The Arizona Republic

Alzheimer’s drug shows brain swelling in patients

- Robert Langreth

Biogen Inc.’s controvers­ial Alzheimer’s drug Aduhelm produced brain swelling in 35% of patients who took the approved dose, although most didn’t experience symptoms, company researcher­s said in a study.

The study in JAMA Neurology found that 362 of 1,029 patients who received the approved dose of the drug experience­d the side effect, which showed up in brain imaging of people in two big clinical trials. While most cases weren’t accompanie­d by symptoms, 94 patients experience­d headache, confusion, dizziness or other effects.

Researcher­s are trying to understand the potential implicatio­ns of the side effects – called amyloid-related imaging abnormalit­ies, or ARIA – now that the drug is on the market and may be used in a wider group of patients than the carefully run clinical trials. Concerns have also risen since a patient with signs of ARIA reportedly died, although there’s no proven link between the side effect and the death.

Ths study in JAMA Neurology is one of the first formal publicatio­ns of data from the company’s two final-stage trials of Aduhelm. Efficacy data from the two studies has not been published in a medical journal, but the company said it’s on track for publicatio­n soon.

About 19% of patients who received the dose had brain bleeding that showed up on imaging, which sometimes overlapped with swelling, the study found. A total of 41% of patients had either brain swelling, bleeding or both. Of those cases, 14 were judged to be serious, including some people who were hospitaliz­ed.

Approved by the U.S. Food and Drug Administra­tion in June, Aduhelm is controvers­ial because the two large trials produced contradict­ory results as to whether it slows Alzheimer’s cognitive decline. Some of FDA’s scientific advisers resigned in protest after the approval, which was based on the drug’s ability to remove an Alzheimer’s-linked protein called amyloid from the brain.

The safety data follows a recent report to the FDA of the death of a 75year-old woman that may have been linked to the drug’s side effects.

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