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A Study of Lacutoclax (LP-108) in Patients With Relapsed/Refractory CLL/SLL

29 de julio de 2026 actualizado 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.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Estimado)

75

Fase

  • Fase 2

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • Jiangsu
      • Nanjing, Jiangsu, Porcelana
        • Reclutamiento
        • The First Affiliated Hospital of Nanjing Medical University
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  1. Patients with confirmed R/R CLL/SLL according to the 2018 International Workshop on Chronic Lymphocytic Leukemia (iwCLL) criteria.
  2. 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.
  3. Have at least one measurable lesion.
  4. Age ≥18 years, regardless of sex.
  5. Eastern Cooperative Oncology Group (ECOG) performance status score ≤2.
  6. Life expectancy ≥ 12 weeks.
  7. Adequate coagulation function, liver and kidney function, bone marrow hematopoietic function.
  8. Toxicities from prior anti-tumor therapy have recovered to Grade ≤1 according to NCI CTCAE v5.0.
  9. 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.
  10. Participation is voluntary, requiring signed informed consent and compliance with the treatment regimen and visit schedule.

Exclusion Criteria:

  1. Known hypersensitivity to Lacutoclax or any of its excipients.
  2. Prior treatment with a BCL-2 family inhibitor.
  3. History of or currently suspected Richter's syndrome.
  4. Known or suspected central nervous system (CNS) involvement.
  5. 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.
  6. 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.
  7. Received corticosteroids for antitumor purposes, herbal medicines for antitumor treatment, or localized radiotherapy within 14 days prior to the first dose of study treatment.
  8. 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.
  9. 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.
  10. Major cardiovascular or cerebrovascular events within 6 months prior to the first dose of study treatment.
  11. Presence of any severe and/or uncontrolled systemic disease.
  12. Impaired cardiac function.
  13. Any uncontrolled systemic infection.
  14. Conditions that may impair oral drug administration or significantly affect absorption or pharmacokinetics of the study drug.
  15. Unable to discontinue moderate or strong CYP3A inhibitors or inducers, or sensitive CYP2C8 substrates during the study period.
  16. Primary autoimmune disease requiring immunosuppressive therapy.
  17. Any other condition that, in the investigator's judgment, makes the patient unsuitable for study participation.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿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
Experimental: Lacutoclax
All participants will receive oral Lacutoclax tablets once daily with dose escalation to a target dose of 400 mg.
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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Overall Response Rate (ORR) assessed by Independent Review Committee (IRC)
Periodo de tiempo: Up to approximately 28 months
Up to approximately 28 months

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
ORR assessed by Investigator(INV)
Periodo de tiempo: Up to approximately 28 months
Up to approximately 28 months
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
Periodo de tiempo: Up to approximately 28 months
Up to approximately 28 months
Time to response (TTR) assessed by IRC and INV, respectively
Periodo de tiempo: Up to approximately 30 months
Up to approximately 30 months
Duration of response (DOR) assessed by IRC and INV, respectively
Periodo de tiempo: Up to approximately 30 months.
Up to approximately 30 months.
Time to first 50% reduction in absolute lymphocyte count (ALC) or normalization of ALC
Periodo de tiempo: Up to approximately 28 months
Up to approximately 28 months
Progression-free survival (PFS) assessed by IRC and INV, respectively
Periodo de tiempo: Up to approximately 30 months
Up to approximately 30 months
Overall Survival
Periodo de tiempo: Up to approximately 30 months
Up to approximately 30 months
Adverse events(AEs) as assessed by CTCAE v5.0
Periodo de tiempo: Up to approximately 30 months
Up to approximately 30 months
Adverse drug reactions (ADRs) related to Lacutoclax
Periodo de tiempo: Up to approximately 30 months
Up to approximately 30 months
Serious adverse events (SAEs)
Periodo de tiempo: Up to approximately 30 months
Up to approximately 30 months
Maximum Plasma Concentration(Cmax)
Periodo de tiempo: From 1 hour prior to administration to 24 hours post-dose
From 1 hour prior to administration to 24 hours post-dose
Time to Maximum Plasma Concentration (Tmax)
Periodo de tiempo: From 1 hour prior to administration to 24 hours post-dose
From 1 hour prior to administration to 24 hours post-dose
Half-life (T1/2)
Periodo de tiempo: 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)
Periodo de tiempo: From 1 hour prior to administration to 24 hours post-dose
From 1 hour prior to administration to 24 hours post-dose

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

14 de julio de 2026

Finalización primaria (Estimado)

30 de marzo de 2028

Finalización del estudio (Estimado)

30 de septiembre de 2029

Fechas de registro del estudio

Enviado por primera vez

20 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

20 de mayo de 2026

Publicado por primera vez (Actual)

27 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

30 de julio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

29 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

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. .

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