Market Overview

Hemispherx Biopharma Says FDA Panel Voted 9-4 Against Ampligen Effocacy

Related HEB
Hemispherx Receives New U.S. Composition of Matter Patent Covering Ampligen(R) Formulations
UPDATE: Hemispherx Biopharma Formally Collaborates With the Swiss Department of Defense, Civil Protection and Sports to Study Alferon(R) Against Tamiflu Resistant Influenza Virus Strains

Hemispherx Biopharma, Inc. (NYSE MKT:HEB) (the "Company" or "Hemispherx") today announced the outcome of the meeting of the Arthritis Advisory Committee (the "AAC") of the U.S. Food and Drug Administration (the "FDA") on the New Drug Application ("NDA") for Ampligen^® for Chronic Fatigue Syndrome ("CFS").

On the question: "Considering the totality of the data, is there substantial evidence of efficacy for Ampligen for the treatment of patients with chronic fatigue syndrome (CFS)?," the AAC voted 9 no, 4 yes and 1 AAC member left the room and did not vote.

Posted-In: News FDA


Related Articles (HEB)

Around the Web, We're Loving...

Partner Network

Get Benzinga's Newsletters