drugset / Trial / NCT05379595

A Study of Amivantamab Monotherapy and in Addition to Standard-of-Care Chemotherapy in Participants With Advanced or Metastatic Colorectal Cancer

NCT05379595

Phase 1/2 Recruiting 225 enrolled Janssen Research & Development, LLC
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the anti-tumor activity of amivantamab as a monotherapy (Cohorts A, B, and C), to assess the recommended phase 2 combination dose (RP2CD) of amivantamab when added to SoC chemotherapy (Ph1b cohorts) and to characterize the safety of amivantamab when added to standard-of care (SoC) chemotherapy in participants with metastatic colorectal cancer (mCRC) (Ph2 cohorts).

Timeline

Start
2022-07-29
Primary completion
2027-04-27
Completion
2030-10-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Amivantamab Monoclonal antibody 700 mg Intravenous
Subject Amivantamab Monoclonal antibody 1050 mg Intravenous
Subject Amivantamab Monoclonal antibody 1400 mg Intravenous
Comparator Irinotecan Small molecule Intravenous
Comparator Leucovorin Small molecule Intravenous
Comparator Oxaliplatin Small molecule Intravenous
Comparator fluorouracil Small molecule Intravenous

Indications