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The drug's failure is a disappointment for patients and advocates, who pressed the FDA and other federal agencies to fund and approve more experimental therapies for the fatal muscle-wasting disease.
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On this episode, a panel of experts delves into the forefront of health care, dissecting the latest advancements and trends.
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The FDA panel voted 17-1 that drugmaker Brainstorm’s stem cell-based treatment has not been shown effective for patients with amyotrophic lateral sclerosis. One panel member abstained from voting.
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The agency reiterated its longstanding position that a lone study by drugmaker Brainstorm doesn't provide convincing evidence that its stem cell-based therapy helps patients with amyotrophic lateral sclerosis.
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After Brian Wallach was diagnosed with ALS, he and his wife Sandra Abrevaya threw themselves into advocating for patients. Everyone up to President Biden took notice.
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The approval came despite a drug-makers' study that failed to meet the company goal of significantly slowing ALS. The drug did make a difference on lab measures of the disease, but the FDA is requiring additional research.
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Patients with insurance coverage say the cost set by drugmaker Amylyx Pharmaceutical is fueling insurance delays or denials, and sometimes exorbitant out-of-pocket expenses.
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The ruling is a remarkable turnaround for the much-debated medication that was previously rejected by the same group this year.
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The vote by the agency's health advisers is a potential setback for patient groups who have lobbied for the medication’s approval for more than a year.
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On Wednesday, a panel of FDA advisers is scheduled to take a nonbinding vote on whether the drug from Amylyx Pharmaceuticals should be approved.