IP Library Granted Patent US 6,939,542
Granted Patent B2
US 6,939,542 · App. 10/369,372 · Granted Sep 6, 2005

Hyaluronidase preparation for ophthalmic administration and enzymatic methods for accelerating clearance of hemorrhagic blood from the vitreous body of the eye

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Quick Facts
Patent No.
US 6,939,542
App. No.
10/369,372
Granted
Sep 6, 2005
Kind
B2
Abstract

A thimerosal-free hyaluronidase preparation wherein the preferred hyaluronidase enzyme is devoid of molecular weight fractions below 40,000 MW, between 60-70,000 MW and above 100,000 MW. Also disclosed is a method for accelerating the clearance of hemorrhagic blood from the vitreous humor of the eye, said method comprising the step of contacting at least one hemorrhage-clearing enzyme (e.g., a β-glucuronidase, matrix metalloproteinase, chondroitinase, chondroitin sulfatase or protein kinase) with the vitreous humor in an amount which is effective to cause accelerated clearance of blood therefrom.

Claims (20)

1. A method for accelerating the clearance of hemorrhagic blood from the vitreous humor of a mammalian eye, said method comprising:

contacting with the vitreous humor an amount of a solution which contains hyaluronidase to provide a dose of at least 1 International Unit of hyaluronidase, said solution being free of thimerosal, and essentially devoid of hyaluronidase molecular weight fractions above 100,000, between 60,000 and 70,000, and below 40,000 as determined by 10% SDS PAGE electrophoresis and wherein said hyaluronidase is defined as causing hydrolysis of the endo-N-acetyl hexosaminic bonds of hyaluronic acid.

2. The method of claim 1 , wherein the dose of hyaluronidase is 1 International Unit.

3. The method of claim 1 , wherein the dose of hyaluronidase is 1-50 International Units.

4. The method of claim 1 , wherein the dose of hyaluronidase is 25-75 International Units.

5. The method of claim 1 , wherein the dose of hyaluronidase is 50-200 International Units.

6. The method of claim 1 , wherein the dose of hyaluronidase is 25 International Units.

7. The method of claim 1 , wherein the dose of hyaluronidase is 50 International Units.

8. The method of claim 1 , wherein the dose of hyaluronidase is 70 International Units.

9. The method of claim 1 , wherein the dose of hyaluronidase is 200 International Units.

10. The method of claim 1 , wherein the dose of hyaluronidase is 10-300 International Units.

11. The method of claim 1 , wherein the contacting step is performed a single time, resulting in the contacting with the vitreous humor of a single dose of at least 1 International Unit of said hyaluronidase.

12. The method of claim 1 , wherein the contacting step is performed at least twice, resulting in the contacting with the vitreous humor of at least two separate doses of said hyaluronidase, each dose being at least 1 International Unit.

13. The method of claim 1 , wherein the solution which contains an amount of hyaluronidase to provide said dose comprises the ingredients hyaluronidase, lactose, and phosphate.

14. The method of claim 13 , wherein the ingredients are dissolved in sterile water, sterile filtered, and lyophilized to a dry composition.

15. The method of claim 14 , wherein the dry composition is dissolved in a balanced salt solution.

16. The method of claim 15 , wherein the solution is a solution for injection.

17. The method of claim 1 , wherein the hyaluronidase is ovine testicular hyaluronidase.

18. A method for accelerating the clearance of hemorrhagic blood from the vitreous humor of a mammalian eye not as an adjunct to vitrectomy, said method comprising:

contacting with the vitreous humor an amount of a solution which contains hyaluronidase to provide a dose of at least 1 International Unit of hyaluronidase, said solution being free of thimerosal, and essentially devoid of hyaluronidase molecular weight fractions above 100,000, between 60,000 and 70,000, and below 40,000 as determined by 10% SDS PAGE electrophoresis, wherein said contacting step is practiced in the absence of vitrectomy, and wherein said hyaluronidase is defined as causing hydrolysis of the endo-N-acetyl hexosaminic bonds of hyaluronic acid.

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Apr 8, 2025
From: BARCLAYS BANK PLC, AS COLLATERAL AGENT
To: SOLTA MEDICAL, INC.; PRECISION DERMATOLOGY, INC.; BAUSCH HEALTH IRELAND LIMITED (F/K/A/ VALEANT PHARMACEUTICALS IRELAND LIMITED); SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD; SANTARUS, INC.; MEDICIS PHARMACEUTICAL CORPORATION; HUMAX PHARMACEUTICAL S.A.; SOLTA MEDICAL IRELAND LIMITED; BAUSCH & LOMB MEXICO, S.A. DE C.V.; BAUSCH+LOMB OPS B.V.; BAUSCH HEALTH AMERICAS, INC.; BAUSCH HEALTH COMPANIES INC.; BAUSCH HEALTH HOLDCO LIMITED; BAUSCH HEALTH MAGYARORSZAG KFT (A/K/A BAUSCH HEALTH HUNGARY LLC); BAUSCH HEALTH POLAND SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA (F/K/A VALEANT PHARMA POLAND SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA); BAUSCH HEALTH US, LLC; BAUSCH HEALTH, CANADA INC. / SANTE BAUSCH, CANADA INC.; ICN POLFA RZESZOW SPOLKA AKCYJNA (A/K/A ICN POLFA RZESZOW S.A.); ORAPHARMA, INC.; PRZEDSIEBIORSTWO FARMACEUTYCZNE JELFA SPOLKA AKCYJNA (A/K/A PRZEDSIEBIORSTWO FARMACEUTYCZNE JELFA S.A.); SOLTA MEDICAL DUTCH HOLDINGS B.V.; V-BAC HOLDING CORP.; VRX HOLDCO LLC; 1261229 B.C. LTD.; 1530065 B.C. LTD.
Reel/Frame 070778/0199 →
NOTICE OF SUCCESSION OF AGENCY Recorded Jan 9, 2015
From: GOLDMAN SACHS LENDING PARTNERS, LLC
To: BARCLAYS BANK PLC, AS SUCCESSOR AGENT
Reel/Frame 034749/0689 →
SECURITY AGREEMENT Recorded Nov 1, 2013
From: BAUSCH & LOMB PHARMA HOLDINGS CORP.
To: GOLDMAN SACHS LENDING PARTNERS LLC, AS COLLATERAL AGENT
Reel/Frame 031533/0859 →
SECURITY AGREEMENT Recorded Sep 4, 2013
From: BAUSCH & LOMB INCORPORATED
To: GOLDMAN SACHS LENDING PARTNERS LLC, AS COLLATERAL AGENT
Reel/Frame 031156/0508 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 15, 2013
From: ISTA PHARMACEUTICALS, LLC
To: BAUSCH & LOMB PHARMA HOLDINGS CORP.
Reel/Frame 031019/0937 →
MERGER Recorded Jan 24, 2013
From: ISTA PHARMACEUTICALS, INC.; INGA ACQUISITION CORPORATION
To: BAUSCH & LOMB INCORPORATED
Reel/Frame 029683/0206 →