CompletedPHASE1, PHASE2NCT02405338
DC Vaccination for Post-remission Therapy in AML
Studying Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Medigene AG
- Principal Investigator
- Yngvar FløisandOslo University Hospital, Rikshospitalet Department of Hematology
- Intervention
- WT1/PRAME vaccination(biological)
- Enrollment
- 20 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2015 – 2019
Study locations (1)
- Oslo University Hospital, Rikshospitalet, Oslo, Norway
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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