- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07609823
A Study of Lacutoclax (LP-108) in Patients With Relapsed/Refractory CLL/SLL
29 de julho de 2026 atualizado por: Guangzhou Lupeng Pharmaceutical Company LTD.
A Phase 2, Open-Label, Single-Arm, Multicenter Study to Evaluate the Efficacy and Safety of Lacutoclax (LP-108) in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
The goal of this clinical trial is to evaluate the efficacy and safety of Lacutoclax, an oral selective BCL-2 inhibitor, in patients with relapsed or refractory chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL).
Lacutoclax is a potent and selective BCL-2 inhibitor with relatively weaker inhibitory activity against BCL-XL and BCL-W.
Preliminary clinical data have demonstrated promising efficacy and an acceptable safety profile in patients with CLL/SLL and other B-cell non-Hodgkin lymphomas (B-NHLs).
This is an open-label, single-arm, multicenter Phase II study evaluating the efficacy and safety of oral Lacutoclax tablets in patients with relapsed or refractory CLL/SLL.
Visão geral do estudo
Status
Recrutamento
Intervenção / Tratamento
Tipo de estudo
Intervencional
Inscrição (Estimado)
75
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: Jianyong Li
- Número de telefone: 025-83781120
- E-mail: lijianyonglm@126.com
Locais de estudo
-
-
Jiangsu
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Nanjing, Jiangsu, China
- Recrutamento
- The First Affiliated Hospital of Nanjing Medical University
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Contato:
- Huayuan Zhu
- Número de telefone: 86-13813810650
- E-mail: huayuan.zhu@hotmail.com
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-
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:
- Patients with confirmed R/R CLL/SLL according to the 2018 International Workshop on Chronic Lymphocytic Leukemia (iwCLL) criteria.
- Patients who had previously received standard therapy, experienced disease progression following the most recent line of treatment (excluding intolerance), and had at least one indication for treatment prior to enrollment.
- Have at least one measurable lesion.
- Age ≥18 years, regardless of sex.
- Eastern Cooperative Oncology Group (ECOG) performance status score ≤2.
- Life expectancy ≥ 12 weeks.
- Adequate coagulation function, liver and kidney function, bone marrow hematopoietic function.
- Toxicities from prior anti-tumor therapy have recovered to Grade ≤1 according to NCI CTCAE v5.0.
- Male patients and female patients of childbearing potential must agree to use effective contraception during the study and for 90 days after the last dose of Lacutoclax. Female patients of childbearing potential must have a negative pregnancy test before study treatment and must not be breastfeeding. Male patients must not donate sperm during the study and for 90 days after the last dose of Lacutoclax.
- Participation is voluntary, requiring signed informed consent and compliance with the treatment regimen and visit schedule.
Exclusion Criteria:
- Known hypersensitivity to Lacutoclax or any of its excipients.
- Prior treatment with a BCL-2 family inhibitor.
- History of or currently suspected Richter's syndrome.
- Known or suspected central nervous system (CNS) involvement.
- Prior allogeneic hematopoietic stem cell transplantation (allo-HSCT), or autologous hematopoietic stem cell transplantation (auto-HSCT) or chimeric antigen receptor T-cell (CAR-T) therapy within 90 days before the first dose of study treatment.
- Received antitumor therapy, investigational agents, major surgery, severe trauma, or live attenuated vaccines within 4 weeks or 5 half-lives prior to the first dose of study treatment.
- Received corticosteroids for antitumor purposes, herbal medicines for antitumor treatment, or localized radiotherapy within 14 days prior to the first dose of study treatment.
- Use of moderate or strong CYP3A inhibitors within 7 days prior to the first dose of study treatment, or consumption of grapefruit, grapefruit juice, starfruit, or Seville oranges within 3 days prior to dosing.
- Prior malignancy other than CLL/SLL within the past 2 years, except for curatively treated basal cell carcinoma, localized squamous cell carcinoma of the skin, carcinoma in situ of the cervix or breast, or other malignancies considered cured.
