| Literature DB >> 31332020 |
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Abstract
The FDA granted accelerated approval to selinexor plus low-dose dexamethasone for triple-class refractory multiple myeloma, despite an advisory panel's concerns about the drug's toxicity and the lack of randomized clinical data. ©2019 American Association for Cancer Research.Entities:
Year: 2019 PMID: 31332020 DOI: 10.1158/2159-8290.CD-NB2019-085
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397