Ravandi, Farhad http://orcid.org/0000-0002-7621-377X
Roboz, Gail J.
Wei, Andrew H.
Döhner, Hartmut
Pocock, Christopher
Selleslag, Dominik
Montesinos, Pau
Sayar, Hamid
Musso, Maurizio
Figuera-Alvarez, Angela
Safah, Hana
Tse, William
Sohn, Sang Kyun
Hiwase, Devendra
Chevassut, Timothy
Pierdomenico, Francesca
La Torre, Ignazia
Skikne, Barry
Bailey, Rochelle
Zhong, Jianhua
Beach, C. L.
Dombret, Herve
Clinical trials referenced in this document:
Documents that mention this clinical trial
Management of adverse events in patients with acute myeloid leukemia in remission receiving oral azacitidine: experience from the phase 3 randomized QUAZAR AML-001 trial
https://doi.org/10.1186/s13045-021-01142-x
Article History
Received: 27 May 2021
Accepted: 17 August 2021
First Online: 28 August 2021
Declarations
:
: The trial was designed and conducted in collaboration with the authors and an independent steering committee and with advice from regulatory agencies, in accordance with principles of the Declaration of Helsinki. The study protocol was approved by an institutional review board or ethics committee at each participating site.
: All patients provided informed written consent. An independent data monitoring committee assessed study conduct and safety outcomes.
: Not applicable.
: F.R. reports honoraria and consulting fees from Bristol Myers Squibb and Celgene; and Research funding from Bristol Myers Squibb. G.J.R. reports Consultancy or Advisory Board or Data and Safety Monitoring Committee: AbbVie, Actinium, Agios, Amphivena, Amgen, Argenx, Array Biopharma, Astex, Astellas, AstraZeneca, Bayer, Bristol Myers Squibb, Celgene, Celltrion, Daiichi Sankyo, Eisai, Epizyme, GlaxoSmithKline, Helsinn, Janssen, Jasper Therapeutics, Jazz, Mesoblast, MEI Pharma (IDMC Chair), Novartis, Orsenix, Otsuka, Pfizer, Roche/Genentech, Sandoz, Takeda (IRC Chair), Trovagene; Research Support: Cellectis. A.H.W. reports study-related fees and personal fees from Celgene; royalties from Walter and Eliza Hall Institute of Medical Research; grants from the Medical Research Future Fund; grants and personal fees from Servier, AbbVie, Novartis, Celgene, Astra Zeneca, and Janssen; and personal fees from Astellas, Pfizer, Macrogenics, and Amgen. H. Döhner reports personal fees from Abbvie, Agios, Astellas, Astex Pharmaceuticals, Helsinn, Janssen, Oxford Biomedicals, and Roche; grants and personal fees from Amgen, Celgene, Jazz Pharmaceuticals, and Novartis; and grants from AROG Pharmaceuticals, Bristol Myers Squibb, Pfizer, and Sunesis. D.S. reports honoraria from Novartis, Celgene, Amgen, Janssen-Cilag, AbbVie, Alexion, GSK, MSD, Pfizer, Sanofi, Takeda, Incyte, and Teva; consultancy for Novartis, Celgene, Amgen, Janssen-Cilag, AbbVie, Alexion, GSK, MSD, Pfizer, Sanofi, Takeda, Incyte, and Teva; and speakers’ bureau participation for Novartis, Celgene, Amgen, MSD, Takeda, and Teva. P.M. reports Research support and advisory board by Celgene-BMS. H.Sayar reports advisory board participation for BMS. H.Safah reports speaker’s bureau participation for Incyte, Celgene/BMS, Sanofi, Karyopharm, and Amgen. D.H. reports research support from Celgene/BMS. H. Dombret reports Research support and advisory board participation for Celgene-BMS. B.S., R.B., J.Z., and C.L.B. are employed at and have equity ownership in Bristol Myers Squibb. I.L.T. was formerly employed at Celgene, a Bristol-Myers Squibb Company, and had equity ownership in Bristol Myers Squibb. C.P., M.M., A.F.-A., W.T., S.K.S., and T.C. report no conflicts.