50
Participants
Start Date
August 31, 2025
Primary Completion Date
December 31, 2028
Study Completion Date
December 31, 2029
Fruquintinib Combined With Chemotherapy
The intervention in this trial involves administering a combination of 5FU-based chemotherapy and fruquintinib to patients with locally advanced unresectable or metastatic colorectal cancer. Patients receive either the FOLFIRI or mFOLFOX6 regimen, both of which include 5-fluorouracil (5FU), leucovorin (LV), and either irinotecan (FOLFIRI) or oxaliplatin (mFOLFOX6). Fruquintinib is given orally once daily for 21 days in each 28-day cycle. The initial dose of fruquintinib is 4 mg daily for the first three patients to assess safety; if no dose-limiting toxicities are observed, the dose is increased to 5 mg daily for subsequent participants. Treatment continues until disease progression, unacceptable toxicity, or patient withdrawal. After six months, patients with stable disease or better transition to a maintenance phase with 5FU and fruquintinib alone.
Houston Methodist Neal Cancer Center, Houston
Takeda Development Center Americas, Inc.
INDUSTRY
The Methodist Hospital Research Institute
OTHER