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Phase 2 study of ATRA and arsenic trioxide for acute promyelocytic leukemia

Phase 2
Conditions
acute promyelocytic leukemia
Registration Number
JPRN-UMIN000012004
Lead Sponsor
Department of Hematology, Hiroshima University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
45
Inclusion Criteria

Not provided

Exclusion Criteria

1. Severe co-morbidity 2. Pregnant and/or lactating woman 3. Patients who have a difficulty to enter the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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