In June 2021, the US Food and Drug Administration (FDA)
granted accelerated approval for aducanumab to treat patients with mild
cognitive impairment (MCI) or mild dementia due to Alzheimer disease
(AD), despite limited evidence of clinical benefit. The 2 phase 3
clinical trials of aducanumab, EMERGE and ENGAGE, were stopped
prematurely based on prespecified futility thresholds.1
Both trials also showed an increased risk of adverse events with
aducanumab, including microhemorrhages and vasogenic brain edema,
headache, and possibly falls.1
Though both trials excluded patients based on age, certain chronic
diseases, and use of antiplatelet agents and anticoagulants, FDA
approval was granted without contraindications or precautions for these
unstudied patient populations. We evaluated whether patients enrolled in
the trials of aducanumab were representative of patients with dementia
enrolled in Medicare by estimating the proportions of Medicare
beneficiaries with AD or MCI who would have been excluded from the
trials.
No comments:
Post a Comment