CA2337399A1 - Ophthalmic compositions for treating ocular hypertension - Google Patents
Ophthalmic compositions for treating ocular hypertension Download PDFInfo
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- CA2337399A1 CA2337399A1 CA002337399A CA2337399A CA2337399A1 CA 2337399 A1 CA2337399 A1 CA 2337399A1 CA 002337399 A CA002337399 A CA 002337399A CA 2337399 A CA2337399 A CA 2337399A CA 2337399 A1 CA2337399 A1 CA 2337399A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/557—Eicosanoids, e.g. leukotrienes or prostaglandins
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
Abstract
Combinations of a prostaglandin, prostaglandin derivative, a hypotensive lip id derived from a prostaglandin or prostaglandin derivative or an ophthalmologically acceptable salt thereof, a .beta.-adrenergic antagonist o r an ophthalmologically acceptable salt thereof and a topical carbonic anhydra se inhibitor or an ophthalmologically acceptable salt thereof are particularly useful in the treatment of ocular hypertension and glaucoma. The combination s are characterized by an improved effect and reduced side-effects.
Description
TITLE OF THE INVENTION
OPHTHALMIC COMPOSITIONS FOR TREATING OCULAR
HYPERTENSION
BACKGROUND OF THE INVENTION
Glaucoma is a degenerative disease of the eye wherein the intraocular pressure is too high to permit normal eye function. As a result, damage may occur to the optic nerve head and result in irreversible loss of visual function. If untreated, glaucoma may eventually lead to blindness. Ocular hypertension, i.e., the condition of elevated intraocular pressure without optic nerve head damage or characteristic glaucomatous visual field defects, is now believed by the majority of ophthalmologists to represent merely the earliest phase in the onset of glaucoma.
Many of the drugs formerly used to treat glaucoma proved not entirely satisfactory. The early methods of treatment of glaucoma employing pilocarpine produced undesirable local effects that made this drug, though valuable, unsatisfactory as a first line drug. J3-adrenergic antagonists are also effective in reducing intraocular pressure. While many of these ~ agents are effective for this purpose, there exist some patients with whom this treatment is not effective or not sufficiently effective. Many of these agents also have other characteristics, e.g., membrane stabilizing activity, that become more apparent with increased doses and render them unacceptable for chronic ocular use.
The 13-adrenergic antagonist (S)-1-{tert-butylamino)-3-[(4-morpholino-1,2,5-thiadiazol-3-yl)-oxy]-2-propanol, timolol, was found to reduce intraocular pressure and to be devoid of many unwanted side effects associated with pilocarpine and, in addition, to possess advantages over many other f3-adrenergic antagonists, e.g., to be devoid of local anesthetic properties, to have a long duration of activity, and to display minimal loss of effect with increased duration of dosing.
Although 13-adrenergic antagonists reduce intraocular pressure, it does not manifest its action by inhibiting the enzyme carbonic anhydrase, and thus they do not take advantage of reducing the contribution to aqueous humor formation made by the carbonic anhydrase pathway.
Agents referred to as carbonic anhydrase decrease the formation of aqueous humor by inhibiting the enzyme carbonic anhydrase. ~'Vhile such carbonic anhydrase inhibitors are now used to treat intraocc lar pressure by systemic routes, they thereby have the distinct disad vantage of inhibiting carbonic anhydrase throughout the entire body. Such a gross disruption of a basic enzyme system is justified only during an acute attack of alarmingly elevated intraocular pressure, or when no other agent is effective.
lZecently, a topically effective carbonic anhydrase inhibitor has become ~.vailable for clinical use. (S, S)-(-)-5,6-Dihydro-4-ethylamino-6-methyl-4H-thieno[2,3-b]thiopyran-2-sulfonamide-7,7-dioxide hydrochloride (dorzolamide HCI; MK507) is the active ingredient in TRUSOPT'M which is prescribed for the treatment of elevated intraocular pressure in ocular hypertension, open-angle glaucoma anc. pseudo-exfoliative glaucoma. Topically effective carbonic anh~~drase inhibitors, for example disclosed in U.S. Patent Nos.
4,386,098; 4,416,890; 4,426,388; 4,668,697; and 4,863,922 and 4,797,413, are now preferred.
F'rostaglandins, or Pgs, are members of a class of organic carboxylic ac; ds that are contained in human and most other mammalian tissues or org;~ns and that exhibit a wide range of physiological activities. Naturally occurring Pgs possess a common structural feature, the prostanoic acid skelton, depicted in Formula I below:
COOH (a-chain) 10 g 6 4 2 ~1) 12 14 16 lg 20 1 \ CH3 (w-chain) 15 1~ 19 S Mme synthetic analogues have somewhat modified skeletons. Th ~ primary PG's are classified based on the structural feature of the five-membered cycle moiety into PGA's, PGB's, PGC's, PGD's PGE's, PGF's PGG's PGH's PGI's and PGJ's and also on the presence or absence of unsaturation and oxidation in the chain moiety as:
Subscript 1 13,14-unsaturated-15-OH, Subscript 2 5,6- and 13,14-diunsaturated -15-OH, Subscript 3 5,6-13,14-, and 17,18-triunsaturated Further, PGFs are subclassified as a or (3 according to the configuration of the hydroxy group at position 9.
Prostaglandins and prostaglandin derivatives are known to lower intraocular pressure. U.S. Patent 4,883,819 to Bito descibes the use and synthesis of PGAs, PGBs and PGCs in reducing intraocular pressure. U.S. Patent 4,824,857 to Goh et al. describes the use and synthesis of PGD2 and derivatives thereof in lowering intraocular pressure including derivatives wherein C-10 is replaced with nitrogen.
U.S. Patent 5,001,153 to Ueno et al. describes the use and synthesis of 13,14-dihydro-15-keto prostaglandins and prostaglandin derivatives to lower intraocular pressure. U.S. Patent 4,599,353 describes the use of eicosanoids and eicosanoid derivatives including prostaglandins and prostaglandin inhibitors in lowering intraocular pressure.
Prostaglandin and prostaglandin derivatives lower intraocular pressure by increasing uveoscleral outflow. This is true for both the F type and A type of Pgs and hence presumably also for the B,C,D,E and J types of prostaglandins and derivatives thereof. A
problem with using prostaglandin derivatives to lower intraocular pressure is that these compounds often induce an initial increase in intraocular pressure.
Since the carbonic anhydrase inhibitor lowers intraocular pressure without accompanying transient ocular hypertension exhibited by the primary Pgs, and since 13-adrenergic antagonists reduce intraocular pressure by manifesting its action by inhibiting a different enzyme than that of the carbonic anhydrase, the combination of the carbonic anhydrase inhibitor, f3-adrenergic antagonists and the prostaglandin derivative can be used for the treatment of diseases and conditions in which the lowering of intraocular pressure is desired, for example glaucoma, ocular hypertension and other disease accompanied by an increase in intraocular pressure.
Thus, when a carbonic anhydrase inhibitor, which takes advantage of reducing the contribution to aqueous humor formation made by the carbonic anhydrase pathway, and a f3-adrenergic antagonist, which takes advantage of reducing the contribution to aqueous humor formation made by the 13-adrenergic pathway, is combined with a prostaglandin or prostaglandin derivative, which increases the outflow of aqueous humor, there is experienced an effect that reduces intraocular pressure below that obtained by any of the medicaments individually.
The combinations disclosed herein are effective either by co-administration of the medicaments in one solution or as a combined therapy achieved by prior administration of one of the components, followed by administration of a different component and ending with the administration of the last component until all three components have been administered. The order in which each component is administered can be varied. For example, as a combined therapy, a carbonic anhydrase inhibitor could be the first administered component, followed the administration of a prostaglandin and ending with the administration of a I3-adrenergic antagonist. The use of a single solution containing the three active medicaments is preferred.
