Alexion Completes Enrollment In AEGIS Study To Evaluate Soliris In Japanese Patients With Genetic Blood Disorder - Quick Facts
Thu. March 20, 2008; Posted: 06:45 AM
(RTTNews) - Alexion Pharmaceuticals Inc. (
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PR Charts ) announced the completion of enrolling patients in AEGIS study, a single registration study to evaluate Soliris as a treatment for patients with paroxysmal nocturnal hemoglobinuria, an acquired genetic blood disorder defined by hemolysis.
The company said it over-enrolled total of 29 patients, who will be treated with Soliris at clinical sites throughout Japan for 12 weeks. The company said it targeted enrollment of 25 patients.
The company said it has set the primary efficacy endpoint of the study as reduction of hemolysis from baseline.
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