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.
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Industries
Company Size
51-200
Company Stage
IPO
Headquarters
South San Francisco, CA
Founded
2015
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Total Funding
$631.1M
Above
Industry Average
Funded Over
6 Rounds
Pliant Therapeutics reported a third-quarter 2026 net loss of $24.4 million, down from $26.3 million a year earlier. The drop reflects lower operating costs after it ended bexotegrast development in IPF in 2025, and a smaller headcount. The company had $142.6 million in cash, cash equivalents and short-term investments as of September 30, 2026. It expects that to fund operations to mid-2028. Enrolment in FORTIFY, a trial of its cancer drug candidate PLN-101095, is ahead of schedule. The trial will enrol up to 102 patients, and interim data is expected in 2027. Pliant also reported encouraging preclinical results for its integrin-based delivery platform. In non-human primates, it saw more than 75% target gene knockdown at eight weeks. It named David Raben as chief medical officer and Craig Blanchette as senior vice president, research (RNAi).
Pliant Therapeutics has appointed Craig Blanchette as senior vice president, research (siRNA). The South San Francisco clinical-stage biotech develops integrin-based therapeutics, and he will help advance its integrin-mediated delivery platform. Blanchette joins from Switch Therapeutics, where as chief scientific officer he built an RNAi discovery team from scratch and advanced two programmes into IND-enabling studies. He previously held roles at Genentech, most recently as head of protein chemistry, and at Lawrence Livermore National Laboratories. "Craig's experience in advancing novel delivery platforms and leading siRNA programs from discovery to clinical development will significantly augment Pliant's deep integrin chemistry and biology expertise," said chief executive officer Bernard Coulie. Pliant granted Blanchette options to buy 300,000 shares as an employment inducement.
Pliant Therapeutics has appointed David Raben as chief medical officer. Dr Raben brings over 30 years of experience in academic translational research, clinical care, and oncology drug development. Dr Raben is a board-certified radiation oncologist. Most recently, he served as chief medical officer at Bicara Therapeutics, where he oversaw clinical development of the company's lead asset across multiple indications. Previously, he held senior positions at Amgen and Genentech, leading oncology programmes and clinical strategy. Before moving to industry, Dr Raben spent more than 20 years as a professor at the University of Colorado Cancer Center. His research focused on combining novel biologic therapies with radiation for patients with advanced cancers. Pliant is developing PLN-101095, a dual-selective inhibitor being investigated for treating solid tumours.
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]
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Industries
Company Size
51-200
Company Stage
IPO
Headquarters
South San Francisco, CA
Founded
2015
Find jobs on Simplify and start your career today
Don't see your dream role? Check out thousands of other roles on Simplify.Browse all jobs