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NCT00426101
Phase 3Interventional
Includes trials conducted after preliminary evidence suggesting effectiveness of the drug has been obtained, and are intended to gather additional information to evaluate the overall benefit-risk relationship of the drug.
View on ClinicalTrials.gov ↗Timeline
- Start date
- Jan 1, 2004
- Primary completion
- Dec 1, 2011
- Completion date
- Dec 1, 2017
- First posted
- —
- Last posted
- —
- Enrollment
- 300
- Arms / groups
- 1 / —
- Source
- AACT · pre-existing
Sponsors
- Karolinska InstituteLead sponsor
- University of FlorenceCollaborator
- St. Anna KinderkrebsforschungCollaborator
- Hospital JP GarrahanCollaborator
- Leiden UniversityCollaborator
- Baylor UniversityCollaborator
- University of LondonCollaborator
- University of CincinnatiCollaborator
- Ehime UniversityCollaborator
- OsakidetzaCollaborator
- Karolinska InstituteOverall official - principal investigator
- Karolinska InstituteReponsible party - principal investigator
- University of HamburgCollaborator
Drugs studied
Indications studied
CDEK-curated fields only — the ClinicalTrials.gov results mirror (baseline measures, adverse events, participant flow) is a separate, currently-dormant pipeline; see MIGRATION_PLAN.md.