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Clinical Trial
Clinical Trial Search
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
-
Vinni Juneja, MD
Disease Types
Sponsors
- Sarah Cannon Development Innovations
- Takeda
ClinicalTrials.gov NCT ID
- NCT07011576