There exists a patient population who will benefit from a combination where the minimal dosage of one, two or three of the medicaments is employed, thus minimizing the possibility of the occurrence of undesirable effects of one, two or three of the medicaments which would be more likely to become apparent with chronic use at the higher dosage.
OPHTHALMIC COMPOSITIONS FOR TREATING OCULAR
HYPERTENSION
BACKGROUND OF THE INVENTION
Glaucoma is a degenerative disease of the eye wherein the intraocular pressure is too high to permit normal eye function. As a result, damage may occur to the optic nerve head and result in irreversible loss of visual function. If untreated, glaucoma may eventually lead to blindness. Ocular hypertension, i.e., the condition of elevated intraocular pressure without optic nerve head damage or characteristic glaucomatous visual field defects, is now believed by the majority of ophthalmologists to represent merely the earliest phase in the onset of glaucoma.
Many of the drugs formerly used to treat glaucoma proved not entirely satisfactory. The early methods of treatment of glaucoma employing pilocarpine produced undesirable local effects that made this drug, though valuable, unsatisfactory as a first line drug. J3-adrenergic antagonists are also effective in reducing intraocular pressure. While many of these ~ agents are effective for this purpose, there exist some patients with whom this treatment is not effective or not sufficiently effective. Many of these agents also have other characteristics, e.g., membrane stabilizing activity, that become more apparent with increased doses and render them unacceptable for chronic ocular use.
The 13-adrenergic antagonist (S)-1-{tert-butylamino)-3-[(4-morpholino-1,2,5-thiadiazol-3-yl)-oxy]-2-propanol, timolol, was found to reduce intraocular pressure and to be devoid of many unwanted side effects associated with pilocarpine and, in addition, to possess advantages over many other f3-adrenergic antagonists, e.g., to be devoid of local anesthetic properties, to have a long duration of activity, and to display minimal loss of effect with increased duration of dosing.
Although 13-adrenergic antagonists reduce intraocular pressure, it does not manifest its action by inhibiting the enzyme carbonic anhydrase, and thus they do not take advantage of reducing the contribution to aqueous humor formation made by the carbonic anhydrase pathway.
Agents referred to as carbonic anhydrase decrease the formation of aqueous humor by inhibiting the enzyme carbonic anhydrase. ~'Vhile such carbonic anhydrase inhibitors are now used to treat intraocc lar pressure by systemic routes, they thereby have the distinct disad vantage of inhibiting carbonic anhydrase throughout the entire body. Such a gross disruption of a basic enzyme system is justified only during an acute attack of alarmingly elevated intraocular pressure, or when no other agent is effective.
lZecently, a topically effective carbonic anhydrase inhibitor has become ~.vailable for clinical use. (S, S)-(-)-5,6-Dihydro-4-ethylamino-6-methyl-4H-thieno[2,3-b]thiopyran-2-sulfonamide-7,7-dioxide hydrochloride (dorzolamide HCI; MK507) is the active ingredient in TRUSOPT'M which is prescribed for the treatment of elevated intraocular pressure in ocular hypertension, open-angle glaucoma anc. pseudo-exfoliative glaucoma. Topically effective carbonic anh~~drase inhibitors, for example disclosed in U.S. Patent Nos.
4,386,098; 4,416,890; 4,426,388; 4,668,697; and 4,863,922 and 4,797,413, are now preferred.
