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BioSante Pharmaceuticals Completes Enrollment in LibiGel(R) Phase III Safety Study

Published in Women's Health Weekly, June 16th, 2011

2011 JUN 16 -- BioSante Pharmaceuticals, Inc. (NASDAQ: BPAX), announced completion of enrollment in its ongoing LibiGel (testosterone gel) Phase III cardiovascular and breast cancer safety study. LibiGel is in development for the treatment of female sexual dysfunction (FSD), specifically, hypoactive sexual desire disorder (HSDD) in menopausal women, for which there is no FDA-approved product.

BioSante has been informed by the LibiGel safety study independent Executive Committee regarding the outcome of the sample size analysis that determines the number of subjects to be enrolled in the LibiGel Phase III safety study. The FDA-agreed sample size analysis...

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