FDA lifts clinical hold on Repros' Proellex

06/13/2010 | Bloomberg Businessweek

The FDA approved Repros Therapeutics' request to conduct another trial of Proellex for use in reducing menstrual bleeding associated with uterine fibroids and endometriosis, lifting a clinical hold that was placed on the drug candidate last year because of liver toxicity. The drugmaker will test lower doses of Proellex on 12 women in a 10-week study comparing the drug with placebo.

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