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- Ensayo clínico NCT07683507
Becotatug Vedotin Plus PD-1 Inhibitor for Head and Neck Squamous Cell Carcinoma
29 de junio de 2026 actualizado por: Feng Liu
A Clinical Study of the Efficacy and Safety of Becotatug Vedotin in Combination With Immune Checkpoint Inhibitors as First-Line or Later-Line Treatment for Head and Neck Squamous Cell Carcinoma
This is a prospective, open-label, non-randomized, two-cohort, single-arm Phase 2 study in adults with unresectable or recurrent/metastatic head and neck squamous cell carcinoma, excluding nasopharyngeal carcinoma.
The study will evaluate the efficacy and safety of Becotatug vedotin, an EGFR-targeted antibody-drug conjugate, in combination with an investigator-selected PD-1 inhibitor.
Participants will enter one of two cohorts based on prior treatment: those who have not received prior systemic treatment for unresectable or recurrent/metastatic disease, and those who have received at least one prior line of treatment.
Becotatug vedotin will be given once every 21 days with the PD-1 inhibitor.
Treatment may continue until disease progression, unacceptable side effects, withdrawal of consent, death, or other protocol-defined reasons.
The main purpose is to assess objective response rate, defined as the percentage of participants whose tumors have a complete or partial response.
Other outcomes include safety, tolerability, progression-free survival, overall survival, disease control rate, and duration of response.
Descripción general del estudio
Estado
Aún no reclutando
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Estimado)
60
Fase
- Fase 2
Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Descripción
Inclusion Criteria:
- Age 18 to 80 years.
- Primary tumor of head and neck squamous cell carcinoma, excluding nasopharyngeal carcinoma.
- Disease assessed as not suitable for complete surgical resection, or the participant refuses surgery despite being considered technically eligible for surgery.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- No obvious contraindications to immunotherapy, radiotherapy, or chemotherapy.
Adequate major organ function, defined as follows:
- Hematologic function: white blood cell count (WBC) ≥4.0 × 10^9/L, absolute neutrophil count (ANC) ≥1.5 × 10^9/L, platelet count (PLT) ≥100 × 10^9/L, and hemoglobin (Hb) ≥90 g/L without blood transfusion, blood products, G-CSF, or other hematopoietic growth factors within 14 days before testing.
- Biochemical function: serum albumin ≥3.0 g/dL (30 g/L), total bilirubin (TBIL) ≤1.5 × upper limit of normal (ULN), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5 × ULN, and blood urea nitrogen (BUN) and serum creatinine (Cr) ≤1.5 × ULN or creatinine clearance ≥60 mL/min calculated by the Cockcroft-Gault formula.
- Adequate coagulation function, defined as international normalized ratio (INR) or prothrombin time (PT) ≤1.5 × ULN. For participants receiving anticoagulant therapy, PT must be within the intended therapeutic range of the anticoagulant.
- Women of childbearing potential must use reliable contraception, have a negative pregnancy test within 7 days before enrollment, and agree to use effective contraception during the study and for 2 months after the last dose of anti-PD-1 antibody. Male participants with female partners of childbearing potential must agree to use effective contraception during the study and for 2 months after the last dose of anti-PD-1 antibody.
- The participant voluntarily agrees to participate in the study, signs the informed consent form, and is willing and able to comply with study visits and follow-up.
Exclusion Criteria:
- Congenital or acquired immunodeficiency, including human immunodeficiency virus (HIV) infection; active hepatitis B infection, defined as HBV-DNA ≥10^4 copies/mL; or hepatitis C infection, defined as positive hepatitis C antibody with HCV-RNA above the lower limit of detection of the assay.
- Known allergy to the study drug or any of its excipients, or a history of severe hypersensitivity reaction to other monoclonal antibodies.
- Any of the following within 6 months before the first dose of study treatment: myocardial infarction, severe or unstable angina, New York Heart Association (NYHA) class II or higher heart failure, or symptomatic congestive heart failure.
- Receipt of a live vaccine within 4 weeks before the first dose of study treatment. Inactivated injectable vaccines for seasonal influenza are permitted, but intranasal live attenuated influenza vaccines are not permitted.
- Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation.
- Known history of psychotropic drug abuse or illicit drug use.
- Pregnant or breastfeeding women.
- Diagnosis of any other malignancy within 5 years before study entry, except for locally treated and cured basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, carcinoma in situ of the cervix, ductal carcinoma in situ of the breast, or papillary thyroid carcinoma.
- Any other serious physical or psychiatric illness or laboratory abnormality that may increase the risk of study participation, interfere with study results, or make the participant unsuitable for this study in the investigator's judgment.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: First-Line Cohort
Participants who have not received prior systemic treatment for unresectable or recurrent/metastatic head and neck squamous cell carcinoma.
|
Becotatug vedotin will be administered at 2.0 mg/kg by intravenous infusion once every 3 weeks in combination with an investigator-selected PD-1 inhibitor.
