- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07609862
A Study of Rocbrutinib in Combination With Lacutoclax in Patients With B-Cell Malignancies
A Phase Ib/II, Open-Label, Multicenter Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of BTK Inhibitor Rocbrutinib in Combination With BCL-2 Inhibitor Lacutoclax in Patients With B-Cell Malignancies
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Lugui Qiu
- Número de teléfono: +86-13821266636
- Correo electrónico: qiulg@ihcams.ac.cn
Ubicaciones de estudio
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Tianjin, Porcelana
- Reclutamiento
- Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences
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Contacto:
- Lugui Qiu
- Número de teléfono: +86-13821266636
- Correo electrónico: qiulg@ihcams.ac.cn
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Age ≥18 years, regardless of sex.
Ib: Histologically confirmed diagnosis of CLL/SLL (per 2018 iwCLL criteria) or B-cell malignancies (per 2022 WHO classification), including: MCL, DLBCL, FL, and WM. Must have received at least one prior line of systemic therapy, with documented disease progression or intolerance.
II: For Treatment-naïve (TN) CLL/SLL patients: Must meet iwCLL treatment indications and no prior systemic therapy. For R/R CLL/SLL patients: at least one prior systemic therapy with documented disease progression or intolerance.
- Have at least one measurable lesion.
- Phase Ib: ECOG performance status ≤1; phase II: ECOG performance status ≤2.
- Life expectancy ≥ 12 weeks.
- Adequate coagulation function, liver and kidney function, bone marrow hematopoietic function.
- 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 study treatment. 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.
- Participation is voluntary, requiring signed informed consent and compliance with the treatment regimen and visit schedule.
Exclusion Criteria:
- Known hypersensitivity or intolerance to Rocbrutinib, Lacutoclax, or any of their excipients; prior treatment with any BCL-2 inhibitor; or prior treatment with both covalent and non-covalent BTK inhibitors.
- Use of systemic corticosteroids at doses equivalent to >20 mg/day of prednisone for ≥3 days within 7 days prior to the first dose.
- 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 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 prior to the first dose.
- History of other active malignancies within the past 3 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.
- Any severe and/or uncontrolled systemic disease, or any other condition that, in the opinion of the investigator, makes the patient unsuitable for participation in the study.
- Any of the following events within 6 months prior to the first dose: Symptomatic arrhythmia, myocardial infarction, intracranial hemorrhage, or Stroke.
- 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, P-gp (P-glycoprotein) inhibitors, sensitive substrates of OATP1B3 or CYP2C8 during the study period.
- Received vaccination with any live-attenuated vaccines within 4 weeks prior to the first dose of study treatment.
- Evidence of an active bleeding constitution or a history of significant hemorrhagic disorders.
- Requirement for ongoing therapy with warfarin or other vitamin K antagonists.
- Presence of an active, uncontrolled, or symptomatic autoimmune disease that requires systemic treatment.
- Any other condition that, in the investigator's judgment, makes the patient unsuitable for study participation.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Lacutoclax+Rocbrutinib
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Phase Ib dose-escalation study of Rocbrutinib in combination with Lacutoclax. Rocbrutinib will be administered at a fixed dose of 150 mg once daily (QD), while Lacutoclax will be dose-escalated. Initial dose levels include Lacutoclax 200 mg QD and 400 mg QD in 28-day treatment cycles.Treatment will continue until disease progression, unacceptable toxicity/intolerance, or completion of the protocol-defined treatment duration, whichever occurs first. In phase II, participants will receive Rocbrutinib monotherapy for 8-12 weeks prior to combination treatment. Upon initiation of combination therapy, Lacutoclax will undergo dose ramp-up to the target dose and will then be administered continuously at the target dose. Treatment will continue until disease progression, unacceptable toxicity/intolerance, or completion of the protocol-defined treatment duration, whichever occurs first. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
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Phase Ib: Dose-limiting toxicity (DLT)
Periodo de tiempo: At the end of Cycle 1 (the length of cycle 1 is 28 days)
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At the end of Cycle 1 (the length of cycle 1 is 28 days)
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Phase Ib: Maximum Tolerated Dose (MTD)
Periodo de tiempo: At the end of Cycle 1 (the length of cycle 1 is 28 days)
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At the end of Cycle 1 (the length of cycle 1 is 28 days)
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Phase Ib: Adverse events as assessed by CTCAE v5.0
Periodo de tiempo: From the first administration to 28 days after the last administration
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From the first administration to 28 days after the last administration
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Phase Ib: Time to Maximum Plasma Concentration (Tmax)
Periodo de tiempo: From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase Ib: Maximum Plasma Concentration (Cmax)
Periodo de tiempo: From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase Ib: Area Under the Plasma Concentration-Time Curve from Time Zero to Time t (AUC0-t)
Periodo de tiempo: From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase Ib: Half-life (t1/2)
Periodo de tiempo: From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase II: Undetectable minimal residual disease (uMRD) rate assessed by flow cytometry
Periodo de tiempo: Up to approximately three years
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Up to approximately three years
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Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
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Phase II: Maximum Plasma Concentration (Cmax)
Periodo de tiempo: From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase II: Time to Maximum Plasma Concentration (Tmax)
Periodo de tiempo: From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase II: Area Under the Plasma Concentration-Time Curve from Time Zero to Time t (AUC0-t)
Periodo de tiempo: From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase II: Half-life (t1/2)
Periodo de tiempo: From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Overall Response Rate(ORR)
Periodo de tiempo: Up to approximately three years
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Up to approximately three years
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Progression-free Survival(PFS)
Periodo de tiempo: Up to approximately three years
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Up to approximately three years
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Overall Survival(OS)
Periodo de tiempo: Up to approximately three years
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Up to approximately three years
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Phase II: Adverse events as assessed by CTCAE v5.0
Periodo de tiempo: From the first administration to 28 days after the last administration
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From the first administration to 28 days after the last administration
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Complete Response Rate (CRR)
Periodo de tiempo: Up to approximately three years
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Up to approximately three years
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Duration of Response (DOR)
Periodo de tiempo: Up to approximately three years
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Up to approximately three years
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Phase Ib: Undetectable Minimal Residual Disease (uMRD) Rate assessed by flow cytometry
Periodo de tiempo: Up to approximately three years
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Up to approximately three years
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades Vasculares
- Enfermedades cardiovasculares
- Procesos Patológicos
- Neoplasias
- Enfermedad crónica
- Atributos de la enfermedad
- Enfermedades del sistema inmunológico
- Neoplasias por tipo histológico
- Enfermedades hematológicas
- Enfermedades linfáticas
- Trastornos linfoproliferativos
- Trastornos inmunoproliferativos
- Linfoma No Hodgkin
- Leucemia de células B
- Linfoma de células B
- Linfoma
- Neoplasias De Células Plasmáticas
- Trastornos hemostáticos
- Paraproteinemias
- Trastornos de proteínas en sangre
- Trastornos hemorrágicos
- Leucemia Linfoide
- Leucemia
- Condiciones Patológicas, Signos y Síntomas
- Enfermedades hemic y linfáticas
- Linfoma de células B grandes, difuso
- Leucemia Linfocítica Crónica De Células B
- Linfoma Folicular
- Linfoma De Células Del Manto
- Macroglobulinemia de Waldenström
Otros números de identificación del estudio
- LP-10822
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .