IP Library Patent Application 12894618
Patent Application
App. No. 12/894,618

USE OF A CHEMICALLY-STABILIZED CHLORITE SOLUTION FOR INHIBITING AN ANTIGEN-SPECIFIC IMMUNE RESPONSE

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
12/894,618
Abstract

Methods of using a stabilized chlorite solution to inhibit antigen-specific immune responses are disclosed. The stabilized chlorite solution, when administered to a mammal in need thereof, can prevent the presentation of antigens by antigen presenting cells. The stabilized chlorite solution therefore is useful in treating, inter alia, auto-immune diseases, treating diseases caused by an inappropriate immune response, treating lymphoproliferative disease and in inhibiting rejection in transplant patients.

Claims (11)

1 - 26 . (canceled)

27 . A method of treating a patient suffering from an autoimmune disease or disease caused by inappropriate immune response, comprising administering to the patient a therapeutically effective amount of WF10, said disease selected from the group consisting of: myasthenia gravis, systemic lupus erythematosus, serum disease, type I diabetes, rheumatoid arthritis, juvenile rheumatoid arthritis, rheumatic fever, Sjörgen syndrome, systemic sclerosis, spondylarthropathies, Lyme disease, sarcoidosis, autoimmune hemolysis, autoimmune hepatitis, autoimmune neutropenia, autoimmune polyglandular disease, autoimmune thyroid disease, multiple sclerosis, inflammatory bowel disease, colitis, Crohn's disease, chronic fatigue syndrome, chronic obstructive pulmonary disease (COPD), graft rejection, graft vs. host response, graft vs. host disease, allergic asthma, allergic rhinitis and atopic dermatitis.

28 . The method of claim 27 , wherein the therapeutically effective amount of WF10 is in a range of from about 0.1 ml/kg to about 1.5 ml/kg body weight of the patient.

29 . The method of claim 27 , wherein the therapeutically effective amount of WF10 is about 0.5 ml/kg body weight of the patient.

30 . The method of claim 28 , wherein WF10 comprises a concentration of about 40 to about 80 mMol ClOC 2 − per liter.

31 . The method of claim 29 , wherein WF10 comprises a concentration of about 60 mMol ClOC 2 − per liter.

32 . The method of claim 27 , wherein the composition comprising WF10 is administered to the patient as 3 to 7 daily infusions.

33 . The method of claim 27 , wherein the composition comprising WF10 is administered to the patient as 5 daily infusions.

34 . The method of claim 33 , wherein the administration is on 5 consecutive days.

35 . The method of claim 27 , wherein the composition comprising WF10 is administered to the patient for more than one treatment, wherein each treatment comprises 5 daily infusions of the composition followed by a rest period.

36 . The method of claim 35 , wherein the rest period is 6 months, one year or two years.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT RECEIVING PARTY PREVIOUSLY RECORDED ON REEL 026594 FRAME 0546. ASSIGNOR CONFIRMS THE CHANGE OF NAME. Recorded Nov 4, 2011
From: DIMETHAID AG
To: NUVO RESEARCH AG
Reel/Frame 027330/0503 →
CHANGE OF NAME Recorded Jul 14, 2011
From: DIMETHAID AG
To: NUVO RESEARCH INC.
Reel/Frame 026594/0546 →