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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.
Industries
Biotechnology
Healthcare
Company Size
51-200
Company Stage
IPO
Headquarters
San Francisco, California
Founded
2015
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Total Funding
$631.1M
Above
Industry Average
Funded Over
6 Rounds
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
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.
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]
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.
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.
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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Industries
Biotechnology
Healthcare
Company Size
51-200
Company Stage
IPO
Headquarters
San Francisco, California
Founded
2015
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