search
Back to results

ASTX727 and FT-2102 in Treating IDH1-Mutated Recurrent/Refractory Myelodysplastic Syndrome or Acute Myeloid Leukemia

Primary Purpose

Acute Myeloid Leukemia, Myelodysplastic Syndrome, Recurrent Acute Myeloid Leukemia

Status
Withdrawn
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
CDA Inhibitor E7727/Decitabine Combination Agent ASTX727
IDH-1 Inhibitor FT-2102
Sponsored by
Vanderbilt-Ingram Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Myeloid Leukemia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Must voluntarily sign an informed consent document (ICF)
  • Morphologically confirmed diagnosis of MDS (inclusive of MDS/MPN) or AML in accordance with World Health Organization (WHO) diagnostic criteria

  • Phase Ib: Subjects may have

    • Relapsed/refractory AML or MDS or
    • Treatment naive AML

  • Phase II Expansion: Subjects may have

    • Relapsed/refractory AML or MDS or
    • Treatment naive AML or
    • Treatment naive MDS
  • For patients with MDS, must have a Revised International Prognostics Scoring System (IPSS-R) risk category of intermediate, high, or very high
  • Confirmed IDH1 R132 mutation
  • A bone marrow biopsy must be performed and tissue collected for entrance to the trial
  • Subjects must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
  • Life expectancy of at least 3 months in the assessment of the investigator
  • Recovery from the non-hematologic toxic effects of prior treatment to grade =< 1, or baseline value according to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version (v)4.03 classification (excluding infertility, alopecia, or grade 1 neuropathy)
  • Must have adequate hepatic and renal function as demonstrated by the following:

ALT (SGPT) and/or AST (SGOT) ≤ 3x upper limit of normal (ULN); Direct bilirubin ≤ 1.5 x ULN(or ≤ 2x ULN if due to Gilbert's disease); Serum creatinine of 1.5 x ULN or creatinine clearance of > 50 mL/min (whichever is lower)

  • Baseline Fridericia's correction formula (QTcF) =< 450 msec (average of the QTcF values of screening triplicate electrocardiography [ECG]swith approximately two-minute intervals ) except for those patients with a bundle branch block (BBB)
  • For fertile men and women, agreement to use effective contraceptive methods for the duration of study participation and 90 days after the last dose of study medication

Exclusion Criteria:

  • Treatment naive patients who are suitable for and willing to receive intensive induction chemotherapy
  • Patients with active, uncontrolled infection. Patients with infection under active treatment and controlled with antibiotics are eligible
  • Concurrent condition that in the investigator's opinion would jeopardize compliance with the protocol
  • Known history of human immunodeficiency virus (HIV), or known active hepatitis A, B, or C infection (hepatitis B carriers with normal liver function test [LFT]s and undetectable viral loads are allowed)
  • Women who are pregnant or nursing
  • Organ transplant recipients other than bone marrow transplant
  • Autologous hematologic stem cell transplant within 3 months of study entry. Allogeneic hematologic stem cell transplant within 6 months. Grade II, or greater, active graft-versus- host disease
  • Use of an investigational drug within 21 days or 5 half-lives (whichever is shorter) prior to the first dose of FT-2102/ASTX727. For investigational drugs for which 5 half-lives is less than 21 days, a minimum of 10 days between termination of the investigational drug and administration of FT-2102/ASTX727 is required
  • Any major surgery, chemotherapy, or immunotherapy within the last 21 days (limited palliative radiation is allowed >= 2 weeks); concurrent hydroxyurea is allowed if less than or equal to 2 grams daily
  • Ongoing immunosuppressive therapy including systemic corticosteroids (prednisone or equivalent =< 20 mg daily allowed as clinically warranted). Patients are allowed to use topical or inhaled corticosteroids
  • Concurrent condition that in the investigator's opinion would jeopardize compliance with the protocol.
  • Patients unable to swallow oral medications, or patients with gastrointestinal conditions (e.g., malabsorption, resection, etc.) deemed by the Investigator to jeopardize intestinal absorption
  • Patients receiving intrathecal chemotherapy for active central nervous system (CNS) disease
  • Patients who have exhibited allergic reactions to a previously administered IDH1 inhibitor
  • Patients with acute promyelocytic leukemia (APL)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Treatment (ASTX727, FT-2102)

    Arm Description

    Patients receive CDA inhibitor E7727/decitabine combination agent ASTX727 PO QD on days 1-5 and IDH-1 inhibitor FT-2102 PO QD or BID on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.

    Outcomes

    Primary Outcome Measures

    Incidence of adverse events (Phase Ib)
    Graded according to Common Terminology Criteria for Adverse Events (CTCAE) version 4.03
    Response rate (Phase II)
    calculated for each cohort, together with 95% confidence intervals based on exact binomial distributions.

