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
2031-05-11

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