Press Releases May 21, 2026 05:29 PM

Pliant Therapeutics Announces Upcoming Presentation at the 2026 American Society of Clinical Oncology Annual Meeting

Pliant Therapeutics to present clinical trial data on PLN-101095 at 2026 ASCO Annual Meeting

By Priya Menon
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Pliant Therapeutics announced a poster presentation at the 2026 ASCO Annual Meeting highlighting their Phase 1b FORTIFY trial, which is evaluating PLN-101095, a dual integrin inhibitor, in combination with pembrolizumab for patients with immune checkpoint inhibitor refractory solid tumors. The trial is actively enrolling multiple patient cohorts and assessing safety, tolerability, and preliminary antitumor activity. This milestone advances Pliant’s clinical development in immuno-oncology.

Pliant Therapeutics Announces Upcoming Presentation at the 2026 American Society of Clinical Oncology Annual Meeting
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Key Points

  • Presentation scheduled for May 30, 2026, at the ASCO Annual Meeting focusing on Phase 1b trial results of PLN-101095 combined with pembrolizumab.
  • PLN-101095 is a first-in-class oral small molecule dual αvβ8/αvβ1 integrin inhibitor targeting ICI-refractory advanced/metastatic solid tumors.
  • The ongoing FORTIFY trial includes patients with NSCLC, high tumor mutational burden tumors, and clear cell renal cell carcinoma, evaluating safety and preliminary efficacy.

Highlights FORTIFY, the Phase 1b indication expansion trial of PLN-101095 
enrolling patients with ICI-refractory solid tumors

SOUTH SAN FRANCISCO, Calif., May 21, 2026 (GLOBE NEWSWIRE) -- Pliant Therapeutics, Inc. (Nasdaq: PLRX) today announced a presentation at the upcoming 2026 American Society of Clinical Oncology (ASCO) Annual Meeting taking place in Chicago, Illinois from May 29 to June 2, 2026.

Poster Presentation

Title: Cohort Expansion of a Phase I Study of PLN-101095, a First-in-Class Dual αvβ8 /αvβ1 Integrin Inhibitor, in Combination with Pembrolizumab in Patients with Advanced Solid Tumors Refractory to Immune Checkpoint Inhibitors

Presenter:Timothy A. Yap, MBBS, Ph.D., University of Texas, M.D. Anderson Cancer CenterSession:Developmental Therapeutics – ImmunotherapyDate:Saturday, May 30, 2026, 1:30 – 4:30 p.m. Central TimeLocation:Hall A, Poster 467b


FORTIFY - PLN-101095 Phase 1b Indication Expansion Trial

PLN-101095 is currently being evaluated in Phase 1a/1b open-label, dose-escalation and indication expansion trial (NCT06270706) to evaluate the safety, tolerability, pharmacokinetics, and preliminary evidence of antitumor activity of PLN-101095 when administered orally in combination with pembrolizumab, in patients with immune checkpoint inhibitor (ICI)-refractory advanced or metastatic solid tumors. Pliant is currently enrolling patients in FORTIFY, a Phase 1b open-label, indication expansion trial enrolling three cohorts of patients with non-small cell lung cancer (NSCLC), tumors with high tumor mutational burden or clear cell renal cell carcinoma. Patients will be treated for 14 days with PLN-101095 dosed at 1,000 mg twice daily as monotherapy, after which pembrolizumab will be added as combination therapy.

About Pliant Therapeutics, Inc.

Pliant Therapeutics is a clinical-stage biopharmaceutical company focused on the discovery and development of integrin-based therapeutics. Pliant’s lead program is PLN-101095, an oral, small molecule, dual-selective inhibitor of αvß8 and αvß1 integrins, that is being developed for the treatment of ICI-refractory advanced or metastatic solid tumors. PLN-101095 is being investigated in FORTIFY, a Phase 1b indication expansion trial enrolling patients with NSCLC, tumors with high tumor mutational burden or clear cell renal cell carcinoma. Pliant’s preclinical research is focused on tissue-specific delivery and internalization of drug payloads utilizing integrin receptor-binding molecules with programs focused on delivering siRNAs to skeletal muscle cells, adipocytes, and renal cells.

For additional information on Pliant, visit www.PliantRx.com and follow us on X, LinkedIn and Facebook.

Investor and Media Contact:
Christopher Keenan
Vice President, Investor Relations and Corporate Communications
Pliant Therapeutics, Inc.
ir@pliantrx.com


Risks

  • The trial is in early Phase 1b stages, so clinical benefit and eventual regulatory approval remain uncertain, impacting biotech and pharmaceutical sectors.
  • Patient enrollment and response variability could influence data outcomes and timelines, introducing execution risks.
  • Competition in immuno-oncology and integrin-targeting therapies may affect commercial viability if superior therapies emerge.

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