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Phase II Study of Becotatug Vedotin Plus Pucotenlimab for Advanced Refractory Solid Tumors With EGFR-Positive

16 de julio de 2026 actualizado por: Tianjin Medical University Second Hospital

ELEVATE Study: A Phase II Single-Arm Open-Label Single-Center Exploratory Trial of Becotatug Vedotin (MRG003) Plus Pucotenlimab (HX008) in Advanced Refractory Solid Tumors With EGFR-Positive

This phase II trial evaluates the combination of Becotatug Vedotin (MRG003), an EGFR-targeting ADC, and Pucotenlimab (HX008), a PD-1 inhibitor, in patients with high EGFR expressing advanced refractory solid tumors. The study is designed to assess clinical efficacy and safety, building on a strong synergistic rationale and promising early-phase data.

Descripción general del estudio

Descripción detallada

Given the substantial unmet medical need for effective treatment options in patients with advanced refractory solid tumors, and grounded in the synergistic rationale of combining EGFR-targeted therapy with immune checkpoint modulation, the encouraging efficacy and manageable safety profiles observed in early phase studies of Becotatug Vedotin (MRG003) andPucotenlimab (HX008) provide a strong rationale for further investigation. Accordingly, a methodologically rigorous phase II clinical trial is warranted to objectively evaluate the clinical efficacy and safety of this dual regimen specifically in patients with high EGFR expressing advanced refractory solid tumors.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

32

Fase

  • Fase 2

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Haitao Wang, Ph.D.
  • Número de teléfono: +86-022-88321190
  • Correo electrónico: peterrock2000@126.com

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

    • Tianjin Municipality
      • Tianjin, Tianjin Municipality, Porcelana, 300211
        • Reclutamiento
        • Tianjin Medical Unversity Second Hospital
        • Contacto:
        • Contacto:
        • Investigador principal:
          • Haitao Wang, Ph.D.
        • Sub-Investigador:
          • Lili Wang, Ph.D.
        • Sub-Investigador:
          • Jinhuan Wang, Ph.D.
        • Sub-Investigador:
          • Hongzheng Li, M.M.
        • Sub-Investigador:
          • Dingkun Hou, Ph.D.

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:

  1. Age≥18 years at the time of signing the informed consent form (ICF).
  2. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 within 7 days prior to the first dose. ECOG 2 is allowable if it is solely attributable to tumor progression, as judged by the investigator.
  3. Life expectancy≥ 12 weeks.
  4. Histologically or cytologically confirmed locally advanced or metastatic solid tumors that have failed standard therapy (progressive disease or intolerance to prior treatment), or for whom standard therapy is currently not applicable or unavailable. There is no limit on the number of prior lines of therapy.
  5. Documentation of EGFR expression status is required for enrollment. If not available, the subject must provide adequate fresh or archival tumor tissue samples for EGFR testing. If adequate tumor specimens cannot be provided, a repeat biopsy may be performed if deemed feasible and safe by the investigator and after obtaining the subject's consent; however, repeat biopsy is not mandatory. In cases where repeat biopsy is not feasible or the subject refuses, eligibility must be jointly confirmed by the investigator and the sponsor.
  6. EGFR expression positive (2+ or 3+) as determined by immunohistochemistry (IHC).
  7. At least one measurable lesion per RECIST version 1.1.
  8. Adequate organ function, as defined by the following criteria (no blood components, cell growth factors, leukopoiesis agents, thrombopoiesis agents, or anemia-correcting drugs are allowed within 14 days prior to the first dose):

    A. White blood cell count (WBC) ≥ 3.0 x 10^9/L; absolute neutrophil count (ANC) ≥ 2.0 x 10^9/L.

    B. Hemoglobin (HB) ≥90 g/L. C. Platelet count ≥ 100x10^9/L. D. Serum albumin ≥ 2.8 g/dL. E. Total bilirubin ≤1.5 x upper limit of normal (ULN); alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3.0 x ULN.

    F. Serum creatinine ≤ 1.5 x ULN or creatinine clearance > 60 mL/min. G. Activated partial thromboplastin time (APTT) and international normalized ratio (INR) ≤ 1.5 x ULN (subjects receiving stable doses of anticoagulants, such as low-molecular-weight heparin or warfarin, with INR within the expected therapeutic range for the anticoagulant, are eligible for screening).

