Third Patient Death Potentially Linked to Lecanemab Days Before Expected FDA Decision (Updated)
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Two days before the FDA is expected to make a decision on Biogen and Eisai's lecanemab, another death possibly linked to the Alzheimer's drug came to light, courtesy of a letter published Wednesday in the New England Journal of Medicine.
The letter to the editor, written by Nicholas J. Reish, M.D., Ph.D. and other physicians at Northwestern, outlines the case of a 65-year-old patient with early Alzheimer’s. The patient had participated in both the randomized Phase III Clarity-AD trial and received three intravenous infusions of the anti-amyloid antibody in the open-label phase.
The patient had cerebral amyloid angiopathy (CAA), according to the autopsy report. CAA is a cerebrovascular disorder in which amyloid beta-peptide accumulates in the walls of small-to-medium-sized cerebral blood vessels and meninges.
Upon suffering a stroke, the patient was treated with intravenous tissue plasminogen activator (t-PA), an emergency stroke-busting medication. According to the authors, the patient then experienced “numerous acute intracerebral hemorrhages” and subsequently died.
The authors went on to write that “the extensive number and variation in sizes of the cerebral hemorrhages in this patient would be unusual as a complication of t-PA solely related to cerebrovascular amyloid.”
The findings “raise the possibility of cerebral hemorrhages and necrotizing vasculopathy associated with t-PA infusion in a patient with cerebrovascular amyloid who had received lecanemab,” the authors concluded.
In a response also published Wednesday in NEJM, Drs. Marwan Sabbagh, M.D. of the Barrow Neurological Institute and Christopher H. van Dyck, M.D. of the Yale School of Medicine, principal investigator, agreed that the case “raises important management issues”, particularly for patients who are homozygous for the APOE ε4 allele.
Sabbagh presented data from Clarity-AD at the 2022 Clinical Trials on Alzheimer's Disease (CTAD) conference in November, where he addressed two deaths that had previously been linked to lecanemab.
In October, an unnamed Clarity-AD investigator attributed a patient’s death to lecanemab. The following month, one day ahead of the CTAD presentation, a report in Science linked a second patient’s death to the drug. Both deaths occurred due to bleeding in the brain.
Sabbagh and Dyck suggested that other factors, including high blood pressure and vasculitis, might have contributed to the stroke patient’s death. They went on to point out that there have been fatal intracerebral hemorrhages after t-PA treatment in people with CAA who were not taking anti-amyloid medications.
When approached for comment, Eisai declined to add to the researchers' response letter due to patient privacy.
Biogen and Eisai have a date with the FDA on Jan. 6.
- Report: Second Patient Death Potentially Linked to Eisai and Biogen’s Lecanemab This will open in a new window
- Eisai & Biogen Address Lecanemab's Safety Concerns at CTAD This will open in a new window
- Biogen Sees Rocky 2022 Finish with Further Aduhelm, Lecanemab Scrutiny This will open in a new window