acute myeloid leukemia
Conditions
Interventions
None listed
Sponsors
National Hospital Organization Nagoya Medical Center IRB
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Registered cases in OCV-501 Phase II study
Exclusion criteria
Exclusion criteria: 1) Cases showing a manifestation of non-participation in this study 2) Cases who the principal investigator deems inappropriate as a research subject
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 5-year disease free survival; OCV-501 group vs. placebo group | — |
Secondary
| Measure | Time frame |
|---|---|
| 5-year overall survival; OCV-501 group vs. placebo group Specific immunological responses to WT-1 and prognosis Level of WT1 mRNA and prognosis | — |
Countries
Japan
Contacts
Public ContactTomoki Naoe
National Hospital Organization Nagoya Medical Center Honorary Director
Outcome results
None listed