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A Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of JNJ-42756493 in Patients With Advanced or Refractory Solid Tumors or Lymphoma

13 de mayo de 2019 actualizado por: Janssen Research & Development, LLC

A Phase 1 Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of JNJ-42756493, a Pan-Fibroblast Growth Factor Receptor (FGFR) Tyrosine Kinase Inhibitor, in Subjects With Advanced or Refractory Solid Tumors or Lymphoma

The purpose of this study is to determine a dose for future development and to evaluate the safety, pharmacokinetics, pharmacodynamics, and efficacy profiles of JNJ-42756493 in Japanese and other Asian patients with advanced or refractory solid tumors or lymphoma.

Descripción general del estudio

Descripción detallada

This is an open-label (identity of assigned study drug will be known), multicenter, 2-part, Phase 1 dose escalation/expansion to evaluate the safety, pharmacokinetics (study of what the body does to a drug), pharmacodynamics (study of what a drug does to the body) and clinical activity of JNJ-42756493 administered orally once daily in 21-day cycles or 28 days cycles of intermittent dosing regimen (7 days on/7 days off) to Japanese and Asian participants >=20 years of age with advanced or refractory solid tumors or lymphoma who are not candidates for approved or available therapies. Approximately 40 participants will be enrolled. In Part 1 Participants will be required to be hospitalized after the first dose on Day 1 of Cycle 1 until Day 2 of Cycle 2 (for daily continuous dosing) or until Day 14 of Cycle 1 (for intermittent dosing), however extension of hospitalization will be allowed until Day 2 of Cycle 2 according to investigators clinical judgment. The Part 1 dose-escalation phase is designed to determine the recommended Phase 2 dose (RP2D) based on safety, pharmacokinetic, and pharmacodynamic data of JNJ-42756493. Participants will be enrolled in sequential cohorts based on the 3+3 dose-escalation scheme; the first cohort will receive the starting dose and subsequent cohorts will receive increased doses of JNJ-42756493. After the last participants in each cohort completes Cycle 1, the Safety Evaluation Team (SET) will evaluate the safety and pharmacokinetic data according to protocol-defined criteria and make the decision whether to escalate the dose in a new cohort. To determine the recommended Phase 2 dose, the SET will review all safety, pharmacokinetic, and pharmacodynamic data from Part 1 before initiation of Part 2. The total number of participants enrolled in Part 1 will depend on the dose level at which the recommended Phase 2 dose is established. After the recommended Phase 2 dose is established, the Part 2 dose-expansion phase will be opened. Part 2 study will be done in a molecularly-defined subset of Participants with gastric adenocarcinoma including gastroesophageal junctions at the RP2D. In Part2, Participants can be hospitalized until Day 8 of Cycle 1 as needed. In addition, extension of hospitalization will be allowed until Day 15 of Cycle 1 according to investigator's clinical judgment. In Part 2, approximately 25 participants will be treated at the recommended Phase 2 dose as 28 days cycles of intermittent dosing regimen in order to evaluate fibroblast growth factor receptor target modulation in tumor, to further elaborate safety, pharmacokinetics, and pharmacodynamics of JNJ-42756493, as well as to evaluate preliminary clinical responses. Participants who are tolerating study drug treatment and achieve clinical responses or stable disease will continue to receive study drug at the same dose until disease progression, unacceptable toxicity, or withdrawal of consent. Serial pharmacokinetic and pharmacodynamic samples will be collected, and safety and efficacy will be monitored throughout the study.

Tipo de estudio

Intervencionista

Inscripción (Actual)

19

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

      • Kashiwa, Japón
      • Matsuyama, Japón
      • Tokyo, Japón

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

20 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Part 1: Histologically or cytologically confirmed solid malignancy or lymphoma that is metastatic or unresectable, and for which standard curative treatment is no longer effective
  • Part 2: Histologically or cytologically confirmed gastric adenocarcinoma including gastroesophageal junctions that is metastatic, locally advanced or unresectable, and for which standard treatment is no longer effective or tolerable
  • Eastern Cooperative Oncology Group performance status score 0 or 1
  • Adequate bone marrow, liver, and renal function according to protocol-defined criteria within the 7 days prior to Day 1 of Cycle 1
  • Laboratory values within protocol -defined parameters
  • Agrees to protocol-defined use of effective contraception
  • Negative urine pregnancy test (urine or serum beta human chorionic gonadotropin [beta-HCG]) at screening for women of child bearing potential

Exclusion Criteria:

