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GNFTF News and Press, Genfit Ord From 04/04/24

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Company Name: Genfit Ord
Stock Symbol: GNFTF
Market: OTC
Website: genfit.com

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GNFTF - GENFIT Reports Full-Year 2023 Financial Results and Provides Corporate Update

Cash and cash equivalents totaled €77.8 million as of December 31, 2023 Revenues amounted to €28.6 million as of December 31, 2023 including a milestone payment of €13.3 million Topline interim data for Phase 2 UNVEIL-IT ® trial in ACLF expect...

GNFTF - Inventiva resumes Phase 3 study for NASH drug, stock up 6%

2024-03-08 13:46:51 ET More on Inventiva Inventiva: Biotech To Consider Despite Short NASH Study Enrollment Pause Inventiva drops after adverse event in Phase 3 trial for NASH drug Seeking Alpha’s Quant Rating on Inventiva Historical earnings data for ...

GNFTF - GENFIT Announces Revenues and Cash Position as of December 31, 2023

Cash and cash equivalents totaled €77.8 million as of December 31, 2023 Revenues amounted to €28.6 million as of December 31, 2023 including a milestone payment of €13.3 million Upcoming FDA PDUFA action date for elafibranor in PBC: June 10, 2024 ...

GNFTF - Inventiva drops after adverse event in Phase 3 trial for NASH drug

2024-02-16 13:52:08 ET More on Inventiva Inventiva reports 9M results Seeking Alpha’s Quant Rating on Inventiva Historical earnings data for Inventiva Financial information for Inventiva Read the full article on Seeking Alpha For furthe...

GNFTF - GENFIT Announces 2024 Financial Calendar  

Lille (France), Cambridge (Massachusetts, United States), Zurich (Switzerland), January 15, 2024 - GENFIT (Nasdaq and Euronext: GNFT) , a late-stage biopharmaceutical company dedicated to improving the lives of patients with rare and life-threatening liver diseases, today announced its prov...

GNFTF - GENFIT Updates 2024 Outlook Following Acceptance of Elafibranor Filings in Primary Biliary Cholangitis (PBC)

US 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 Application (MAA) for elafibranor. Acceptance triggers a first milestone payment. ...

GNFTF - Ipsen confirms U.S. FDA grants priority review for New Drug Application for elafibranor for the treatment of rare cholestatic liver disease, PBC

New Drug Application granted priority review with PDUFA date set for June 10, 2024 European Medicines Agency (EMA) has also validated the Marketing Authorization Application (MAA) for elafibranor Investigational elafibranor is the first novel second-line treatment for primary bili...

GNFTF - GENFIT Announces Publication in the Journal of Hepatology on the Accurate Performance of NIS2+(TM) as a Screening Tool for the Enrollment of Patients in MASH Clinical Trials

The paper published in Journal of Hepatology demonstrates that NIS2+™ technology could significantly reduce liver biopsy failure rate and maximizes accuracy of patient selection for MASH 1 clinical trials Growing body of clinical evidence: this is the third ...

GNFTF - GENFIT Highlights ACLF Development Strategy at "ACLF Day" during AASLD The Liver Meeting® 2023

GENFIT highlighted new focus and development strategy in Acute On-Chronic Liver Failure (ACLF) ACLF is a very serious condition affecting ~294,000 1 2 patients with chronic liver diseases in the USA and Europe every year and is associated with multi-organ failure and h...

GNFTF - GENFIT: Results from Ipsen's ELATIVE® pivotal Phase III trial of elafibranor in PBC presented as late breaking data at AASLD congress and published in New England Journal of Medicine

ELATIVE® Phase III trial confirms potential for investigational elafibranor as a novel, first-in-class, dual PPAR α,δ agonist for patients with Primary Biliary Cholangitis. Elafibranor demonstrates significant improvements in biomarkers of disease progression versus pla...

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