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Rimegepant Plus Glofitamab and CD19 CAR-T Therapy in R/R LBCL

23 de maio de 2026 atualizado por: Zhao Weili, Ruijin Hospital

A Study to Evaluate the Efficacy and Safety of Rimegepant Plus Glofitamab and CD19 CAR-T Cell Therapy in Patients With High-Risk Relapsed/Refractory Large B-Cell Lymphoma

This study is designed to evaluate the efficacy and safety of rimegepant in combination with glofitamab and CD19 CAR-T cell therapy in patients with high-risk relapsed/refractory large B-cell lymphoma. Eligible patients will be randomized to receive glofitamab plus CD19 CAR-T cell therapy with or without rimegepant. The primary endpoint is complete response rate at 6 months after CAR-T cell infusion.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Estimado)

100

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

  • Nome: Weili Zhao
  • Número de telefone: +862164370045 Ext. 610707
  • E-mail: zwl_trial@163.com

Estude backup de contato

Locais de estudo

    • China
      • Shanghai, China, China, 200020
        • Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
        • Contato:

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:

  • Able to understand and voluntarily sign the written informed consent form.
  • Age 18 years or older.
  • Histologically confirmed large B-cell lymphoma with CD19 and CD20 expression.
  • Relapsed or refractory disease after at least one prior line of systemic therapy.
  • Prior treatment must have included an anthracycline-containing chemotherapy regimen and an anti-CD20 monoclonal antibody.
  • Considered suitable by the investigator to receive glofitamab and CD19 CAR-T cell therapy.
  • Presence of at least one high-risk feature, including extranodal involvement, bulky disease, or TP53 abnormality.
  • ECOG performance status of 0 to 2.
  • Life expectancy of at least 12 weeks.
  • Adequate bone marrow, hepatic, renal, pulmonary, and cardiac function as determined by the investigator.
  • Participants of reproductive potential must agree to use effective contraception during the study period.
  • Able and willing to comply with the study protocol, in the investigator's judgment.

Exclusion Criteria:

