Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

A Study of PLX51107 in Advanced Malignancies

20 de diciembre de 2018 actualizado por: Plexxikon

A Phase 1b/2a, Two-Part, Dose Escalation and Expansion Study to Assess the Safety, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of PLX51107 in Subjects With Advanced Hematological Malignancies and Solid Tumors

The purpose of this research study is to evaluate safety, pharmacokinetics, pharmacodynamics, and preliminary efficacy of the investigational drug PLX51107 in subjects with advanced solid tumors (including lymphoma), and advanced hematological malignancies

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Actual)

50

Fase

  • Fase 1

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.

Ubicaciones de estudio

    • New York
      • New York, New York, Estados Unidos, 10032
        • Columbia University Medical Center
    • Ohio
      • Columbus, Ohio, Estados Unidos, 43212
        • The Ohio State University Stephanie Spielman Comprehensive Breast Center
    • Pennsylvania
      • Philadelphia, Pennsylvania, Estados Unidos, 19107
        • Thomas Jefferson University
    • South Carolina
      • Charleston, South Carolina, Estados Unidos, 29425
        • MUSC/ Hollings Cancer Center
    • Texas
      • San Antonio, Texas, Estados Unidos, 78229
        • South Texas Accelerated Research Therapeutics

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

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  1. Confirmed diagnosis of a relapsed or refractory malignancy in 1 of 2 treatment groups:

    1. Group A: Subjects with any solid tumor (including lymphomas).
    2. Group B: Subjects with relapsed or refractory AML, Subjects with relapsed or refractory high-risk MDS, defined as revised International Prognostic Scoring System (IPSS-R) intermediate or greater disease.
  2. Age ≥18 years.
  3. Eastern Cooperative Oncology Group (ECOG) performance status 0 to 2.
  4. Life expectancy ≥3 months in the judgment of the investigator.
  5. Adequate organ function.
  6. Group A subjects must have measurable or evaluable disease per the appropriate disease criteria.
  7. Women of child-bearing potential must have a negative serum pregnancy test at Screening and must agree to use an effective form of contraception from the time of the negative pregnancy test up to 6 months after the last dose of study drug. Effective forms of contraception include abstinence, hormonal contraceptive in conjunction with a barrier method, or a double barrier method. Women of non-child-bearing potential may be included if they are either surgically sterile or have been postmenopausal for ≥1 year.
  8. Fertile men must agree to use an effective method of birth control during the study and for up to 6 months after the last dose of study drug.
  9. All associated clinically significant toxicity from previous cancer therapy must be resolved (to ≤Grade 1 or baseline) prior to study treatment administration (Grade 2 alopecia is allowed).
  10. Willingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirements.

Exclusion Criteria:

  1. Prior exposure to a bromodomain inhibitor, such as OTX-015 or CPI-0610.
  2. Allogenic or autologous transplant for hematological malignancy with infusion of stem cells within 90 days before Cycle 1 Day 1, or on active immunosuppressive therapy for graft-versus-host disease (GVHD) or GVHD prophylaxis within 2 weeks of Cycle 1 Day 1.
  3. Known uncontrolled fungal, bacterial, and/or viral infection ≥Grade 2.
  4. Uncontrolled autoimmune hemolytic anemia or thrombocytopenia.
  5. For Group A: Subjects with a history of brain metastases are ineligible. This includes previously treated brain metastases. For Group B (subjects with AML): Active symptomatic CNS involvement of AML. Subjects with previously treated leptomeningeal disease that has been effectively treated are eligible.
  6. A diagnosis of acute promyelocytic leukemia (APL) or chronic myeloid leukemia (CML) in blast crisis.
  7. Known or suspected allergy to the investigational agent or any agent given in association with this trial.
  8. Women who are pregnant or are breast feeding.
  9. Clinically significant cardiac disease
  10. Inability to take oral medication or significant nausea and vomiting, malabsorption, or significant small bowel resection that, in the opinion of the Investigator, would preclude adequate absorption.
  11. Subject with known human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV) infection or is known to be a carrier of hepatitis B or C.
  12. Strong CYP3A4 and CYP2C8 inhibitors or inducers or CYP3A4 substrate drugs with a narrow therapeutic range taken within 14 days or 5 drug half-lives before start of study drug.
  13. Active secondary malignancy
  14. Major surgery or significant traumatic injury within 14 days prior to therapy
  15. Receipt of anti-cancer therapy 14 days prior to Cycle 1 Day 1
  16. Presence of any other medical, psychological, familial, sociological, or geographic condition potentially hampering compliance with the study protocol Subjects who are participating in any other therapeutic clinical study (observational or registry trials are allowed).
  17. Subjects who have Burkitt's lymphoma or Burkitt-like lymphoma.
  18. Subjects on active anticoagulation therapy including warfarin, factor Xa inhibitors, thrombin inhibitors, or heparin.
  19. Subjects with documented hepatic metastases involving >50% of the hepatic parenchyma.

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: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Treatment Group A
Open label, sequential PLX51107 dose escalation in approximately 30 solid tumor subjects.
Experimental: Treatment Group B
Open label, sequential PLX51107 dose escalation in approximately 30 subjects with acute myeloid leukemia (AML) or high-risk myelodysplastic syndrome (MDS).

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Safety of PLX51107 as measured by adverse events and serious adverse events.
Periodo de tiempo: 1 year
1 year
Area under the concentration-time curve (AUC) of PLX51107.
Periodo de tiempo: 1 year
1 year
Maximum observed concentration (Cmax) of PLX51107.
Periodo de tiempo: 1 year
1 year
Time to peak concentration (Tmax) of PLX51107.
Periodo de tiempo: 1 year
1 year
Half life (t1/2) of PLX51107.
Periodo de tiempo: 1 year
1 year

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Overall Response Rate (ORR)
Periodo de tiempo: 1 year
ORR is defined as the total number of patients with the best overall response according to standard criteria for the relevant malignancy divided by the total number of treated patients and expressed as a percentage.
1 year
Duration Of Response (DOR).
Periodo de tiempo: 1 year
DOR is defined as the time from the initial objective response to disease progression or death, whichever occurs first.
1 year
Progression-Free Survival (PFS).
Periodo de tiempo: 1 year
PFS time is defined as the time from the first dose of PLX51107 to disease progression or death, whichever occurs first.
1 year
Overall Survival (OS).
Periodo de tiempo: 1 year
OS is defined as the first dose of study drug until the date of death from any cause.
1 year

Colaboradores e Investigadores

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

Patrocinador

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

1 de marzo de 2016

Finalización primaria (Actual)

1 de septiembre de 2018

Finalización del estudio (Actual)

1 de septiembre de 2018

Fechas de registro del estudio

Enviado por primera vez

12 de febrero de 2016

Primero enviado que cumplió con los criterios de control de calidad

12 de febrero de 2016

Publicado por primera vez (Estimar)

17 de febrero de 2016

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

24 de diciembre de 2018

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

20 de diciembre de 2018

Última verificación

1 de diciembre de 2018

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

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. .

Suscribir