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Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies (TG02-101)

5 de mayo de 2016 actualizado por: Tragara Pharmaceuticals, Inc.

Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies

This is a multicenter, open-label, dose escalation Phase 1 study.

Descripción general del estudio

Descripción detallada

This is a multicenter, open-label, dose escalation, Phase 1/1b study.

For Parts 1, 2, and 3 of the study, the primary objective is to determine the highest dose of TG02 citrate that can safely be given to patients with different types of hematological malignancy.

For Part 4, the primary objective is to evaluate the safety and tolerability of once-weekly dosing at the maximum-tolerated dose/ Recommended Phase 2 Dose of TG02 in combination with carfilzomib.

This study consists of four parts:

  • Part 1: single agent TG02 in acute leukemia patients
  • Part 2: single agent TG02 in multiple myeloma patients
  • Part 3: TG02 in combination with carfilzomib in multiple myeloma patients
  • Part 4: TG02 in combination with carfilzomib in carfilzomib refractory multiple myeloma patients.

Tipo de estudio

Intervencionista

Inscripción (Anticipado)

120

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

    • Colorado
      • Denver, Colorado, Estados Unidos, 80218
        • RMCC
    • Georgia
      • Atlanta, Georgia, Estados Unidos, 30322
        • EMORY
    • Illinois
      • Chicago, Illinois, Estados Unidos, 60612
        • Rush
    • Indiana
      • Indianapolis, Indiana, Estados Unidos, 46202
        • IU
    • New Jersey
      • Hackensack, New Jersey, Estados Unidos, 07601
        • HUMC
    • New York
      • New York City, New York, Estados Unidos, 10021
        • Cornell
    • Ohio
      • Columbus, Ohio, Estados Unidos, 43210
        • OSU
    • Tennessee
      • Nashville, Tennessee, Estados Unidos, 37203
        • SCRI
    • Texas
      • Houston, Texas, Estados Unidos, 77030
        • MDACC

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

Part 1 Inclusion Criteria:

  • Relapsed AML, ALL, CML in blast crisis, or MDS
  • 65+ yrs with AML not eligible for standard frontline chemo
  • Interval from prior treatment to time of study drug at least 5 half-lives for cytotoxic/ noncytotoxic agents.
  • Persistent clinically significant toxicities from prior chemo ≤ Grd 1
  • ECOG PS 0-2
  • Lab values:

    • Cr ≤ 2X ULN
    • ALT and/or AST ≤2.5 X ULN
    • Total bilirubin ≤1.5 X ULN unless considered due to Gilbert's syndrome
  • Negative pregnancy test
  • Can take oral med

Part 2 Inclusion Criteria:

  • Relapsed multiple myeloma. At least ≥1 line of therapy and progressed after ≥1 prior therapy
  • Measurable disease defined as at least one of the following:

    • Serum M ≥500 mg/dL
    • Urine M ≥200 mg per 24hr
    • Involved FLC ≥10 mg/dL and abnormal FLC ratio in serum (<0.26 or >1.65)
    • Measurable soft tissue plasmacytoma
  • Persistent clinically significant toxicities from prior chemo ≤ Grd 1
  • ECOG PS 0-2
  • Lab values:

    • ANC of >1000/mm3
    • Platelets ≥50,000/mm3
    • Cr ≤2X the ULN
    • ALT and/or AST ≤2.5X ULN
    • Total bilirubin ≤1.5X ULN, unless considered due to Gilbert's syndrome
  • Negative pregnancy test
  • Can take oral med

Part 3 Inclusion Criteria:

  • Measurable disease defined as at least one of the following:

    • Serum M ≥500 mg/dL
    • Urine M protein ≥200 mg per 24hr
    • Involved FLC level ≥10 mg/dL and abnormal FLC ratio in serum (<0.26 or >1.65)
  • Meet at least one of the criteria below:

    • a. ≥2 prior therapies including proteasome inhibitor and immunomodulatory agent (IMiD)
    • b. ≥1 prior therapy and one of the following abnormalities: 17p del, p53, 1q amp, 1p del, t(4;14)
  • Interval from prior treatment to time of study drug at least 5 half-lives or 3 wks, which ever is shorter, for noncytotoxic agents
  • Persistent clinically significant toxicities from prior chemo ≤ Grd 1 or Grd 2 neuropathy without pain
  • ECOG PS 0-2
  • Lab values:

