A Study to Evaluate the Adverse Events, and Efficacy of Intravenous (IV) of Telisotuzumab Adizutecan in Combination With IV Oxaliplatin, Fluorouracil, Folinic Acid/Leucovorin, Bevacizumab, Panitumumab in Adult Participants With Metastatic Colorectal Cancer

CRC is the third most common type of cancer diagnosed worldwide with developed countries at highest risk. The purpose of this study is to assess adverse events and change in disease activity when telisotuzumab adizutecan is given in combination with oxaliplatin, fluorouracil (5FU), leucovorin (LV) (FOLFOX), and bevacizumab or panitumumab. Telisotuzumab adizutecan is an investigational drug being developed for the treatment of mCRC. Fluorouracil and leucovorin are drugs approved for the treatment of mCRC. This study will be divided into two stages, with the first stage treating participants wi

Trial Details

NCT ID
NCT06820463
Phase
PHASE2
Sponsor
AbbVie
Status
RECRUITING
Cancer Type
Colorectal Cancer
Interventions
  • Telisotuzumab Adizutecan
  • Fluorouracil
  • Oxaliplatin
  • Leucovorin
  • Bevacizumab
  • Panitumumab
Locations (sample)
  • Duarte, California, United States|34.13945,-117.97729
  • New Haven, Connecticut, United States|41.30815,-72.92816
  • Hinsdale, Illinois, United States|41.80086,-87.93701
  • Boston, Massachusetts, United States|42.35843,-71.05977
  • Kansas City, Missouri, United States|39.09973,-94.57857

Key Eligibility Criteria

  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  • Laboratory values meeting the criteria within the protocol.
  • Has measurable disease per response evaluation criteria in solid tumors (RECIST) v1.1.

For full eligibility, visit ClinicalTrials.gov.

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