Pliant Therapeutics

Pliant Therapeutics

Develops integrin-targeted therapies for fibrosis

Overview

Pliant Therapeutics develops drugs to treat fibrotic diseases. The company focuses on inhibiting integrin pathways involved in tissue scarring to stop disease progression and potentially restore normal organ function. Its products work by targeting fibrosis-related mechanisms at the molecular level, guided by medicinal chemistry and advanced screening technologies, and advancing candidates through clinical trials toward commercialization. Pliant differentiates itself through deep expertise in integrin biology and fibrosis, aiming to create best-in-class therapies that can address multiple fibrotic indications and provide targeted, effective treatments. The company’s goal is to transform the treatment of fibrotic diseases by halting progression and reversing fibrosis, improving patient outcomes and organ function.

About Pliant Therapeutics

Simplify's Rating
Why Pliant Therapeutics is rated
C-
Rated C on Competitive Edge
Rated C on Growth Potential
Rated D+ on Differentiation

Industries

Biotechnology

Healthcare

Company Size

51-200

Company Stage

IPO

Headquarters

San Francisco, California

Founded

2015

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Simplify's Take

What believers are saying

  • FORTIFY dosed its first patient April 30, 2026, expanding PLN-101095 into oncology.
  • Pliant reported $159.6 million cash on June 30, 2026, funding into 2H 2028.
  • Updated 2026 data showed biomarker activation and generally tolerable safety, supporting continued enrollment.

What critics are saying

  • BEACON-IPF failed in June 2025, ending Pliant's fibrosis flagship program.
  • Pliant cut 45% of staff in May 2025, signaling severe portfolio damage.
  • Ongoing PLRX shareholder litigation ties February 2025 disclosure failures to a 60% stock crash.

What makes Pliant Therapeutics unique

  • PLN-101095 is oral dual αvβ8/αvβ1 inhibition, targeting checkpoint-resistant solid tumors.
  • Pliant pairs integrin blockade with pembrolizumab, a differentiated TGF-beta suppression strategy.
  • AACR 2026 showed one complete response and three partial responses in refractory tumors.

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Funding

Total Funding

$631.1M

Above

Industry Average

Funded Over

6 Rounds

Notable Investors:
Post IPO Equity funding comparison data is currently unavailable. We're working to provide this information soon!
Post IPO Equity Funding Comparison
Coming Soon

Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

401(k) Company Match

Remote Work Options

Flexible Work Hours

Professional Development Budget

Wellness Program

Mental Health Support

Gym Membership

Phone/Internet Stipend

Home Office Stipend

Paid Vacation

Paid Sick Leave

Paid Holidays

Parental Leave

Family Planning Benefits

Fertility Treatment Support

Employee Stock Purchase Plan

Performance Bonus

Relocation Assistance

Employee Referral Bonus

Student Loan Assistance

Adoption Assistance

Childcare Support

Elder Care Support

Pet Insurance

Bereavement Leave

Commuter Benefits

Meal Benefits

Legal Services

Employee Discounts

Company Social Events

Stock Price

Growth & Insights and Company News

Headcount

6 month growth

9%

1 year growth

-4%

2 year growth

-1%
Associated Press
Aug 11th, 2026
Pliant Therapeutics reports strong enrollment in FORTIFY Phase 1b oncology trial, appoints two directors

Pliant Therapeutics reported second quarter 2026 financial results and announced the appointment of two oncology drug development experts to its board of directors. The clinical-stage biotechnology company appointed Flavia Borellini and Robert Iannone, who bring extensive experience in global oncology drug development and commercialisation. The company is experiencing strong enrollment in FORTIFY, a Phase 1b trial of PLN-101095 in combination with pembrolizumab for immune checkpoint inhibitor-refractory advanced or metastatic solid tumours. The trial will enroll up to 102 patients across three cohorts, with interim data expected in 2027. Research and development expenses decreased to $16.7 million from $32.2 million year-over-year. Net loss fell to $22.4 million from $43.3 million in the prior-year quarter. As of 30 June 2026, Pliant had cash and investments of $159.6 million, expected to fund operations into the second half of 2028.

GlobeNewswire
May 21st, 2026
Pliant Therapeutics announces upcoming presentation at the 2026 American Society of Clinical Oncology Annual Meeting.

Pliant Therapeutics announces upcoming presentation at the 2026 American Society of Clinical Oncology Annual Meeting. 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 | Presenter: | Timothy A. Yap, MBBS, Ph.D., University of Texas, M.D. Anderson Cancer Center | | Session: | Developmental Therapeutics - Immunotherapy | | Date: | Saturday, May 30, 2026, 1:30 - 4:30 p.m. Central Time | | Location: | 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 α[v] ß[8] and α[v] ß[1] 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. [email protected]

The Globe and Mail
Mar 18th, 2026
Pliant Therapeutics announces upcoming presentation of Phase 1 clinical trial of PLN-101095 in patients with solid tumors at the 2026 AACR Annual Meeting.