F'rostaglandins, or Pgs, are members of a class of organic carboxylic ac; ds that are contained in human and most other mammalian tissues or org;~ns and that exhibit a wide range of physiological activities. Naturally occurring Pgs possess a common structural feature, the prostanoic acid skelton, depicted in Formula I below:
COOH (a-chain) 10 g 6 4 2 ~1) 12 14 16 lg 20 1 \ CH3 (w-chain) 15 1~ 19 S Mme synthetic analogues have somewhat modified skeletons. Th ~ primary PG's are classified based on the structural feature of the five-membered cycle moiety into PGA's, PGB's, PGC's, PGD's PGE's, PGF's PGG's PGH's PGI's and PGJ's and also on the presence or absence of unsaturation and oxidation in the chain moiety as:
Subscript 1 13,14-unsaturated-15-OH, Subscript 2 5,6- and 13,14-diunsaturated -15-OH, Subscript 3 5,6-13,14-, and 17,18-triunsaturated Further, PGFs are subclassified as a or (3 according to the configuration of the hydroxy group at position 9.
Prostaglandins and prostaglandin derivatives are known to lower intraocular pressure. U.S. Patent 4,883,819 to Bito descibes the use and synthesis of PGAs, PGBs and PGCs in reducing intraocular pressure. U.S. Patent 4,824,857 to Goh et al. describes the use and synthesis of PGD2 and derivatives thereof in lowering intraocular pressure including derivatives wherein C-10 is replaced with nitrogen.
U.S. Patent 5,001,153 to Ueno et al. describes the use and synthesis of 13,14-dihydro-15-keto prostaglandins and prostaglandin derivatives to lower intraocular pressure. U.S. Patent 4,599,353 describes the use of eicosanoids and eicosanoid derivatives including prostaglandins and prostaglandin inhibitors in lowering intraocular pressure.
Prostaglandin and prostaglandin derivatives lower intraocular pressure by increasing uveoscleral outflow. This is true for both the F type and A type of Pgs and hence presumably also for the B,C,D,E and J types of prostaglandins and derivatives thereof. A
problem with using prostaglandin derivatives to lower intraocular pressure is that these compounds often induce an initial increase in intraocular pressure.
Since the carbonic anhydrase inhibitor lowers intraocular pressure without accompanying transient ocular hypertension exhibited by the primary Pgs, and since 13-adrenergic antagonists reduce intraocular pressure by manifesting its action by inhibiting a different enzyme than that of the carbonic anhydrase, the combination of the carbonic anhydrase inhibitor, f3-adrenergic antagonists and the prostaglandin derivative can be used for the treatment of diseases and conditions in which the lowering of intraocular pressure is desired, for example glaucoma, ocular hypertension and other disease accompanied by an increase in intraocular pressure.
Thus, when a carbonic anhydrase inhibitor, which takes advantage of reducing the contribution to aqueous humor formation made by the carbonic anhydrase pathway, and a f3-adrenergic antagonist, which takes advantage of reducing the contribution to aqueous humor formation made by the 13-adrenergic pathway, is combined with a prostaglandin or prostaglandin derivative, which increases the outflow of aqueous humor, there is experienced an effect that reduces intraocular pressure below that obtained by any of the medicaments individually.
The combinations disclosed herein are effective either by co-administration of the medicaments in one solution or as a combined therapy achieved by prior administration of one of the components, followed by administration of a different component and ending with the administration of the last component until all three components have been administered. The order in which each component is administered can be varied. For example, as a combined therapy, a carbonic anhydrase inhibitor could be the first administered component, followed the administration of a prostaglandin and ending with the administration of a I3-adrenergic antagonist. The use of a single solution containing the three active medicaments is preferred.
There exists a patient population who will benefit from a combination where the minimal dosage of one, two or three of the medicaments is employed, thus minimizing the possibility of the occurrence of undesirable effects of one, two or three of the medicaments which would be more likely to become apparent with chronic use at the higher dosage.
SUMMARY OF THE INVENTION
This invention relates to novel ophthalmic compositions comprising a pharmaceutically acceptable carrier, a topical carbonic anhydrase inhibitor or an ophthamologically acceptable salt thereof, a !3-adrenergic antagonist or an ophthamologically acceptable salt thereof and a prostaglandin or prostaglandin derivative thereof such as a hypotensive lipid derived from PGF2a prostaglandins.
