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Clinical trial of lanifibranor in adult patients with nonalcoholic steatohepatitis without cirrhosis and stage 2/grade 3 liver fibrosis
THE AIM OF THIS STUDY IS TO SEE IF A DRUG NOT YET APPROVED BY ANY REGULATORY AUTHORITY FOR MARKETING, CALLED LANIFIBIBRANOR, WILL HELP IN THE TREATMENT OF NON-ALCOHOLIC STEATOHEPATITIS (NASH) WITHOUT CIRRHOSIS AND LIVER FIBROSIS STAGE (THE AMOUNT OF SCARRING) GRADE 2 (F2)/GRADE 3(F3) AND IF IT IS SAFE TO USE IN PEOPLE.
Technical Summary
- PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY TO EVALUATE THE LONG-TERM SAFETY AND EFFICACY OF LANIFIBRANOR IN ADULT PATIENTS WITH NON-ALCOHOLIC STEATOHEPATITIS (NASH) WITHOUT CIRRHOSIS AND LIVER FIBROSIS STAGE GRADE 2 (F2)/GRADE 3 (F3)
- Code EudraCT: 2020-004986-38
- Protocol number: 337HNAS20011
- Promoter: Inventiva
- Molecule/Drug: lanifibrano
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* The trials only admit a limited number of patients and are subject to inclusion and exclusion criteria. The specialist who assesses your case will inform you of the conditions required to participate in the clinical trial.
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