    • ANC of >1000/mm3 independent of G-CSF
    • Platelets ≥50,000/mm3 independent of transfusion
    • MDRD calculated or measured CrCl of ≥30 mL/min
    • ALT and/or AST ≤3X ULN
    • Total bilirubin ≤2X ULN, unless considered due to Gilbert's syndrome
  • Negative pregnancy test
  • Can take oral med

Part 4 Inclusion Criteria:

  • Measurable disease defined as at least one of the following:

    • Serum M ≥500 mg/dL
    • Urine M protein ≥200 mg per 24hr
    • Involved FLC level ≥10 mg/dL and an abnormal FLC ratio in serum (<0.26 or >1.65)
  • Received prior therapies including:

    • a. bortezomib
    • b. an IMiD
    • c. carfilzomib. Demonstrated disease progression on or within 60d of completion of carfilzomib therapy
  • Interval from prior treatment to time of study drug at least 5 half-lives or 3 wks, which ever is shorter, for noncytotoxic agents.
  • Persistent clinically significant toxicities from prior chemo ≤ Grd 1, or Grd 2 neuropathy without pain.
  • ECOG PS 0-2
  • Lab values:

    • ANC of >1000/mm3 independent of G-CSF
    • Platelets ≥50,000/mm3 independent of transfusion
    • MDRD calculated or measured CrCl of ≥30 mL/min
    • ALT and/or AST ≤3X ULN
    • Total bilirubin ≤2X ULN, unless considered due to Gilbert's syndrome
  • Negative pregnancy test
  • Can take oral med

Parts 1 and 2 Exclusion Criteria:

  • Previous allogenic hematopoietic transplant within 90 d
  • Concurrent severe or uncontrolled medical disease that would compromise the safety or compromise the ability of the patient to complete the study
  • Prolonged QTC interval >450ms
  • Symptomatic CNS metastases
  • Known HIV or AIDS
  • Actively treated for a second malignancy
  • Pregnant or nursing women

Part 3 Exclusion Criteria:

  • Multiple myeloma of IgM subtype, POEMS, plasma cell leukemia
  • Corticosteroids discontinued ≥7 days of initiating therapy
  • Previous chemo within 2 wks
  • Hx of ventricular arrhythmia or symptomatic conduction abnormality within 12m
  • CHF, symptomatic ischemia, conduction abnormalities uncontrolled by conventional intervention, myocardial infarction within 6m
  • Prolonged QTc interval (males >450ms, females >470ms)
  • Previous allogeneic hematopoietic transplant within 90 days of study enrollment, Active GVHD requiring treatment.
  • Concurrent severe or uncontrolled medical disease that would compromise the safety or compromise the ability of the patient to complete the study
  • Symptomatic CNS metastases
  • Known HIV or AIDS
  • Prior or 2nd malignancy, except non-melanoma skin cancer, completely resected cervical or prostate cancer (with PSA of less than or equal to 0.1 ng/ml), or other cancer for which the subject has received curative therapy at least 3 yrs prior to study entry
  • Treatment-related MDS
  • Significant neuropathy (Grd 3-4 or Grd 2 with pain) at the time of 1st dose
  • Primary AL amyloidosis
  • Pleural effusions requiring thoracentesis or ascites requiring paracentesis
  • Pregnant or nursing women

Part 4 Exclusion Criteria:

