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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


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

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