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A randomized, open-label, phase II study of azacitidine (AZA) in combination with durvalumab in patients (pts) with previously untreated higher-risk myelodysplastic syndromes (MDS) or acute myeloid leukemia (AML) ineligible for hematopoietic stem cell transplantation (HSCT). |
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Consulting or Advisory Role - Celgene |
Research Funding - Celgene |
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Honoraria - Abbvie; Agios; Amgen; Astex Pharmaceuticals; Celator; Celgene; Novartis; Seagen; Sunesis Pharmaceuticals |
Consulting or Advisory Role - Abbvie; Agios; Amgen; Astex Pharmaceuticals; Celator; Celgene; Novartis; Seagen; Sunesis Pharmaceuticals |
Research Funding - Arog; Bristol-Myers Squibb; Celgene; Novartis; Pfizer |
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No Relationships to Disclose |
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Consulting or Advisory Role - Celgene |
Speakers' Bureau - Celgene |
Research Funding - AstraZeneca; Celgene; Novartis |
Travel, Accommodations, Expenses - Celgene; Novartis |
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Consulting or Advisory Role - Abbvie; Agios; Amgen; Bristol-Myers Squibb; Celator; Celgene; Fujifilm; Juno Therapeutics; Karyopharm Therapeutics; Merck; Novartis; Ono Pharmaceutical; Roche/Genentech; Theradex |
Research Funding - Agios (Inst); Celator (Inst); Karyopharm Therapeutics (Inst); Novartis (Inst) |
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No Relationships to Disclose |
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Stock and Other Ownership Interests - Celgene |
Travel, Accommodations, Expenses - Celgene |
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Stock and Other Ownership Interests - Celgene |
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No Relationships to Disclose |