TrialSignal
Clinical trial intelligence report
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.
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 13, 2026
NCT ID
NCT07466017
Status
RECRUITING
Phase
Phase 2
Sponsor
Cascade Pharmaceuticals, Inc
Executive brief
Investment-Ready Snapshot
Cascade Pharmaceuticals, Inc. is advancing CS060380 in a Phase II trial to evaluate its efficacy and safety in combination with semaglutide for treating MASH and obesity. The market for obesity and related liver diseases is significant, with increasing prevalence globally. The combination therapy approach may provide a competitive edge against existing treatments, particularly as semaglutide has shown promise in weight management. Successful trial outcomes could position Cascade favorably in a growing market, but diligence is required regarding regulatory pathways and potential competition from other obesity and liver disease therapies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT07466017
Indication
Metabolic Dysfunction-associated Steatohepatitis (MASH)
Modality
small molecule
Target
CS060380 is a THR-beta agonist targeting metabolic dysfunction-associated steatohepatitis (MASH) and obesity.
Intervention
semaglutide, CS060380, Placebo
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.