Clinical Trials /

IDH2 (AG 221) Inhibitor in Patients With IDH2 Mutated Myelodysplastic Syndrome



patients with MDS (Myelodysplastic Syndrome) and mutated IDH2 patients will be treated with AG221 (IDH2 inhibitor)

Related Conditions:
  • Acute Myeloid Leukemia
  • Myelodysplastic Syndromes
Recruiting Status:



Phase 2

Trial Eligibility



  • Brief Title: IDH2 (AG 221) Inhibitor in Patients With IDH2 Mutated Myelodysplastic Syndrome
  • Official Title: A Single-arm Phase II Multicenter Study of IDH2 (AG-221) Inhibitor in Patients With IDH2 Mutated Myelodysplastic Syndrome

Clinical Trial IDs

  • NCT ID: NCT03744390


  • Myelodysplastic Syndromes
  • Leukemia Acute Myeloid




patients with MDS (Myelodysplastic Syndrome) and mutated IDH2 patients will be treated with AG221 (IDH2 inhibitor)

Detailed Description

      Myelodysplastic syndrome (MDS) are clonal hematopoietic stem cell disorders characterized by
      ineffective hematopoiesis leading to blood cytopenia, especially anemia, and often evolving
      to Acute myeloblastic Leukemia (AML). Main prognostic factors of MDS, for progression to AML
      and survival, include the number and importance of cytopenias, percent marrow blasts and bone
      marrow cytogenetic abnormalities. These factors are combined in an International Prognostic
      Scoring System (IPSS) that distinguishes 4 subgroups with significantly different risk of
      progression to AML and survival (low, intermediate 1 (int 1), intermediate 2 (int 2), high).
      Low and int 1 subgroups are often grouped together as "favorable " or low risk MDS, and int 2
      and high subgroups are " unfavorable " or high risk MDS.

      On the other hand, only 50 to 60% of the patients respond to Azacitidine, and most responders
      relapse within 12 to 15 months resulting in a median survival of only about 6 months in these
      patients,. As a result there is a need for new therapies in patients who fail to respond to
      azacitidine or decitabine and for whom there is currently no establish treatment.

      Isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) are key metabolic enzymes that convert
      isocitrate to α-ketoglutarate. IDH1/2 mutations define distinct subsets of cancers, including
      low-grade gliomas and secondary glioblastomas, chondrosarcomas, intrahepatic chol-, and
      hematologic angiosarcomas c malignancies. Somatic point mutations in IDH1/2 confer a
      gain-of-function in cancer cells, resulting in the accumulation and secretion in vast excess
      of an antimetabolite, the D-2-hydroxyglutarate (D-2HG). Overproduction of D-2HG interferes
      with cellular metabolism and epigenetic regulation, contributing to oncogenesis. Indeed, high
      levels of D-2HG inhibit alpha-ketoglutarate-dependent dioxygenases, including histone and DNA
      demethylases, leading to histone and DNA hypermethylation and finally a block in cell

      preclinical studies have demonstrated that inhibition of IDH1/2-mutant enzymes decreases
      intracellular D-2-hydroxyglutarate (D-2HG) levels, reverses epigenetic dysregulation, and
      releases the differentiation block.

      AG-221, a selective inhibitor of the IDH2 mutant enzyme Overall, in myeloid malignancies,
      AG221 have been mainly used in generally heavily pretreated AML, with about 40% of responses
      in patients with the respective IDH 1 and IDH2 mutations, and a median response duration
      exceeding 1 year when CR or PR was achieved.

      Based on these results, the investigators hypothesize that the IDH2 inhibitor (AG 221) may be
      an effective therapeutic option in patient with IDH2 mutation-positive myelodysplastic
      syndrome This is an open-label, single-arm multicenter, phase II study

      The efficacy of AG 221 will be studied in 3 different groups of MDS patients with IDH-1

        -  Cohort A:Higher risk MDS (IPSS int-2, high) without response (CR,PR,stable disease with
           HI) after at least 6 cycles of azacitidine or relapse after a response but without overt
           progression (defined by at least doubling of marrow blasts, compared to pre azacitidine
           bone marrow, or by AML progression beyond 30% blasts)

        -  Cohort B:Untreated higher risk MDS (IPSS int-2, high) without life threatening
           cytopenias (ie red blood cell (ANC) < 500/mm3 or any recent severe infection and/or
           platelets below 30,000/mm3 and any bleeding symptom). Azacitidine will be added after 3
           cycles of AG-221 in the absence of response

        -  Cohort C: Lower risk MDS with anemia resistant to erythropoietic stimulating agents
           (primary or secondary resistance)

Trial Arms

AG-221ExperimentalSubjects enrolled will receive continuous 28-day cycles of AG-221 - 100 mg.
  • AG-221

Eligibility Criteria


        Patients must meet all of the following criteria to participate in the study:

          1. Myelodysplastic syndrome according to World Health Organization (WHO) classification
             including non-proliferative AML up to 29% of Bone marrow (BM) blast

