Topically applicable pharmaceutical preparation
A topical pharmaceutical preparation for administering a slightly soluble PDE4 inhibitor is described. A surprisingly good systemic bioavailability is observed with this dosage form.
1 - 17 . (canceled)
18 . A method for treating a patient suffering from a dermatosis comprising administering to said patient in need thereof a therapeutically effective and pharmacologically suitable amount of a topical pharmaceutical preparation comprising an active pharmaceutical ingredient chosen from roflumilast, a salt of roflumilast, the N-oxide of roflumilast and a salt thereof, wherein said administration takes place by dermal administration.
19 . The method according to claim 18 , where the dermatosis is chosen from psoriasis vulgaris, toxic and allergic contact eczema, atopic eczema, seborrhoeic eczema, lichen simplex, sunburn, pruritus in the genitoanal region, alopecia greata, hypertrophic scars, discoid lupus erythematosus, follicular and extensive pyodermas, endogenous and exogenous acne, acne rosacea or other proliferative, inflammatory and allergic skin disorders.
20 . The method according to claim 18 , where the dermatosis is chosen from psoriasis vulgaris and atopic eczema.
in which
R1 is difluoromethoxy,
R2 is cyclopropylmethoxy and
R3 is 3,5-dichloropyrid-4-yl.
22 . The method according to claim 18 , wherein the topical pharmaceutical preparation is a semisolid dosage form chosen from a solution ointment, a suspension ointment, a cream, a gel and a paste.
23 . The method according to claim 18 , wherein the topical pharmaceutical preparation is a transdermal therapeutic system (TTS).
24 . A method for treating a patient suffering from an acute or chronic airway disorder or disorder of the arthritic type comprising administering to said patient in need thereof a therapeutically effective amount of a topical pharmaceutical preparation comprising an active pharmaceutical ingredient chosen from roflumilast, a salt of roflumilast, the N-oxide of roflumilast and a salt thereof, wherein said administration takes place by dermal administration.
25 . The method according to claim 24 , wherein said acute and chronic airway disorder is chosen from bronchitis, allergic bronchitis, bronchial asthma, and COPD, and wherein said disorder of the arthritic type is chosen from rheumatoid arthritis, rheumatoid spondylitis, and osteoarthritis.
26 . The method according to claim 24 , where roflumilast is a compound of the formula I
in which
R1 is difluoromethoxy,
R2 is cyclopropylmethoxy and
R3 is 3,5-dichloropyrid-4-yl.
27 . The method according to claim 24 , wherein the topical pharmaceutical preparation is a semisolid dosage form chosen from a solution ointment, a suspension ointment, a cream, a gel and a paste.
28 . The method according to claim 24 , wherein the topical pharmaceutical preparation is a transdermal therapeutic system (TTS).
29 . A method for treating a patient suffering from an eye disorder comprising administering to said patient in need thereof a therapeutically effective amount of a topical pharmaceutical preparation comprising an active pharmaceutical ingredient chosen from roflumilast, a salt of roflumilast, the N-oxide of roflumilast and a salt thereof.
30 . The method according to claim 29 , where the disease is allergic conjunctivitis, conjunctivitis caused by bacteria, viruses or fungi, inflammatory states after intraocular lens implantation, inflammation of the optic nerve (neuritis nervi optici), keratitis, dry eye syndrome (keratitis sicca), uveitis, glaucoma, retinal oedema, retinitis pigmentosa or diabetic retinopathy.
31 . A method according to claim 29 , where the disease is allergic conjunctivitis, conjunctivitis caused by bacteria, viruses or fungi, inflammatory states after intraocular lens implantation or uveitis.
32 . The method according to claim 29 , where roflumilast is a compound of the formula I
in which
R1 is difluoromethoxy,
R2 is cyclopropylmethoxy and
R3 is 3,5-dichloropyrid-4-yl.
33 . The method according to claim 29 , wherein the topical pharmaceutical preparation is a semisolid dosage form chosen from a solution ointment, a suspension ointment, a cream, a gel and a paste.