You’re using a public version of DrugPatentWatch with 5 free searches available | Register to unlock more free searches. CREATE FREE ACCOUNT

Last Updated: April 26, 2024

Claims for Patent: 7,914,542


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 7,914,542
Title:Devices, systems and methods for treating benign prostatic hyperplasia and other conditions
Abstract: Devices, systems and methods for compressing, cutting, incising, reconfiguring, remodeling, attaching, repositioning, supporting, dislocating or altering the composition of tissues or anatomical structures to alter their positional or force relationship to other tissues or anatomical structures. In some applications, the invention may be used to used to improve patency or fluid flow through a body lumen or cavity (e.g., to limit constriction of the urethra by an enlarged prostate gland).
Inventor(s): Lamson; Theodore Charles (Pleasanton, CA), Makower; Joshua (Los Altos, CA), Catanese, III; Joseph (San Leandro, CA), Welch; Jacqueline Nerney (Pacifica, CA), Walke; Amrish Jayprakash (Santa Clara, CA), Vidal; Claude (Santa Barbara, CA), Redmond; Russell J. (Goleta, CA), Collinson; Michael (Goleta, CA)
Assignee: Neotract, Inc. (Pleastanton, CA)
Application Number:11/838,036
Patent Claims:1. A method for treating a condition in a human or animal subject wherein the prostate gland is causing undesirable constriction of the urethra, said method comprising the steps of: A) inserting an introducer device into the subject's body; B) advancing a cutting device from the introducer device; C) using the cutting device to cut at least a portion of the prostate such that the constriction of the urethra is lessened; placing a first anchor at a first location on, in or adjacent to the prostate; placing a second anchor at a second location on, in or adjacent to the prostate; and placing a connecting member between the first and second anchors, said connecting member drawing at least one of said first and second anchors toward the other thereby compressing at least a portion of the prostate.

2. A method according to claim 1 wherein the introducer device inserted in Step A comprises a scope lumen and a working lumen and wherein a scope is inserted into the scope lumen and the cutting device is advanced through the working lumen.

3. A method according to claim 2 further comprising the step of using the scope to view at least a portion of the performance of the method.

4. A method according to claim 1 wherein Step A comprises inserting the introducer into the urethra and advancing it to a position within the urethra where the urethra is substantially surrounded by the prostate gland.

5. A method according to claim 1 wherein Step A comprises inserting the introducer into the urethra and advancing the introducer to a position within the urethra distal to the prostate gland.

6. A method according to 1 wherein Step A comprises inserting the introducer into the urethra and advancing the introducer into the urinary bladder.

7. A method according to claim 1 wherein Step A comprises inserting the introducer to a position within the urethra and wherein Steps B and C comprise forming an opening in the wall of the urethra, advancing either the introducer or the cutting apparatus though the opening formed in the wall of the urethra and thereafter causing the cutting apparatus to form a cut that extends through the capsule of the prostate gland.

8. A method according to claim 7 wherein the opening formed in the wall of the urethra is no greater than 2 mm in its greatest cross-dimension.

9. A method according to claim 7 further comprising the step of closing the opening formed in the urethra.

10. A method according to claim 1 wherein Step B comprises advancing the cutting device into the prostate gland.

11. A method according to claim 1 wherein Step B comprises advancing a guide to a position within or near the prostate and advancing the cutting device over or through said guide.

12. A method according to claim 11 wherein the guide comprises a guidewire and wherein the cutting device comprises a guidewire lumen that facilitates advancement of the cutting device over the guidewire.

13. A method according to claim 11 further comprising the step of anchoring the guide.

14. A method according to claim 13 wherein the step of anchoring the guide comprises anchoring a distal portion of the guide.

15. A method according to claim 13 wherein the guide is advanced through the prostate into the urinary bladder and wherein the guide is anchored in a way that deters a distal portion of the guide from being pulled out of the urinary bladder.

16. A method according to claim 1 wherein Step C comprises using the cutting device to form a subcapsular cut within the prostate gland.

17. A method according to claim 1 wherein Step C comprises using the cutting device to form a cut through the capsule of the prostate gland.

18. A method according to claim 1 wherein Step C comprises using the cutting device to form a cut that extends through subcapsular prostate tissue and through the capsule of the prostate gland.

19. A method according to claim 1 further comprising administering a local, regional or general anesthetic to the subject.

20. A method according to claim 19 wherein a local anesthetic is injected into the prostate before performance of Step C.

21. A method according to claim 1 wherein the cutting device comprises an elongate shaft and a cutting element that is deployable from the shaft.

