The Patient Experience of Premenopausal Women Treated with Bremelanotide for Hypoactive Sexual Desire Disorder: RECONNECT Exit Study Results.
Koochaki. Patricia P; Revicki. Dennis D; Wilson. Hilary H; Pokrzywinski. Robin R; Jordan. Robert R; Lucas. Johna J; Williams. Laura A LA; Sadiq. Amama A; Krop. Julie J
Key Findings
- Bremelanotide significantly increased self‑reported sexual desire and physical arousal in women with HSDD
- Placebo participants reported only modest benefits, mainly related to treatment perception and partner communication
- Patient‑reported outcomes confirmed the primary trial’s efficacy results, highlighting real‑world quality‑of‑life improvements
Practical Outcomes
- For biohackers interested in sexual health, bremelanotide appears to be an effective, prescription‑only option for boosting desire in pre‑menopausal women, but it requires medical supervision and proper dosing. It’s not a DIY supplement, so the practical step is to consult a qualified clinician to discuss eligibility, dosing protocols, and potential side effects.
Summary
A study of up to 242 pre‑menopausal women showed that the peptide bremelanotide (also called PT‑141) noticeably boosted sexual desire, physical arousal, and overall sexual satisfaction compared with a placebo, and participants reported better communication with partners. The findings are based on patient‑filled exit surveys and interviews after a double‑blind trial.
Abstract
<b><i>Background:</i></b> Hypoactive sexual desire disorder (HSDD) has a significant negative impact on women's overall health and relationships with their partners. Primary analyses from the RECONNECT clinical trials demonstrated statistically significant and clinically meaningful improvements in sexual desire and related distress with bremelanotide relative to placebo in premenopausal women with HSDD. Exit surveys and patient interviews were conducted to evaluate the impact of HSDD and bremelanotide treatment from the patient's perspective. <b><i>Materials and Methods:</i></b> Upon completion of the double-blind study but before participation in the open-label extension, up to 250 participants were recruited to complete the quantitative exit survey (17 questions). A subset of up to 90 patients was invited to participate in the telephone interview (17 questions). Patients who volunteered to participate remained blinded to study drug until the survey and interviews were completed. <b><i>Results:</i></b> Quantitative exit surveys were completed by 242 RECONNECT participants; 80 of these women also completed qualitative telephone exit interviews. Participants who received bremelanotide described increased feelings of sexual desire, physical arousal, and improvements in overall quality of their sexual activities in their partner relationship. In comparison, women taking placebo reported benefits that did not include the physiological responses described by women receiving bremelanotide, such as positive experiences of seeking HSDD treatment and improved communication with their partner. <b><i>Conclusions:</i></b> Exit surveys and patient interviews support the primary findings from RECONNECT and provide quantitative and qualitative assessments of the impact of HSDD on patients' quality of life and the patients' perspectives on the impact of bremelanotide. Clinical trial numbers NCT02333071, NCT02338960.
Study Information
pubmed
2021
2021-02-03T00:00:00.000Z
10.1089/jwh.2020.8460
11
17