Trial Profile

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy, Safety, and Tolerability of Treatment With DD01 for 48 Weeks in Overweight/Obese Subjects With MASLD/MASH

Status: Active, no longer recruiting

Phase of Trial: Phase II

Latest Information Update: 23 Jun 2025

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At a glance

16 Jun 2025 Primary endpoint (Proportion of subjects who achieve at least 30% liver fat reduction measured by MRI-PDFF) has been met.
16 Jun 2025 Results published in the D&D Pharmatech Media Release
24 Feb 2025 Planned primary completion date changed from 1 Mar 2025 to 1 Apr 2025.

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