Exhibit 99.1
Pliant Therapeutics Announces Next Steps Following DSMB Recommendation
on BEACON-IPF, a Phase 2b/3 Trial in Patients with Idiopathic Pulmonary Fibrosis
Pliant has initiated assembly of outside panel of world-renowned experts
to review BEACON-IPF trial data
SOUTH SAN FRANCISCO, CA., February 13, 2025 - Pliant Therapeutics, Inc. (Nasdaq: PLRX) today announced that, per the charter of the trials
independent Data Safety Monitoring Board (DSMB), the Company has initiated the assembly of an outside expert panel to review unblinded data from the ongoing BEACON-IPF Phase 2b trial of bexotegrast in patients
with idiopathic pulmonary fibrosis (IPF). The panel, consisting of world-renowned experts in pulmonary diseases and biostatistics, will provide an independent recommendation to Pliant regarding the BEACON-IPF
trial. Subsequently, the panel will serve as part of an expanded DSMB with the goal to reach a consensus recommendation regarding BEACON-IPF. The decision to assemble the outside panel was taken as the Company
has not been able, through review of blinded data, to determine the rationale for the DSMBs recommendation to pause enrollment and dosing in the trial. The Company expects this process to conclude in two to four weeks.
Following the DSMBs previously announced recommendation, Pliant voluntarily paused enrollment and dosing in the
BEACON-IPF clinical trial. Pliant is committed to remaining blinded ensuring the data integrity of the BEACON-IPF 2b clinical trial with the goal of maintaining its
potential to serve as a registrational trial.
About Pliant Therapeutics, Inc.
Pliant Therapeutics is a late-stage biopharmaceutical company and leader in the discovery and development of novel therapeutics for the treatment of fibrotic
diseases. Pliants lead product candidate, bexotegrast (PLN-74809), is an oral, small molecule, dual selective inhibitor of αvß6 and
αvß1 integrins that is in development in the lead indication for the treatment of idiopathic pulmonary fibrosis, or IPF.
Bexotegrast has received Fast Track Designation and Orphan Drug Designation from the U.S. Food and Drug Administration (FDA) and Orphan Drug Designation from the European Medicines Agency in IPF. Pliant has initiated
BEACON-IPF, an adaptive Phase 2b/3 trial of bexotegrast in IPF. Pliant is conducting a Phase 1 study for its third clinical program, PLN-101095, a small molecule,
dual-selective inhibitor of αvß8 and αvß1 integrins, that is being developed for the treatment of
solid tumors. In addition, Pliant has received regulatory clearance for the conduct of a Phase 1 study of PLN-101325, a monoclonal antibody agonist of integrin α7ß1 targeting muscular dystrophies.
For
additional information, please visit: www.PliantRx.com. Follow us on social media X, LinkedIn, and Facebook.
Forward-Looking Statements
Statements contained in this
press release regarding matters that are not historical facts are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as may, will, expect,
anticipate, estimate, intend, and similar