Status:
COMPLETED
Study of FF-10501-01 in Patients With Relapsed or Refractory Hematological Malignancies
Lead Sponsor:
Fujifilm Pharmaceuticals U.S.A., Inc.
Conditions:
AML
CMML
Eligibility:
All Genders
18+ years
Phase:
PHASE1
PHASE2
Brief Summary
A Phase 1/2a Dose Escalation Study of FF-10501-01 in Patients with Relapsed or Refractory Hematological Malignancies to determine the safety and tolerability. A total of 6 cohorts will be enrolled in ...
Detailed Description
Subjects will receive FF-10501-01 orally on a twice daily schedule for 14, 21 or 28 days repeated every 28 days (=1 cycle). Disease assessments, including analysis of blood and bone marrow aspirates, ...
Eligibility Criteria
Inclusion
- Confirmed advanced hematologic malignancies;
- Phase 1:
- High-risk MDS/CMML (defined as ≥ 10% peripheral blood or marrow blasts and/or IPSS score ≥ 1.5) and relapsed or refractory to prior therapy
- AML relapsed or refractory to prior therapy, or ≥ 60 years of age and not a candidate for other therapies
- Phase 2a:
- MDS/CMML, relapsed from, or refractory to, prior HMA therapy; the latter defined as failure to achieve clinical remission (CR), partial remission (PR) or hematologic improvement (HI) after previous HMA therapy (≥ 4 cycles of azacitidine or decitabine), or progression during, or toxicity to previous HMA therapy precluding further HMA treatment, and,
- Bone marrow blast count ≥ 10% or peripheral blast count ≥ 5%, or IPSS-R score ≥ 3.5.
- At least 3 weeks beyond the last chemotherapy, targeted anticancer agent, major surgery or experimental treatment and recovered from all acute toxicities (≤ Grade 1). Hydroxyurea used to control peripheral blast counts is permitted up to Day 7 of treatment on study.
- Adequate performance status: ECOG ≤ 2;
- Adequate renal and hepatic function:
- creatinine ≤ 2.0 mg/dL, or calculated creatinine clearance ≥ 45 mL/min
- total bilirubin ≤ 2 times the upper limit of normal (ULN)
- ALT/AST ≤ 2 times ULN
- Negative serum pregnancy test
- Ability to provide written informed consent
Exclusion
- Known history of coronary artery disease, angina, myocardial infarction, congestive heart failure, cardiac arrhythmia or any other type of heart disease present within the last 6 months
- Known family history of hereditary heart disease
- QT interval corrected for rate (QTc) \> 450 msec on the electrocardiogram (ECG) obtained at Screening
- Concomitant medication(s) that may cause QTc prolongation or induce Torsades de Pointes, with the exception of anti-microbials that are used as standard of care to prevent or treat infections and other such drugs that are considered by the Investigator to be essential for the care of the patient.
- Presence of active central nervous system (CNS) leukemia. Subjects adequately treated for CNS leukemia documented by 2 consecutive cerebrospinal fluid samples negative for leukemia cells are eligible. Subjects with no history of CNS leukemia will not be required to undergo cerebrospinal fluid sampling for eligibility.
- Known positive for HIV, hepatitis B virus surface antigen (HBsAg), or hepatitis C virus (HCV).
- Active infection requiring IV anti-infective usage within the last 7 days prior to study treatment.
- Any other medical intervention or condition which could compromise adherence to study requirements or confound the interpretation of study results.
- Pregnant or breast-feeding.
- Treatment with any investigational product within 28 days prior to Screening.
Key Trial Info
Start Date :
July 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 15 2019
Estimated Enrollment :
55 Patients enrolled
Trial Details
Trial ID
NCT02193958
Start Date
July 1 2014
End Date
October 15 2019
Last Update
March 19 2025
Active Locations (2)
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1
Cleveland Clinic at Taussig Cancer Center
Cleveland, Ohio, United States, 44195
2
M D Anderson Cancer Center
Houston, Texas, United States, 77030