A Study of UBT251 in Participants With Metabolic Dysfunction-Associated Steatohepatitis (MASH)

This is a registry record, not a result. A trial being listed, recruiting or completed says nothing by itself about whether the compound works or is safe.

Registry numberNCT07145151
StatusRecruiting
PhasePhase 2
SponsorThe United Bio-Technology (Hengqin) Co., Ltd.
Enrollment156 participants
DesignInterventional, Randomized, Parallel, Masking: Triple
ConditionsMetabolic Dysfunction-associated Steatohepatitis (MASH)
InterventionsUBT251; Placebo
StartSep 30, 2025
Primary completionJun 4, 2027
Study completionAug 31, 2027
Results postedNot yet
Registry last updatedNov 20, 2025

Compounds on this site that cite this trial

What the registry says the trial is about

This is a multicenter, randomized, double-blind, placebo-controlled Phase 2 clinical study evaluating the efficacy and safety of UBT251 in MASH subjects. Subjects will be randomly assigned to UBT251 2mg-dose, 4mg-dose,6mg-dose and placebo groups. The entire trial cycle includes a 6-week screening period, a 48-week double-blind treatment period, and a 4-week follow-up period.

Primary outcomes

These are what the trial was designed to measure first. They are registered in advance, which is what makes a later result checkable.

Outcome measureTime frame
Percentage of Participants With MASH resolution With no Worsening of Fibrosis on Liver HistologyBaseline, Week 48

25 secondary outcomes also registered. See the registry record for the full list.

Source: ClinicalTrials.gov (U.S. National Library of Medicine). Last checked against the registry on Nov 1, 2026. See the trial changes feed for what has changed recently.