We therefore believe that it’s likely that if approved, bremelanotide product label would not have alcohol restrictions or a significant risk evaluation and mitigation program. We are also conducting pre-launch and commercial activities for our bremelanotide female sexual dysfunction program. These include pricing, insurance reimbursement, packaging and trade name activities. In light of above events and significant progress of the bremelanotide Phase 3 clinical trials, we have received significant interest from potential licensing partners. We believe that there is a substantial U.S. and global market for bremelanotide and we continue to make progress with our licensing activities.
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