New Hemophilia A Treatment Option to Get FDA Review - Monthly Prescribing Reference
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Daily Record
New Hemophilia A Treatment Option to Get FDA ReviewMonthly Prescribing ReferenceThe BLA submission is based on results from the LEOPOLD (Long-Term Efficacy Open-Label Program in Severe Hemophilia A Disease) clinical trials, which evaluated BAY 81-8973 in adults and children using two-and three-times-per-week prophylaxis ...FDA Accepts Bayer's Biologics License Application for Investigational ...PR Newswire (press release)all 4 news articles »
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