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FORTIFI-HN01: A Study of Ficerafusp Alfa (BCA101) or Placebo in Combination With Pembrolizumab in First-Line PD-L1-pos, R or M HNSCC

RecruitingPhase 2/3

A Multicenter, Randomized, Double-blind, Phase 2/3 Study of Ficerafusp Alfa (BCA101) or Placebo in Combination With Pembrolizumab for First-Line Treatment of PD-L1-positive, Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
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.

About the study

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).

What is being tested

Sponsor: Bicara Therapeutics · Participants: 650 · Started: Jan 28, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT06788990

Locations in the U.S.

AlabamaUniversity of Alabama Hospital (Site # 0137), Birmingham
ArizonaMayo Clinic Hospital (Site #0147), Phoenix
CaliforniaUC San Diego Moores Cancer Center (Site #0107), La Jolla
UCLA Department of Medicine - Hematology/Oncology (Site #0106), Los Angeles
UC Davis (Site#0144), Sacramento
University of California San Francisco (Site #0130), San Francisco
Stanford Cancer Institute (Site #0150), Stanford
ColoradoRocky Mountain Cancer Centers, LLP (Site #0122), Aurora
Rocky Mountain Regional VAMC (Site #0124), Aurora
University of Colorado Cancer Center (UCCC) - Anschutz Medical Campus (Site#0121), Aurora
DelawareChristianaCare Helen F. Graham Cancer Center and Research Institute (Site # 127), Newark
FloridaMayo Clinic Florida (Site #0148), Jacksonville
Cancer Care Centers of Brevard (Site #0136), Palm Bay
Moffit Cancer Center (Site #0105), Tampa
IllinoisCaptain James A Lovell Federal Health Care Center-VA North Chicago (Site # 133), Chicago
IowaUniversity of Iowa Hospitals & Clinics (Site#0140), Iowa City
KansasUniversity of Kansas Medical Center Research Institute, Inc. (Site #0149), Westwood
KentuckyUniversity of Kentucky, Markey Cancer Center (Site # 109), Lexington
Norton Cancer Institute (Site#0111), Louisville
The University of Louisville, James Graham Brown Cancer Center (Site#0115), Louisville
MarylandUniversity of Maryland Medical Group (Site #0112), Baltimore
MassachusettsDana-Farber Cancer Institute (Site#0101), Boston
Massachusetts General Hospital (Site #0131), Boston
MichiganUniversity of Michigan (Site # 161), Ann Arbor
MinnesotaSite #0156, Maplewood
Mayo Clinic Cancer Center - Rochester (Site #0146), Rochester
MissouriWashington University School of Medicine (Site #0114), St Louis
New JerseyHackensack Meridian Health (Site # 119), Hackensack
Rutgers- Cancer Institute (Site #0145), Newark
New YorkMemorial Sloan Kettering Cancer Center (Site#0142), New York
Mount Sinai (Site #0155), New York
North CarolinaDuke University Health System (Site#0118), Durham
OhioMercy Hospital (Site#0154), Canton
University of Cincinnati Cancer Institute (Site#0117), Cincinnati
Cleveland Clinic (Site #0108), Cleveland
University Hospitals Seidman Cancer Center (Site #0151), Cleveland
OregonProvidence Portland Medical Center (Site #0113), Portland
PennsylvaniaUPMC Hillman Cancer Center (Site #0103), Pittsburgh
VA Pittsburgh Healthcare System (Site #0123), Pittsburgh
Rhode IslandLifespan Cancer Institute (Site #0132), Providence
South CarolinaMedical University of South Carolina (MUSC) (Site#0104), Charleston
TennesseeSCRI-Oncology Partners (Site#0126), Nashville
Vanderbilt-Ingram Cancer Center (Site #0116), Nashville
TexasMD Anderson Cancer Center (Site#0102), Houston
SCRI- Texas Oncology- Central South (Site #0152), Waco
VirginiaUniversity of Virginia (Site#0134), Charlottesville
Richmond Department of Veterans Affairs (Site #0138), Richmond
Virginia Commonwealth University (VCU) Massey Cancer Center (Site #0129), Richmond
WashingtonSwedish Cancer Institute - North Campus Edmonds (Site # 0160), Edmonds
Swedish Cancer Institute (Site # 0159), Seattle
University of Washington - Seattle Cancer Care Alliance (Site #0125), Seattle
Northwest Cancer Specialists, PC (Site#0120), Vancouver
WisconsinUniversity of Wisconsin Hospital and Clinics (Site #0157), Madison
William S. Middleton Memorial Veteran's Hospital (Site #0141), Madison
Advocate Aurora Research Institute (Site # 0153), Milwaukee

Conditions

From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.