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Indevus Pharmaceuticals Provides Update on PRO 2000 Program
Date:2/15/2008

of funding and access to scientific expertise. The development of an effective microbicide is critical to the fight against HIV."

MDP 301 is a multi-national, randomized, double-blind, placebo-controlled Phase III trial designed to examine the safety and effectiveness of PRO 2000 in preventing HIV infection in women. The MDP selected two PRO 2000 strengths (0.5% and 2.0%) for testing against placebo. Participants also receive a standard HIV prevention package. The trial opened in October 2005, and is currently underway at clinical centers in South Africa, Tanzania, Uganda and Zambia. Approximately 7,730 women have been enrolled in the trial to date and enrollment is expected to be completed later this year. The IDMC will continue to monitor the trial carefully until its planned completion in late 2009.

HPTN 035 is a multi-national, randomized, placebo-controlled trial designed to examine the safety and effectiveness of PRO 2000 and another candidate vaginal microbicide (BufferGel, Reprotect, Inc.) in preventing HIV infection in women. One PRO 2000 strength, 0.5%, is being tested in comparison with a placebo and no treatment. The trial involves seven clinical centers in South Africa, Malawi, Zimbabwe, Zambia, and the United States. The trial opened in February 2005, and 3,100 healthy women were enrolled before planned recruitment ended in July 2007. An NIAID Data and Safety Monitoring Board (DSMB) reviewed the unblinded data from the trial on six separate occasions, most recently in November 2007, and each time has found no safety concerns and recommended proceeding as planned. Completion of the HPTN 035 trial is expected this summer.

About Indevus

Indevus Pharmaceuticals, Inc. is a specialty pharmaceutical company engaged in the acquisition, development and commercialization of products to treat conditions in urology and endocrinology. The Company's approved products include SANCTURA XR(TM) and SANCTURA(R) for overactive bladder, VANTAS(
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