US2004224023A1PendingUtilityA1
Compositions and methods for treating or preventing diseases of body passageways
Est. expiryMay 24, 2016(expired)· nominal 20-yr term from priority
A61P 9/10A61P 31/06A61P 35/00A61P 9/00A61P 43/00A61P 31/04A61P 27/02A61K 31/00A61K 9/5146A61K 31/28A61K 9/1647A61K 9/1075A61P 1/04A61K 9/5192A61K 9/5153A61P 13/08A61P 1/00A61K 47/34A61K 31/335A61K 9/12A61K 9/1652A61K 31/337A61K 9/167A61K 9/10A61P 11/00A61P 13/00A61K 9/7007A61K 9/5138A61P 15/00A61K 9/0024A61P 13/02A61P 11/08A61K 9/70A61K 9/1635A61K 9/5031A61K 33/24
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Claims
Abstract
The present invention provides methods for treating or preventing diseases associated with body passageways, comprising the step of delivering to an external portion of the body passageway a therapeutic agent. Representative examples of therapeutic agents include anti-angiogenic factors, anti-proliferative agents, anti-inflammatory agents, and antibiotics.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A method for treating or preventing diseases associated with body passageways, comprising delivering to an external portion of said body passageway a therapeutic agent.
2 . A method for treating or preventing diseases associated with body passageways, comprising delivering to smooth muscle cells of said body passageway, via the adventia, a therapeutic agent.
3 . The method according to claim 1 wherin said therapeutic agent is an anti-angiogenic factor.
4 . The method according to claim 1 wherein said therapeutic agent further comprises a polymeric carrier.
5 . The method according to claim 3 wherein said polmeric carrier is formed into microspheres having an average size of between 0.5 and 200 μm.
5 . The method according to claim 3 wherein said polymeric carrier is poly(ethylene-vinyl acetate) (40% crosslinked).
6 . The method according to claim 3 wherein said polymeric carrier is copolymer of lactic acid and glycolic acid.
7 . The method according to claim 3 wherein said polymeric carrier is poly (caprolactone).
8 . The method according to claim 3 wherein said polymeric carrier is poly (lactic acid).
9 . The method according to claim 3 wherein said polymeric carrier is a copolymer of poly(lactic acid) and poly(caprolactone).
10 . The method according to claim 1 wherein said therapeutic agent is a compound which disrupts microtubule function.
11 . The method according to claim 10 wherein said compound which disrupts microtubule function is paclitaxel, or an analogues or derivative thereof.
12 . The method according to claim 1 wherein said body passageway is selected from the group consisting of arteries, the esophagus, the stomach, the duodenum, the small intestine, the large intestine, biliary tracts, the ureter, the bladder, the urethra, lacrimal ducts, the trachea, bronchi, bronchiole, nasla airways, eustachian tubes, the external auditory canal, and fallopian tubes.
13 . The method according to claim 12 wherein said therapeutic agent is delivered to an artery by direct injection via an outer wall of the artery into the adventia.Join the waitlist — get patent alerts
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