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RecruitingSquamous Cell Carcinoma of Head and Neck

A Study of Amivantamab in Addition to Standard of Care Agents (SOC) Compared With SOC Alone in Participants With Recurrent/Metastatic Head and Neck Cancer

Eligible age

18+ yrs

Accepts

All genders

Locations

21 states

Healthy volunteers

No

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About this study

The purpose of this study is to compare anti-tumor activity of amivantamab in addition to pembrolizumab and carboplatin versus pembrolizumab, 5-fluorouracil (FU), and platinum therapy (carboplatin or cisplatin) in participants with refractory/metastatic (R/M) head and neck squamous cell carcinoma (HNSCC). HNSCC is a type of cancer that develops in the head and neck regions, including the outer tissue layer of the mouth and throat. This study will focus on participants with HNSCC who are treatment-naive (have not received prior treatment) in the R/M setting.

Sponsor: Janssen Research & Development, LLC

You may qualify if…

  • Be more than or equal to (\>=) 18 years of age (or the legal age of majority in the jurisdiction in which the study is taking place, whichever is greater)
  • Have histologically or cytologically confirmed recurrent/metastatic (R/M) HNSCC that is considered incurable by local therapies: a. eligible primary tumor locations are the oral cavity, oropharynx, hypopharynx, or larynx; b. Must not have a primary tumor site of nasopharynx or primary tumor of unknown location; c. Must have documented local testing results per local regulations; d. Human papillomavirus (HPV) status must be known for participants with primary tumor location in oropharynx via p16 test, HPV DNA test, or high-risk HPV in situ hybridization (ISH). Any known p16, HPV DNA, or high-risk HPV ISH status of tumor must be negative
  • Be treatment-naive for systemic therapy in the R/M setting
  • Have an ECOG performance status of 0 or 1
  • Have measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST) version (v).1.1

You may not qualify if…

  • Have an uncontrolled illness
  • Have untreated brain metastases or history of known presence of leptomeningeal disease
  • Have a history of clinically significant cardiovascular disease
  • Inadequate organ or bone marrow function
  • Known allergies, hypersensitivity, contraindications, or intolerance to excipients of: Amivantamab, Pembrolizumab, Carboplatin, Cisplatin, 5-FU and Hyaluronidase

Where it's recruiting

Arizona

Chandler · Tucson

California

Fullerton · La Jolla · Los Angeles · Murrieta

Connecticut

Hartford · New Haven

Florida

Fort Myers · Miami · Orlando · St. Petersburg

Georgia

Atlanta · Macon

Illinois

Chicago · O'Fallon

Kentucky

Lexington

Maryland

Baltimore

Michigan

Ann Arbor · Detroit

Missouri

St Louis

Nebraska

Lincoln

Source: ClinicalTrials.gov · NCT07276399 · last updated 2026-07-31

A Study of Amivantamab in Addition to Standard of Care Agents (SOC) Co · TrialPath