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Wednesday, July 17, 2019 11:45:50 AM
I really think that it is men who will appreciate the therapeutic benefits of PT-141 aka Vyleesi the most. Men as they get older can experience ED. Let’s say after age 50. If it were to happen just a few times the anxiety of not knowing what is going to happen can make it even more likely to happen. Sexual performance is related to confidence.
I know that many men do not need any help. That is great for them. The ones that do need help know how important it is to perform well at those crucial moments when a man is lucky enough to have the opportunity to experience life at its very best.
Not so much is ever really on the line for women. Artificial lubrication can solve the problem for them to a large degree. If PT-141 is to be a blockbuster I think that PTN should be thinking about the male market much more that the female market.
If women love it too that is great. I am all for women enjoying sex more. Men would benefit from dosing their dates and partners along with themselves. I think that the FDA was worried about a party drug phenomenon. I think that the FDA has a bias against benefiting men. If a drug can benefit women then it has a priority. Why is it this way?
Men might enhance themselves privately and not tell their date about any pharmacology to make it seem as though they are naturally a total stud. That would impress women more than confiding that the man has used a drug.
Viagra does not work for some men. A combination of viagra or Cialis with Vyleesi could be the ultimate synergistic combination for men. I wonder whether that combination has been tried by anybody. I do not see the combination being discussed anywhere.
Some women might complain that their man wanted sex all night and that it was a problem for them. That is another reason why a man might want to have his date share the pharmacological enhancement.
The take home message is that performance is a bigger issue for men than it is for women.
Recent PTN News
- Palatin Announces Exercise of Warrants for Approximately $6.1 Million Gross Proceeds • PR Newswire (US) • 06/21/2024 12:00:00 PM
- Palatin Announces the Initiation of a Phase 2 Clinical Study of Bremelanotide Co-Administered with a PDE5i for the Treatment of Erectile Dysfunction (ED) • PR Newswire (US) • 06/20/2024 11:30:00 AM
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- Form 8-K - Current report • Edgar (US Regulatory) • 05/15/2024 12:40:59 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 05/15/2024 12:04:24 PM
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- Palatin Announces FDA Clearance of IND Application for the Co-Administration of Bremelanotide with Tirzepatide (GLP-1) for the Treatment of Obesity • PR Newswire (US) • 05/02/2024 11:30:00 AM
- Palatin to Host Virtual KOL Event "Beyond GLPs: The Multiple Roles for Novel Melanocortin Receptor 4 Agonists in Treating Obesity and Weight Loss Maintenance" on May 8, 2024 • PR Newswire (US) • 04/30/2024 11:30:00 AM
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- Palatin Announces Results of PL9643 MELODY-1 Pivotal Phase 3 Clinical Trial in Patients with Dry Eye Disease (DED) • PR Newswire (US) • 02/28/2024 12:30:00 PM
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- Palatin Announces Database Lock for PL9643 MELODY-1 Pivotal Phase 3 Clinical Trial in Patients with Dry Eye Disease (DED) • PR Newswire (US) • 02/05/2024 12:30:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 02/01/2024 10:16:03 PM
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- Palatin Provides Corporate Update and Highlights Strategic Priorities for Calendar Year 2024 • PR Newswire (US) • 01/08/2024 03:33:00 PM
- Cosette Pharmaceuticals Acquires Vyleesi® (Bremelanotide Injection) from Palatin Technologies Inc. • Business Wire • 01/03/2024 01:00:00 PM
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