A Study of Ficlatuzumab in Combination With Cetuximab in Participants With Recurrent or Metastatic (R/M) HPV Negative Head and Neck Squamous Cell Carcinoma

Recruiting now · Phase 3 · Has a placebo group

Conditions studied: Metastatic Head-and-neck Squamous-cell Carcinoma, Recurrent Head and Neck Squamous Cell Carcinoma

In brief

The purpose of this study is to compare the efficacy and safety of ficlatuzumab plus cetuximab compared to placebo plus cetuximab in participants with recurrent/metastatic (R/M) HPV-negative Head and Neck Cancer. The primary hypothesis is that ficlatuzumab combined with cetuximab is superior to cetuximab alone in terms of progression-free survival and/or overall survival.

Key facts

Study ID: NCT06064877
Run by: AVEO Pharmaceuticals, Inc.
People needed: 410
Starts: 2024-01-11
Expected to finish: 2027-11-01
Last updated by the study team: 2026-04-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Male or female and ≥ 18 years of age
Histologically and/or cytologically confirmed primary diagnosis of R/M HNSCC
Participants with oropharyngeal cancer will be required to have proof of p16 negative status submitted on the basis of a pathology report
At least 1 measurable lesion by contrast CT or MRI scan according to RECIST v.1.1. Such lesions must not have been previously irradiated; if the measurable lesion(s) has been irradiated, clear progression must be documented
Participants must have failed prior therapy with an anti-PD-1/PD-L1 ICI and with platinum-based chemotherapy administered in combination or sequentially, in either the locally advanced or R/M setting. Failure of prior treatment may be due to progression of disease or intolerance to treatment
Patient's tumor must be considered inoperable and incurable
Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 with a life expectancy of at least 12 weeks
For women of childbearing potential (WOCBP), documentation of negative serum pregnancy test within 30 days of randomization
For WOCBP and male participants whose sexual partners are of childbearing potential, agreement to use an effective method of contraception during the study and for at least 5 months after the last dose of study treatment. Birth control methods which may be considered highly effective include methods that achieve a failure rate of less than 1% per year when used consistently and correctly.
Ability to give written informed consent and comply with protocol requirements
Patients with feeding tubes are eligible for the study.
Archived tissue sample must be submitted to the Sponsor-designated laboratory within 60 days of randomization for c-Met analysis (if a tissue sample is not available, a fresh biopsy may be required prior to enrollment)

You may not qualify if…

Participants who have received > 2 prior lines of anticancer therapy or prior treatment with cetuximab/alternative EGFR inhibitors for the treatment of R/M HNSCC
History of severe allergic or anaphylactic reactions or hypersensitivity to recombinant proteins or excipients in the investigational agent or cetuximab
Known or suspected untreated and uncontrolled brain metastases or leptomeningeal carcinomatosis Note: Participants with locally treated brain metastases are eligible provided 2 weeks have elapsed since local therapy. Participants are allowed to continue steroid taper during the start of study treatment.
Prior treatment with any other investigational drug or biologic agent or radiation therapy before a washout has been completed (must be completed prior to randomization):
2 weeks (14 days) or 5 half-lives, whichever is shorter, for chemotherapeutic agents, small molecules, and checkpoint inhibitors
3 weeks (21 days) or 5 half-lives, whichever is shorter, for antibody-drug conjugates
4 weeks (28 days) for cell therapies
2 weeks (14 days) for radiation therapy
Any unresolved and significant toxicity (National Cancer Institute Common Terminology Criteria for Adverse Events [NCI-CTCAE] version 5.0) Grade 2 or greater from previous anticancer therapy (including radiation therapy), other than alopecia
Significant cardiovascular disease, including: Cardiac failure New York Heart Association class III or IV; Myocardial infarction, severe or unstable angina within 6 months prior to randomization; History of serious ventricular arrhythmia (i.e., ventricular tachycardia or ventricular fibrillation)
Any other medical condition or psychiatric condition that, in the opinion of the Investigator, might interfere with the participant's involvement in the study or interfere with the interpretation of study results
History of prior malignancy within 2 years prior to randomization (except for adequately treated non-melanoma skin cancer, carcinoma in situ of the breast or cervix, superficial bladder cancer, or early-stage prostate cancer, without evidence of recurrence; participants may or may not be on maintenance therapy)
Participants who are positive for hepatitis B virus (HBV) or hepatitis C virus (HCV) with indication of acute or chronic hepatitis (as defined in protocol)
Radiographic evidence (historical or at screening) of interstitial lung disease or idiopathic pulmonary fibrosis
Female participants who are pregnant or breastfeeding
A full list of inclusion and exclusion criteria can be found in the protocol.

Where it is running

Oncology Consultants — Houston, Texas, United States (enrolling)
University of California Los Angeles — Los Angeles, California, United States (enrolling)
The University of Arizona Cancer Center — Tucson, Arizona, United States (enrolling)
Banner MD Anderson Cancer Center — Gilbert, Arizona, United States (enrolling)
AdventHealth Medical Group Oncology & Hematology at Orlando — Orlando, Florida, United States (enrolling)
Moffitt Cancer Center — Tampa, Florida, United States (enrolling)
Emory University — Atlanta, Georgia, United States (enrolling)
Yale School of Medicine - Smilow Cancer Hospital — New Haven, Connecticut, United States (enrolling)
The George Washington University — Washington D.C., District of Columbia, United States (enrolling)
Mary Bird Perkins Cancer Center — Baton Rouge, Louisiana, United States (enrolling)
MaineHealth Institute for Research — South Portland, Maine, United States (enrolling)
University of Maryland — Baltimore, Maryland, United States (enrolling)
Massachusetts General Hospital — Boston, Massachusetts, United States (enrolling)
Dana Farber Cancer Institute — Boston, Massachusetts, United States (enrolling)
Siteman Cancer Center - Washington University — St Louis, Missouri, United States (enrolling)
Northwell Health Cancer Institute — Lake Success, New York, United States (enrolling)
Manhattan Eye, Ear & Throat Hospital — New York, New York, United States (enrolling)
University of Illinois Cancer Center — Chicago, Illinois, United States (enrolling)
University of Kansas Cancer Center — Westwood, Kansas, United States (enrolling)
Ohio State University, James Cancer Hospital and Solove Research Institute — Columbus, Ohio, United States (enrolling)
Fox Chase Cancer Center — Philadelphia, Pennsylvania, United States (enrolling)
University of Pittsburgh Medical Center - Hillman Cancer Center — Pittsburgh, Pennsylvania, United States (enrolling)
Medical University of South Carolina (MUSC) — Charleston, South Carolina, United States (enrolling)
MD Anderson Cancer Center — Houston, Texas, United States (enrolling)
VCU Massey Cancer Center — Richmond, Virginia, United States (enrolling)

Full record on ClinicalTrials.gov

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