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- Ensaio Clínico NCT07684950
Lisaftoclax Plus Pirtobrutinib in Relapsed or Refractory Mantle Cell Lymphoma After BTK-Targeted Therapy
A Prospective Phase 2 Study of Lisaftoclax Plus Pirtobrutinib in Patients With Relapsed or Refractory Mantle Cell Lymphoma After Failure of BTK-Targeted Therapy
This prospective, open-label, phase 2 study will evaluate the efficacy and safety of lisaftoclax in combination with pirtobrutinib in adults with relapsed or refractory mantle cell lymphoma following failure of prior BTK-targeted therapy.
The study includes two cohorts. Cohort 1 will enroll participants who experienced stable disease, disease progression, or intolerance following treatment with a covalent BTK inhibitor. Cohort 2 is an exploratory cohort enrolling participants who experienced stable disease, disease progression, or intolerance following treatment with a non-covalent BTK inhibitor other than pirtobrutinib or a BTK degrader.
Participants will receive oral pirtobrutinib 200 mg once daily in combination with oral lisaftoclax. Lisaftoclax will be administered using a dose ramp-up schedule, followed by a target dose of 600 mg once daily. Treatment will continue until disease progression, unacceptable toxicity, withdrawal of consent.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 2
Contactos e Locais
Locais de estudo
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Henan
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Zhengzhou, Henan, China
- Henan Cancer Hospital
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Investigador principal:
- Keshu Zhou
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Contato:
- Keshu Zhou
- Número de telefone: 13674902391
- E-mail: drzhouks77@163.com
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-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
Participants must meet all of the following criteria:
- Age 18 years or older.
- Histologically and immunophenotypically confirmed mantle cell lymphoma.
- At least one measurable lesion.
- Received at least one prior systemic treatment regimen that included a BTK-targeted therapy, including a covalent BTK inhibitor, non-covalent BTK inhibitor, or BTK degrader, and had stable disease, disease progression, or intolerance during or after the most recent BTK-targeted therapy.
- Eastern Cooperative Oncology Group performance status of 0 to 2.
Adequate hepatic, renal, and bone marrow function, defined as all of the following:
* Aspartate aminotransferase and alanine aminotransferase ≤3 × upper limit of normal;
- Total bilirubin ≤1.5 × upper limit of normal;
- Creatinine clearance ≥30 mL/min;
- Absolute neutrophil count ≥0.5 × 10^9/L;
- Platelet count ≥30 × 10^9/L. Supportive treatment is permitted.
- Participants of reproductive potential must agree to use effective contraception during study treatment and for 3 months after the last dose of study treatment.
- Willing and able to comply with study procedures and follow-up assessments.
- Able to understand and voluntarily sign the informed consent form before screening.
Exclusion Criteria:
1. Known hypersensitivity to pirtobrutinib, lisaftoclax, or any component or excipient of either study drug.
2. Concurrent participation in another clinical study. 3. Prior treatment with any BCL-2 inhibitor. 4. Active central nervous system involvement, including parenchymal or leptomeningeal disease.
5. Clinically significant uncontrolled cardiac or cardiovascular disease, or a history of myocardial infarction within 6 months before the planned initiation of pirtobrutinib.
6. Uncontrolled active severe systemic bacterial, viral, fungal, or parasitic infection.
7. Current treatment with strong CYP3A4 inhibitors or inducers and/or strong P-glycoprotein inhibitors.
8. Positive human immunodeficiency virus test. 9. Active hepatitis B or hepatitis C infection, except:
- Participants with detectable hepatitis B virus DNA whose disease is controlled may be enrolled at the investigator's discretion, provided that concurrent antiviral therapy is administered;
Participants with a history of hepatitis C virus infection who have completed antiviral treatment and have a viral load below the lower limit of quantification may be enrolled.
10. Pregnant or breastfeeding women. 11. Unable to complete protocol-required study visits or procedures, including follow-up visits, or unable to comply with study requirements.