22. A method according to claim 21 wherein Step C comprises causing the cutting member to emit energy to facilitate formation of said cut.

23. A method according to claim 22 wherein the cutting member is caused to emit radiofrequency energy.

24. A method according to claim 1 further comprising the step of maintaining separation of opposing surface of the cut for at least a period of time after formation of the cut.

25. A method according to claim 24 wherein the step of maintaining separation of opposing surface of the cut for at least a period of time after formation of the cut comprises implanting space occupying matter within the cut.

26. A method according to claim 25 wherein the space occupying matter is substantially resorbable.

27. A method according to claim 26 wherein the space occupying matter comprises is not substantially resorbable.

28. A method according to claim 24 wherein the step of maintaining separation of opposing surface of the cut for at least a period of time after formation of the cut comprises implanting a device within the cut.

29. A method according to claim 25 wherein the device implanted within the cut is substantially resorbable.

30. A method according to claim 26 wherein the device implanted within the cut is not substantially resorbable.

31. A method according to claim 1 further comprising the step of delivering a therapeutic substance to a location within or near the prostate gland.

32. A method according to claim 31 wherein the therapeutic substance is selected from the group consisting of: hemostatic agents; antimicrobial agents; antibiotics; antifungals; antiprotozoals; antivirals; antimicrobial metals; hemostatic and/or vasoconstricting agents; pseudoephedrine; xylometazoline; oxymetazoline; phenylephrine; epinephrine; cocaine; local anesthetic agents; lidocaine; cocaine; bupivacaine; hormones; anti-inflammatory agents; corticosteroids; non-steroidal anti-inflammatory agents; hormonally active agents; agents that enhance potency; substances that dissolve, degrade, cut, break, weaken, soften, modify or remodel connective tissue or other tissue; enzymes; collagenase; trypsin; EDTA; trypsin combined with EDTA; hyaluronidase; tosyllysylchloromethane (TLCM)); chemotherapeutic or antineoplastic agents; substances that prevent adhesion formation; hyaluronic acid gel; space occupying substances; substances that promote desired tissue ingrowth into an anchoring device or other implanted device; substances that promote or facilitate epithelialization; substances that create a coagulative lesion which is subsequently resorbed causing the tissue to shrink, substances that cause the prostate to decrease in size; phytochemicals that cause the prostate to decrease in size; alpha-1a-adrenergic receptor blocking agents; 5-alpha-reductase inhibitors; smooth muscle relaxants and agents that inhibit the conversion of testosterone to dihydrotestosterone.

33. A method according to claim 31 wherein the step of delivering a therapeutic substance to a location within or near the prostate gland comprises injecting said therapeutic substance into or near the prostate gland.

34. A method according to claim 31 wherein the step of delivering a therapeutic substance to a location within or near the prostate gland comprises placing a substance eluting implant in or near the prostate gland.

35. A method according to claim 34 wherein the substance eluting implant comprises a substance eluting device.

36. A method according to claim 34 wherein the substance eluting implant comprises a substance eluting material.

37. A method according to claim 34 wherein the substance eluting implant is positioned within the cut.

38. A method according to claim 37 wherein the substance eluting implant is further operative to maintain separation of opposing surface of the cut for at least a period of time after formation of the cut.

39. A method according to claim 1 further comprising the step of: forming a lesion within the tissue which subsequently causes shrinkage of the tissue.

40. A method according to claim 39 wherein a coagulative lesion is formed by heating the tissue.

41. A method according to claim 40 wherein the coagulative lesion subsequently becomes resorbed thereby causing the tissue to shrink.

42. A method according to claim 1 further comprising the step of implanting at least one tissue compressing device to compresses the prostate in a manner that lessens constriction of the urethra.

43. A method according to claim 1 wherein Step C comprises using the cutting device to form a cut within the capsule of the prostate gland.

Details for Patent 7,914,542

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Bausch & Lomb Incorporated VITRASE hyaluronidase Injection 021640 05/05/2004 ⤷  Try a Trial 2025-05-20
Bausch & Lomb Incorporated VITRASE hyaluronidase Injection 021640 12/02/2004 ⤷  Try a Trial 2025-05-20
Amphastar Pharmaceuticals, Inc. AMPHADASE hyaluronidase Injection 021665 10/26/2004 ⤷  Try a Trial 2025-05-20
Akorn, Inc. HYDASE hyaluronidase Injection 021716 10/25/2005 ⤷  Try a Trial 2025-05-20
Smith & Nephew, Inc. SANTYL collagenase Ointment 101995 06/04/1965 ⤷  Try a Trial 2025-05-20
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.