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FDA skeptical of experimental ALS treatment pushed by patient advocates - Vimarsana News

FDA skeptical of experimental ALS treatment pushed by patient advocates

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,

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

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,

Source: wvnews.com
ALS Advocates Push for Approval of Experimental Drug, Even as FDA Expresses Doubts - Vimarsana News

ALS Advocates Push for Approval of Experimental Drug, Even as FDA Expresses Doubts

WASHINGTON (AP) — The Food and Drug Administration meets this week to consider approval of an experimental treatment for Lou Gehrig’s disease, the culmination of a yearslong lobbying effort by

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

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,

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

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 s...

Source: wdio.com