAY), a biopharmaceutical company focused...
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07.02.Bilia AB: Full-Year Report 1 Jan - 31 Dec 2023268Stable results in Sweden and Western Europe Fourth quarter 2023Net turnover amounted to SEK 10,108 M (10,425), a decrease of 3 per cent.Operational earnings amounted to SEK 414 M (574).Sweden and Western...
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05.02.Tharimmune, Inc.: Tharimmune Announces Dosing of First Patient in Phase 1 Clinical Trial of TH104, its Lead Candidate for Pruritus in Primary Biliary Cholangitis241Phase 1 clinical trial dosing of first patient complete; primary objective to assess safety/tolerability and absolute bioavailability of TH104Phase 1 study expected to be completed in 1Q24 with topline...
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08.01.Compugen to Receive $10 Million Milestone Payment Following Dosing of First Patient in AstraZeneca Phase 3 Rilvegostomig Trial in Biliary Tract Cancer664HOLON, Israel, Jan. 8, 2024 /PRNewswire/ -- Compugen Ltd. (Nasdaq: CGEN) (TASE: CGEN) a clinical-stage cancer immunotherapy company and a pioneer in computational target discovery, today announced...
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19.12.23Eisai Submits Marketing Authorization Application in Japan for Anticancer Agent Tasurgratinib for Biliary Tract Cancer with Fgfr2 Gene Fusion285TOKYO, Dec 19, 2023 - (JCN Newswire) - Eisai Co., Ltd. announced today that it has submitted a marketing authorization application in Japan for its in-house discovered fibroblast growth factor (FGF)...
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18.12.23Eisai files biliary tract cancer drug tasurgratinib in Japan6
18.12.23CymaBay seeks FDA approval for primary biliary cholangitis therapy4
08.12.23GENFIT S.A.: GENFIT Updates 2024 Outlook Following Acceptance of Elafibranor Filings in Primary Biliary Cholangitis (PBC)345US Food and Drug Administration (FDA) has granted Priority Review for New Drug Application (NDA) for elafibranor in PBC, and European Medicine Agency (EMA) has also validated the Marketing Authorization...
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27.11.23Tharimmune, Inc.: Tharimmune Reports Positive Phase 1 Data on TH104, its Lead Therapeutic Candidate, for Chronic Pruritis in Primary Biliary Cholangitis251Phase 1 ex-US trial achieved primary objective of predictable pharmacokinetic profiling with favorable safety and tolerabilityCompany expects to engage FDA on Phase 2 trial design and expects topline...
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