          2. Age ≥ 18 years

          3. Belonging to one of the following categories:

               1. higher risk MDS (IPSS int-2, high) without response to azacitidine (Complete
                  response (CR),Partial Response (PR), stable disease with HI) after at least 6
                  cycles , or relapsing after a response but without overt progression (defined by
                  at least doubling of marrow blasts, compared to pre azacitidine bone marrow, or
                  AML progression beyond 30% blasts)

               2. Untreated higher risk MDS (IPSS int-2, high) without life threatening cytopenia
                  including absolute neutrophil count (ANC) <500/mm3 or any recent severe
                  infections and/or platelets below 30,000/mm3 and any bleeding symptom

               3. Lower risk MDS with resistance or loss of response to a previous treatment with
                  epoetin alpha/ beta (≥60000 U/w) or Darbopoetin (≥250 ug/w) given for at least 12
                  weeks and red blood cell (RBC) transfusion requirement at least 2 U/8 weeks in
                  the previous 16 weeks.

          4. Presence of IDH2 mutation in either blood or marrow prior to start of therapy

          5. Normal renal function, defined by creatinine less than 1.5 times the upper limit of
             normal, creatinine clearance (Modification of diet in renal disease) (MDRD) ≥ 50

          6. Normal liver function, defined by total bilirubin and transaminases less than 1.5
             times the upper limit of normal.

          7. Adequate cardiac ejection fraction (>40%)

          8. Patient is not known to be refractory to platelet transfusions.Written informed

          9. Patient must understand and voluntarily sign consent form.

         10. Patient must be able to adhere to the visit schedule as outlined in the study and
             follow protocol requirements.

         11. Eastern Cooperative Oncology Group (ECOG) performance status 0-2 at the time of

         12. Female subjects of child-bearing potential must agree to undergo medically supervised
             pregnancy test prior to starting study drug. The first pregnancy test will be
             performed at screening (within 7 days prior to first study drug administration), and
             on the day of the first study drug administration and confirmed negative prior to
             dosing and Day 1 before dosing all subsequent cycles.

         13. Female subjects with reproductive potential must have a negative serum pregnancy test
             within 7 days prior to the start of therapy. Subjects with reproductive potential are
             defined as sexually mature women who have not undergone a hysterectomy, bilateral
             oophorectomy or tubal occlusion or who have not been naturally postmenopausal (i.e.,
             who have not menstruated at all) for at least 24 consecutive months (i.e., has had
             menses at any time in the preceding 24 consecutive months). Females of reproductive
             potential as well as fertile men and their partners who are female of reproductive
             potential must agree to abstain from sexual intercourse or to use two highly effective
             forms of contraception from the time of giving informed consent, during the study and
             for 120 days (females and males) following the last dose of AG-221. A highly effective
             form of contraception is defined as hormonal oral contraceptives, injectables,
             patches, intrauterine devices.

        Male patients must :

        Agree the need for the use of a condom if engaged in sexual activity with a woman of
        childbearing potential during the entire period of treatment, even if disruption of
        treatment and during 3 months after end of treatment.

        Agree to learn about the procedures for preservation of sperm before starting treatment


        A patient meeting any of the following criteria is not eligible to participate in the

          1. Severe infection or any other uncontrolled severe condition.

          2. Significant cardiac disease - New York Heart Association (NYHA) Class III or IV or
             having suffered a myocardial infarction in the last 6 months.

          3. Less than 14 days since prior treatment with growth factors (EPO, G-CSF).

          4. Use of investigational agents within 30 days or any anticancer therapy within 2 weeks
             before the study entry with the exception of hydroxyurea. The patient must have
             recovered from all acute toxicity from any previous therapy.

          5. Subject has a heart-rate corrected QT interval using Fridericia's method (QTcF) ≥ 470
             msec or any other factor that increases the risk of QT prolongation or arrhythmic
             events (e.g., heart failure, hypokalemia, family history of long QT interval
             syndrome). Subjects with prolonged QTcF interval in the setting of bundle branch block
             may participate in the study.

          6. Active cancer or cancer during the year prior to trial entry other than basal cell
             carcinoma, or carcinoma in situ of the cervix or breast.

          7. Patient already enrolled in another therapeutic trial of an investigational drug.

          8. Known HIV infection or active hepatitis B or C.

          9. Women who are or could become pregnant or who are currently breastfeeding.

         10. Any medical or psychiatric contraindication that would prevent the patient from
             understanding and signing the informed consent form.

         11. Patient eligible for allogeneic stem cell transplantation.

         12. Known allergies to AG-221 or any of its excipients.

         13. No affiliation to a health insurance system.
Maximum Eligible Age:90 Years
Minimum Eligible Age:18 Years
Eligible Gender:All
Healthy Volunteers:No

Primary Outcome Measures

Measure:Overall hematological response
Time Frame:6 months
Safety Issue:
Description:Overall hematological response

Secondary Outcome Measures

Measure:Duration Response
Time Frame:3 years
Safety Issue:
Description:Duration Response
Measure:Progression IPSS
Time Frame:3 years
Safety Issue:
Description:Progression IPSS


Phase:Phase 2
Primary Purpose:Interventional
Overall Status:Recruiting
Lead Sponsor:Groupe Francophone des Myelodysplasies

Last Updated

December 2, 2020