FDA approves controversial new drug designed to slow progression of ALS

The Food and Drug Administration on Thursday approved a controversial new drug designed to slow the progression of Lou Gehrig’s disease, a victory for patients and advocates despite limited evidence that the drug is effective.

The Medicine, from Massachusetts Amylyx Pharmaceuticalsjoint only a handful of medicine agency-approved for life-threatening neurodegenerative disease and its symptoms.

The disease, also called amyotrophic lateral sclerosis, or ALS, affects nerve cells needed for activities like walking, talking, and eating. There is no known cure, and most people live only two to five years after diagnosis. according to the ALS association.

The FDA’s decision was based on a single Phase 2 clinical trial of 137 ALS patients that found people who took Amylyx’s drug, which will be sold under the name Relivrio, lived about 10 months longer than those who did not receive it. The drug also appears to delay hospitalizations.

The drug, taken in pill form, is a combination of two existing products: sodium phenylbutyratewhich is prescribed to treat a metabolic disorder, and taurursodiol, an over-the-counter supplement used to help prevent liver disease.

Amylyx said she was still working out what she would charge for the drug. It may be priced similar to an older ALS drug, edaravone, which costs around $170,000 a year, according to a report from the Institute for Clinical and Economic Review.

The endorsement is likely to engender some disagreement among neurologists who treat ALS.

Generally, the FDA requires at least two well-controlled clinical trials to demonstrate that a drug is effective, or a single “statistically very convincing” trial, said Holly Fernandez Lynch, assistant professor of medical ethics at the University of Pennsylvania. Amylyx’s trial, she said, failed to meet agency standards.

Concerns about the trial results were raised in March, when the drug was first presented to an FDA advisory panel. In background papers published before that meeting, agency scientists questioned the persuasiveness of the Amylyx trial. The committee narrowly voted against recommending the drug for approval.

The FDA, however, took the unusual step of convening a second advisory committee six months later, after Amylyx submitted additional analysis of its trial data. During this meeting, the advisory committee backtracked, vote to recommend the drug.

The positive vote came despite another lackluster review from FDA scientists as well as concerns from several advisory committee members about whether clinical trial data provided by Amylyx showed clear evidence that the drug slows disease progression. .

The agency’s review of the drug has been compared to Biogen’s Alzheimer’s drug, Aduhelm. This drug received full FDA approval in 2021, although the advisory committee voted overwhelmingly against his recommendationciting a lack of evidence of its effectiveness.

Amylyx’s drug approval suggests the FDA is willing to show the most flexibility for life-threatening conditions for which there is an “unmet treatment need,” Lynch said.

However, the decision could pose other challenges for the agency, she added, as it may not prompt the company to prove that the drug works.

“It’s also up to the payers to decide whether the evidence is sufficient to support coverage, so in that sense it may just kick in,” she said.

Proponents say that while questions remain about the drug’s effectiveness, patients should be allowed to at least try the drug.

“We need new treatments as soon as possible if we are to turn ALS into a viable disease and eventually cure it,” Larry Falivena, a member of the ALS Association, an advocacy group, said in an email.

Amylyx is currently conducting a larger Phase 3 clinical trial of the drug, which it expects to complete in late 2023 or early 2024.

At the September advisory committee meeting, company representatives agreed to pull the drug from the market if the results of those trials showed it was not effective. The drug has already received conditional approval in Canada.

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