Metastatic Colorectal Cancer Clinical Trial
Official title:
Phase 2 Study of Panitumumab Plus Irinotecan Followed by Panitumumab Plus AMG 479 in Subjects With Metastatic Colorectal Carcinoma Expressing Wild Type KRAS and Refractory to Oxaliplatin-or Irinotecan- and Oxaliplatin-containing Regimens to Evaluate Mechanisms of Acquired Resistance to Panitumumab
This study is designed to evaluate the mechanism(s) of resistance to the anti-epidermal growth factor receptor (EGFR) antibody panitumumab given in combination with irinotecan in metastatic colorectal carcinoma (mCRC) patients with wild-type Kirsten rat sarcoma-2 virus oncogene (KRAS) tumor status at the time of initial diagnosis.
In Part 1, all participants will undergo a baseline tumor biopsy and will receive
panitumumab with irinotecan. Participants who respond or have stable disease will continue
to receive treatment until radiographically-confirmed disease progression. These
participants will then undergo a second tumor biopsy and blood sampling and then proceed to
Part 2 of the study. Participants with radiographically confirmed disease progression at the
time of the first tumor measurement will undergo blood sampling and proceed directly to Part
2.
In Part 2, participants will receive panitumumab with ganitumab. In both parts of the study,
panitumumab and irinotecan (Part 1) and panitumumab and ganitumab (Part 2) will be
administered every 2 weeks until disease progression, intolerability, withdrawal of consent,
death, or unless otherwise indicated by the study team.
;
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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