A RANDOMISED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTRE, PHASE 3 STUDY EVALUATING EFFICACY AND SAFETY OF LANIFIBRANOR FOLLOWED BY AN ACTIVE TREATMENT EXTENSION IN ADULT PATIENTS WITH NON-CIRRHOTIC NON-ALCOHOLIC STEATOHEPATITIS (NASH) AND FIBROSIS 2 (F2)/FIBROSIS 3 (F3) STAGE OF LIVER FIBROSIS

Registry ID
337HNAS20011
Source registry
HEALTH_CANADA
Status
Ongoing
Phase
PHASE3
Study type
INTERVENTIONAL
Sponsor
INVENTIVA S.A
Start date
2024-04-19
Last update
2021-07-16

Conditions

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