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Postmarket Safety Actions for Novel Oncology Drugs Granted FDA’s Accelerated Approval

Year: 2026
Type: article
Study design: Observational Study
Abstract: This cross-sectional study examines postmarket safety actions for novel oncology drugs that received accelerated Food and Drug Administration (FDA) approval.
Language: English
Subfield: Toxicology
Open Access status: gold
Estimated APC paid: $3,000
OpenAlex ID: W7123908162
FWCI: 22.99
Cites: 5
Cited by: 4
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