US2020254029A1PendingUtilityA1
Use of gram negative species to treat atopic dermatitis
Assignee: THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY DEPT OF HEALTH AND HUMAN SERVICPriority: Apr 19, 2016Filed: Apr 14, 2020Published: Aug 13, 2020
Est. expiryApr 19, 2036(~9.7 yrs left)· nominal 20-yr term from priority
A61P 17/04A61K 9/0014A61K 35/74A61K 9/06
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Claims
Abstract
Pharmaceutical compositions are disclosed that includes a therapeutically effective amount of a purified viable Gram negative bacteria and a pharmaceutically acceptable carrier. The pharmaceutical compositions are formulated for topical administration. Methods of treating atopic dermatitis using these pharmaceutical compositions are also disclosed.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A kit, comprising:
a) a first container comprising a pharmaceutical composition, wherein the pharmaceutical composition comprises:
at least one strain of Roseomonas mucosa , wherein said strain of Roseomonas mucosa comprises a nucleic acid sequence selected from the group consisting of SEQ ID NO: 10, SEQ ID NO: 11, and SEQ ID NO: 12, wherein the at least one strain of Roseomonas mucosa is isolated and viable, and wherein the pharmaceutical composition is lyophilized; and
b) instructions for reconstituting the pharmaceutical composition for topically applying to skin of a subject.
2 . The kit of claim 1 , wherein the first container further comprises a pharmaceutically acceptable carrier.
3 . The kit of claim 2 , wherein the pharmaceutically acceptable carrier comprises sucrose.
4 . The kit of claim 3 , wherein the pharmaceutically acceptable carrier is sucrose.
5 . The kit of claim 1 , further comprising a second container.
6 . The kit of claim 5 , wherein the second container comprises a pharmaceutically acceptable carrier.
7 . The kit of claim 6 , wherein the pharmaceutically acceptable carrier in the second container comprises a cream, gel, foam, ointment, or liquid.
8 . The kit of claim 7 , wherein the liquid is water.
9 . The kit of claim 1 , wherein said strain of Roseomonas mucosa is isolated from a subject that does not have atopic dermatitis.
10 . The kit of claim 1 , wherein the subject is an adult.
11 . The kit of claim 1 , wherein the subject is a child.
12 . The kit of claim 1 , wherein the subject is an infant.
13 . The kit of claim 1 , wherein said strain of Roseomonas mucosa comprises the nucleic acid sequence of SEQ ID NO: 10.
14 . The kit of claim 1 , wherein said strain of Roseomonas mucosa comprises the nucleic acid sequence of SEQ ID NO: 11.
15 . The kit of claim 1 , wherein said strain of Roseomonas mucosa comprises the nucleic acid sequence of SEQ ID NO: 12.
16 . The kit of claim 1 , wherein the at least one strain of Roseomonas mucosa comprises a mixture of three strains of Roseomonas mucosa , wherein each of said strains comprises one of the nucleic acid sequences selected from the group consisting of SEQ ID NO: 10, SEQ ID NO: 11, and SEQ ID NO: 12.
17 . The kit of claim 1 , wherein the at least one strain of Roseomonas mucosa is present in the pharmaceutical composition in a total amount of 10 4 to 10 12 colony forming units.
18 . The kit of claim 1 , wherein the at least one strain of Roseomonas mucosa is present in the pharmaceutical composition in a total amount of about 10 3 colony forming units.Join the waitlist — get patent alerts
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