  9. No contraindications to chemotherapy, targeted therapy, or immunotherapy.
  10. No history of immune-related diseases.
  11. No uncontrolled pneumonia or pulmonary infection.
  12. Females of childbearing potential must agree to use effective contraception during the trial; a serum or urine pregnancy test must be negative within 72 hours before the start of chemotherapy.
  13. Subjects must be compliant, able to undergo treatment and follow-up, and willing to comply with the study requirements as specified in the protocol.
  14. For male subjects with partners of childbearing potential, effective medical contraception must be used from the signing of the ICF until 6 months after the last dose.
  15. Subjects must voluntarily sign the ICF and be able to comply with the protocol-specified visits and procedures.

Exclusion Criteria:

  1. Presence of uncontrolled serious medical conditions, including severe cardiac disease, cerebrovascular disease, uncontrolled diabetes, uncontrolled hypertension, uncontrolled infection, active peptic ulcer, etc.
  2. History of allergy or hypersensitivity to any component of monoclonal antibody-based agents, or known allergic constitution.
  3. Uncontrolled cardiac symptoms or diseases, such as:

    • New York Heart Association (NYHA) Class ≥ II heart failure, or left ventricular ejection fraction (LVEF) < 50% on echocardiography;
    • Unstable angina;
    • Myocardial infarction within 1 year;
    • Clinically significant supraventricular or ventricular arrhythmias requiring intervention (including QTc interval≥470 ms).
  4. Severe infection (CTC AE > Grade 2) within 4 weeks before the first dose, such as severe pneumonia requiring hospitalization, bacteremia, infectious complications, etc.; evidence of active pulmonary inflammation on baseline chest imaging; signs or symptoms of infection or need for oral or intravenous antibiotics (excluding prophylactic antibiotics) within 2 weeks before the first dose.
  5. Unexplained fever > 38.5 ℃ during screening or before the first dose (subjects with tumor fever, as judged by the investigator, may be enrolled).
  6. Active autoimmune disease or history of autoimmune disease (e.g., interstitial pneumonia, colitis, hepatitis, hypophysitis, vasculitis, nephritis, hyperthyroidism, hypothyroidism, including but not limited to these). Exceptions include: autoimmune-mediated hypothyroidism treated with stable doses of thyroid-replacement hormones; type 1 diabetes mellitus controlled with stable insulin; vitiligo; or childhood asthma/allergy that has resolved and requires no intervention in adulthood.
  7. History of immunodeficiency, including HIV-positive status, other acquired or congenital immunodeficiency diseases, or history of organ transplantation or allogeneic bone marrow transplantation.
  8. Untreated chronic hepatitis B, or hepatitis B virus (HBV) DNA > 500 IU/mL, or active hepatitis C virus (HCV) infection. Subjects with inactive hepatitis B surface antigen (HBsAg) carriers, treated and stabilized hepatitis B (HBV DNA < 500 IU/mL), or cured hepatitis C may be enrolled.
  9. History of interstitial lung disease (excluding radiation pneumonitis that has not been treated with corticosteroids) or non-infectious pneumonitis.
  10. Active pulmonary tuberculosis infection by history or CT findings, or history of active tuberculosis within 1 year before enrollment, or history of active tuberculosis more than 1 year ago without adequate treatment.
  11. Prior receipt of any of the following treatments:

    A. Any investigational drug within 4 weeks before the first dose. B. Last dose of anticancer therapy (including chemotherapy, radiotherapy, targeted therapy, etc.) ≤ 4 weeks before the first dose.

    C. Systemic corticosteroids (>10 mg/day prednisone equivalent) or other immunosuppressive agents within 2 weeks before the first dose, except for local inflammation prophylaxis, anti-allergy, or anti-emetic use. Inhaled or topical corticosteroids, and adrenal hormone replacement doses > 10 mg/day prednisone equivalent, are permitted in the absence of active autoimmune disease.

    D. Prior anti-cancer vaccine, or live vaccine within 4 weeks before the first dose.

    E. Major surgery or severe trauma within 4 weeks before the first dose. F. Concurrent enrollment in another clinical study.

