Bremelanotide clinical trials
Every study registered on ClinicalTrials.gov that lists Bremelanotide as an intervention, as of the data edition — what is being tested, in whom, by whom, and how far it has got.
- Registered studies
- 10
- Active or recruiting
- 1
- Completed
- 9
- With posted results
- 4
- Planned or actual enrollment
- 2,644participants, summed
| Phase | Studies | Breakdown |
|---|---|---|
| Phase 1 | 1 | 1 completed, 0 active or recruiting, 0 stopped, 0 other |
| Phase 2 | 4 | 3 completed, 1 active or recruiting, 0 stopped, 0 other |
| Phase 3 | 3 | 3 completed, 0 active or recruiting, 0 stopped, 0 other |
| Phase 4 | 2 | 2 completed, 0 active or recruiting, 0 stopped, 0 other |
Conditions studied
- Hypoactive Sexual Desire Disorder5
- Obesity1
- Female Sexual Arousal Disorder1
- Nausea1
- Lactating Mother1
- Sexual Arousal Disorder1
- Kidney Disease1
Lead sponsors
- Palatin Technologies, Inc6
- Imperial College Healthcare NHS Trust1
- Kwang Dong Pharmaceutical co., ltd.1
- AMAG Pharmaceuticals, Inc.1
- Cosette Pharmaceuticals, Inc.1
The registry, study by study
Registration is not evidence of benefit; many registered studies never publish. Status and dates are as reported by sponsors to ClinicalTrials.gov.
| Study | Phase | Status | Start | n | Sponsor |
|---|---|---|---|---|---|
| NCT06565611A Phase 2 Study Evaluating the Co-Administration of Bremelanotide With Tirzepatide for the Treatment of Obesity | Phase 2 | Active, not recruiting | Aug 2024 | 108 | Palatin Technologies, Inc |
| NCT06867835Single Dose of Vyleesi in Lactating Female Subjects to Measure the Concentration of Bremelanotide in Breast Milk | Phase 4 | Completed | Jul 2025 | 10 | Cosette Pharmaceuticals, Inc. |
| NCT05709444A Phase IIb, Multicenter, Open-Label, Prospective Study of Bremelanotide in Diabetic Kidney Disease | Phase 2 | Completed | Dec 2022 | 16 | Palatin Technologies, Inc |
| NCT04943068A Phase 3, Bridging, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Trial to Evaluate the Efficacy and Safety of Subcutaneously Administered Bremelanotide in Premenopausal Women With Hypoactive Sexual Desire Disorder (With or Without Decreased Arousal) | Phase 3 | Completed | May 2021 | 193 | Kwang Dong Pharmaceutical co., ltd. |
| NCT04179734Role of the Melanocortin-4 Receptor in Hypoactive Sexual Desire DisorderResults posted | Phase 4 | Completed | Oct 2019 | 40 | Imperial College Healthcare NHS Trust |
| NCT03973047Study to Evaluate Rate of Nausea in Healthy Premenopausal Female Subjects Treated With Single Dose of Bremelanotide Alone or With Zofran | Phase 1 | Completed | Jun 2019 | 228 | AMAG Pharmaceuticals, Inc. |
| NCT023389602. Study to Evaluate the Efficacy/Safety of Bremelanotide in Premenopausal Women With Hypoactive Sexual Desire DisorderResults posted | Phase 3 | Completed | Jan 2015 | 714 | Palatin Technologies, Inc |
| NCT023330711. Study to Evaluate the Efficacy/Safety of Bremelanotide in Premenopausal Women With Hypoactive Sexual Desire DisorderResults posted | Phase 3 | Completed | Dec 2014 | 723 | Palatin Technologies, Inc |
| NCT01382719Bremelanotide in Premenopausal Women With Female Sexual Arousal Disorder and/or Hypoactive Sexual Desire DisorderResults posted | Phase 2 | Completed | Jun 2011 | 612 | Palatin Technologies, Inc |
| NCT00425256Evaluate the Safety and Efficacy of Bremelanotide in Women With Female Sexual Arousal Disorder (FSAD) | Phase 2 | Completed | Feb 2006 | — | Palatin Technologies, Inc |
Run this search on ClinicalTrials.gov → Query term: bremelanotide OR PT-141