Palatin Technologies Announces Completion of All Patient Visits In Phase 3 Clinical Trials of Bremelanotide for Hypoactive Sexual Desire Disorder | Boulder Peptide Symposium

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Palatin Technologies Announces Completion of All Patient Visits In Phase 3 Clinical Trials of Bremelanotide for Hypoactive Sexual Desire Disorder

Palatin Technologies Announces Completion of All Patient Visits In Phase 3 Clinical Trials of Bremelanotide for Hypoactive Sexual Desire Disorder

Source: Palatin Technologies, Inc. & reported by http://www.prnewswire.com/
CRANBURY, N.J., Aug. 4, 2016 /PRNewswire/ -- Palatin Technologies, Inc. (NYSE MKT: PTN) today announced that the last patient visits in the Company's reconnect studies, consisting of two pivotal Phase 3 clinical trials of bremelanotide for the treatment of female hypoactive sexual desire disorder (HSDD), have been completed.

"We are very excited with the completion of the last patient visits in our Phase 3 reconnect studies," said Carl Spana, Ph.D., President and Chief Executive Officer of Palatin. "Patient enrollment and last patient out of the studies were concluded on time. We now look forward to data verification and database lock, which we anticipate occurring in late September, with topline data announced shortly thereafter."

Each Phase 3 study is a multicenter (~80 sites), randomized, placebo controlled, parallel-group, eight month trial with an open-label extension phase. The studies are designed to evaluate the efficacy and safety of subcutaneous bremelanotide, delivered by an autoinjector pen, in premenopausal women with HSDD as an on-demand, as-needed treatment.

Read more: http://www.prnewswire.com/news-releases/palatin-technologies-announces-completion-of-all-patient-visits-in-phase-3-clinical-trials-of-bremelanotide-for-hypoactive-sexual-desire-disorder-300308981.html


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