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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01204164
Recruitment Status : Completed
First Posted : September 17, 2010
Last Update Posted : May 6, 2016
Sponsor:
Information provided by (Responsible Party):
Tragara Pharmaceuticals, Inc.

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

Condition or disease Intervention/treatment Phase
AML ALL Blast Crisis MDS Multiple Myeloma Drug: TG02 citrate Drug: Carfilzomib Drug: Dexamethasone Phase 1

Detailed Description:

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.

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 120 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Study Start Date : August 2010
Actual Primary Completion Date : March 2016
Actual Study Completion Date : April 2016


Arm Intervention/treatment
Experimental: TG02 in AL
Single agent TG02 citrate in acute leukemia patients
Drug: TG02 citrate
TG02 citrate capsules given orally.
Other Name: No other names.

Experimental: TG02 in MM
Single Agent TG02 citrate in multiple myeloma patients
Drug: TG02 citrate
TG02 citrate capsules given orally.
Other Name: No other names.

Experimental: TG02 + CFZ in MM
TG02 in combination with carfilzomib and dexamethasone in multiple myeloma patients
Drug: TG02 citrate
TG02 citrate capsules given orally.
Other Name: No other names.

Drug: Carfilzomib
Carfilzomib per PI
Other Name: Kyprolis

Experimental: TG02 + CFZ + DEX in CFZ refractory MM
TG02 in combination with carfilzomib and dexamethasone in carfilzomib refractory multiple myeloma patients
Drug: TG02 citrate
TG02 citrate capsules given orally.
Other Name: No other names.

Drug: Carfilzomib
Carfilzomib per PI
Other Name: Kyprolis

Drug: Dexamethasone
Dexamethasone (Oral or IV)
Other Name: Ozurdex, Maxidex, Decadron, Baycadron




Primary Outcome Measures :
  1. Maximum Tolerated Dose [ Time Frame: 28 days ]
    Maximum Tolerated Dose refers to the highest dose of TG02 administered that will produce the desired effect without unacceptable toxicity.


Secondary Outcome Measures :
  1. Safety [ Time Frame: 28 days ]
    Safety data will include vital signs, ECGs, PE findings, clinical laboratory parameters, ECOG PS, AEs/SAEs and concomitant medications.

  2. Pharmacokinetics of TG02 [ Time Frame: 28 days ]
    Plasma will be analyzed to determine TG02 concentration.

  3. Clinical Benefit Response [ Time Frame: 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).

  4. Overall Response Rate [ Time Frame: 28 days ]
    Overall Response Rate is defined as the sum of patients with sCR, CR, VGPR and PR.

  5. Progression-Free Survival [ Time Frame: 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.

  6. Overall Survival [ Time Frame: 28 days ]
    Overall Survival is time to death, which is measured from the date of first study drug administration until the date of death.

  7. Duration of Response [ Time Frame: 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.

  8. Pharmacodynamics [ Time Frame: 28 days ]
    Pharmacodynamic sampling may include whole blood and bone marrow at baseline and post-treatment for pathway determination if available.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01204164


Locations
Layout table for location information
United States, Colorado
RMCC
Denver, Colorado, United States, 80218
United States, Georgia
Emory
Atlanta, Georgia, United States, 30322
United States, Illinois
Rush
Chicago, Illinois, United States, 60612
United States, Indiana
IU
Indianapolis, Indiana, United States, 46202
United States, New Jersey
HUMC
Hackensack, New Jersey, United States, 07601
United States, New York
Cornell
New York City, New York, United States, 10021
United States, Ohio
OSU
Columbus, Ohio, United States, 43210
United States, Tennessee
SCRI
Nashville, Tennessee, United States, 37203
United States, Texas
MDACC
Houston, Texas, United States, 77030
Sponsors and Collaborators
Tragara Pharmaceuticals, Inc.
Investigators
Layout table for investigator information
Study Director: T Parrott Tragara Pharmaceuticals
Layout table for additonal information
Responsible Party: Tragara Pharmaceuticals, Inc.
ClinicalTrials.gov Identifier: NCT01204164    
Other Study ID Numbers: TG02-101
First Posted: September 17, 2010    Key Record Dates
Last Update Posted: May 6, 2016
Last Verified: May 2016
Keywords provided by Tragara Pharmaceuticals, Inc.:
AML
ALL
MDS
CML in blast crisis
Multiple Myeloma
Carfilzomib refractory
Additional relevant MeSH terms:
Layout table for MeSH terms
Multiple Myeloma
Hematologic Neoplasms
Blast Crisis
Neoplasms, Plasma Cell
Neoplasms by Histologic Type
Neoplasms
Hemostatic Disorders
Vascular Diseases
Cardiovascular Diseases
Paraproteinemias
Blood Protein Disorders
Hematologic Diseases
Hemorrhagic Disorders
Lymphoproliferative Disorders
Immunoproliferative Disorders
Immune System Diseases
Neoplasms by Site
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Leukemia, Myeloid
Leukemia
Cell Transformation, Neoplastic
Carcinogenesis
Neoplastic Processes
Myeloproliferative Disorders
Bone Marrow Diseases
Chronic Disease
Disease Attributes
Pathologic Processes
Dexamethasone
Anti-Inflammatory Agents