drugset / Trial / NCT06575400

A Study to Test How Well Different Doses of BI 3804379 Are Tolerated by Healthy People and Patients With Metabolic Dysfunction-associated Steatohepatitis (MASH)

NCT06575400 ↗

Phase 1 Recruiting 124 enrolled Boehringer Ingelheim
RandomizedSequentialSingle-blindTreatment

Summary

The main objectives of this trial are to investigate safety, tolerability and pharmacokinetics (PKs) of BI 3804379 in healthy male and female participants and in stable patients with advanced liver fibrosis due to MASH following administration of single rising doses and administration of multiple rising doses.

Timeline

Start
2024-09-12
Primary completion
2028-02-02
Completion
2028-03-20

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 3804379 Unknown — Subcutaneous