12. Any other clinically significant current or prior medical condition that, in the investigator's judgment, may pose a risk to participant safety or interfere with study assessments, procedures, or completion.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Não randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Cohort 1: Prior Covalent BTK Inhibitor Therapy
Participants with relapsed or refractory mantle cell lymphoma who experienced stable disease, disease progression, or intolerance following prior treatment with at least one covalent BTK inhibitor will receive lisaftoclax in combination with pirtobrutinib.
|
Lisaftoclax will be administered orally once daily.
During Cycle 1, participants will undergo dose ramp-up with 20 mg on Day 1, 50 mg on Day 2, 100 mg on Day 3, 200 mg on Day 4, and 400 mg on Day 5.
The target dose of 600 mg once daily will begin on Day 6 and continue thereafter.
Each treatment cycle is 28 days.
Treatment will continue until disease progression, unacceptable toxicity, withdrawal of consent, or another protocol-defined reason for discontinuation.
Pirtobrutinib will be administered orally at a dose of 200 mg once daily beginning on Day 1 of Cycle 1.
Each treatment cycle is 28 days.
Treatment will continue until disease progression, unacceptable toxicity, withdrawal of consent, or another protocol-defined reason for discontinuation.
|
|
Experimental: Cohort 2: Prior Non-Covalent BTK Inhibitor or BTK Degrader Therapy
Participants with relapsed or refractory mantle cell lymphoma who experienced stable disease, disease progression, or intolerance following prior treatment with a non-covalent BTK inhibitor other than pirtobrutinib or a BTK degrader will receive lisaftoclax in combination with pirtobrutinib.
|
Lisaftoclax will be administered orally once daily.
During Cycle 1, participants will undergo dose ramp-up with 20 mg on Day 1, 50 mg on Day 2, 100 mg on Day 3, 200 mg on Day 4, and 400 mg on Day 5.
The target dose of 600 mg once daily will begin on Day 6 and continue thereafter.
Each treatment cycle is 28 days.
Treatment will continue until disease progression, unacceptable toxicity, withdrawal of consent, or another protocol-defined reason for discontinuation.
Pirtobrutinib will be administered orally at a dose of 200 mg once daily beginning on Day 1 of Cycle 1.
Each treatment cycle is 28 days.
Treatment will continue until disease progression, unacceptable toxicity, withdrawal of consent, or another protocol-defined reason for discontinuation.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Complete Response Rate at 6 Months in Cohort 1
Prazo: At 6 months after initiation of study treatment
|
The proportion of participants in Cohort 1 who achieve a complete response at 6 months after initiation of study treatment, as assessed by the investigator according to the Lugano 2014 response criteria.
|
At 6 months after initiation of study treatment
|
|
Overall Response Rate in Cohort 2
Prazo: From the first dose of study treatment until disease progression, assessed up to 36 months
|
The proportion of participants in Cohort 2 who achieve a best overall response of complete response or partial response, as assessed by the investigator according to the Lugano 2014 response criteria.
|
From the first dose of study treatment until disease progression, assessed up to 36 months
|
Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
|
Duration of Response
Prazo: From the first documented response until disease progression or death, whichever came first, assessed up to 36 months
|
From the first documented response until disease progression or death, whichever came first, assessed up to 36 months
|
|
Progression-Free Survival
Prazo: From the first dose of study treatment until disease progression or death, whichever came first, assessed up to 36 months
|
From the first dose of study treatment until disease progression or death, whichever came first, assessed up to 36 months
|
|
Overall Survival
Prazo: From the first dose of study treatment until death from any cause, assessed up to 36 months
|
From the first dose of study treatment until death from any cause, assessed up to 36 months
|
|
Minimal Residual Disease Negativity Rate
Prazo: At baseline, assessed up to 4 weeks. Interim response assessment, from the first dose of study treatment till 3 cycles. End of induction treatment, from the first dose of study treatment till 3 cycles. Following period, every 6 months during follow-up.
|
At baseline, assessed up to 4 weeks. Interim response assessment, from the first dose of study treatment till 3 cycles. End of induction treatment, from the first dose of study treatment till 3 cycles. Following period, every 6 months during follow-up.
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Number of Participants With Treatment-Emergent Adverse Events
Prazo: From the first dose of study treatment through 30 days after the last dose
|
From the first dose of study treatment through 30 days after the last dose
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- 2026-204
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