Treatment will continue until disease progression, unacceptable toxicity, withdrawal of consent, death, or other protocol-defined reasons for discontinuation.
|
|
Experimental: Previously Treated Cohort
Participants who have received at least one prior line of systemic treatment for unresectable or recurrent/metastatic head and neck squamous cell carcinoma.
|
Becotatug vedotin will be administered at 2.0 mg/kg by intravenous infusion once every 3 weeks in combination with an investigator-selected PD-1 inhibitor.
Treatment will continue until disease progression, unacceptable toxicity, withdrawal of consent, death, or other protocol-defined reasons for discontinuation.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Objective Response Rate (ORR)
Periodo de tiempo: From enrollment until disease progression, death, withdrawal of consent, start of new anti-cancer therapy, loss to follow-up, or end of study, up to 2 years.
|
Objective response rate is defined as the percentage of participants who achieve a complete response (CR) or partial response (PR) as assessed by investigators according to RECIST v1.1.
ORR will be evaluated separately in each cohort.
|
From enrollment until disease progression, death, withdrawal of consent, start of new anti-cancer therapy, loss to follow-up, or end of study, up to 2 years.
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Progression-Free Survival (PFS)
Periodo de tiempo: From enrollment to disease progression or death from any cause, up to 2 years.
|
Progression-free survival is defined as the time from enrollment to the first documented disease progression or death from any cause, whichever occurs first.
|
From enrollment to disease progression or death from any cause, up to 2 years.
|
|
1-Year and 2-Year Progression-Free Survival Rate
Periodo de tiempo: At 1 year and 2 years after enrollment.
|
The 1-year and 2-year progression-free survival rates are defined as the percentage of participants who remain alive and free of disease progression at 1 year and 2 years after enrollment.
|
At 1 year and 2 years after enrollment.
|
|
1-Year and 2-Year Overall Survival Rate
Periodo de tiempo: At 1 year and 2 years after enrollment.
|
The 1-year and 2-year overall survival rates are defined as the percentage of participants who remain alive at 1 year and 2 years after enrollment.
|
At 1 year and 2 years after enrollment.
|
|
Duration of Response (DoR)
Periodo de tiempo: From the first documented CR or PR to disease progression or death from any cause, up to 2 years.
|
Duration of response is defined as the time from the first documented CR or PR to the first documented disease progression or death from any cause, whichever occurs first.
This measure will be evaluated in participants who achieve CR or PR.
|
From the first documented CR or PR to disease progression or death from any cause, up to 2 years.
|
|
Disease Control Rate (DCR)
Periodo de tiempo: From enrollment until disease progression, death, withdrawal of consent, start of new anti-cancer therapy, loss to follow-up, or end of study, up to 2 years.
|
Disease control rate is defined as the percentage of participants who achieve CR, PR, or stable disease (SD) as assessed by investigators according to RECIST v1.1.
DCR will be evaluated separately in each cohort.
|
From enrollment until disease progression, death, withdrawal of consent, start of new anti-cancer therapy, loss to follow-up, or end of study, up to 2 years.
|
|
Incidence and Severity of Adverse Events
Periodo de tiempo: From signing informed consent to 90 days after the last dose of study treatment.
|
Adverse events (AEs), serious adverse events (SAEs), immune-related adverse events, adverse events of special interest, infusion-related reactions, laboratory abnormalities, vital signs, physical examination findings, electrocardiogram findings, and echocardiography findings will be evaluated and summarized by severity, relationship to study treatment, action taken, and outcome.
AEs will be graded according to NCI-CTCAE v5.0 and coded using MedDRA.
|
From signing informed consent to 90 days after the last dose of study treatment.
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Estimado)
1 de julio de 2026
Finalización primaria (Estimado)
31 de diciembre de 2027
Finalización del estudio (Estimado)
31 de diciembre de 2029
Fechas de registro del estudio
Enviado por primera vez
29 de junio de 2026
Primero enviado que cumplió con los criterios de control de calidad
29 de junio de 2026
Publicado por primera vez (Actual)
6 de julio de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
6 de julio de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
29 de junio de 2026
Última verificación
1 de junio de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Neoplasias por sitio
- Neoplasias
- Neoplasias por tipo histológico
- Neoplasias de Cabeza y Cuello
- Neoplasias Glandulares y Epiteliales
- Carcinoma
- Carcinoma De Células Escamosas
- Carcinoma de células escamosas de cabeza y cuello
- Agentes antineoplásicos inmunológicos
- Agentes antineoplásicos
- Mecanismos moleculares de acción farmacológica.
- Acciones farmacológicas
- Acciones y usos químicos
- Usos terapéuticos
- Inhibidores de puntos de control inmunitarios
Otros números de identificación del estudio
- SH9H-2026-T260-2
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .