MedPath

Pierre Fabre Acquires Global Rights to Next-Generation EGFR Inhibitors for NSCLC Treatment

a month ago3 min read

Key Insights

  • Pierre Fabre Laboratories acquired worldwide rights to PFL-721 and PFL-241 from Antares Therapeutics, expanding their oncology pipeline with mutant-specific EGFR inhibitors targeting unmet needs in non-small cell lung cancer.

  • PFL-721 is a dual EGFR exon 20 and HER2 exon 20 inhibitor transitioning to dose optimization in first-in-human trials, while PFL-241 is a brain-penetrant fourth-generation EGFR inhibitor addressing C797S resistance mutations.

  • EGFR mutations drive approximately 14-38% of NSCLC tumors globally, representing a significant patient population with substantial therapeutic needs.

Pierre Fabre Laboratories announced the acquisition of worldwide rights to two promising EGFR inhibitors, PFL-721 and PFL-241, from Antares Therapeutics, Inc., a spin-out of Scorpion Therapeutics. The deal expands Pierre Fabre's previous agreement with Scorpion Therapeutics and positions the French pharmaceutical company to lead global clinical development of both programs targeting non-small cell lung cancer (NSCLC).

Advanced EGFR Targeting Mechanisms

PFL-721 represents a mutant-specific EGFR exon 20 and HER2 exon 20 inhibitor with best-in-class potential. The compound is preparing to transition to dose optimization within its ongoing first-in-human trial in NSCLC patients. This dual targeting approach addresses specific mutation profiles that have historically presented therapeutic challenges.
PFL-241 offers a different strategic advantage as a mutant-specific, brain-penetrant fourth-generation EGFR inhibitor. Currently in dose escalation within its first-in-human trial, PFL-241 specifically targets C797S resistance mutations in NSCLC patients. The brain-penetrant properties of this compound address a critical unmet need, as central nervous system metastases represent a significant challenge in NSCLC management.

Addressing Significant Market Need

NSCLC represents the most common subtype of lung cancer, with EGFR mutations serving as the most frequent oncogenic drivers. According to epidemiological data, various EGFR mutations occur in approximately 14-38 percent of NSCLC tumors, with prevalence varying by geographic region. This substantial patient population underscores the clinical significance of developing targeted therapies that can address both primary mutations and resistance mechanisms.

Strategic Portfolio Consolidation

"With this agreement with Antares, Pierre Fabre Laboratories now own the global rights for all the assets within our R&D portfolio: exarafenib, PFL-002 (formerly VERT-002), PFL-721 and PFL-241," said Francesco Hofmann, Head of Research and Development for Medical Care at Pierre Fabre Laboratories. "The R&D team is fully engaged and committed to progress the clinical development of these programs, aiming at providing novel and differentiated precision medicines to patient populations with significant unmet needs."
The acquisition represents a strategic consolidation that gives Pierre Fabre complete control over their oncology pipeline. The company's portfolio now encompasses multiple approaches to EGFR inhibition, from early-generation compounds to advanced fourth-generation inhibitors designed to overcome resistance mechanisms.

Company Profile and Therapeutic Focus

Pierre Fabre Laboratories operates as the world's second-largest dermo-cosmetics company and ranks among Europe's leading pharmaceutical laboratories. The company's Medical Care division focuses on five main therapeutic areas: oncology, dermatology, rare diseases, primary care, and family health care. This acquisition strengthens their oncology capabilities and demonstrates their commitment to precision medicine development in cancer treatment.
Subscribe Icon

Stay Updated with Our Daily Newsletter

Get the latest pharmaceutical insights, research highlights, and industry updates delivered to your inbox every day.

© Copyright 2025. All Rights Reserved by MedPath