drugset / Trial / NCT05671835

Study of TTI-101 in Participants With Idiopathic Pulmonary Fibrosis

NCT05671835

Phase 2 Completed 100 enrolled Tvardi Therapeutics, Incorporated
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to evaluate the safety and tolerability of oral daily administration of TTI-101 over a 12-week treatment duration in participants with idiopathic pulmonary fibrosis (IPF).

Timeline

Start
2023-05-15
Primary completion
2025-08-14
Completion
2025-08-14

Drugs

EvaluationDrugModalityDoseRoute
Subject C-188-9 Small molecule 400 mg Oral
Subject C-188-9 Small molecule 800 mg Oral