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To Evaluate the Efficacy, Safety, and Tolerability of BBT-877 in Patients With IPF

Idiopathic Pulmonary Fibrosis Clinical Trial

Official title:
A Phase 2, Randomized, Double-blind, Placebo-controlled, 24-Week Study to Evaluate the Efficacy, Safety, and Tolerability of BBT-877, as Mono- or add-on Therapy, in Patients With Idiopathic Pulmonary Fibrosis (IPF)

Clinical Trial Summary

This is a Phase 2, multicenter, randomized, double-blind, placebo-controlled, study to evaluate the efficacy, safety, and tolerability of 200 mg twice daily (BID) of BBT-877 in patients with IPF, with or without AF approved background therapies (pirfenidone or nintedanib).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05483907
Study type Interventional
Source Bridge Biotherapeutics, Inc.
Contact Bridge Biotherapeutics, Inc.
Phone +82-31-8092-3280
Email clinicaltrials.gov_inquiries@Bridgebiorx.com
Status Recruiting
Phase Phase 2
Start date April 12, 2023
Completion date December 31, 2024
View Details
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