    Secondary Outcome Measures

    To confirm the phase II recommended dosing level (1b)
    Pharmacokinetics parameters (1b)
    analysis of plasma concentrations during the dose escalation phase of the study
    Reduction of bone marrow blasts (phase II)
    Overall survival (Phase II)
    Time from randomization to death due to any cause
    Event-Free Survival (Phase II)
    Time from start of treatment to event that treatment was intended to prevent or delay
    Measure change in levels of 2-HG in the blood and blood cells after treatment (Phase II)
    Compare 2-HG change to clinical response (Phase II)

    Full Information

    First Posted
    July 5, 2019
    Last Updated
    July 1, 2020
    Sponsor
    Vanderbilt-Ingram Cancer Center
    Collaborators
    Astex Pharmaceuticals, Inc., Novo Nordisk A/S
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT04013880
    Brief Title
    ASTX727 and FT-2102 in Treating IDH1-Mutated Recurrent/Refractory Myelodysplastic Syndrome or Acute Myeloid Leukemia
    Official Title
    A Phase IB/II Study to Evaluate the Safety, Tolerability, and Efficacy of ASTX727 and FT-2102 in IDH1-Mutated Myelodysplastic Syndrome or Acute Myeloid Leukemia
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2020
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Loss of funding
    Study Start Date
    August 27, 2019 (Actual)
    Primary Completion Date
    March 31, 2021 (Anticipated)
    Study Completion Date
    March 31, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Vanderbilt-Ingram Cancer Center
    Collaborators
    Astex Pharmaceuticals, Inc., Novo Nordisk A/S

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    Yes
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    This phase Ib/II trial studies the side effects and best dose of FT-2102 when given together with ASTX727 in treating patients with IDH1-mutated myelodysplastic syndrome or acute myeloid leukemia that has come back (recurrent) or does not respond to treatment (refractory). ASTX727 is an oral deoxyribonucleic acid (DNA) methyltransferase (DNMT) inhibitor. DNA methylation is necessary for cell differentiation and development. Changes to the methylation profile can lead to DNA instability which can cause diseases like cancer. DNMT inhibitors target and inhibit these changes. FT-2102 is an isocitrate dehydrogenase 1 (IDH1) inhibitor. IDH1 is a type of protein involved in metabolism, or the process of providing the body's cells with energy. FT-2102 may stop the abnormal IDH1 protein and may reduce 2-HG levels in diseased cells to levels found in normal cells. Giving ASTX727 and FT-2102 may work better in treating patients with myelodysplastic syndrome or acute myeloid leukemia compared to ASTX727 and FT-2102 alone.
    Detailed Description
    PRIMARY OBJECTIVES: To evaluate the safety of IDH-1 inhibitor FT-2102 (FT-2102) in combination with CDA inhibitor E7727/decitabine combination agent ASTX727 (ASTX727) in myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) patients with IDH1 R132 mutations. (Phase Ib) To evaluate the response rate (overall response rate [ORR], complete response [CR], complete remission with partial hematologic recovery (CRh), complete remission with incomplete blood count recovery [CRi], morphologic leukemia-free state [MLFS], partial response [PR]) of the combination of ASTX727 and the IDH1-inhibitor, FT-2102 in subjects with myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) with IDH1 R132 mutations. (Phase II) SECONDARY OBJECTIVES: To confirm the phase II recommended dosing level of FT-2102 and ASTX727 in combination. (Phase Ib) To determine the pharmacokinetics of FT-2102 and ASTX727 in combination. (Phase Ib) To determine the reduction of bone marrow blasts. (Phase II) To determine the overall survival and event-free survival. (Phase II) To determine the levels of 2-HG in the blood and blood cells after treatment. (Phase II) To determine the relationship of 2-HG reduction to clinical response. (Phase II) OUTLINE: This is a phase Ib, dose-escalation of IDH-1 inhibitor FT-2102 followed by a phase II study. Patients receive CDA inhibitor E7727/decitabine combination agent ASTX727 orally (PO) once daily (QD) on days 1-5 and IDH-1 inhibitor FT-2102 PO QD or twice daily (BID) on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up at 30 days, every 3 months for 12 months, and then periodically for up to 5 years.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Acute Myeloid Leukemia, Myelodysplastic Syndrome, Recurrent Acute Myeloid Leukemia, Recurrent Myelodysplastic Syndrome, Refractory Acute Myeloid Leukemia, Refractory Myelodysplastic Syndrome

