Almost half of cancer drugs that received accelerated approval didn’t end up improving quality of life or survival after five years of follow-up, Harvard University researchers found, underscoring the uncertainty around a commonly used regulatory pathway for the treatments.
In a paper published in JAMA Sunday, the researchers from Harvard’s Program on Regulation, Therapeutics and Law looked at 129 cancer drugs granted accelerated approval between 2013 and 2023. Oncology drugs make up 80% of all accelerated approvals, the researchers noted.
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