Status:
COMPLETED
Phase 1 Study of SGI-110 in Patients With Acute Myeloid Leukemia
Lead Sponsor:
Otsuka Pharmaceutical Co., Ltd.
Conditions:
Acute Myeloid Leukemia
Eligibility:
All Genders
20+ years
Phase:
PHASE1
Brief Summary
To evaluate the tolerability and pharmacokinetics of SGI-110 when administered subcutaneously to Japanese patients with acute myeloid leukemia (AML).
Eligibility Criteria
Inclusion
- Male or female patients with a diagnosis of AML (WHO classification 2008).
- Patients, 20 years of age or older, who are unresponsive to standard chemotherapy or have relapsed following standard chemotherapy
- Patients, 65 years of age or older, who are not eligible for standard intensive chemotherapy
- Patients with ECOG performance status (PS) of 0 to 2
- Patients with adequate organ function
- Women of child-bearing potential must not be pregnant or breast feeding (pregnancy test will be performed at Screening). Women of child bearing potential and all men with female partners of child bearing potential must practice two medically acceptable methods of birth control and must not become pregnant or father a child while receiving treatment with SGI-110 and for 3 months following last dosing.
- Patients who have undergone prior allogeneic hematopoietic stem cell transplantation must have no evidence of active graft-versus host disease (GVHD) and must be off immunosuppressive therapy by ≥2 weeks prior to IMP administration.
Exclusion
- Patients with acute promyelocytic leukemia accompanied by t(15;17)(q22;q12) or (PML/RARA) karyotype abnormalities (include other variant types of APL)
- Patients with multiple cancers (except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other cancer from which the subject has been disease free for at least 3 years)
- Subjects with life-threatening illnesses other than AML or MDS, uncontrolled medical conditions or organ system dysfunction which, in the investigator's opinion, could compromise the subject's safety, or put the study outcomes at risk.
- Patients with poorly controlled arrhythmias, or any Class 3 or 4 cardiac disease as defined by the New York Heart Association Functional Classification
- Patients with symptomatic central nervous system involvement.
Key Trial Info
Start Date :
January 7 2015
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 31 2019
Estimated Enrollment :
21 Patients enrolled
Trial Details
Trial ID
NCT02293993
Start Date
January 7 2015
End Date
May 31 2019
Last Update
March 5 2021
Active Locations (3)
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1
kinki Region
Kyoto, Japan
2
Kanto
Region, Japan
3
Kyusyu
Region, Japan