Resmiterom Efficacy & Safety in Patients With MASH

NCT07249788 · Status: RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 165

Last updated 2025-12-03

No results posted yet for this study

Summary

Phase 4 clinical trial study aims to further evaluate the safety and therapeutic efficacy of Resmetirom in Pakistani patients with fibroscan proven MASH.

Conditions

  • MASH - Metabolic Dysfunction-Associated Steatohepatitis

Interventions

DRUG

Resmetirom

1st FDA approved MASH therapy

Sponsors & Collaborators

  • Nabiqasim Industries (Pvt) Ltd

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-10-17
Primary Completion
2026-10-16
Completion
2026-12-31

Countries

  • Pakistan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07249788 on ClinicalTrials.gov