Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies (TG02-101)
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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
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
AML ALL Blast Crisis MDS Multiple Myeloma | Drug: TG02 citrate Drug: Carfilzomib Drug: Dexamethasone | Phase 1 |
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.
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
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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 |
- 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.
- Safety [ Time Frame: 28 days ]Safety data will include vital signs, ECGs, PE findings, clinical laboratory parameters, ECOG PS, AEs/SAEs and concomitant medications.
- Pharmacokinetics of TG02 [ Time Frame: 28 days ]Plasma will be analyzed to determine TG02 concentration.
- 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).
- Overall Response Rate [ Time Frame: 28 days ]Overall Response Rate is defined as the sum of patients with sCR, CR, VGPR and PR.
- 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.
- 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.
- 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.
- Pharmacodynamics [ Time Frame: 28 days ]Pharmacodynamic sampling may include whole blood and bone marrow at baseline and post-treatment for pathway determination if available.

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

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
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 |
Study Director: | T Parrott | Tragara Pharmaceuticals |
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 |
AML ALL MDS |
CML in blast crisis Multiple Myeloma Carfilzomib refractory |
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 |