US2016367493A1PendingUtilityA1
Method and improved pharmaceutical composition for enhancing transdermal delivery of pde-5 inhibitor
Assignee: TRITECH BIOPHARMACEUTICALS CO LTDPriority: Dec 26, 2011Filed: Jun 16, 2016Published: Dec 22, 2016
Est. expiryDec 26, 2031(~5.4 yrs left)· nominal 20-yr term from priority
A61P 9/00A61P 43/00A61P 15/00A61P 11/00A61P 15/10A61K 47/16A61K 47/10A61K 9/0014A61K 9/7023A61K 31/4985A61K 47/08A61K 47/22A61K 31/53A61K 9/06A61K 31/519A61K 47/186
26
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The present disclosure relates to the use of an agent that enhances transdermal delivery of a PDE-5 inhibitor. More particularly, the present disclosure provides improved method and composition that promotes transdermal delivery of a PDE-5 inhibitor for the treatment of the PDE-5 mediated conditions and/or diseases.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A transdermal pharmaceutical gel or patch composition comprising:
an effective amount of vardenafil or a pharmaceutically acceptable salt thereof and an enhancer for enhancing transdermal delivery of vardenafil; wherein the enhance is cocamidopropyl betaine, and vardenafil and the enhancer are present in a ratio from about 20:1 to 2:1 by weight in the transdermal pharmaceutical gel or patch composition; and a pharmaceutically acceptable excipient.
2 . The transdermal pharmaceutical gel or patch composition of claim 1 , wherein vardenafil and the enhancer are present in the transdermal pharmaceutical gel or patch composition in a ratio of about 17:1.
3 . The transdermal pharmaceutical gel or patch composition of claim 1 , wherein vardenafil and the enhancer are present in the transdermal pharmaceutical gel or patch composition in a ratio of about 10:1.
4 . The transdermal pharmaceutical gel or patch composition of claim 1 , wherein vardenafil and the enhancer are present in the transdermal pharmaceutical gel or patch composition in a ratio of about 3:1.
5 . The transdermal pharmaceutical gel or patch composition of claim 1 , wherein vardenafil is not in a crystalline state.
6 . A method for enhancing transdermal delivery of vardenafil in a subject comprising administering to the subject an effective amount of the transdermal pharmaceutical gel or patch composition of claim 1 .
7 . The method of claim 6 , wherein vardenafil and the enhancer are present in the transdermal pharmaceutical gel or patch composition in a ratio of about 17:1 by weight.
8 . The method of claim 6 , wherein vardenafil and the enhancer are present in the transdermal pharmaceutical gel or patch composition in a ratio of about 10:1 by weight.
9 . The method of claim 6 , wherein vardenafil and the enhancer are present in the transdermal pharmaceutical gel or patch composition in a ratio of about 3:1 by weight.
10 . The method of claim 6 , wherein vardenafil is not in a crystalline state.Join the waitlist — get patent alerts
Track US2016367493A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.