A Phase 1/1b, Multicenter, Open-Label, Dose-Escalation Study of FT 2102 as a Single Agent and in Combination with Azacitidine in Patients with Acute Myeloid Leukemia or Myelodysplastic Syndrome with an IDH1 Mutation
A study for patients with Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome using study drugs FT 2102
Sponsor: Forma Therapeutics
Enrolling: Male and Female Patients
IRB Number: AAAQ7654
U.S. Govt. ID: NCT02719574
Contact: Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu
Additional Study Information: The purpose of this study is to test the safety and effectiveness of an experimental medication, FT-2102, in the treatment of acute myeloid leukemia or myelodysplastic syndrome. Patients will receive either FT-2102 alone or in combination with cytarabine or azacitidine, an approved drug commonly used in the treatment of AML and MDS. Subjects will remain on study until they experience intolerable side effects, their disease worsens, or they or the study doctor decides to stop.
This study is closed
Investigator
Joseph Jurcic, MD
Do You Qualify?
Have you been diagnosed with Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS)? Yes No
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For more information, please contact:
Research Nurse Navigator
cancerclinicaltrials@cumc.columbia.edu
212-342-5162