Pliant Therapeutics announces upcoming presentation of Phase 1 clinical trial of PLN-101095 in patients with solid tumors at the 2026 AACR Annual Meeting. Pliant Therapeutics, Inc. - GlobeNewswire - Wed Mar 18, 8:00AM CDT SOUTH SAN FRANCISCO, Calif., March 18, 2026 (GLOBE NEWSWIRE) - Pliant Therapeutics, Inc. (Nasdaq: PLRX), a clinical-stage biotechnology company focused on the discovery and development of integrin-based therapeutics, today announced the presentation of data from the Phase 1 trial of PLN-101095 at the upcoming American Association for Cancer Research (AACR) Annual Meeting taking place in San Diego, California from April 17-22, 2026. The abstract was selected for oral presentation as part of the Clinical Trials Mini Symposium. Oral Presentation Title: First-in-human phase I study of PLN-101095, a first-in-class dual α[v] β[8] /α[v] β[1] integrin inhibitor, as monotherapy and in combination with pembrolizumab in patients with advanced solid tumors refractory to immune checkpoint inhibitors (ICI) Presenter: Timothy A. Yap, M.D., Ph.D., University of Texas, M.D. Anderson Cancer Center Session: CTMS01: Updates in Anticancer Immunotherapies Date: Saturday, April 18, 2026 Presentation Time: 10:21 a.m. - 10:31 a.m. Pacific Time Location: Ballroom 6A - Upper Level - San Diego Convention Center Oncology Program PLN-101095 is an oral, small molecule, dual selective inhibitor of αvβ8 and αvβ1 integrins designed to overcome checkpoint resistance by blocking TGF-β activation in the tumor microenvironment. Pliant is currently conducting a Phase 1a/1b open-label, dose-escalation and indication expansion trial to evaluate the safety, tolerability, pharmacokinetics, and preliminary evidence of antitumor activity of PLN-101095, as monotherapy and in combination with pembrolizumab, in patients with immune checkpoint inhibitor (ICI)-refractory advanced or metastatic solid tumors. About Pliant Therapeutics, Inc. Pliant Therapeutics is a clinical-stage biopharmaceutical company focused on the discovery and development of integrin-based therapeutics. The Company's lead program is PLN-101095, a small molecule, dual-selective inhibitor of αvß8 and αvß1 integrins, that is being developed for the treatment of solid tumors. Pliant's early-stage platform includes preclinical research focused on tissue-specific delivery and internalization of drug payloads utilizing integrin receptor-binding molecules. For additional information, please visit: www.PliantRx.com. Follow us on social media X, LinkedIn and Facebook. Investor and Media Contact: Christopher Keenan Vice President, Investor Relations and Corporate Communications Pliant Therapeutics, Inc. [email protected] This article contains syndicated content. We have not reviewed, approved, or endorsed the content, and may receive compensation for placement of the content on this site. For more information please view the Barchart Disclosure Policy here.

Associated Press
Mar 11th, 2026
Pliant Therapeutics' PLN-101095 shows deep responses in checkpoint inhibitor refractory tumors

Pliant Therapeutics has raised $120 million in a Series C round, valuing the company at $1.45 billion, as it advances PLN-101095, an oral inhibitor targeting checkpoint-resistant cancers. Phase 1 data showed four responses, including one complete response, in 10 heavily pretreated immune checkpoint inhibitor-refractory patients. Responding patients showed significant increases in plasma interferon gamma after 14 days of PLN-101095 monotherapy before adding pembrolizumab. The company has initiated a Phase 1b indication expansion trial across non-small cell lung cancer, clear cell renal cell carcinoma and high tumour mutational burden cancers. First patient enrolment is anticipated in the second quarter, with interim data expected in 2027. Pliant reported $192.4 million in cash and investments as of December 31, 2025, sufficient to fund operations into the second half of 2028.

ETFDailyNews.com
Sep 17th, 2025
Acadian Asset Management LLC Makes New Investment in Pliant Therapeutics, Inc. $PLRX

Acadian Asset Management LLC bought a new position in shares of Pliant Therapeutics, Inc. (NASDAQ:PLRX – Free Report) in the 1st quarter, Holdings Channel reports. The institutional investor bought 1,220,446 shares of the company’s stock, valued at approximately $1,642,000. Several other institutional investors and hedge funds have also recently added to or reduced their stakes […]

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