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A Study of YL201 in Combination With Serplulimab in Participants With Treatment-naïve Extensive-stage Small Cell Lung Cancer

20 de agosto de 2026 actualizado por: MediLink Therapeutics (Suzhou) Co., Ltd.

A Phase III, Multicenter, Randomized, Controlled, Open-label Clinical Study to Evaluate the Efficacy and Safety of YL201 in Combination With Serplulimab Versus Carboplatin and Etoposide in Combination With Serplulimab as First-line Treatment in Participants With Treatment-naïve Extensive-stage Small Cell Lung Cancer

This trial is a registrational Phase III, randomized, open-label, multicenter study to compare the efficacy and safety of YL201 in combination with serplulimab versus standard-of-care carboplatin and etoposide in combination with serplulimab as first-line treatment in patients with extensive-stage small cell lung cancer.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Estimado)

442

Fase

  • Fase 3

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

Ubicaciones de estudio

    • Guangdong
      • Guangzhou, Guangdong, Porcelana, 510060
        • Reclutamiento
        • Sun Yat-sen University Cancer Center
        • Contacto:
          • Study Coordinator
    • Liaoning
      • Shenyang, Liaoning, Porcelana, 110042
        • Reclutamiento
        • Liaoning Cancer Hospital & Institute
        • Contacto:
          • Study Coordinator

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. Voluntarily sign the written informed consent form and comply with the protocol requirements
  2. Age ≥18 years.
  3. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  4. Histologically or cytologically confirmed extensive-stage small cell lung cancer (ES-SCLC).
  5. No prior systemic treatment for ES-SCLC.
  6. At least one extracranial measurable lesion according to RECIST v1.1.
  7. Adequate organ function.
  8. Life expectancy ≥3 months.

Exclusion Criteria:

  1. Any histological types of transformed SCLC or combined SCLC.
  2. History of immune-related adverse events (irAEs) of CTCAE Grade ≥3 during prior immunotherapy, or unresolved adverse events from previous antitumor therapy.
  3. Major surgery (excluding diagnostic procedures) or severe trauma within 4 weeks prior to randomization or planned major surgery during the study period.
  4. History of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation.
  5. Presence of active brain metastases, brainstem metastases, or leptomeningeal metastases.
  6. Presence of severe and uncontrolled cardiovascular or cerebrovascular disease.
  7. History of interstitial lung disease (ILD) /pneumonitis requiring steroid treatment, or current diagnosis of ILD/pneumonitis, or concurrent pulmonary disease leading to clinically severe impairment of respiratory function.
  8. Active autoimmune or inflammatory diseases within 2 years prior to randomization.
  9. Severe infection within 4 weeks prior to randomization, or active infection requiring intravenous anti-infective therapy within 2 weeks or oral anti-infective therapy within 1 week prior to randomization.
  10. Known active tuberculosis or active syphilis infection.
  11. History of immunodeficiency or positive for human immunodeficiency virus (HIV) antibodies test.
  12. Active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection. Participants with inactive HBV infection must receive antiviral therapy throughout the study.
  13. History of other primary malignancies within 5 years prior to randomization.
  14. Known hypersensitivity to any component of the investigational product.
  15. Females who are pregnant or breastfeeding, or who plan to become pregnant or breastfeed during the study period.
  16. Any condition that, in the opinion of the investigator, would make the participant unsuitable for study 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: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: YL201 in combination with serplulimab
Participants will receive YL201 in combination with serplulimab until disease progression or unacceptable toxicity, whichever occurs first. The total number of treatment cycles of YL201 in this study is not fixed, and the maximum duration of serplulimab treatment is 2 years.

YL201 will be administered by intravenous infusion at a dose of 2.0 mg/kg on Day 1 of each 3-week cycle.

