PARIS--(BUSINESS WIRE)-- Regulatory News: BioAlliance Pharma SA (Paris:BIO), a company dedicated to the treatment of cancer and AIDS patients and supportive care, today announced the submission of its New Drug Application (NDA) to the United States Food and Drug Administration (FDA), as planned, for the approval of Loramyc®, Mucoadhesive Buccal Tablets (MBT), developed for the treatment of OroPharyngeal Candidiasis. If approved, Strativa Pharmaceuticals, the specialty pharma division of Par Pharmaceutical, Inc. (NYSE: PRX), the BioAlliance Pharma’s partner for commercialization in the USA, could launch Loramyc® in the second half of 2010.