  • Multiple myeloma of IgM subtype, POEMS, plasma cell leukemia
  • Previous chemo within 2 wks
  • Hx ventricular arrhythmia or symptomatic conduction abnormality within 12m
  • CHF, symptomatic ischemia, conduction abnormalities uncontrolled by conventional intervention, and myocardial infarction within 6m
  • Prolonged QTc interval (males >450ms, females >470ms)
  • Previous allogeneic hematopoietic transplant within 90 days. Active GVHD requiring treatment
  • Concurrent severe or uncontrolled medical disease that would compromise the safety or compromise the ability of the patient to complete study
  • Symptomatic CNS metastases
  • Known HIV or AIDS
  • Prior or 2nd malignancy, except non-melanoma skin cancer, completely resected cervical or prostate cancer (with PSA of less than or equal to 0.1 ng/ml), or other cancer for which the subject has received curative therapy at least 3 yrs prior to study entry
  • Treatment-related MDS
  • Significant neuropathy (Grd 3-4 or Grd 2 with pain) at the time of 1st dose
  • Primary AL amyloidosis
  • Pleural effusions requiring thoracentesis or ascites requiring paracentesis
  • Pregnant or nursing women

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 de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: TG02 in AL
Single agent TG02 citrate in acute leukemia patients
TG02 citrate capsules given orally.
Otros nombres:
  • Sin otros nombres.
Experimental: TG02 in MM
Single Agent TG02 citrate in multiple myeloma patients
TG02 citrate capsules given orally.
Otros nombres:
  • Sin otros nombres.
Experimental: TG02 + CFZ in MM
TG02 in combination with carfilzomib and dexamethasone in multiple myeloma patients
TG02 citrate capsules given orally.
Otros nombres:
  • Sin otros nombres.
Carfilzomib per PI
Otros nombres:
  • Kyprolis
Experimental: TG02 + CFZ + DEX in CFZ refractory MM
TG02 in combination with carfilzomib and dexamethasone in carfilzomib refractory multiple myeloma patients
TG02 citrate capsules given orally.
Otros nombres:
  • Sin otros nombres.
Carfilzomib per PI
Otros nombres:
  • Kyprolis
Dexamethasone (Oral or IV)
Otros nombres:
  • Ozurdex, Maxidex, Decadron, Baycadron

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Maximum Tolerated Dose
Periodo de tiempo: 28 days
Maximum Tolerated Dose refers to the highest dose of TG02 administered that will produce the desired effect without unacceptable toxicity.
28 days

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Safety
Periodo de tiempo: 28 days
Safety data will include vital signs, ECGs, PE findings, clinical laboratory parameters, ECOG PS, AEs/SAEs and concomitant medications.
28 days
Pharmacokinetics of TG02
Periodo de tiempo: 28 days
Plasma will be analyzed to determine TG02 concentration.
28 days
Clinical Benefit Response
Periodo de tiempo: 28 days
Clinical Benefit Response is defined as the sum of all response categories for Overall Response Rate (ORR is defined as the sum of patients with sCR, CR, VGPR and PR) plus minimal response (MR).
28 days
Overall Response Rate
Periodo de tiempo: 28 days
Overall Response Rate is defined as the sum of patients with sCR, CR, VGPR and PR.
28 days
Progression-Free Survival
Periodo de tiempo: 28 days
Progression-Free Survival is the time to disease progression or death, which is measured from the date of first study drug administration until the first date that recurrent or progressive disease is objectively documented or the date of death.
28 days
Overall Survival
Periodo de tiempo: 28 days
Overall Survival is time to death, which is measured from the date of first study drug administration until the date of death.
28 days
Duration of Response
Periodo de tiempo: 28 days
Duration of Response is the duration from first observation of response to the first documentation of disease progression, with deaths from causes other than disease progression censored. For the purposes of the calculation of the DOR, the date at which the response status was first observed rather than the date of confirmation is used as the start date.
28 days
Pharmacodynamics
Periodo de tiempo: 28 days
Pharmacodynamic sampling may include whole blood and bone marrow at baseline and post-treatment for pathway determination if available.
28 days

Colaboradores e Investigadores

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

Investigadores

  • Director de estudio: T Parrott, Tragara Pharmaceuticals

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 agosto de 2010

Finalización primaria (Actual)

1 de marzo de 2016

Finalización del estudio (Actual)

1 de abril de 2016

Fechas de registro del estudio

Enviado por primera vez

14 de septiembre de 2010

Primero enviado que cumplió con los criterios de control de calidad

15 de septiembre de 2010

Publicado por primera vez (Estimar)

17 de septiembre de 2010

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

6 de mayo de 2016

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

5 de mayo de 2016

Última verificación

1 de mayo de 2016

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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