In 2007 Pfizer (PFE) formed a partnership with Bristol-Myers
Squibb (BMY) to develop the anti-coagulant drug "Eliquis" that
reduces blood clotting. In this partnership, Pfizer and Bristol-Myers share the
profits 60:40 respectively. The FDA approved this drug in late 2012 and both
companies are now moving ahead to develop supplements to treat patients more
effectively.
After receiving approval for Eliquis, Pfizer and
Bristol-Myers Squibb also received approval from the FDA for its supplemental
New Drug Application, or sNDA, in July 2013. A sNDA is an application that
enables the company to innovate or make changes in a drug that has already been
approved. Eliquis is used to treat venous thromboembolism, or VTE, patients and
reduces the probability of deep vein thrombosis, or DVT, a blood clot in veins.Read
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