In one aspect of the invention a composition comprising 0.025 to 5% (w/w) of a compound of the structural formula II
Z
Q
~~-S02NH2 S (II) an individual diastereomer, an individual enantiomer or mixture thereof, or an ophthalmologically acceptable salt thereof, wherein:
I5 A is carbon or nitrogen, preferably carbon;
Z is -NHR or -OR, preferably -NHR;
R is C,_6alkyl, either straight or branched chain, preferably C~_4alkyl such as ethyl, propyl or isobutyl;
Q is {H, H), oxo or thioxo;
R' is (a) hydrogen, (b) C,_~alkyl, preferably methyl, ethyl or n-propyl, or (c) C,_4alkoxy-C,_4alkyl, preferably 3-methoxypropyl or ethoxymethyl; and X is -S(O)2- or -C(O)-, preferably -S(O)2-; 0.01 to 1.0% of a 13-adrenergic antagonist such as betaxolol, bufenolol, carteolol, levobunolol, metipranolol, timolol or an ophthalmologically acceptable salt thereof, preferably betaxolol or timolol, 0.005 to 2%
(w/w) of a prostaglandin such as 13,14-dihydro-15 (R)-17-phenyl-18,19,20-trinor-PGF2oc ester, or 13, 14-dihydro-15-keto-20-ethyl-PGF2a, or a prostaglandin derivative such as a hypotensive lipid derived from PGF2a prostaglandins and their traps and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material is disclosed. Said composition can optionally contain a gum belonging to the group consisting of gellan gum or xanthan gum.
Another aspect of the invention is concerned with the use of the novel ophthalmic compositions in the treatment of ocular hypertension or glaucoma.
DETAILED DESCRIPTION OF THE INVENTION
This invention relates to novel ophthalmic combinations comprising a pharmaceutically acceptable carrier, a topical carbonic anhydrase inhibitor or an ophthamologically acceptable salt thereof, 13-adrenergic antagonist or an ophthamologically acceptable salt thereof and a prostaglandin or prostaglandin derivative thereof, which are used in the treatment of ocular hypertension and glaucoma.
Another aspect of this invention is realized when in the compounds of structural formula II A is carbon; and wherein R is -CH~CH~ and R' is -CH3; or R is -CH2CH2CH~ and R' is CHZCH~CHZOCH~; or R is -CHZCH; and R' is -CHZCH~CH3; or R is -CHZCH~(CH~)2 and R' is hydrogen; or R is -CH~CH~ and R' is -CH~OCH~CH~; and carbons 4 and 6 of the topical carbonic anhydrase inhibitor both have S absolute stereochemical configuration.
Another aspect of this invention is realized when in the compounds of structural formula II A is nitrogen; and wherein R is -CHzCH~ and R' is -CHI; or R is -CHZCHZCH~ and R' is -CHZCH2CH20CH~; or R is -CH~CH3 and R' is -CH2CHZCHj; or R is -CHZCH2(CH~)2 and R' is hydrogen; or R is -CH,CH~ and R' is -CH20CH2CH3.
A preferred topical carbonic anhydrase inhibitor for use in the novel compositions of the present invention is 5,6-dihydro-4-ethylamino-6-methyl-4H-thieno-[2,3-bJthiopyran-2-sulfonamide-7,7 dioxide hydrochloride or 2H-thieno[3,2-e)-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-l,l-dioxide and their trans and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material.
_ 'j _ The carbon atoms to which Z and R' are bonded may be chiral. When named according to absolute configuration, e.g., (R,S) or (S,S), the first letter represents the chirality the carbon atom to which Z
is bonded and the second letter represents the chirality of A when A is carbon. The carbonic anhydrase inhibitors of this invention accordingly may be used as diastereomeric mixtures or single enantiomers or as racemlc mixtures.
