SHR2554 Plus Liposomal Mitoxantrone as First-line Treatment for Peripheral T-cell Lymphoma (PTCL)
An Open-label, Multicenter, Phase Ib/II Exploratory Clinical Study of EZH2 Inhibitor SHR2554 in Combination With Liposomal Mitoxantrone for the First-line Treatment of Peripheral T-cell Lymphoma
Visão geral do estudo
Status
Status
Condições
Condições
Intervenção / Tratamento
Intervenção / Tratamento
Tipo de estudo
Tipo de estudo
Inscrição (Estimado)
Inscrição
Estágio
Estágio
- Fase 2
- Fase 1
Contactos e Locais
Contato de estudo
Contato de estudo
- Nome: Liang Huang
- Número de telefone: +86 022-23608126
- E-mail: huangliang@ihcams.ac.cn
Critérios de participação
Critérios de elegibilidade
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- Age ≥18 years old,regardless of gender;
- Centrally confirmed histopathological/cytologic diagnosis of PTCL with the following subtypes:Peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS);Follicular helper T (TFH) cell lymphoma of lymph nodes, including angioimmunoblastic, follicular, NOS; Enteropathy-associated T-cell lymphoma(EATL); Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL)and any other PTCL subtypes deemed by the investigator to be eligible for inclusion.
- No prior anti-tumor therapy.
- There must be at least one measurable or evaluable lesion that meets the Lugano 2014 criteria for lymphoma: Measurable lesion: Nodal lesions with major diameter greater than 1.5cm and minor diameter greater than 1.0cm as assessed by PET/CT or Computed Tomography (CT) and/or Magnetic Resonance Imaging (MRI); Or the length of extranodal lesions >1.0cm; 2)Evaluable lesions: PET-CT showed increased uptake in lymph nodes or extranodal regions (higher than liver) and imaging features consistent with lymphoma;
- ECOG performance status score: 0-2;
- Expected survival time ≥3 months;
- Have adequate organ and bone marrow functiont;
- No concurrent hemophagocytic lymphohistiocytosis (HLH). If a patient has clinically diagnosed HLH, enrollment eligibility will be determined by the investigator based on an evaluation of the patient's general physical condition following targeted anti-HLH therapy.
- Women of childbearing potential must have a negative serum pregnancy test within 7 days before the first dose of medication; Effective contraception should be used from the time of informed consent until 6 months after the last dose of study drug.
- Capable of understanding the study procedures and voluntarily signing a written informed consent form (ICF).;
Exclusion Criteria:
- Prior treatment with epigenetic agents before enrollment;
- Patients with a history of severe cardiac disease, history of radiation therapy to the mediastinal/pericardial region, cumulative anthracycline dose > 550 mg (doxorubicin equivalent), prior use of mitoxantrone, baseline left ventricular ejection fraction (LVEF) < 50%, or history of exposure to other cardiotoxic drugs;
- History of other primary aggressive malignancies that are not in remission, or have been in remission for less than 3 years;
- Primary central nervous system (CNS) lymphoma or secondary CNS involvement.
- Known allergy or hypersensitivity to the study drugs or their related metabolites;
- Currently participating in another clinical study, or less than 4 weeks elapsed from the end of treatment in a previous clinical study to the planned start of study treatment;
- Pregnant or lactating women;
- Active infections;
- Medical History and Concurrent Conditions;
- History of Human Immunodeficiency Virus (HIV) infection and/or Acquired Immunodeficiency Syndrome (AIDS);
- Patients with mental disorders or those unable to provide informed consent
- Any other condition deemed by the investigator to be unsuitable for study enrollment;
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Número de braços
Armas e Intervenções
Grupo de Participantes / BraçoGrupo de Participantes / Braço |
Intervenção / TratamentoIntervenção / Tratamento |
|---|---|
|
Experimental: SHR2554 combined with Liposomal Mitoxantrone
|
Patients will receive 6 cycles of SHR2554 combined with liposomal mitoxantrone as induction therapy.
All patients who achieve a complete response (CR) after induction therapy are eligible for transplantation.
Patients achieving CR or partial response (PR), as well as those post-transplantation, may receive SHR2554 maintenance therapy in 28-day cycles.
Maintenance therapy will continue until disease progression or other reasons for discontinuation.
The maximum duration of SHR2554 administration in the maintenance phase will not exceed 24 months.
|
O que o estudo está medindo?
Medidas de resultados primários
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Incidence of Dose-Limiting Toxicities (DLT)
Prazo: Cycle 1 (28 days)
|
Adverse events (AE) defined as DLT events per protocol
|
Cycle 1 (28 days)
|
|
Complete response (CR) rate
Prazo: up to 6 months after enrollment
|
The proportion of subjects evaluated as complete response (CR) according to Lugano 2014 efficacy evaluation criteria
|
up to 6 months after enrollment
|
Medidas de resultados secundários
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Adverse events(AE)
Prazo: From the first day of medication to 28 days after the last dose
|
The safety of the drug was evaluated by NCI-CTC AE 6.0 standard.
Hematologic and non-hematologic toxicity.
|
From the first day of medication to 28 days after the last dose
|
|
Objective response rate (ORR)
Prazo: up to 6 months after enrollment
|
The proportion of subjects evaluated as complete response (CR) and partial response (PR) according to Lugano 2014 efficacy evaluation criteria
|
up to 6 months after enrollment
|
|
Duration of Response (DOR)
Prazo: up to 2.5 years post first treatment
|
The time from the first assessment of CR/PR to the first assessment of PD or death from any cause in the subject
|
up to 2.5 years post first treatment
|
|
Duration of complete response (CR)
Prazo: up to 2.5 years post first treatment
|
The time from the first assessment of CR to the first assessment of PD or death from any cause in the subject
|
up to 2.5 years post first treatment
|
|
Progression-free Survival (PFS)
Prazo: Up to 2.5 years
|
From the time subjects were enrolled to the time of disease progression (in any way) or death from any cause.
|
Up to 2.5 years
|
|
Overall survival (OS)
Prazo: Up to 2.5 years
|
From the date of inclusion to date of death, irrespective of cause.
|
Up to 2.5 years
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Início do estudo
Conclusão Primária (Estimado)
Conclusão Primária
Conclusão do estudo (Estimado)
Conclusão do estudo
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Primeira postagem
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última Atualização Postada
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Outros números de identificação do estudo
Outros números de identificação do estudo
- IIT2026083
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
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 .