drugset / Trial / NCT06385080

A Study of Amivantamab Alone or in Addition to Other Treatment Agents in Participants With Head and Neck Cancer

NCT06385080

Phase 1/2 Recruiting 287 enrolled Janssen Research & Development, LLC
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine safety and preliminary efficacy of amivantamab monotherapy, amivantamab in addition to pembrolizumab, amivantamab in addition to paclitaxel and amivantamab in addition to pembrolizumab and carboplatin in participants with recurrent/metastatic head and neck cancer. The study will also confirm the recommended Phase 2 combination dose (RP2CD) for amivantamab in addition to paclitaxel. The safety and preliminary efficacy of amivantamab in addition to pembrolizumab will also be determined in perioperative (before and after surgery) setting in participants with resectable locally advanced head and neck squamous cell carcinoma (HNSCC).

Timeline

Start
2024-04-22
Primary completion
2032-12-27
Completion
2032-12-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Amivantamab Monoclonal antibody 2400 mg Subcutaneous
Subject Amivantamab Monoclonal antibody 3360 mg Subcutaneous
Background Carboplatin Small molecule 5 unknown Intravenous
Background Paclitaxel Small molecule 175 mg/m2 Intravenous
Background Pembrolizumab Monoclonal antibody 200 mg Intravenous