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Clinical Trial Summary

The primary objective of this study is to evaluate the efficacy of subcutaneous azacitidine in combination with durvalumab as compared with subcutaneous azacitidine alone in adults with previously untreated, higher risk MDS who are not eligible for HSCT or in adults ≥ 65 years old with previously untreated AML who are not eligible for HSCT, with intermediate or poor cytogenetic risk.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02775903
Study type Interventional
Source Celgene
Contact
Status Completed
Phase Phase 2
Start date June 3, 2016
Completion date December 27, 2021

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