Clinical trials: design, endpoints and interpretation of outcomes
- PMID: 34997213
- PMCID: PMC12727137
- DOI: 10.1038/s41409-021-01542-0
Clinical trials: design, endpoints and interpretation of outcomes
Conflict of interest statement
MO is a consultant for Daiichi Sankyo, Biosight, and Merck and is on independent data safety monitoring boards for Celgene and Glycomimetics. RPG is a consultant to BeiGene Ltd., Fusion Pharma LLC, LaJolla NanoMedical Inc., Mingsight Parmaceuticals Inc. CStone Pharmaceuticals, NexImmune Inc. and Prolacta Bioscience; advisor to Antengene Biotech LLC, Medical Director, FFF Enterprises Inc.; partner, AZAC Inc.; Board of Directors, Russian Foundation for Cancer Research Support; and Scientific Advisory Board: StemRad Ltd.
References
-
- Zheng C, Dai R, Gale R, Zhang M. Causal inference in randomized clinical trials. Bone Marrow Transplantation 2019; 55(1): 4–8. - PubMed
-
- Jabbour J, Manana B, Zahreddine A, Al-Shaar L, Bazarbachi A, Blaise D et al. Vitamins and minerals intake adequacy in hematopoietic stem cell transplant: results of a randomized controlled trial. Bone Marrow Transplantation 2021; 56(5): 1106–1115. - PubMed
-
- DiNardo CD, Jonas BA, Pullarkat V, Thirman MJ, Garcia JS, Wei AH et al. Azacitidine and venetoclax in previously untreated acute myeloid leukemia. New England Journal of Medicine 2020; 383(7): 617–629. - PubMed
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