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 1, Phase 2
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Treatment (ASTX727, FT-2102)
    Arm Type
    Experimental
    Arm Description
    Patients receive CDA inhibitor E7727/decitabine combination agent ASTX727 PO QD on days 1-5 and IDH-1 inhibitor FT-2102 PO QD or BID on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.
    Intervention Type
    Drug
    Intervention Name(s)
    CDA Inhibitor E7727/Decitabine Combination Agent ASTX727
    Other Intervention Name(s)
    ASTX727
    Intervention Description
    Given by mouth
    Intervention Type
    Drug
    Intervention Name(s)
    IDH-1 Inhibitor FT-2102
    Other Intervention Name(s)
    FT 2102, FT-2102, IDH1-R132 Inhibitor FT-2102
    Intervention Description
    Given by mouth
    Primary Outcome Measure Information:
    Title
    Incidence of adverse events (Phase Ib)
    Description
    Graded according to Common Terminology Criteria for Adverse Events (CTCAE) version 4.03
    Time Frame
    Up to 30 days
    Title
    Response rate (Phase II)
    Description
    calculated for each cohort, together with 95% confidence intervals based on exact binomial distributions.
    Time Frame
    Approximately 12 months
    Secondary Outcome Measure Information:
    Title
    To confirm the phase II recommended dosing level (1b)
    Time Frame
    At 28 days
    Title
    Pharmacokinetics parameters (1b)
    Description
    analysis of plasma concentrations during the dose escalation phase of the study
    Time Frame
    Approximately 12 months
    Title
    Reduction of bone marrow blasts (phase II)
    Time Frame
    Approximately 12 months
    Title
    Overall survival (Phase II)
    Description
    Time from randomization to death due to any cause
    Time Frame
    Up to 2 years
    Title
    Event-Free Survival (Phase II)
    Description
    Time from start of treatment to event that treatment was intended to prevent or delay
    Time Frame
    Up to 2 years
    Title
    Measure change in levels of 2-HG in the blood and blood cells after treatment (Phase II)
    Time Frame
    Up to 12 months
    Title
    Compare 2-HG change to clinical response (Phase II)
    Time Frame
    Up to 12 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Must voluntarily sign an informed consent document (ICF) Morphologically confirmed diagnosis of MDS (inclusive of MDS/MPN) or AML in accordance with World Health Organization (WHO) diagnostic criteria Phase Ib: Subjects may have Relapsed/refractory AML or MDS or Treatment naive AML Phase II Expansion: Subjects may have Relapsed/refractory AML or MDS or Treatment naive AML or Treatment naive MDS For patients with MDS, must have a Revised International Prognostics Scoring System (IPSS-R) risk category of intermediate, high, or very high Confirmed IDH1 R132 mutation A bone marrow biopsy must be performed and tissue collected for entrance to the trial Subjects must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 Life expectancy of at least 3 months in the assessment of the investigator Recovery from the non-hematologic toxic effects of prior treatment to grade =< 1, or baseline value according to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version (v)4.03 classification (excluding infertility, alopecia, or grade 1 neuropathy) Must have adequate hepatic and renal function as demonstrated by the following: ALT (SGPT) and/or AST (SGOT) ≤ 3x upper limit of normal (ULN); Direct bilirubin ≤ 1.5 x ULN(or ≤ 2x ULN if due to Gilbert's disease); Serum creatinine of 1.5 x ULN or creatinine clearance of > 50 mL/min (whichever is lower) Baseline Fridericia's correction formula (QTcF) =< 450 msec (average of the QTcF values of screening triplicate electrocardiography [ECG]swith approximately two-minute intervals ) except for those patients with a bundle branch block (BBB) For fertile men and women, agreement to use effective contraceptive methods for the duration of study participation and 90 days after the last dose of study medication Exclusion Criteria: Treatment naive patients who are suitable for and willing to receive intensive induction chemotherapy Patients with active, uncontrolled infection. Patients with infection under active treatment and controlled with antibiotics are eligible Concurrent condition that in the investigator's opinion would jeopardize compliance with the protocol Known history of human immunodeficiency virus (HIV), or known active hepatitis A, B, or C infection (hepatitis B carriers with normal liver function test [LFT]s and undetectable viral loads are allowed) Women who are pregnant or nursing Organ transplant recipients other than bone marrow transplant Autologous hematologic stem cell transplant within 3 months of study entry. Allogeneic hematologic stem cell transplant within 6 months. Grade II, or greater, active graft-versus- host disease Use of an investigational drug within 21 days or 5 half-lives (whichever is shorter) prior to the first dose of FT-2102/ASTX727. For investigational drugs for which 5 half-lives is less than 21 days, a minimum of 10 days between termination of the investigational drug and administration of FT-2102/ASTX727 is required Any major surgery, chemotherapy, or immunotherapy within the last 21 days (limited palliative radiation is allowed >= 2 weeks); concurrent hydroxyurea is allowed if less than or equal to 2 grams daily Ongoing immunosuppressive therapy including systemic corticosteroids (prednisone or equivalent =< 20 mg daily allowed as clinically warranted). Patients are allowed to use topical or inhaled corticosteroids Concurrent condition that in the investigator's opinion would jeopardize compliance with the protocol. Patients unable to swallow oral medications, or patients with gastrointestinal conditions (e.g., malabsorption, resection, etc.) deemed by the Investigator to jeopardize intestinal absorption Patients receiving intrathecal chemotherapy for active central nervous system (CNS) disease Patients who have exhibited allergic reactions to a previously administered IDH1 inhibitor Patients with acute promyelocytic leukemia (APL)
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Paul Ferrell, MD
    Organizational Affiliation
    Vanderbilt Medical Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    ASTX727 and FT-2102 in Treating IDH1-Mutated Recurrent/Refractory Myelodysplastic Syndrome or Acute Myeloid Leukemia

    We'll reach out to this number within 24 hrs