FDA trims use of contentious Alzheimer’s drug amid backlash
WASHINGTON (AP) — A month after approving a controversial new Alzheimer’s drug, U.S. health regulators on Thursday signed off on new prescribing instructions that are likely to limit its use.
The Food and Drug Administration said the change is intended to address confusion among physicians and patients about who should get the drug, which has faced an intense public backlash since its approval last month.
The new drug label emphasizes that the drug, Aduhelm, is appropriate for patients with mild symptoms or early-stage Alzheimer’s but has not been studied in patients with more advanced disease. That’s a big change from the original FDA instructions, which said simply that the drug was approved for Alzheimer’s disease in general.
Drugmaker Biogen announced the change in a release Thursday, stating that the update is intended to “clarify” the patient group studied in the company trials that led to approval. The FDA first approached the company about narrowing the label and OK’d the language.
When the drug was first approved, a top FDA official told reporters the drug was “relevant to all stages of Alzheimer’s disease.”
The FDA’s OK last month quickly sparked controversy over Aduhelm’s $56,000-a-year price-tag and questionable benefits. Three of FDA’s outside advisers resigned over the decision with Harvard researcher Dr. Aaron Kesselheim calling it the “worst drug approval decision in recent U.S. history.”
On Thursday, Kesselheim tweeted that the change was “a welcome step” but added that the FDA and Biogen should do much more to combat “misperceptions about this drug.”
Sweeping changes to drug labels are rare, particularly only a few weeks after approval.
“It’s a responsible move by both the FDA and Biogen to maximize the safety while giving the drug the best chance to work,” said Dr. Ronald Petersen of the Mayo Clinic, who has consulted for Biogen and other drugmakers. The drug’s side effects include brain swelling and bleeding.
Aduhelm hasn’t been shown to reverse or significantly slow the disease. But the FDA said that its ability to reduce clumps of plaque in the brain is likely to slow dementia. Many experts say there is little evidence to support that claim.
Biogen is required to conduct a follow-up study to definitively answer whether the drug slows mental decline. Other Alzheimer’s drugs only temporarily ease symptoms.
Two congressional committees in the House have launched an investigation into the FDA’s review of the drug. And lawmakers in the Senate have called for hearings into the drug’s cost and impact on federal spending.
The narrower label may ease some of those concerns by shrinking the number of patients likely to get the drug, which requires monthly IVs. Many hospitals have already stated that they plan to limit the drug’s use to patients with earlier stage disease. Doctors could still prescribe the drug for more advanced patients, though insurers might refuse to pay for it, citing the FDA label.
“It was pretty troubling that the previous label was so broad and included groups of patients in whom the drug had never been tested,” said Dr. Suzanne Schindler of Washington University in St. Louis. “I think this is a positive change because it better reflects the patients in whom the drug was actually studied.”
Wall Street analysts said the change wouldn’t significantly impact projected sales for Biogen. Michael Yee of Jefferies said in a research note that the company already planned to target the drug for the 1 million to 2 million Americans with mild Alzheimer’s.
Follow Matthew Perrone on Twitter: @AP_FDAwriter
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