  12. Dementia, altered mental status, or any psychiatric condition that would interfere with understanding or providing informed consent or completing questionnaires.
  13. History of allergy or hypersensitivity to any component of the study treatments.
  14. Known history of allogeneic organ or allogeneic hematopoietic stem cell transplantation.
  15. Active hepatitis B (HBsAg positive, requiring HBV-DNA testing; HBV-DNA≥500 IU/mL or above the lower limit of detection, whichever is higher) or active hepatitis C (HCV antibody positive with HCV-RNA above the lower limit of detection). Note: Subjects who are HBsAg positive are required to receive anti-HBV therapy during the study treatment period.
  16. Positive HIV test or history of acquired immunodeficiency syndrome (AIDS); known active syphilis infection.
  17. Major surgery within 4 weeks before the first dose, or anticipated to require major surgery during the study period.
  18. Rapid deterioration of clinical condition during the screening period (e.g., significant changes in performance status).
  19. Local or systemic disease not caused by malignancy, or disease/symptoms secondary to the tumor, that would pose a higher medical risk or introduce uncertainty in survival assessment, such as leukemoid reaction, cachexia, etc.
  20. Any condition that, in the investigator's opinion, would interfere with evaluation of the study drug, compromise subject safety, or confound interpretation of study results, or any other condition rendering the subject unsuitable for participation.

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: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Becotatug Vedotin+Pucotenlimab
In this study, Becotatug Vedotin will be given at a dose of 2.0 mg/kg via intravenous infusion on Day 1 of every 3 week cycle (Q3W). Pucotenlimab will be administered intravenously at 3.0 mg/kg (or as a flat dose of 200 mg) also on Day 1 of each Q3W cycle.
Becotatug Vedotin will be given at a dose of 2.0 mg/kg via intravenous infusion on Day 1 of every 3 week cycle (Q3W).
Otros nombres:
  • MRG003
Pucotenlimab will be administered intravenously at 3.0 mg/kg (or as a flat dose of 200 mg) also on Day 1 of each Q3W cycle.
Otros nombres:
  • HX008

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Objective Response Rate (ORR)
Periodo de tiempo: Up to approximately 2 years.
Objective Response Rate (ORR) assessed according to the evaluation criteria for the efficacy of solid tumors (RECIST v1.1).
Up to approximately 2 years.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Supervivencia general (OS)
Periodo de tiempo: Desde la administración del tratamiento hasta una duración máxima de 24 meses.
Tiempo desde el inicio del tratamiento hasta la muerte debido a cualquier causa.
Desde la administración del tratamiento hasta una duración máxima de 24 meses.
Adverse Events (AEs)
Periodo de tiempo: From treatment administration up to a maximum duration of 24 months.
Number of participants with adverse effects of treatment. Frequency and severity of adverse effects of treatment as assessed by NCI CTCAE.
From treatment administration up to a maximum duration of 24 months.
Progression Free Survival(PFS)
Periodo de tiempo: From treatment administration up to a maximum duration of 24 months.
The time from the beginning of the patient's treatment to the disease progression or death for any reason.Based on RECIST criteria v1.1.
From treatment administration up to a maximum duration of 24 months.
Radiological Progression-Free Survival(rPFS)
Periodo de tiempo: From treatment administration up to a maximum duration of 24 months.
Progression-free survival (PFS) based on radiographic assessment by the investigator using RECIST version 1.1
From treatment administration up to a maximum duration of 24 months.
Disease Control Rate(DCR)
Periodo de tiempo: From treatment administration up to a maximum duration of 24 months.
The disease control rate (DCR), defined as the proportion of patients achieving a best overall response of complete response, partial response, or stable disease, as assessed by the investigator using RECIST v1.1.
From treatment administration up to a maximum duration of 24 months.
Duration of Response(DoR)
Periodo de tiempo: From treatment administration up to a maximum duration of 24 months.
Duration of response (DoR) is defined as the time from the first documented objective response (complete response or partial response) until the date of disease progression or death, as assessed by the investigator using RECIST version 1.1.
From treatment administration up to a maximum duration of 24 months.

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
EGFR Expression Level and Efficacy Correlation
Periodo de tiempo: From treatment administration up to a maximum duration of 24 months.
Exploratory analysis evaluating the association between baseline EGFR expression levels (H-score or IHC) and ORR/PFS.
From treatment administration up to a maximum duration of 24 months.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Colaboradores

Investigadores

  • Investigador principal: Haitao Wang, Ph.D., Tianjin Medical University Second Hospital

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 agosto de 2026

Finalización primaria (Estimado)

31 de agosto de 2028

Finalización del estudio (Estimado)

31 de diciembre de 2028

Fechas de registro del estudio

Enviado por primera vez

12 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

16 de julio de 2026

Publicado por primera vez (Actual)

17 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

17 de julio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

16 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • PAN-CANCER-EGFR-MH

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

Due to the exploratory nature and limited sample size of this phase II study, IPD will not be share.

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. .

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