drugset / Trial / NCT04273802

CPX-351 in Higher Risk Myelodysplastic Syndromes

NCT04273802

Phase 1/2 Completed 40 enrolled Groupe Francophone des Myelodysplasies
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Study of the efficacy of CPX-351 treatment in patients with higher risk myelodysplastic syndromes : as first line treatment or after hypomethylating agents failure

Timeline

Start
2020-04-29
Primary completion
2021-08-27
Completion
2022-07-06

Drugs

EvaluationDrugModalityDoseRoute
Subject CPX-351 Other / unclassified 60 unknown Intravenous
Subject CPX-351 Other / unclassified 100 unknown Intravenous