PARIS--(BUSINESS WIRE)-- Regulatory News: BioAlliance Pharma SA (Paris:BIO), today announced that it had successfully completed patient enrolment in the pivotal phase III clinical trial performed with a view to registering Loramyc® in the US, for the treatment of oropharyngeal candidiasis. With 540 patients enrolled by 40 specialist clinical centers in the USA, Canada and South Africa, the company has achieved its target ahead of schedule. The trial results are expected in the first half of 2008. The company plans to file a market authorization application in the second half of next year, subject to the FDA’s regulatory requirements.
