IP Library Granted Patent US 12,016,848
Granted Patent B2
US 12,016,848 · App. 18/453,674 · Granted Jun 25, 2024

Roflumilast formulations with an improved pharmacokinetic profile

Inventor: David Osborne (Fort Collins, CO)
Assignee: Arcutis Biotherapeutics, Inc.
A61K31/44A61K9/0014A61K9/06A61K9/145A61K45/06A61K47/10C09K15/06
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Quick Facts
Patent No.
US 12,016,848
App. No.
18/453,674
Granted
Jun 25, 2024
Kind
B2
Abstract

An improved a method of treating a patient having a disorder responsive to PDE-4 inhibition by administering roflumilast. The improvement involves administering the roflumilast topically in a composition having a roflumilast release profile that produces in the patient a flattened plasma concentration time curve and a reduced Cmax relative to oral administration of a PDE4-inhibiting amount of roflumilast. Such disorders include inflammatory disorders such as inflammatory dermatoses, including psoriasis, atopic dermatitis and seborrheic dermatitis. Such disorders also include inflammatory diseases in a variety of organs, especially the lungs (asthma, COPD). Because of reduced side effects with topical administration due to the improved pharmacokinetics (PK) characteristics, it may be possible to provide higher systemic exposures (AUCs) with topical administration, resulting in greater therapeutic efficacy than with the oral route of administration.

Claims (19)

1. A topical roflumilast pharmaceutical composition comprising:

(i) roflumilast in an amount of 0.05-1.0% w/w;

(ii) water;

(iii) a hydrophobic component;

(iv) a solvent comprising diethylene glycol monoethyl ether; and

(v) a surfactant;

wherein said topical roflumilast composition is an emulsion, and

wherein said topical roflumilast composition has a roflumilast absorption profile that produces in a patient following administration, a plasma concentration time curve having a delayed Tmax relative to oral administration of roflumilast.

2. The composition of claim 1 , wherein the surfactant comprises a blend of ceteraryl alcohol, dicetyl phosphate, and ceteth-10 phosphate.

3. The composition of claim 1 , wherein the hydrophobic component comprises petrolatum.

4. The composition of claim 2 , wherein the hydrophobic component comprises petrolatum.

5. The composition of claim 1 , wherein said Tmax is between about 3 and 9 hours at steady state.

6. The composition of claim 2 , wherein said Tmax is between about 3 and 9 hours at steady state.

7. The composition of claim 3 , wherein said Tmax is between about 3 and 9 hours at steady state.

8. The composition of claim 4 , wherein said Tmax is between about 3 and 9 hours at steady state.

9. The composition of claim 5 , wherein said Tmax is between about 8 and 9 hours at steady state.

10. The composition of claim 6 , wherein said Tmax is between about 8 and 9 hour at steady state.

11. The composition of claim 7 , wherein said Tmax is between about 8 and 9 hours at steady state.

12. The composition of claim 8 , wherein said Tmax is between about 8 and 9 hours at steady state.

Assignments (2)
SECURITY INTEREST Recorded Aug 9, 2024
From: ARCUTIS BIOTHERAPEUTICS, INC.
To: SLR INVESTMENT CORP.
Reel/Frame 068236/0418 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 1, 2024
From: OSBORNE, DAVID
To: ARCUTIS BIOTHERAPEUTICS, INC.
Reel/Frame 066758/0595 →
Continuity (7)
Continuation 17155679 · Feb 5, 2021
Continuation In Part 17102056 · Nov 23, 2020
Continuation 16136804 · Sep 20, 2018
Continuation 15848505 · Dec 20, 2017
Continuation 15676356 · Aug 14, 2017
Division 15616409 · Jun 7, 2017
Related Publication 20240000760A1 · Jan 4, 2024
Cited By (1)
US 12,310,956