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Experimental treatment pushed by ALS patients gets day before FDA, but agency unconvinced it works

The Food and Drug Administration meets this week to consider a much-debated treatment for Lou Gehrig’s disease. The deadly neurological disease has few treatment options. NurOwn, a stem cell therapy, is at the center of a yearslong lobbying campaign by patients seeking access to experimental medicines. But the FDA has repeatedly rebuffed drugmaker Brainstorm. The agency says the company's only study failed to show a benefit for patients. The review is the starkest test yet of FDA's commitment to “regulatory flexibility” to help patients with rare, deadly conditions. Advocates see reasons for optimism. The FDA has approved two new treatments for ALS in the past year after intense lobbying by patients.

Experimental ALS treatment gets its day before an unconvinced FDA

Experimental ALS treatment gets its day before an unconvinced FDA
usf.edu - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from usf.edu Daily Mail and Mail on Sunday newspapers.

FDA to consider new ALS treatment that patients want | News

The Food and Drug Administration is considering a much-debated new treatment for Lou Gehrig’s disease, a deadly neurological disease that has few treatment options.

FDA to consider new ALS treatment that patients want

FDA to consider new ALS treatment that patients want
poststar.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from poststar.com Daily Mail and Mail on Sunday newspapers.

FDA to consider new ALS treatment that patients want

The Food and Drug Administration is considering a much-debated new treatment for Lou Gehrig’s disease, a deadly neurological disease that has few treatment options.

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