Still another aspect of this invention is realized when the prostaglandin isl l, 15-dipivaloyl PGF2a, 11-pivaloyl prostaglandin F2a hydroxyethyl ester, (+)-(Z)-sodium-7-[1R, 2R, 3R, 5S)-3,5-dihydroxy-2-[(E)-1-octenyl)cyclopentyl)-5-heptenoate sesquihydrate, [ 1 a,2(3,3a,5a]methyl-5-cis-2-(phenylethylsulfonamidomethyl)-3,5-dihydroxycyclopentyl heptenoate, (+-)-5-[6-(1-hydroxy)hexyl)-1,3-benzodioxol-5-yl)-pentanol, 15-pivaloyl PGFa, 7-[3a,5a dihydroxy-2-(3a-hydroxy-5--lE-pentenyl)cyclopentyl)-5Z-heptenoic acid, isopropyl (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl)cyclopentyl)-5-heptenoate, 13,14-dihydro-15(R)-17-phenyl-18,19,20-trinor-PGF2a esters, 13,14-dihydro-15-keto-20-ethyl-PGF2a isopropyl ester, (+)-isopropyl fluprostenol, [2R(lE, 3R),3S(4Z),4R)-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl)-4-heptanoate, 13,14-dihydro-PGF2p isoprpopyl esters, or 13,14-dihydro-15-keto-20-ethyl-PGFZa isopropyl ester trimethylphenol-l -acetate.
Another aspect of this invention is realized when hypotensive lipids derived from a prostaglandin or prostaglandin derivative such as lipids derived from PGFZa prostaglandins, in which the carboxylic acid group on the a-chain link of the basic prostaglandin _g_ structure is replaced with electrochemically neutral substituents, is used.
An example of a hypotensive lipid is that in which the carboxylic acid group is replaced with a C,_6 alkoxy group such as OCH~ (PGF2~ 1-OCH3), or a hydroxy group (PGF2~ 1-OH).
In another aspect of this invention, the novel ophthalmic compositions of this invention comprise a pharmaceuticallly acceptable carrier, a therapeutically effective amount of 7-[3a,5a dihydroxy-2-(3a-hydroxy-5--lE-pentenyl)cyclopentyl]-SZ-heptenoic acid;
isopropyl (Z)-7-[(1R,2R,3R,SS)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]-5-heptenoate;
(+)-(Z)-sodium-7-[1R, 2R, 3R, SS)-3,5-dihydroxy-2-[(E)-1-octenyl]cyclopentyl]-5-heptenoate sesquihydrate;
13,14-dihydro-15-keto-20-ethyl-PGF2a isopropyl ester trimethylphenol-1-acetate; (+)-isopropyl fluprostenol; 13,14-dihydro-PGF2p isoprpopyl esters; [2R(lE, 3R),3S(4Z),4R]-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate; or hypotensive lipids derived from a prostaglandin or prostaglandin derivative such as lipids derived from PGF2a prostaglandins wherein the COON is replaced with electrochemically neutral substituents like C,_6 alkoxy or hydroxy, 13-adrenergic antagonists such as betaxolol, bufenolol, carteolol, levobunolol, metipranolol, timolol or an ophthalmologically acceptable salt thereof and a topical carbonic anhydrase inhibitor belonging to the group consisting of 5,6-dihydro-4-ethylamino-6-methyl-4H-thieno-[2,3-b]thiopyran-2-sulfonamide-7,7 dioxide hydrochloride or 2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-1,1-dioxide and their traps and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material.
The term "prostaglandin or prostaglandin derivative", within this invention refers to those naturally occurring prostaglandins that are useful for lowering intraocular pressure, specifically prostaglandins A,B,C,D,E,F and J class as well as synthetically modified prostaglandins including but not limited to 15-keto (oxo group in place of OH at 15) 13,14-dihydro (single bond in place of double bond between positions 13 and 14), and esters thereof.
