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The Company previously announced favorable results from a preliminary analysis of a Phase II clinical trial with Cylexin evaluating its ability to reduce reperfusion injury following the surgical removal of chronic blood clots from the lungs in an orphan drug indication, pulmonary thromboendarterectomy (PDE). SAN DIEGO--(BUSINESS WIRE)--April 30, 1996--Cytel Corporation (NASDAQ:CYTL) announced today that results of a Phase II clinical trial with its selectin blocker, Cylexin(TM), demonstrated evidence of a clinical benefit suggesting reduction of reperfusion injury following pulmonary thromboendarterectomy (PTE), the surgical removal of chronic blood clots from the lungs. Cytel is currently engaged in Phase II clinical trials with its nead drug candidates, Theradigm-HBV, targeting hepatitis B infection, and Cylexin, designed to prevent reperfusion injury upon restoration of blood flow following treatment for heart attack and pulmonary thromboendarterectomy (PTE), a type of lung surgery. |
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