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A Study of BL-M14D1 in Combination With Atezolizumab in Patients With Extensive-stage Small Cell Lung Cancer

24 de agosto de 2026 atualizado por: Sichuan Baili Pharmaceutical Co., Ltd.

A Phase II Clinical Study to Evaluate the Efficacy and Safety of BL-M14D1 for Injection in Combination With Atezolizumab in Patients With Extensive-stage Small Cell Lung Cancer

This Phase II study is a clinical study exploring the efficacy and safety of BL-M14D1 in combination with Atezolizumab in patients with extensive-stage small cell lung cancer.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Estimado)

36

Estágio

  • Fase 2

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

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, China
        • Recrutamento
        • Shanghai East Hospital
        • Contato:
          • Caicun Zhou

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 informed consent form and comply with the protocol requirements;
  2. No gender restriction;
  3. Age: ≥18 years;
  4. Expected survival time ≥3 months;
  5. Histopathologically and/or cytologically confirmed extensive-stage small cell lung cancer that is incurable or for which there is currently no standard treatment;
  6. Agree to provide archived tumor tissue specimens from the primary or metastatic lesion within 3 years, or fresh tissue samples;
  7. Must have at least one measurable lesion as defined by RECIST v1.1;
  8. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
  9. Toxicities from prior anti-tumor therapy have recovered to ≤ Grade 1 as defined by NCI-CTCAE v6.0;
  10. No severe cardiac dysfunction, with left ventricular ejection fraction (LVEF) ≥50%;
  11. Organ function levels must meet the required criteria;
  12. Urine protein ≤1+ or ≤1000 mg/24h;
  13. For premenopausal women with childbearing potential, a pregnancy test must be performed within 7 days before the start of treatment. Serum pregnancy testing must rule out pregnancy, and the patient must not be breastfeeding. All enrolled trial participants (regardless of gender) should take adequate barrier contraceptive measures throughout the entire treatment period and for 7 months after the end of treatment.

Exclusion Criteria:

  1. Use of chemotherapy, biological therapy, immunotherapy, etc., within 4 weeks or 5 half-lives before the first dose;
  2. Previous treatment with ADC drugs using topoisomerase I inhibitors as toxins;
  3. Small cell carcinoma with non-small cell carcinoma components indicated by pathology must be excluded;
  4. Use of immunomodulatory drugs within 2 weeks before the first dose of the study;
  5. Receiving long-term systemic corticosteroid therapy at a dose >10 mg/day of prednisone or equivalent before the first dose;
  6. History of severe cardiovascular or cerebrovascular diseases;
  7. Prolonged QTc interval, complete left bundle branch block, etc.;
  8. Active autoimmune diseases and inflammatory diseases;
  9. Diagnosis of another malignancy within 5 years before the first dose;
  10. Hypertension poorly controlled by two antihypertensive drugs;
  11. Patients with poorly controlled blood glucose;
  12. History of ILD/interstitial pneumonia treated with corticosteroids, etc.;
  13. Concomitant pulmonary diseases leading to clinically severe impairment of respiratory function;
  14. Presence of massive serous cavity effusion, or serous cavity effusion with symptoms, etc.;
  15. Imaging findings indicating that the tumor has invaded or encased major blood vessels in the chest, neck, pharynx, etc.;
  16. Any thrombotic event within 6 months before randomization;
  17. Patients with active central nervous system metastases;
  18. History of allergy to recombinant humanized antibodies or chimeric human-mouse antibodies, or allergy to any excipient components of the investigational drug, etc.;
  19. Previous organ transplantation or allogeneic hematopoietic stem cell transplantation;
  20. Cumulative anthracycline dose >360 mg/m² during prior (neo)adjuvant anthracycline therapy;
  21. Positive for human immunodeficiency virus antibody, active tuberculosis, active hepatitis B virus infection, or active hepatitis C virus infection;
  22. Active infections requiring systemic treatment, or occurrence of severe infection within 4 weeks before informed consent;
  23. Receipt of other unapproved clinical study drugs or treatments within 4 weeks before the first dose;
  24. Pregnant or breastfeeding women;
  25. History of severe neurological or psychiatric disorders;
  26. Presence of serious non-healing wounds, ulcers, or fractures within 4 weeks before signing informed consent;
  27. Clinically significant bleeding or obvious bleeding tendency within 4 weeks before signing informed consent;
  28. History of intestinal obstruction, inflammatory bowel disease, extensive bowel resection, or presence of Crohn's disease, ulcerative colitis, or chronic diarrhea;
  29. Trial participants who plan to receive or have received live vaccines within 28 days before the first dose;
  30. Other conditions deemed by the investigator to be unsuitable for participation in this clinical trial.

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: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: BL-M14D1+ Atezolizumab
Participants receive BL-M14D1+ Atezolizumab for the first cycle (3 weeks). Participants with clinical benefit could receive additional treatment for more cycles. The administration will be terminated because of disease progression or intolerable toxicity occurring or other reasons.
Administração por infusão intravenosa durante um ciclo de 3 semanas.
Administration by intravenous infusion for a cycle of 3 weeks.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Objective Response Rate (ORR)
Prazo: Up to approximately 12 months
ORR is defined as the percentage of participants, who has a CR (disappearance of all target lesions) or PR (at least a 30% decrease in the sum of diameters of target lesions). The percentage of participants who experiences a confirmed CR or PR is according to RECIST 1.1.
Up to approximately 12 months
Treatment-Emergent Adverse Event (TEAE)
Prazo: Up to approximately 12 months
TEAE is defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally emerging, or any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a pre-existing condition during the treatment of BL-M14D1 . The type, frequency and severity of TEAE will be evaluated during the treatment of BL-M14D1.
Up to approximately 12 months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Progression-free survival (PFS)
Prazo: Up to approximately 12 months
Progression-free survival (PFS) as assessed by BICR is defined as the time between the date subjects were randomized and the first observation of disease progression (based on BICR's image-based assessment) or death.
Up to approximately 12 months
Disease Control Rate (DCR)
Prazo: Up to approximately 12 months
The DCR is defined as the percentage of participants who has a CR, PR, or Stable Disease (SD: neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progressive disease [PD: at least a 20% increase in the sum of diameters of target lesions and an absolute increase of at least 5 mm. The appearance of one or more new lesions is also considered PD]).
Up to approximately 12 months
Duration of Response (DOR)
Prazo: Up to approximately 12 months
The DOR for a responder is defined as the time from the participant's initial objective response to the first date of either disease progression or death, whichever occurs first.
Up to approximately 12 months
Overall Survival (OS)
Prazo: Up to approximately 12 months
Overall survival (OS) is defined as the time between the day the subject is randomized and the subject's death.
Up to approximately 12 months
Cmax
Prazo: Up to approximately 12 months
Maximum serum concentration (Cmax) of BL-M14D1 will be investigated.
Up to approximately 12 months
Tmax
Prazo: Up to approximately 12 months
Time to maximum serum concentration (Tmax) of BL-M14D1 will be investigated.
Up to approximately 12 months
Ctrough
Prazo: Up to approximately 12 months
Ctrough is defined as the lowest serum concentration of BL-M14D1 prior to the next dose will be administered.
Up to approximately 12 months
ADA (anti-drug antibody)
Prazo: Up to approximately 12 months
Frequency of anti-BL-M14D1 antibody (ADA) will be investigated.
Up to approximately 12 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)

9 de julho de 2026

Conclusão Primária (Estimado)

1 de dezembro de 2027

Conclusão do estudo (Estimado)

1 de dezembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

12 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

12 de junho de 2026

Primeira postagem (Real)

17 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

25 de agosto de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

24 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

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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