LivingGLP1
Study S003309

A 52-week Double-blind, Randomized, Placebo-controlled, Phase 2 Study to Assess the Efficacy and Safety of SAR425899 for the Treatment of Non-alcoholic Steatohepatitis (NASH)

Registration

Registration
NCT03437720
Acronym
Restore
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
WITHDRAWN
Enrollment
0
Start
2019-05-23
Primary completion
2021-08-25
Lead sponsor
Sanofi
Conditions
Non-alcoholic Steatohepatitis; Type 2 Diabetes Mellitus
Interventions
DRUG:SAR425899; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
EUDRACT_NUMBER:2017-002371-26; OTHER:U1111-1191-5486; NIH:2017

Registered primary outcomes

  • Resolution of Non-alcoholic steatohepatitis (NASH) [Week 52]

Linked records (0)

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