Prostaglandins of the F class, particularly PGF2«
derivatives are known to be particularly potent at lowering intraocular pressure. PGF2« prostaglandin derived hypotensive lipids, in which the carboxylic acid group on the a-chain link of the basic prostaglandin structure is replaced with electrochemically neutral substituents, are also known to be particularly potent at lowering intraocular pressure. In particular, the hypotensive lipids intended for the claimed invention are those compounds which increase aqueous humor outflow without any meaningful interaction with the FP prostaglandin receptor and little or no stimulation of the other prostanoid receptors (DP, EPl-4, IP, TP).
Examples of such lipids are taught in US Patent Nos. 4,494,274;
5,034,413; 5,656,635; 5,516,791, 5,385,945, 5,688,819, 5,352,708 and 5,607978 all incorporated herein by reference.
Although Formula I shows a basic skeleton having twenty carbon atoms, the prostaglandin compounds used in the present invention are not limited to those having the same number of carbon 10 atoms. The carbon atoms in Formula (I) are numbered 2 to 7 on the (a-chain starting from the a-carbon atom adjacent to the carboxylic carbon atom which is numbered I and towards the five membered ring 8 to 12 on the ring starting from the carbon atom on which the a-chain is attached, and 13 to 20 on the w-chain starting from the carbon atom adjacent to the ring. When the number of carbon atoms is decreased on the a-chain, the number is deleted in order starting from position 2 and when the number of carbon atoms is increased in the a-chain compounds are named as stbstituted derivatives having, substituents at position 1 in place of carboxy group at C-1. Similarly, when the number of carbon atoms is decreased in the w-chain, the number is deleted in order starting from position 20 and when the number of carbon atoms is increased on the co-chain, compounds are named as substituted derivatives having respective substituent at position 20.
Thus, 13,14-dihydro-15-keto-PG compounds having 10 carbon atoms in the c~-chain are 13,14-dihydro-15-keto-20-ethyl PGs. The term prostaglandin derivative also includes esters of the C-1 carboxyl group, such as the C1-5 alkyl esters.
The hypotensive lipids contemplated by the claimed invention include PGFZa lipid analogs which, unlike PGF2a" exhibit no meaningful interaction with recombinant or constitutively expressed FP
receptors (human, moust, cat). Further the PGFZa lipid analogs exhibit only either minimal or absent interaction with other prostanoid receptors (DP, EP,_4, TP). Even with their inability to interact with with prostanoid receptors the subject PGFZa lipid analogs, having electrochemically neutral substituents, are potent and efficacious at lowering elevated intraocular pressure (IOP). Examples of such lipids are taught in US Patent Nos. 4,494,274; 5,034,413; 5,656,635;
5,385,945, 5,688,819, 5,352,708 and 5,607978 all incorporated herein by reference. A particular ocular hypotensive agent is referred to as I5 AGN 192024, disclosed in VanDenburgh et al., Investigative Oph. and Vis. Sci. March 15, 1998, Vol. 39, No.4. p. S258 abstract 1177 and at the May 10-15, 1998 Association for Research in Vision and Ophthalmology (ARVO) meeting by Allergan of Irvine, California.
