Metastatic Head and Neck Squamous Cell CarcinomaRecurrent Head and Neck Squamous Cell Carcinoma
Investigational drug(s) / intervention(s)
Ficerafusp alfaPembrolizumab (KEYTRUDA®)Placebo
Ficerafusp alfa: Investigational
Pembrolizumab (KEYTRUDA®): Immunotherapy agent used in combination with investigational agent
Placebo: Placebo Control
Study summary
Ficerafusp alfa is directed against two targets, Epidermal Growth Factor Receptor (EGFR) and Transforming Growth Factor beta (TGF-β).
This study intends to evaluate the safety and efficacy of ficerafusp alfa in combination with pembrolizumab versus placebo with pembrolizumab in 1L PD-L1-positive, recurrent or metastatic Head and Neck Squamous Cell Carcinoma (HNSCC).
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Age ≥18 years on the day the Informed Consent Form is signed.
* Histologically or cytologically confirmed R or M HNSCC. Eligible primary tumor locations are oral cavity, hypopharynx, larynx or oropharynx (with documented HPV-negative disease if presenting with OPSCC). Note: primary tumor location of paranasal sinuses and nasopharynx, any histology are excluded.
* No prior systemic therapy administered in the R or M setting; and completed systemic therapy \>6 months prior if given as part of multimodal treatment for locoregionally advanced disease in the adjuvant or definitive setting.
* Archival tumor tissue or willing to undergo pretreatment biopsy at Screening if archival tissue is insufficient or unavailable.
* PD-L1 CPS ≥1.
* Measurable disease based on RECIST 1.1.
* Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
* Adequate organ function, as defined in the protocol.
Exclusion Criteria:
* Disease suitable for local therapy administered with curative intent.
* Prior treatment with anti-TGFβ therapy.
* Prior therapy with an anti-EGFR antibody (exception: radio sensitizing agents and multimodal treatment for locoregionally advanced disease).
* Prior history of Grade ≥2 intolerance or hypersensitivity reaction to anti-EGFR therapy or other murine proteins.
* Prior therapy with an immune checkpoint inhibitor completed within 6 months prior to study treatment initiation.
* Progressive disease \<6 months from completion of curative intent systemic therapy for locoregionally advanced HNSCC.
* Life expectancy less than 3 months.
* Known active central nervous system metastases, history of spinal cord compression from tumor involvement, a history of carcinomatous meningitis, or leptomeningeal disease are excluded.
* Current active major bleeding, or a recent major bleeding episode within 4 weeks prior to enrollment.
* Subject participated in another clinical study or received treatment with another investigational drug must wait at least 5 half-lives of the treatment received or 4 weeks (whichever is shorter) following prior therapy.
* Active autoimmune disease requiring systemic treatment in the past 2 years.
* Subjects with chronic hepatitis B virus (HBV) infection with active disease who meet the criteria for anti-HBV therapy and are not on a suppressive antiviral therapy prior to initiation of study treatment.
* Subjects with a known history of hepatitis C virus (HCV) who have not completed curative antiviral treatment or have an HCV viral load above the limit of quantification at Screening.
* Known history of human immunodeficiency virus (HIV).
* Receipt of any organ transplantation, including autologous and allogeneic stem cell transplantation, with the exception of transplants that do not require immunosuppression.
* Known to be diagnosed and/or treated for any other additional malignancy within 2 years prior to randomization with the exception of the following: curatively treated basal cell carcinoma or squamous cell carcinoma of the skin, and curatively resected in situ cervical cancer, and curatively resected in situ breast cancer, and low-risk early stage prostate cancer.
* Any condition requiring systemic treatment with either corticosteroids (\>10 mg daily of prednisone or equivalent) or other immunosuppressive medication within 7 days prior to the first dose of study treatment, except for topical, intranasal, intrabronchial, or ocular steroids.
* Use of a live or live attenuated vaccine within 4 weeks prior to Screening.
Other Inclusion/Exclusion criteria may apply as defined in the protocol.
Primary outcome measure(s)
Phase 2 - Incidence and severity of TEAEs, treatment-treatment emergent SAEs TEAEs leading to dose interruption, dose reduction, or permanent discontinuation. — Up to 30 days post end of treatment for TEAEs (90 days for SAEs). To assess safety and tolerability of ficerafusp alfa with pembrolizumab.
Phase 2 - Objective Response Rate (ORR) per RECIST 1.1 by blinded independent central review (BICR) — Approximately 1 year. ORR is defined as the proportion of subjects in the DDS who have a confirmed CR or PR per RECIST 1.1. by BICR.
Phase 3 - Objective Response Rate (ORR) per RECIST 1.1 by BICR. — Approximately 2 years. ORR is defined as the proportion of subjects in the DDS who have a confirmed CR or PR per RECIST 1.1. by BICR.
Phase 3 - Overall Survival (OS) — Approximately 3 years. OS: Defined as the time from the randomization to death due to any cause.
Trial sites (203)
Facility
City
Region
Status
Site # 0137
Birmingham
Alabama
Recruiting
Site #0147
Phoenix
Arizona
Recruiting
Site #0107
La Jolla
California
Recruiting
Site #0106
Los Angeles
California
Recruiting
Site#0144
Sacramento
California
Recruiting
Site #0130
San Francisco
California
Recruiting
Site #0150
Stanford
California
Recruiting
Site #0122
Aurora
Colorado
Recruiting
Site #0124
Aurora
Colorado
Recruiting
Site#0121
Aurora
Colorado
Recruiting
Site #0148
Jacksonville
Florida
Recruiting
Site #0136
Palm Bay
Florida
Recruiting
Site #0105
Tampa
Florida
Recruiting
Site#0140
Iowa City
Iowa
Recruiting
Site #0149
Westwood
Kansas
Recruiting
Site#0111
Louisville
Kentucky
Recruiting
Site#0115
Louisville
Kentucky
Recruiting
Site #0112
Baltimore
Maryland
Recruiting
Site #0131
Boston
Massachusetts
Recruiting
Site#0101
Boston
Massachusetts
Recruiting
Site #0156
Maplewood
Minnesota
Recruiting
Site #0146
Rochester
Minnesota
Recruiting
Site #0114
St Louis
Missouri
Recruiting
Site #0145
Newark
New Jersey
Recruiting
Site #0155
New York
New York
Recruiting
Site#0142
New York
New York
Recruiting
Site#0118
Durham
North Carolina
Recruiting
Site#0154
Canton
Ohio
Recruiting
Site#0117
Cincinnati
Ohio
Recruiting
Site #0151
Cleveland
Ohio
Recruiting
Site #0108
Cleveland
Ohio
Recruiting
Site #0113
Portland
Oregon
Recruiting
Site #0103
Pittsburgh
Pennsylvania
Recruiting
Site #0123
Pittsburgh
Pennsylvania
Recruiting
Site #0132
Providence
Rhode Island
Recruiting
Site#0104
Charleston
South Carolina
Recruiting
Site#0126
Nashville
Tennessee
Recruiting
Site #0116
Nashville
Tennessee
Recruiting
Site#0102
Houston
Texas
Recruiting
Site #0152
Waco
Texas
Recruiting
+ 163 more sites — see the full list on the official registry below.
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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