IP Library Granted Patent US 9,481,716
Granted Patent B2
US 9,481,716 · App. 14/005,789 · Granted Nov 1, 2016

Treatment for peanut allergy

Inventors: Andrew Clark (Cambridge, GB); Pamela Ewan (Cambridge, GB)
Assignee: Cambridge Univeristy Hospitals NHS Foundation Trust
C07K14/415A61K39/35A61K2039/542A61K2039/545
View Patent ↗
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 9,481,716
App. No.
14/005,789
Granted
Nov 1, 2016
Kind
B2
Abstract

The present invention relates to oral immunotherapy for the desensitization of patients who are hypersensitive to peanut allergen. The immunotherapy comprises increasing the oral dose daily dose of peanut protein administered to the patient at intervals of at least 2 weeks in a series of increments from an initial dose to a maximum dose, the series of dose increments including 2 mg, 5 mg, 12.5 mg, 25 mg, 50 mg, 100 mg, 200 mg, 400 mg and 800 mg; administering a daily oral dose of the maximum dose of peanut protein for at least 2 years and then administering a weekly oral dose of the maximum dose of peanut protein for at least 2 years.

Claims (8)

1. A method of treating an individual with peanut allergy which comprises:

(1) orally administering a series of daily oral doses of peanut protein to the individual with peanut allergy, beginning with an initial daily oral dose and then increasing to a maximum daily oral dose,

wherein the series of daily oral doses consists of doses consisting of 2 mg, 5 mg, 12.5 mg, 25 mg, 50 mg, 100 mg and 200 mg of peanut protein, and wherein each of the doses in the series of daily oral doses is increased after at least 2 weeks of daily administration until the maximum daily oral dose in the series of daily oral doses is reached, and

(2) orally administering the maximum daily oral dose in the series of daily oral doses to the individual with peanut allergy daily for at least 1 year.

2. The method according to claim 1 wherein the peanut protein is administered as peanut flour.

3. The method according to claim 2 wherein the peanut flour is admixed with a carrier for administration.

4. The method according to claim 3 wherein the carrier is a dairy or dairy substitute product.

5. The method according to claim 1 , further comprising measuring levels of anti-peanut IgE in the serum of the individual with peanut allergy, wherein the level of anti-peanut IgE in the serum of the individual is reduced or eliminated by the treatment.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 14, 2016
From: CLARK, ANDREW; EWAN, PAMELA
To: CAMBRIDGE UNIVERSITY HOSPITALS NHS FOUNDATION TRUST
Reel/Frame 039158/0122 →
Priority Claims (1)
GB 1104537.4 · Mar 17, 2011 · national
Continuity (1)
Related Publication 20140093541A1 · Apr 3, 2014