A Phase 2 Multicenter Randomized Double-blind Placebo-controlled Study to Evaluate the Safety Tolerability Pharmacokinetics and Efficacy of TTI-101 in Participants with Idiopathic Pulmonary Fibrosis

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A Phase 2 Multicenter Randomized Double-blind Placebo-controlled Study to Evaluate the Safety Tolerability Pharmacokinetics and Efficacy of TTI-101 in Participants with Idiopathic Pulmonary Fibrosis

Brief description of study

This multicenter, randomized, double-blind, placebo-controlled, parallel-group clinical study is designed to evaluate the safety and tolerability of 3 dose levels of TTI-101 vs placebo in participants with idiopathic pulmonary fibrosis (IPF). Following a screening period of up to 28 days, 100 participants will be randomly assigned (1:1:1:1) to receive 1 of 3 dose levels of TTI-101 or matching placebo.

Clinical Study Identifier: s23-00399

ClinicalTrials.gov Identifier: NCT05671835

Principal Investigator: Rany Condos.

Other Investigators: Daniel H. Sterman, John S Munger, Nathaniel Clardy Nelson.

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