Compositions and methods for treatment of protease mediated disease

US12186368B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12186368-B2
Application numberUS-202016825221-A
CountryUS
Kind codeB2
Filing dateMar 20, 2020
Priority dateJun 2, 2011
Publication dateJan 7, 2025
Grant dateJan 7, 2025

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

A method is provided for a condition related to the activity of a protease through the administration of a θ-defensin, analog, or derivative is described. Suitable proteases include metalloproteases and cysteine proteases such as Cathepsin-C. The θ-defensin, analog, or derivative can be effectively administered parenterally, topically, or orally.

First claim

Opening claim text (preview).

What is claimed is: 1. A method of inhibiting a metalloprotease and a cysteine protease in a subject in need thereof, comprising: injectably administering to the subject in need thereof a θ-defensin in an amount effective to inhibit the metalloprotease and the cysteine protease; wherein the θ-defensin is administered intravenously, subcutaneously, or intraperitoneally; and wherein the administration reduces TNF-alpha mediated inflammation in the subject. 2. The method of claim 1 , wherein the θ-defensin is a mini-θ-defensin. 3. The method of claim 1 , wherein the θ-defensin is selected from the group consisting of SEQ. ID NO. 8, SEQ. ID NO. 11, SEQ. ID NO. 12, SEQ. ID NO.13, SEQ. ID NO. 14, SEQ. ID NO. 15, SEQ. ID NO. 16, SEQ. ID NO. 17, and SEQ. ID NO. 18. 4. The method of claim 1 , wherein the θ-defensin is selected from the group consisting of SEQ. ID NO. 8, SEQ. ID NO. 14, and SEQ. ID NO. 15. 5. The method of claim 1 , wherein the mini-θ-defensin is selected from the group consisting of SEQ. ID NO. 11, SEQ. ID NO. 12, and SEQ. ID NO.13. 6. The method of claim 1 , wherein the mini-θ-defensin is SEQ. ID NO. 12. 7. The method of claim 1 , wherein the cysteine protease is Cathepsin-C. 8. The method of claim 1 , wherein the θ-defensin is formulated for injection. 9. A method of inhibiting a metalloprotease or a cysteine protease in a subject in need thereof, comprising: administering to the subject in need thereof a θ-defensin in an amount effective to inhibit the metalloprotease or the cysteine protease, wherein the θ-defensin is a mini-θ-defensin. 10. The method of claim 9 , wherein the mini-θ-defensin is selected from the group consisting of SEQ. ID NO. 11, SEQ. ID NO. 12, and SEQ. ID NO.13. 11. The method of claim 10 , wherein the mini-θ-defensin is SEQ. ID NO. 12. 12. The method of claim 1 , wherein the θ-defensin is administered by intravenous injection. 13. The method of claim 1 , wherein the θ-defensin is administered by intravenous infusion. 14. The method of claim 1 , wherein the θ-defensin is administered by subcutaneous injection. 15. The method of claim 1 , wherein the θ-defensin is administered by intraperitoneal injection.

Assignees

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Classifications

  • Mouth and digestive tract, i.e. intraoral and peroral administration · CPC title

  • Cationic antimicrobial peptides, e.g. defensins · CPC title

  • comprising three rotors · CPC title

  • combined with a spraying device · CPC title

  • using rotating elements · CPC title

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What does patent US12186368B2 cover?
A method is provided for a condition related to the activity of a protease through the administration of a θ-defensin, analog, or derivative is described. Suitable proteases include metalloproteases and cysteine proteases such as Cathepsin-C. The θ-defensin, analog, or derivative can be effectively administered parenterally, topically, or orally.
Who is the assignee on this patent?
Univ California
What technology area does this patent fall under?
Primary CPC classification A61K38/10. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Jan 07 2025 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 4 related publications on this page (citations in our corpus or others sharing the same primary CPC).