IP Library Granted Patent US 9,861,631
Granted Patent B2
US 9,861,631 · App. 14/679,598 · Granted Jan 9, 2018

Methods and compositions for safe and effective treatment of erythema

Inventors: Michael Graeber (Lawrenceville, NJ); Christian Loesche (Hegenheim, FR); Philip Freidenreich (Yardley, PA); Yin-sang Liu (Princeton Junction, NJ); Matthew James Leoni (Titusville, NJ)
Assignee: Galderma Laboratories, L.P.
A61K31/498A61K9/0014A61K9/06A61K31/194A61K45/06
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Quick Facts
Patent No.
US 9,861,631
App. No.
14/679,598
Granted
Jan 9, 2018
Kind
B2
Abstract

Improved methods and compositions for safe and effective treatment of erythema or a symptom associated with erythema in a subject are described. The methods involve topically applying to an affected skin area a topical composition comprising about 0.3% to about 10% by weight of brimonidine and a pharmaceutically acceptable carrier.

Claims (19)

1. A method of treating facial erythema associated with rosacea in a subject in need thereof, comprising once daily topically administering to a skin area of the subject affected by the facial erythema a topical composition comprising, relative to the total weight of the composition:

0.5% by weight of brimonidine tartrate;

about 8.0% to about 30.0% by weight in total of one or more polyols;

about 0.20% to about 4.0% by weight of a gelling agent; and

a pharmaceutically acceptable carrier,

wherein the topical administration results in more reduction of the facial erythema compared to a vehicle control as measured by a 12 hour success profile evaluated on both Clinician's Erythema Assessment scores and Patient's Self Assessment scales without causing unacceptable drug related adverse events, and the 12 hour success profile comprises at least a 1-grade improvement of the facial erythema.

2. The method of claim 1 , wherein the 12 hour success profile further comprises about 1 hour to about 8 hours of a 2-grade improvement of the facial erythema.

3. The method of claim 1 , wherein the 12 hour success profile further comprises about 3 hours to about 6 hours of a 2-grade improvement of the facial erythema.

4. The method of claim 1 , wherein the gelling agent comprises a carbomer, and the topical composition comprises about 0.5% to about 2.0% by weight of the carbomer relative to the total weight of the composition.

5. The method of claim 4 , wherein the carbomer is selected from the group consisting of carbomer 934P, carbomer 974P, and carbomer 980.

6. The method of claim 5 , wherein the topical composition comprises a first polyol and a second polyol, and the amount of each of the first and second polyols in the composition is independently about 4 to 15% by weight relative to the total weight of the composition.

7. A method of treating facial erythema associated with rosacea in a subject in need thereof, comprising once daily topically administering to a skin area of the subject affected by the facial erythema a topical composition comprising, relative to the total weight of the composition:

0.5% by weight of brimonidine tartarate;

about 5.0% to about 30.0% by weight of at least one polyol;

about 0.5% to about 2.0% by weight of a gelling agent; and

a pharmaceutically acceptable carrier,

wherein the gelling agent comprises a carbomer selected from the group consisting of carbomer 934P, carbomer 974P, and carbomer 980, and

wherein the topical administration results in more reduction of the facial erythema compared to a vehicle control as measured by a 12 hour success profile evaluated on both Clinician's Erythema Assessment scores and Patient's Self Assessment scales without causing unacceptable drug related adverse events, and the 12 hour success profile comprises at least a 1-grade improvement of the facial erythema and about 1 hour to about 8 hours or about 3 hours to about 6 hours of a 2-grade improvement of the facial erythema.

8. The method of claim 7 , wherein the topical composition further comprises a preservative selected from the group consisting of sodium benzoate, phenoxyethanol, benzyl alcohol, methylparaben, imidazolidinyl urea and diazolidinyl urea.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 23, 2025
From: GALDERMA LABORATORIES, L.P.
To: NESTLE SKIN HEALTH SA
Reel/Frame 071810/0089 →
MERGER AND CHANGE OF NAME Recorded Jul 23, 2025
From: NESTLE SKIN HEALTH SA; GALDERMA HOLDINGS SA
To: GALDERMA HOLDING SA
Reel/Frame 072205/0883 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 20, 2016
From: GALDERMA RESEARCH AND DEVELOPMENT
To: GALDERMA LABORATORIES, L.P.
Reel/Frame 039800/0367 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 7, 2015
From: GRAEBER, MICHAEL; LOESCHE, CHRISTIAN; FREIDENREICH, PHILIP; LIU, YIN-SANG; LEONI, MATTHEW JAMES
To: GALDERMA RESEARCH & DEVELOPMENT
Reel/Frame 035347/0495 →
Continuity (4)
Continuation 14097912 · Dec 5, 2013
Continuation 13637040
Provisional Application 61282754 · Mar 26, 2010
Related Publication 20150209350A1 · Jul 30, 2015