- Major cardiovascular or cerebrovascular events within 6 months prior to the first dose of study treatment.
- Presence of any severe and/or uncontrolled systemic disease.
- Impaired cardiac function.
- Any uncontrolled systemic infection.
- Conditions that may impair oral drug administration or significantly affect absorption or pharmacokinetics of the study drug.
- Unable to discontinue moderate or strong CYP3A inhibitors or inducers, or sensitive CYP2C8 substrates during the study period.
- Primary autoimmune disease requiring immunosuppressive therapy.
- Any other condition that, in the investigator's judgment, makes the patient 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: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Lacutoclax
All participants will receive oral Lacutoclax tablets once daily with dose escalation to a target dose of 400 mg.
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Participants will first undergo a dose ramp-up period of at least 4 days (Cycle 0: C0D1-C0D4), followed by continuous administration at the target dose of 400 mg once daily starting from Cycle 1.
Each treatment cycle will last 28 days.
Treatment will continue until disease progression, unacceptable toxicity, or fulfillment of other criteria for treatment discontinuation.
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Prazo |
|---|---|
|
Overall Response Rate (ORR) assessed by Independent Review Committee (IRC)
Prazo: Up to approximately 28 months
|
Up to approximately 28 months
|
Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
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ORR assessed by Investigator(INV)
Prazo: Up to approximately 28 months
|
Up to approximately 28 months
|
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Complete response(CR) plus complete response with incomplete bone marrow recovery (CRi) rate (CRi applicable only to patients with CLL) assessed by IRC and INV, respectively
Prazo: Up to approximately 28 months
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Up to approximately 28 months
|
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Time to response (TTR) assessed by IRC and INV, respectively
Prazo: Up to approximately 30 months
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Up to approximately 30 months
|
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Duration of response (DOR) assessed by IRC and INV, respectively
Prazo: Up to approximately 30 months.
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Up to approximately 30 months.
|
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Time to first 50% reduction in absolute lymphocyte count (ALC) or normalization of ALC
Prazo: Up to approximately 28 months
|
Up to approximately 28 months
|
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Progression-free survival (PFS) assessed by IRC and INV, respectively
Prazo: Up to approximately 30 months
|
Up to approximately 30 months
|
|
Overall Survival
Prazo: Up to approximately 30 months
|
Up to approximately 30 months
|
|
Adverse events(AEs) as assessed by CTCAE v5.0
Prazo: Up to approximately 30 months
|
Up to approximately 30 months
|
|
Adverse drug reactions (ADRs) related to Lacutoclax
Prazo: Up to approximately 30 months
|
Up to approximately 30 months
|
|
Serious adverse events (SAEs)
Prazo: Up to approximately 30 months
|
Up to approximately 30 months
|
|
Maximum Plasma Concentration(Cmax)
Prazo: From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
|
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Time to Maximum Plasma Concentration (Tmax)
Prazo: From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
|
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Half-life (T1/2)
Prazo: From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
|
|
Area Under the Plasma Concentration-Time Curve from Time Zero to Time t(AUC0-t)
Prazo: From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
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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 (Real)
14 de julho de 2026
Conclusão Primária (Estimado)
30 de março de 2028
Conclusão do estudo (Estimado)
30 de setembro de 2029
Datas de inscrição no estudo
Enviado pela primeira vez
20 de maio de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
20 de maio de 2026
Primeira postagem (Real)
27 de maio de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
30 de julho de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
29 de julho de 2026
Última verificação
1 de julho de 2026
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
- Processos Patológicos
- Neoplasias
- Doença crônica
- Atributos da doença
- Doenças do sistema imunológico
- Neoplasias por Tipo Histológico
- Doenças Hematológicas
- Doenças Linfáticas
- Distúrbios Linfoproliferativos
- Distúrbios imunoproliferativos
- Leucemia de Células B
- Leucemia Linfóide
- Leucemia
- Condições Patológicas, Sinais e Sintomas
- Doenças hemic e linfáticas
- Recorrência
- Leucemia Linfocítica Crônica de Células B
Outros números de identificação do estudo
- LP-10821
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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