Skip to main content
UK clinical trials - updated daily from ClinicalTrials.gov
TrialConnect
← Back to Search
Looking for participantsPhase2/Phase3

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

Sponsor: Bicara Therapeutics

NCT ID: NCT06788990

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Ficerafusp alfa (drug), Pembrolizumab (KEYTRUDA®) (drug), Placebo (drug)
How long the study runs
Study runs about 54 months (dates as stated)
About the drug or intervention
Ficerafusp alfa — drug: Investigational · Pembrolizumab (KEYTRUDA®) — drug: Immunotherapy agent used in combination with investigational agent · Placebo — drug: Placebo Control
Patient visit burden
Not specified by the sponsor

In plain English

This study is for adults with head and neck cancer that has come back (recurrent) or spread to other parts of the body (metastatic). It tests whether a new drug called ficerafusp alfa (BCA101) works better than a dummy medicine (placebo) when given together with an existing drug called pembrolizumab. It is run by Bicara Therapeutics for people who have not yet had drug treatment for recurrent or metastatic disease.

Who can take part

  • Aged 18 or over.
  • Confirmed recurrent or metastatic head and neck squamous cell carcinoma (a type of head and neck cancer) in the mouth, voice box, throat areas listed, or oropharynx (part of the throat behind the mouth). If the cancer started in the oropharynx, it must be HPV-negative (not linked to a common virus).
  • No previous drug treatment for recurrent or metastatic disease. If you had drug treatment earlier as part of treatment for locally advanced disease, it must have finished more than 6 months ago.
  • Willing to provide stored tumour tissue, or have a small sample of tissue taken (a biopsy) before the study starts, if stored tissue is not available.
  • Tumour must test positive for PD-L1 (a protein on cancer cells) with a score of at least 1.
  • Cancer that can be measured on scans.
  • Able to carry out light activity (performance status score of 0 or 1).
  • Good working organs, such as the liver and kidneys, as defined in the study plan.

Who may not be able to

  • Cancer that could be treated with local treatment (such as surgery or radiotherapy) aiming to cure it.
  • Previous treatment that targets a protein called TGF-beta.
  • Previous treatment with a type of drug called an anti-EGFR antibody (with some exceptions, such as drugs given with radiotherapy or as part of earlier treatment for locally advanced disease).
  • A past moderate or worse allergic reaction or bad reaction to anti-EGFR treatment or similar proteins.
  • Treatment with an immune checkpoint inhibitor (a type of immunotherapy drug) within the last 6 months.
  • Cancer that got worse within 6 months of finishing earlier curative drug treatment for locally advanced head and neck cancer.
  • Life expectancy of less than 3 months.
  • Cancer that has spread to the brain or spinal cord, or affects the lining of the brain or spinal cord.
  • Current serious bleeding, or a serious bleed within the last 4 weeks.
  • Taking part in another clinical study, or having another experimental drug, within a set waiting period (4 weeks or 5 half-lives, whichever is shorter).
  • An active autoimmune disease needing treatment in the past 2 years.
  • Hepatitis B infection that is active and not being treated with antiviral medicine.
  • Hepatitis C that has not been cured or still shows up in blood tests.
  • Known HIV infection.
  • Having had an organ transplant or stem cell transplant (unless the transplant does not need drugs that damp down the immune system).
  • Another cancer diagnosed or treated in the past 2 years (with some exceptions, such as treated skin cancers and very early prostate cancer).
  • Needing steroid tablets (more than 10 mg prednisone a day) or other drugs that damp down the immune system in the last 7 days (creams, nose sprays, lung inhalers or eye drops are allowed).
  • Having had a live vaccine (a vaccine containing a weakened live germ) in the last 4 weeks.
  • Other criteria in the study plan may also apply.

What taking part involves

  • • Being given either ficerafusp alfa (BCA101) or a dummy medicine (placebo) — which one you get is decided by chance.
  • • Your medicine is given together with pembrolizumab, an existing immunotherapy drug.

Time commitment: Not stated — ask the trial team about how many visits are needed and how long the study lasts; you may need to provide stored tumour tissue or have a biopsy before the study starts.

