Clinical Trial

Trial Protocol ID USOR 24246: Ph2 Study of Fruquintinib plus FOLFIRI as 2L Treatment for mCRC

Trial Description

A Phase II Study Investigating Fruquintinib plus FOLFIRI as Second-Line Treatment for Participants with Metastatic Colorectal Cancer (mCRC)

MOA: Fruquintinib is a highly selective and potent VEGFR inhibitor.

Key Eligibility Criteria:

  • Subjects must have confirmed mCRC
  • Genetic aberrations are allowed, excludes MSI-H and BRAF V600
  • Subjects must have received 1L therapy that included oxaliplatin, a
    fluoropyrimidine, and a BEV-based agent
    • FOLFOXIRI + BEV and SOX + BEV regimens not permitted
    • Must have completed minimum of 2 cycles of first-line therapy
  • Subjects that received more than 1 prior systemic treatment or any
    treatment including FOLFIRI or irinotecan-based therapy are
    excluded
  • Participants who received neo/adjuvant oxaliplatin and a
    fluoropyrimidine and progressed within 6 months are not eligible due
    to lack of BEV exposure
  • ECOG score ≤ 2

Contact us regarding Clinical Trials at MOHRSCH@usoncology.com or call us at 877-664-7724

Investigator

  • Photo of Vinni Juneja, MD Vinni Juneja, MD

Disease Types

Sponsors

  • Sarah Cannon Development Innovations
  • Takeda

ClinicalTrials.gov NCT ID

  • NCT07011576