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Samples in periodicals archive:
FROM A MEETING OF THE FDA'S ARTHRITIS ADVISORY COMMITTEE SILVER SPRING, MD.
gov Meetings, Workshops and Congressional Testimony: Tuesday, 6/21 - Arthritis Advisory Committee discusses supplemental biologics license application for ILARIS (canakinumab), proposed for treatment of gouty arthritis.
FROM THE FDA'S ARTHRITIS ADVISORY COMMITTEE AND THE DRUG SAFETY AND RISK MANAGEMENT COMMITTEE
Members of the FDA's Arthritis Advisory Committee considered canakinumab, a monoclonal antibody that neutralizes interleukin-1 beta, a promising treatment, and all but one panelist agreed that the 150-mg subcutaneous dose that was studied in two phase III trials was shown to be effective in treating an attack of gouty arthritis in this population.
Food and Drug Administration (FDA) Arthritis Advisory Committee voted overwhelmingly (13 to 2) to recommend BENLYSTA for approval as a treatment for the autoimmune disease lupus.
At a meeting of the FDA's Arthritis Advisory Committee in June, members proposed guidelines that could be used to design trials of drugs for fibromyalgia, a syndrome for which clinical research has historically been difficult to pursue because of its heteregenicity of symptoms and varied response to treatment.
After the FDA Arthritis Advisory Committee met on November 16, 2010 to consider the BENLYSTA BLA, the FDA requested some additional information from HGS, which has been submitted.
FDA Arthritis Advisory Committee voted 13 to 2 to recommend approval of the treatment developed by Human Genome Sciences (HGS) and GlaxoSmithKline.