Roche gets breakthrough status for Alzheimer's test Elecsys

ZURICH: The U.S. Food and Drug Administration has granted Roche an accelerated review for its Elecsys product used to diagnose Alzheimer’s disease, the Swiss drugmaker said.
The FDA gave breakthrough device designation to Elecsys, which examines the cerebrospinal fluid in adult patients with cognitive impairment who are being evaluated for Alzheimer’s disease or other causes of dementia.
(Reporting by John Revill; Editing by Amrutha Gayathri)
Alzheimer's diseaseAlzheimer's testbreakthrough device designationbreakthrough statuscerebrospinal fluidcognitive impairmentdementiaElecsysRocheU.S. Food and Drug Administration
Source : REUTERSNext Story
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