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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 atualizado 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.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Estimado)

442

Estágio

  • Fase 3

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

    • Guangdong
      • Guangzhou, Guangdong, China, 510060
        • Recrutamento
        • Sun Yat-sen University Cancer Center
        • Contato:
          • Study Coordinator
    • Liaoning
      • Shenyang, Liaoning, China, 110042
        • Recrutamento
        • Liaoning Cancer Hospital & Institute
        • Contato:
          • Study Coordinator

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
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,

Outros nomes:
  • 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 Ativo: 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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Overall survival (OS)
Prazo: 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
Prazo: 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 resultados secundários

Medida de resultado
Descrição da medida
Prazo
Progression-free survival (PFS) as assessed by investigator
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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
Prazo: Up to approximately 30 months
PK parameters of YL201 and serplulimab will be evaluated.
Up to approximately 30 months
Anti-drug antibody (ADA)
Prazo: Up to approximately 30 months
Frequency of anti-YL201 antibody (ADA) will be investigated.
Up to approximately 30 months

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

18 de agosto de 2026

Conclusão Primária (Estimado)

1 de junho de 2029

Conclusão do estudo (Estimado)

1 de abril de 2030

Datas de inscrição no estudo

Enviado pela primeira vez

28 de julho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

28 de julho de 2026

Primeira postagem (Real)

31 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

24 de agosto de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

20 de agosto de 2026

Última verificação

1 de agosto de 2026

Mais Informações

Termos relacionados a este estudo

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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