LivingGLP1
Study S000174

A Randomized, Double-blind, Placebo-controlled, Parallel-group Phase II Study to Evaluate the Efficacy and Safety of CS060380 Tablets in Patients With Metabolic Dysfunction-associated Steatohepatitis (MASH) and Obesity.

Registration

Registration
NCT07466017
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
130
Start
2026-04-02
Primary completion
2027-04-30
Lead sponsor
Cascade Pharmaceuticals, Inc
Conditions
Metabolic Dysfunction-associated Steatohepatitis (MASH); Obesity
Interventions
DRUG:semaglutide; DRUG:CS060380; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:2024LP01824; OTHER:CS060380-MASH-CN-II-03

Registered primary outcomes

  • Percentage change in liver fat content from baseline to Week 36 (MRI-PDFF) [Baseline, Week 36]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0012449A Placebo-Controlled Trial of Subcutaneous Semaglutide in Nonalcoholic Steatohepatitis.
Newsome PN, The New England journal of medicine
2021Randomized trialPMID 33185364DOIregistry reference BACKGROUND:33185364