  • Has had chemotherapy, radiotherapy, immunotherapy, or treatment with an investigational anticancer agent within 3 weeks (nitrosoureas and mitomycin C within 6 weeks) before the first administration of study drug (localized radiation therapy for palliative purposes and ongoing luteinizing hormone-releasing hormone agonists and antagonists for patients with prostate cancer, bisphosphonates and denosumab are permitted
  • History or current condition of uncontrolled cardiovascular disease as defined in the protocol
  • Taking medications known to have a risk of causing QTc prolongation and Torsades de Pointes or known as strong CYP3A inhibitors or inducers
  • Left ventricular ejection fraction less than (<) 50 percent (%) as assessed by echocardiography (or multi-gated acquisition [MUGA]) performed at screening
  • Uncontrolled intercurrent illness including, but not limited to, poorly controlled hypertension or diabetes, ongoing active infection, psychiatric illness, or a risk of gastrointestinal perforation

Woman who is pregnant, breast-feeding, or planning to become pregnant or is a man who plans to father a child, while the participant is enrolled in this study and is within 3 or 5 months, respectively, after the last dose of the study drug

  • Not recovered from reversible, clinically significant toxicity of prior anticancer therapy
  • Presence of any medical condition that requires intact wound healing capacity and is expected to endanger participant safety if wound healing capacity would be severely reduced during administration of the investigational agent
  • Major surgery within 4 weeks before enrollment
  • Known human immunodeficiency virus infection
  • Known hepatitis B or C (except hepatocellular carcinoma)
  • Active, symptomatic, or untreated brain metastasis

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: Part 1: Dose Escalation (Daily Dosing)
Dose escalation of JNJ-42756493 is to occur until a dose at which <33 percent of participants experience a dose-limiting toxicity, the maximum concentration of JNJ-42756493 is less than the protocol-defined cardiovascular threshold, and JNJ-42756493 is biologically active. Participants will receive study drug once day on Day 1 of Cycle 1 followed by a 2-day drug-free period (Days 2 and 3 of Cycle 1) and continues throughout the 21 day cycle. For all subsequent cycles once a day for 21 days.
JNJ-42756493 dose escalation starting at dose of 2 mg orally daily for 21-day cycles and 28 day cycles Intermitting dosing regimen (7 days on and 7 days off) up to the maximum tolerated dose in order to determine the recommended Phase 2 dose.
Experimental: Part 1: Dose Escalation (Intermittent Dosing)
Intermitting dosing regimen will be 28 days (7 days on and 7 days off). Participants will receive JNJ-42756493 on Days 1 to 7 and Days 15 to 21 of each cycle; JNJ-42756493 will not be administered on Days 8 to 14 and Days 22 to 28 of each cycle.
JNJ-42756493 dose escalation starting at dose of 2 mg orally daily for 21-day cycles and 28 day cycles Intermitting dosing regimen (7 days on and 7 days off) up to the maximum tolerated dose in order to determine the recommended Phase 2 dose.
Experimental: Part 2: Dose Expansion
Participants will receive the recommended Phase 2 JNJ-42756493 dose determined in Part 1 as Intermitting dosing regimen (28 days, 7 days on and 7 days off). Participants who are tolerating study drug treatment and achieve clinical responses or stable disease will continue to receive study drug at the same dose until disease progression, unacceptable toxicity, or withdrawal of consent.
Recommended Phase 2 JNJ-42756493 dose determined in Part 1 administered orally for 28-days cycles (Intermitting dosing regimen).

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Número de participantes afectados por eventos adversos por clasificación de órganos del sistema (SOC) de MedDRA y término preferido (PT)
Periodo de tiempo: Hasta 30 días después de la última dosis del medicamento del estudio
Hasta 30 días después de la última dosis del medicamento del estudio

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Maximum observed plasma concentration of JNJ-42756493
Periodo de tiempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Minimum observed plasma concentration of JNJ-42756493
Periodo de tiempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Time correspondent to the maximum observed plasma concentration of JNJ-42756493
Periodo de tiempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Area under the plasma concentration-time curve from time 0 to 24 hours of JNJ-42756493
Periodo de tiempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Half-life of JNJ-42756493
Periodo de tiempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Apparent volume of distribution of JNJ-42756493
Periodo de tiempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Total clearance of drug of JNJ-42756493
Periodo de tiempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Accumulation index of JNJ-42756493
Periodo de tiempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Number of participants with complete response
Periodo de tiempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Number of participants with partial response
Periodo de tiempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Number of participants with stable disease
Periodo de tiempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Number of participants with progressive disease
Periodo de tiempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28

Colaboradores e Investigadores

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

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el 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)

21 de agosto de 2013

Finalización primaria (Actual)

28 de enero de 2016

Finalización del estudio (Actual)

28 de enero de 2016

Fechas de registro del estudio

Enviado por primera vez

26 de julio de 2013

Primero enviado que cumplió con los criterios de control de calidad

10 de octubre de 2013

Publicado por primera vez (Estimar)

14 de octubre de 2013

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

15 de mayo de 2019

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

13 de mayo de 2019

Última verificación

1 de mayo de 2019

Más información

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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