Monday, December 23, 2024
Health

Pierre Fabre Laboratories and Scorpion Therapeutics Announce First Patient Dosed in Phase I/II Clinical Trial of PFL-241/STX-241, a Mutant-Selective Inhibitor Intended To Treat Locally Advanced or Metastatic Non-Small Cell Lung Cancer


PFL-241/STX-241 is a highly selective, and potentially best-in-class fourth generation epidermal growth factor receptor (“EGFR”) inhibitor

One of two EGFR programs being developed with Scorpion Therapeutics

CASTRES, France and BOSTON, Oct. 8, 2024 /PRNewswire/ — Pierre Fabre Laboratories, a global player in oncology, and Scorpion Therapeutics, Inc. (“Scorpion”), a pioneering clinical-stage oncology company dedicated to transforming the lives of cancer patients by redefining the frontier of precision medicine, today announced that the first patient has been dosed in a Phase I/II, first-in-human dose-escalation, dose-optimization and dose-expansion trial. This clinical trial evaluates PFL-241/STX-241, a highly differentiated, orally bioavailable, highly selective tyrosine kinase inhibitor (“TKI”) targeting epidermal growth factor receptor (“EGFR”) Exon 19 or 21 mutations with the co-occurring C797S mutation, a known resistance mechanism to 3rd generation EGFR inhibitors.

Pierre Fabre Laboratories and Scorpion Therapeutics Announce First Patient Dosed in Phase I/II Clinical Trial of PFL-241/STX-241, a Mutant-Selective Inhibitor Intended To Treat Locally Advanced or Metastatic Non-Small Cell Lung Cancer Driven by EGFR Exon 19 or 21 and Co-occurring C797S Mutations

The PFL-241/STX-241 Phase I/II trial is an open label, multi-center study that aims to assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and preliminary clinical efficacy of PFL-241/STX-241 as a monotherapy in patients with locally advanced or metastatic non-small cell lung cancer (“NSCLC”) harboring EGFR Exon 19 or 21 mutations with the co-occurring C797S mutation.

NSCLC is the most common form of lung cancer and EGFR mutations are one of its most common disease drivers, occurring in up to 38 percent of tumors, depending on geography1,2,3.

“We are eager to begin the clinical evaluation of PFL-241/STX-241, our mutant-selective 4th generation EGFR inhibitor, a molecule with differentiated properties that we believe has the potential to become a best-in-class therapeutic option for patients developing resistance to current targeted therapy,” said Francesco Hofmann, Head of Research and Development for Medical Care at Pierre Fabre Laboratories. “The initiation of this clinical trial highlights our team’s engagement and execution in strong partnership with Scorpion Therapeutics, and we look forward to demonstrating how patients could potentially benefit from this targeted therapy.”

PDF:  https://mma.prnewswire.com/media/2525480/Pierre_Fabre_Laboratories.pdf

Logo: https://mma.prnewswire.com/media/2525481/Pierre_Fabre_and_Scorpio_Logo.jpg

 

Pierre Fabre Laboratories Media Contact:

Laure Bregeon-Sgandurra

Pierre Fabre Laboratories

[email protected] 

Scorpion Therapeutics Contacts: 

Media Contact:

Ethan Metelenis

Precision AQ

[email protected] 

Investor Contact:

Emiley Demick

Precision AQ

[email protected] 

 

 

Pierre Fabre and Scorpio Logo

Cision View original content to download multimedia:https://www.prnewswire.co.uk/news-releases/pierre-fabre-laboratories-and-scorpion-therapeutics-announce-first-patient-dosed-in-phase-iii-clinical-trial-of-pfl-241stx-241-a-mutant-selective-inhibitor-intended-to-treat-locally-advanced-or-metastatic-non-small-cell-lung-ca-302269906.html





Source link