US2017007638A1PendingUtilityA1
Novel interstitial therapy for immediate symptom relief and chronic therapy in interstitial cystitis
Est. expiryJan 28, 2024(expired)· nominal 20-yr term from priority
Inventors:C. Lowell Parsons
A61P 13/10A61P 13/02A61K 31/24A61K 31/728A61K 31/445A61K 31/167A61K 9/0034A61K 9/08A61K 31/727A61K 45/06A61K 31/737
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Claims
Abstract
The present invention relates to a disorder of the lower urinary tract, and in particular, reducing the symptoms (including treatment) of interstitial cystitis in vivo. In a preferred embodiment, the present invention relates to treatment formulations and methods for reducing interstitial cystitis in patients.
Claims
exact text as granted — not AI-modified1 - 22 . (canceled)
23 . A composition for intravesical instillation into the bladder, wherein said composition consists of:
(i) a heparinoid selected from the group consisting of sodium pentosanpolysulfate, chondroitin sulfate, and hyaluronic acid; (ii) a local anesthetic agent selected from the group consisting of lidocaine, bupivacaine, and mepivacaine, (iii) a buffer selected from the group consisting of phosphate buffer, sodium bicarbonate buffer, and Tris buffer, and (iv) optionally an osmolar component selected from the group consisting of sodium chloride, dextrose, dextran 40, dextran 60, starch and mannitol,
wherein said composition treats interstitial cystitis or at least one symptom thereof when instilled into the bladder;
wherein, when the heparinoid is sodium pentosanpolysulfate, the sodium pentosanpolysulfate is present in about 1 mg to about 600 mg per unit dose;
wherein, when the heparinoid is chondroitin sulfate, the chondroitin sulfate is present in about 1 mg to about 10,000 mg per unit dose; and
wherein, when the heparinoid is hyaluronic acid, the hyaluronic acid is present in about 5 mg to about 600 mg per unit dose.
24 . The composition of claim 23 , wherein the heparinoid is sodium pentosanpolysulfate.
25 . The composition of claim 23 , wherein the buffer is phosphate buffer.
26 . The composition of claim 23 , wherein the local anesthetic agent is lidocaine.
27 . The composition of claim 26 wherein the lidocaine is present in the composition in the quantity of 10 mg up to 400 mg lidocaine per unit dose.
28 . The composition of claim 23 wherein the heparinoid is sodium pentosanpolysulfate, the buffer is phosphate buffer, and the local anesthetic is lidocaine.
29 . The composition of claim 23 wherein the osmolar component is present in a sufficient amount so that the final solution is substantially isotonic.
30 . The composition of claim 28 wherein the osmolar component is selected from the group consisting of sodium chloride, dextrose, dextran 40, and dextran 60.
31 . The composition of claim 23 wherein the heparinoid is selected from the group consisting of chondroitin sulfate and hyaluronic acid.
32 . The composition of claim 23 wherein the local anesthetic agent is selected from the group consisting of bupivacaine and mepivacaine.
33 . A composition for intravesical instillation into the bladder, wherein said composition consists of an aqueous solution of:
(i) a heparinoid selected from the group consisting of sodium pentosanpolysulfate, chondroitin sulfate, and hyaluronic acid; (ii) a local anesthetic agent other than cocaine, (iii) a buffer selected from the group consisting of phosphate buffer, sodium bicarbonate buffer, and Tris buffer, and (iv) optionally an osmolar component selected from the group consisting of sodium chloride, dextrose, dextran 40, dextran 60, starch and mannitol,
wherein the composition has a pH from about 7 to about 12, and
wherein the composition treats interstitial cystitis or at least one symptom thereof when instilled into the bladder.
34 . The composition of claim 33 wherein the heparinoid is sodium pentosanpolysulfate.
35 . The composition of claim 33 wherein the local anesthetic agent other than cocaine is selected from the group consisting of lidocaine, bupivacaine, and mepivacaine.
36 . The composition of claim 35 wherein the local anesthetic agent is lidocaine.
37 . The composition of claim 36 wherein lidocaine is present in the composition in the quantity of 10 mg up to 400 mg lidocaine per unit dose.
38 . The composition of claim 23 wherein the buffer is sodium bicarbonate buffer.
39 . The composition of claim 23 wherein the buffer is Tris buffer.
40 . The composition of claim 33 wherein the buffer is sodium bicarbonate buffer.
41 . The composition of claim 33 wherein the buffer is Tris buffer.Join the waitlist — get patent alerts
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