Plain-English summary (AI-generated) from registry data. Not eligibility advice — only the trial team can confirm whether you can take part. Use the eligibility checker to see how your health profile matches this trial.

Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
650
Started
2025-01-28
Last checked
2026-07

Plain English Summary

What is this study?

  • • Testing a new treatment for metastatic head and neck squamous cell carcinoma
  • • Phase2/Phase3 - 650 participants
  • • Ficerafusp alfa is directed against two targets, Epidermal Growth Factor Receptor (EGFR) and Transforming Growth Factor beta (TGF-β)

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with metastatic head and neck squamous cell carcinoma

Where?

  • • Aberdeen - Site #0504
  • • Birmingham - Site #0512
  • • Cambridge - Site #0513
  • • Glasgow - Site # 0510
  • • +11 more UK sites

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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).

More detail

The mechanism of action of ficerafusp alfa involves dual targeting of two cancer targets, EGFR and TGF-β, which are known to drive solid tumor growth and metastasis. Phase 2 of the study will identify an optimal biologic dose (OBD) supported by the safety, tolerability, PK, PD, and efficacy data of ficerafusp alfa. In this part, eligible subjects will be randomized to one of three treatment arms at a 1:1:1 ratio: * Arm A: ficerafusp alfa 1500 mg once weekly (QW) + pembrolizumab 200 mg every three weeks (Q3W). * Arm B: ficerafusp alfa 750 mg QW + pembrolizumab 200 mg Q3W. * Arm C (control): placebo QW + pembrolizumab 200 mg Q3W. The primary objective for the phase 3 portion is to compare the efficacy in subjects treated with ficerafusp alfa at the selected OBD in combination with pembrolizumab versus placebo with pembrolizumab. Eligible subjects will be randomized 2:1 in the treatment versus control arm during the phase 3 portion.

Metastatic Head and Neck Squamous Cell CarcinomaRecurrent Head and Neck Squamous Cell Carcinoma

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

Biomarkers mentioned

PD-L1EGFR

What the study is looking for

  • ✓Age ≥18 years on the day the agreement to take part Form is signed.
  • ✓Archival tumor tissue or willing to undergo pretreatment biopsy at Screening if archival tissue is insufficient or...
  • ✓PD-L1 CPS ≥1.
  • ✓cancer that can be measured on scans based on (standard scan measurements).
  • ✓activity scale (ECOG) performance status of 0 or 1.

Who cannot take part

  • ✗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...
  • ✗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.
See the full 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.

Where Is This Study? (15 UK sites)

Site #0504

Aberdeen AB25 2ZN, United Kingdom

Recruiting
Site contact (verified)

Site #0512

Birmingham B15 2TH, United Kingdom

Recruiting
Site contact (verified)

Site #0513

Cambridge CB2 0QQ, United Kingdom

Recruiting
Site contact (verified)

Site # 0510

Glasgow G12 0YN, United Kingdom

Recruiting
Site contact (verified)

Site #0511

Leeds LS9 7TF, United Kingdom

Recruiting
Site contact (verified)

Site #0507

Liverpool L7 8YA, United Kingdom

Recruiting
Site contact (verified)

Site #0505

London SW3 6JJ, United Kingdom

Recruiting
Site contact (verified)

Site #0502

London WC1E 6AG, United Kingdom

Recruiting
Site contact (verified)

Site #0508

Manchester M20 4BX, United Kingdom

Recruiting
Site contact (verified)

Site #0506

Middlesex HA6 2RN, United Kingdom

Recruiting
Site contact (verified)

Newcastle University (Site # 509)

Newcastle upon Tyne NE7 7DN, United Kingdom

Recruiting
Site contact (verified)

Site #0503

Nottingham NG5 1PB, United Kingdom

Recruiting
Site contact (verified)

Site #0515

Oxford OX3 7LE, United Kingdom

Recruiting
Site contact (verified)

Site # 0514

Portsmouth PO6 3LY, United Kingdom

Recruiting
Site contact (verified)

Site # 0501

Sutton SM2 5PT, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Medical Affairs

Sponsor contact

CONTACT

1-617-468-4219 FORTIFI_inquiries@bicara.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-07