IP Library Patent Application 16563435
Patent Application
App. No. 16/563,435

METHOD FOR REDUCING SIDE EFFECTS FROM ADMINISTRATION OF PHOSPHODIESTERASE-4 INHIBITORS

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Patent No.
US None
App. No.
16/563,435
Abstract

A method for altering the PK profile of a pharmaceutical formulation containing a PDE-4 inhibitor, such as roflumilast, to reduce the spike in Cmax. The spike in Cmax is reduced by topically administering the PDE-4 inhibitor in combination with one or more phosphate ester surfactants. Reducing the spike in Cmax will reduce gastrointestinal side effects and result in better patient compliance.

Claims (23)

1 . A method for reducing gastrointestinal side effects in a patient suffering from gastrointestinal side effects or likely to suffer from gastrointestinal side effects due to administration of a PDE-4 inhibitor drug, comprising administering to said patient, a composition comprising a PDE-4 inhibitor drug at a concentration sufficient to provide a systemic effect of the drug in combination with a phosphate ester surfactant comprising cetostearyl alcohol, dicetyl phosphate and ceteth-10 phosphate.

2 . The method of claim 1 wherein the composition is administered topically.

3 . The method of claim 1 wherein the PDE-4 inhibitor drug is selected from the group consisting of apremilast, cilomilast, crisaborole, ibudilast, piclamilast, roflumilast, and rolipram.

4 . The method of claim 3 wherein the PDE-4 inhibitor drug is roflumilast.

5 . The method of claim 1 wherein the composition is in the form of a semisolid.

6 . The method of claim 1 wherein the composition further comprises diethylene glycol monoethyl ether.

7 . The method according to claim 4 , wherein said roflumilast is in an amount of 0.005-2% w/w.

8 . The method according to claim 7 , wherein said roflumilast is in an amount of 0.05-1% w/w.

9 . The method according to claim 8 , wherein said roflumilast is in an amount of 0.1-0.5% w/w.

10 . The method according to claim 3 , wherein said roflumilast is in an amount of 0.3% w/w.

11 . The method according to claim 1 , wherein said composition is selected from the group consisting of an oil in water emulsion, a thickened aqueous gel, a thickened hydroalcoholic gel, a hydrophilic gel, and a hydrophilic or hydrophobic ointment.

12 . The method according to claim 1 , wherein said roflumilast composition further comprises at least one additional component selected from the group consisting of a solvent, moisturizer, surfactant or emulsifier, polymer or thickener, anti-foaming agent, preservative, antioxidant, sequestering agent, stabilizer, buffer, pH adjusting solution, skin penetration enhancer, film former, dye, pigment, and fragrance.

13 . The method according to claim 1 , wherein said roflumilast composition further comprises an additional active agent selected from the group consisting of nonsteroidal anti-inflammatory drugs (NSAIDs), Apremilast, JAK inhibitors, leukotriene inhibitors, mast cell stabilizers, Anthralin, Azathioprine, Tacrolimus, Coal tar, Methotrexate, Methoxsalen, Salicylic acid, Ammonium lactate, Urea, Hydroxyurea, 5-fluorouracil, Propylthouracil, 6-thioguanine, Sulfasalazine, Mycophenolate mofetil, Fumaric acid esters, Corticosteroids, Corticotropin, Vitamin D analogues, Acitretin, Tazarotene, Cyclosporine, Resorcinol, Colchicine, bronchodialators, and antibiotics.

14 . The method according to claim 1 , wherein said patient is suffering from asthma or chronic obstructive pulmonary disease (COPD).

15 . The method according to claim 1 , wherein said patient is suffering from an inflammatory condition.

16 . The method according to claim 13 , wherein said patient is suffering from atopic dermatitis.

17 . The method according to claim 1 , wherein the composition is administered in a semi-solid or a liquid form.

18 . The method according to claim 17 , wherein the composition is administered in a form selected from the group consisting of an emulsion, suspension, ointment, oil, cream, gel, paste, transdermal patch, spray, and foam.

19 . The method according to claim 18 , wherein the composition is administered in the form of a foam.

20 . A method for reducing a spike in Cmax resulting from administration of a PDE-4 inhibitor drug, comprising administering to said patient, a composition comprising a PDE-4 inhibitor drug at a concentration sufficient to provide a systemic effect of the drug in combination with a phosphate ester surfactant, wherein said phosphate ester surfactant comprises cetostearyl alcohol, dicetyl phosphate and ceteth-10 phosphate.

21 . A composition comprising a PDE-4 inhibitor drug in combination with a phosphate ester surfactant comprising cetostearyl alcohol, dicetyl phosphate and ceteth-10 phosphate.

22 . The composition according to claim 21 , wherein the composition is in a form selected from the group consisting of an emulsion, suspension, ointment, oil, cream, gel, paste, transdermal patch, spray, and foam.

23 . The method according to claim 22 , wherein the composition is in the form of a cream or a foam.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 23, 2024
From: WELGUS, HOWARD; THURSTON, ARCHIE W., JR.; OSBORNE, DAVID W.
To: ARCUTIS INC.
Reel/Frame 067194/0196 →
CHANGE OF NAME Recorded Apr 23, 2024
From: ARCUTIS, INC.
To: ARCUTIS BIOTHERAPEUTICS, INC.
Reel/Frame 067194/0520 →
SECURITY INTEREST Recorded Dec 22, 2021
From: ARCUTIS BIOTHERAPEUTICS, INC.
To: SLR INVESTMENT CORP., AS AGENT
Reel/Frame 058463/0187 →