Treatment will continue until disease progression or unacceptable toxicity, whichever occurs first. The total number of treatment cycles of YL201 in this study is not fixed,

Otros nombres:
  • Tam-Peli
  • Tambotatug Pelitecan

Serplulimab will be administered by intravenous infusion at a dose of 300mg on Day 1 of each 3-week cycle.

Treatment will continue until disease progression or unacceptable toxicity. The maximum treatment duration for serplulimab will be 2 years.

Comparador activo: Carboplatin and etoposide in combination with serplulimab
Participants will receive 4 cycles of carboplatin plus etoposide in combination with serplulimab as induction therapy, followed by maintenance treatment with serplulimab for up to 2 years.

Serplulimab will be administered by intravenous infusion at a dose of 300mg on Day 1 of each 3-week cycle.

Treatment will continue until disease progression or unacceptable toxicity. The maximum treatment duration for serplulimab will be 2 years.

Carboplatin will be administered by intravenous infusion at a dose of AUC 5 on Day 1 of each 3-week cycle.

Carboplatin treatment will be administered for up to 4 cycles.

Etoposide will be administered by intravenous infusion at a dose of 100 mg/m2 on Days 1 to 3 of each 3-week cycle.

Etoposide treatment will be administered for up to 4 cycles.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Overall survival (OS)
Periodo de tiempo: Up to approximately 5 years
OS duration is defined as the difference in time from the date of randomization to the date of death due to any cause. OS was estimated using KM methodology.
Up to approximately 5 years
Progression-free survival (PFS) as assessed by BIRC
Periodo de tiempo: Up to approximately 30 months
PFS, as assessed by Blinded Independent Review Committee (BIRC), is defined as the time from randomization to the first documented progressive disease (PD) based on BIRC imaging assessment, or death from any cause, whichever occurs first.
Up to approximately 30 months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Progression-free survival (PFS) as assessed by investigator
Periodo de tiempo: Up to approximately 30 months
PFS assessed by investigator is defined as the time from randomization to the first documented PD based on investigator assessment, or death from any cause, whichever occurs first.
Up to approximately 30 months
Objective response rate (ORR)
Periodo de tiempo: Up to approximately 30 months
ORR is defined as the percentage of participants with (confirmed) complete response or partial response as assessed according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
Up to approximately 30 months
Disease control rate (DCR)
Periodo de tiempo: Up to approximately 30 months
DCR is defined as the percentage of participants with (confirmed) complete response, partial response, or stable disease as assessed according to RECIST v1.1
Up to approximately 30 months
Duration of response (DOR)
Periodo de tiempo: Up to approximately 30 months
DOR is defined as the time from the first documented objective response to the first documented disease progression or death from any cause, whichever occurs first.
Up to approximately 30 months
Time to response (TTR)
Periodo de tiempo: Up to approximately 30 months
TTR is defined as the time from randomization to the first documented objective response.
Up to approximately 30 months
Treatment Emergent Adverse Event (TEAE)
Periodo de tiempo: Up to approximately 30 months

Treatment-emergent adverse events (TEAEs) are defined as any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new onset or worsening) that occurs after initiation of YL201, or any worsening of a pre-existing condition during YL201 treatment.

TEAEs will be graded and summarized by type, frequency, and severity according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE), version 6.0.

Up to approximately 30 months
Pharmacokinetic (PK) characteristics
Periodo de tiempo: Up to approximately 30 months
PK parameters of YL201 and serplulimab will be evaluated.
Up to approximately 30 months
Anti-drug antibody (ADA)
Periodo de tiempo: Up to approximately 30 months
Frequency of anti-YL201 antibody (ADA) will be investigated.
Up to approximately 30 months

Colaboradores e Investigadores

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

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 (Actual)

18 de agosto de 2026

Finalización primaria (Estimado)

1 de junio de 2029

Finalización del estudio (Estimado)

1 de abril de 2030

Fechas de registro del estudio

Enviado por primera vez

28 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

28 de julio de 2026

Publicado por primera vez (Actual)

31 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

24 de agosto de 2026

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

20 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

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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