  • History of hypersensitivity to any study treatment or related compounds.
  • Active or uncontrolled infection requiring systemic treatment.
  • History of allogeneic hematopoietic stem cell transplantation or organ transplantation.
  • Uncontrolled or clinically significant viral infection as defined by the protocol.
  • Known central nervous system involvement by lymphoma or clinically significant central nervous system disease that may interfere with study treatment or safety assessment.
  • Severe or uncontrolled cardiovascular disease.
  • Severe autoimmune disease or immune-mediated disease that may interfere with study treatment or safety assessment.
  • Known or suspected history of hemophagocytic lymphohistiocytosis.
  • Recent thromboembolic event before screening.
  • History of another malignancy within 5 years before screening, except adequately treated carcinoma in situ or non-melanoma skin cancer.
  • Receipt of prohibited anticancer therapy, immunosuppressive therapy, live attenuated vaccine, or other prohibited treatment within the protocol-specified period before enrollment.
  • Pregnant or breastfeeding women, or participants planning pregnancy during the study period.
  • Concurrent participation in another interventional clinical trial.
  • Need for prohibited concomitant medications that cannot be discontinued or substituted.
  • Any condition that, in the investigator's judgment, makes the participant unsuitable for study treatment or 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: Rimegepant Plus Glofitamab and CD19 CAR-T Cell Therapy
Participants will receive rimegepant in combination with glofitamab and CD19 CAR-T cell therapy. Rimegepant will be administered orally at 75 mg every other day from the first day of lymphodepleting chemotherapy until Day 90 after CAR-T cell infusion. Glofitamab will be given with obinutuzumab pretreatment and step-up dosing, followed by CD19 CAR-T cell therapy after lymphodepleting chemotherapy. Participants with CR, PR, or SD after CAR-T cell infusion may continue glofitamab consolidation according to the study protocol.
Rimegepant will be administered orally at 75 mg every other day from the first day of lymphodepleting chemotherapy until Day 90 after CAR-T cell infusion.
Glofitamab will be administered intravenously with step-up dosing. Participants will receive 2.5 mg on Cycle 1 Day 8, 10 mg on Cycle 1 Day 15, and 30 mg on Cycle 2 Day 1. Participants with CR, PR, or SD after CAR-T cell infusion may continue glofitamab consolidation at 30 mg on Day 1 of each 21-day cycle for four cycles.
Obinutuzumab will be administered intravenously at 1000 mg on Cycle 1 Day 1 as pretreatment before glofitamab.
Participants will receive CD19-directed CAR-T cell therapy after lymphodepleting chemotherapy. The specific CAR-T product and dose will be determined according to the approved product label, institutional standard practice, and investigator discretion.
Fludarabine will be administered as part of lymphodepleting chemotherapy before CD19 CAR-T cell infusion.
Cyclophosphamide will be administered as part of lymphodepleting chemotherapy before CD19 CAR-T cell infusion.
Comparador Ativo: Glofitamab Plus CD19 CAR-T Cell Therapy
Participants will receive glofitamab in combination with CD19 CAR-T cell therapy. Glofitamab will be given with obinutuzumab pretreatment and step-up dosing, followed by CD19 CAR-T cell therapy after lymphodepleting chemotherapy. Participants with CR, PR, or SD after CAR-T cell infusion may continue glofitamab consolidation according to the study protocol.
Glofitamab will be administered intravenously with step-up dosing. Participants will receive 2.5 mg on Cycle 1 Day 8, 10 mg on Cycle 1 Day 15, and 30 mg on Cycle 2 Day 1. Participants with CR, PR, or SD after CAR-T cell infusion may continue glofitamab consolidation at 30 mg on Day 1 of each 21-day cycle for four cycles.
Obinutuzumab will be administered intravenously at 1000 mg on Cycle 1 Day 1 as pretreatment before glofitamab.
Participants will receive CD19-directed CAR-T cell therapy after lymphodepleting chemotherapy. The specific CAR-T product and dose will be determined according to the approved product label, institutional standard practice, and investigator discretion.
Fludarabine will be administered as part of lymphodepleting chemotherapy before CD19 CAR-T cell infusion.
Cyclophosphamide will be administered as part of lymphodepleting chemotherapy before CD19 CAR-T cell infusion.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Complete Response Rate at 6 Months
Prazo: 6 months after CAR-T cell infusion
Complete response rate at 6 months is defined as the proportion of participants who achieve complete response at 6 months after CAR-T cell infusion.
6 months after CAR-T cell infusion

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Objective Response Rate
Prazo: Up to 24 months
Objective response rate is defined as the proportion of participants who achieve complete response or partial response.
Up to 24 months
Complete Response Rate at Day 28
Prazo: Day 28 after CAR-T cell infusion
Complete response rate at Day 28 is defined as the proportion of participants who achieve complete response at Day 28 after CAR-T cell infusion.
Day 28 after CAR-T cell infusion
Complete Response Rate at 3 Months
Prazo: 3 months after CAR-T cell infusion
Complete response rate at 3 months is defined as the proportion of participants who achieve complete response at 3 months after CAR-T cell infusion.
3 months after CAR-T cell infusion
Progression-Free Survival
Prazo: Up to 24 months
Progression-free survival is defined as the time from randomization to disease progression or death from any cause, whichever occurs first.
Up to 24 months
Duration of Response
Prazo: Up to 24 months
Duration of response is defined as the time from the first documented response to disease progression or death from any cause, whichever occurs first.
Up to 24 months
Overall Survival
Prazo: Up to 24 months
Overall survival is defined as the time from randomization to death from any cause.
Up to 24 months
Adverse Events
Prazo: Up to 24 months
Incidence and severity of adverse events will be assessed throughout the study.
Up to 24 months

Colaboradores e Investigadores

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

Patrocinador

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 (Estimado)

1 de maio de 2026

Conclusão Primária (Estimado)

1 de novembro de 2028

Conclusão do estudo (Estimado)

1 de abril de 2029

Datas de inscrição no estudo

Enviado pela primeira vez

23 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

23 de maio de 2026

Primeira postagem (Real)

29 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

29 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

23 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

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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