in the development of pharmaceutical products
that address conditions of the male and female reproductive
systems. Proellex, the Company's lead compound, a PRM (progesterone
receptor modulator) has recently completed a successful U.S.
three-month Phase 2 clinical trial for the treatment of uterine
fibroids, a condition that affects numerous women of childbearing
age in the United States and results in a significant number of
hysterectomies each year. Proellex has recently completed a
six-month European Phase 1/2 study for the treatment of
endometriosis, a condition that affects approximately 5.5 million
women in the United States and Canada. Androxal(TM), the Company's
other program in late clinical development, is designed to restore
normal testosterone production by the testes and has recently
completed a six-month U.S. non-pivotal Phase 3 clinical trial for
the treatment of testosterone deficiency in men due to secondary
hypogonadism. According to industry sources, approximately 13
million men in the United States experience testosterone
deficiency. The Company is planning meetings with the FDA for all
three programs to lay out the remaining clinical program pathway
required before a New Drug Application may be submitted for each
product candidate.
For more information, please visit the Company's website at
http://www.reprosrx.com.
Any statements that are not historical facts contained in this
release are forward-looking statements that involve risks and
uncertainties, including Repros' ability to have success in the
clinical development of its technologies, the timing of enrollment
in such clinical studies and the accuracy of such studies, Repros'
ability to raise additional capital on acceptable terms or at all,
and such other risks which are identified in the Company's Annual
Report on Form 10-K for the year ended December 31, 2006, and
Repros' Quarterly Report on Form 10-Q for the quarter ended March
31, 2007, as they may be updated by the Comp
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