PT141 10mg Bremelanotide for Women Sexual Enhance PT-141 10mg/Vial Female Enhancement Polypeptide for Male Erectile Dysfunction PT-141, Bremelanotide, PT141 10mg/Vial 189691-06-3 Treat Sexual Dysfunction 99% Purity
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Bremelanotide (formerly known as PT-141, brand Rekynda) is a peptide candidate drug developed by Palatin Technologies as a treatment for female sexual dysfunction
Our main product in late development is bremelanotide, a novel melanocortin 4- receptor agonist, which is currently under investigation to help restore the natural sexual desire of postmenopausal women with HSDD. The mechanism of action of Brumino Peptide involves helping to activate the brain's internal pathways involved in the normal response of the body.
Bremelanotide has been studied in more than 3,000 clinical trials, more than 2,500 people. Phase 3 Reconnection The purpose of the study was to demonstrate the efficacy of bupretum as a treatment for postmenopausal women with HSDD, to monitor side effects and to collect information that would enable safe use of aspergillus nigari.
Subcutaneous injection of Bremeranotide is under the skin using a single automatic syringe. The automatic syringe has no visible needles. In the Phase 3 clinical trial, women gave the naupivacin - the automatic syringe was the rest by pressing the automatic syringe on the thigh or abdomen.
Women do not have to take daily triclosan. Bremelanotide is required only before expected sexual activity.
In our recently completed Phase 2B clinical trial, 1.25 mg and 1.75 mg doses of bruylamin peptide significantly increased the number of sexual arousal, sexual desire and sexual satisfaction events and reduced the pain associated with premenopausal women with FSD.
Sexually active sexual dysfunction (HSDD) and HSDD combination of female sexual awakening in women were observed efficacy.
The percentage of women receiving 1.75 mg of bromidolide was significantly higher than 55%, clinically significant compared with at least the baseline of sexual events, compared with 37% of women receiving placebo. In addition, a significant increase in the percentage of women compared with placebo also achieved clinically significant improvements in sexual function, as measured by FSFI (53% vs 29%), and clinically relevant for sexual dysfunction The reduction was compared with FSDS-DAO (69% vs 45%).
Of the FSD
Bremelanotide was well tolerated during the trial. The most common type of treatment for sudden malignancy in the braniline peptide group is facial flushing, nausea and vomiting, with severity mainly mild to moderate. The study was given to 394 patients. According to a pre-determined blood pressure standard, 26 patients were discontinued; these patients were evenly distributed on placebo and bilumino-administered doses. As a result of adverse events, another 12 patients stopped the study (placebo 2, rumpletin 10). The most common cause of withdrawal is nausea and vomiting. No serious adverse events occurred during the trial.
We have extensive clinical experience with bremelanotide. More than 2,500 patients received diphtheria in 30 clinical studies, with intranasal or subcutaneous preparations, with FSD and erectile dysfunction.
We presented the results of the Phase 2B trial at national and international scientific
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