US6054429A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Epidural method of producing analgesia
Assignee: Jazz Pharmaceuticals International Ltd
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Filing: 1996-03-08
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Granted: 2000-04-25
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Expires: 2016-03-08
Abstract
Abstract A improved method of treating pain is disclosed. The method includes administering to a subject an N-type voltage-sensitive calcium channel blocking omega conopeptide which is characterized by its ability to (a) inhibit electrically stimulated contraction of the guinea pig ileum, and (b) bind selectively to omega conopeptide MVIIA binding sites present in neuronal tissue. The method includes administering the omega conopeptide epidurally, preferably so that the compound is in prolonged or sustained contact with the epidural region.
Inventors
- 👤 S. Scott Bowersox
- 👤 Theresa Gadbois
- 👤 Mark Raymond Pettus
- 👤 Robert R. Luther
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-23 10:46
CPC Classifications
C; C07; C07K; C07K14/00; C07K14/435; A; A61; A61K; A61K38/00
Claims Analysis
Total Claims: 10
Claim 1
Independent Claim
132 words
In a method of producing analgesia in a mammalian subject by administering to the subject, an omega conopeptide composition which is effective (a) to inhibit electrically stimulated contraction of the guinea pig ileum, and (b) to bind selectively to omega conopeptide MVIIA binding sites present in neuronal tissue, wherein the activities of the omega conopeptide in inhibition of guinea pig ileum and in binding to the MVIIA binding site are within the ranges of such activities of omega-conotoxins MVIIA and TVIA, the improvement comprising administering said omega conopeptide composition via a spinal epidural route over a period of time such that said conopeptide is in prolonged contact with the epidural region, at a dosage that is in the range of an effective intrathecal analgesic dose administered over an equivalent period of time.
Claim 2
Dependent Claim
132 words
In a method of producing analgesia in a mammalian subject by administering to the subject, an omega conopeptide composition which is effective (a) to inhibit electrically stimulated contraction of the guinea pig ileum, and (b) to bind selectively to omega conopeptide MVIIA binding sites present in neuronal tissue, wherein the activities of the omega conopeptide in inhibition of guinea pig ileum and in binding to the MVIIA binding site are within the ranges of such activities of omega-conotoxins MVIIA and TVIA, the improvement comprising administering said omega conopeptide composition via a spinal epidural route over a period of time such that said conopeptide is in prolonged contact with the epidural region, at a dosage that is in the range of an effective intrathecal analgesic dose administered over an equivalent period of time.
Claim 3
Dependent Claim
13 words
The method of claim 1, wherein said epidural administering is via continuous infusion.
Claim 4
Dependent Claim
16 words
The method of claim 2, wherein said dosage is measured over a twenty-four hour time period.
Claim 5
Dependent Claim
20 words
The method of claim 1, wherein said prolonged contact is effected by administering said conopeptide in a sustained release formulation.
Claim 6
Dependent Claim
29 words
The method of claim 1, wherein said administering is carried out in the absence in said composition of an agent for enhancing permeation of the conopeptide through meningeal membranes.
Claim 7
Dependent Claim
32 words
The method of claim 5, wherein said analgesia is produced in a patient experiencing neuropathic pain, and said administering is effective to prevent further progression of a neuropathic condition underlying said pain.
Claim 8
Dependent Claim
61 words
The method of claim 1, wherein said conopeptide is selected from the group consisting of conopeptides identified by SEQ ID NO: 1 (MVIIA/SNX-111), SEQ ID NO: 7 (TVIA/SNX-185), SEQ ID NO: 30 (SNX-236), SEQ ID NO: 2 (SNX-159), SEQ ID NO: 32 (SNX-239), SEQ ID NO: 33 (SNX-199), SEQ ID NO: 35 (SNX-273), SEQ ID NO: 36 (SNX-279), and derivatives thereof.
Claim 9
Dependent Claim
16 words
The method of claim 7, wherein said conopeptide is identified by SEQ ID NO: 1 (MVIIA/SNX-111).
Claim 10
Dependent Claim
59 words
The method of claim 1, wherein said activity to bind selectively to omega conopeptide MVIIA binding sites is further evidenced by a selectivity ratio of binding at said MVIIA binding site to binding at a site 2 omega conopeptide binding site which is within the range of selectivity ratios determined for omega conopeptides MVIIA/SNX-111, SNX-199, SNX-236, SNX-239 and TVIA/SNX-185.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 2003-04-25 | 2003-10-25 | 2004-04-25 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 2007-04-25 | 2007-10-25 | 2008-04-25 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2011-04-25 | 2011-10-25 | 2012-04-25 | $7700.00 | Window Closed / Lapsed |