The novel ophthalmic formulations of this invention comprise about 0.025 to 5% (w/w), usually about 0.5 to 3% (w/w) and more preferably about 0.7 to about 2% (w/w) of the carbonic anhydrase inhibitors discussed herein, preferably 5,6-dihydro-4-ethylamino-6-methyl-4H-thieno-[2,3-b]thiopyran-2-sulfonamide-7,7 dioxide hydrochloride or 2H-thieno[3,2-a]-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-1,1-dioxide and their trans and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material, 0.01 to 1.0%, preferably about 0.1 to 0.5% {w/w) of a f3-adrenergic antagonist such as betaxolol, bufenolol, carteolol, levobunolol, metipranolol, timolol or an ophthalmologically acceptable salt thereof, and about 0.001 to 2.0% (w/w), preferably about 0.1 to 1 % (w/w) of the prostaglandin or prostaglandin derivatives discussed herein, preferably 13,14-dihydro-15(R)-17-phenyl-18,19,20-trinor-PGF2a esters or 13, 14-dihydro-15-keto-20-ethyl-PGF2a isopropryl esters, and more preferably isopropyl 7-[3a,5a dihydroxy-2-(3a-hydroxy-5--lE-pentenyl)cyclopentylJ-SZ-heptenoic acid;
isopropyl (Z)-7-[(1R,2R,3R,SS)-3,S-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]-5-heptenoate;
(+)-(Z)-sodium-7-[1R, 2R, 3R, SS)-3,5-dihydroxy-2-[(E)-1-octenyl]cyclopentyl]-5-heptenoate sesquihydrate;
13,14-dihydro-15-keto-20-ethyl-PGF2a isopropyl ester trimethylphenol-1-acetate, (+)-isopropyl fluprostenol; 13,14-dihydro-PGF~p isoprpopyl esters; [2R(lE, 3R),3S(4Z),4R]-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanylJ-4-heptanoate; or a hypotensive lipid derived from a prostaglandin or prostaglandin derivative such as lipids derived from PGF2~, prostaglandins, in which the carboxylic acid on the a-chain has been replaced by an electrochemically neutral substituent, to be administered on a 1 to 2 times a day schedule.
A novel method of this invention comprises the topical ocular administration of about 0.025 to about 5 mg per day, preferably about 0.25 to about 3 mg per day of a carbonic anhydrase inhibitor, concomitant, prior or previous administration of about 0.005 to about 1 mg per day, preferably about 0.05 to about 0.5 mg per day of (3-adrenergic antagonist and concomitant, prior, or previous administration of about 0.001 to 2 mg per day, preferably about 0.1 to 1.0 mg per day, of prostaglandin or prostaglandin derivative to each eye.
Suitable subjects for the administration of the formulation of the present invention include mammals, primates, man, and other animals, particularly man and domesticated animals such as cats and dogs. For topical ocular administration the novel formulations of this invention may take the form of solutions, gels, ointments, suspensions or solid inserts, formulated so that a unit dosage comprises a therapeutically effective amount of each active component or some submultiple thereof.
Typical ophthalmologically acceptable carriers for the novel formulations are, for example, water, mixtures of water and water-miscible solvents such as lower alkanols or aralkanols, vegetable oils, polyalkylene glycols, petroleum based jelly, ethyl cellulose, ethyl oleate, carboxymethylcellulose, polyvinylpyrrolidone, isopropyl myristate and other conventionally employed acceptable carriers. The pharmaceutical preparation may also contain non-toxic auxiliary substances such as emulsifying, preserving, wetting agents, bodying agents and the like, as for example, polyethylene glycols 200, 300, 400 and 600, carbowaxes 1,000, 1,500, 4,000, 6,000 and 10,000, antibacterial components such as quaternary ammonium compounds, phenylmercuric salts known to have cold sterilizing properties and which are non-injurious in use, thimerosal, benzalkonium chloride, methyl and propyl paraben, benzyldodecinium bromide, benzyl alcohol, phenylethanol, buffering ingredients such as sodium chloride, sodium borate, sodium acetate, or gluconate buffers, and other conventional ingredients such as sorbitan monolaurate, triethanolamine, polyoxyethylene sorbitan monopalmitylate, dioctyl sodium sulfosuccinate, monothioglycerol, thiosorbitol, ethylenediamine tetra acetic acid, and the like. Additionally, suitable ophthalmic vehicles can be used as carrier media for the present purpose including conventional phosphate buffer vehicle systems, isotonic boric acid vehicles, isotonic sodium chloride vehicles, isotonic sodium borate vehhicles and the like.
The formulation may also include a gum such as gellan gum at a concentration of 0.1 % to 2% by weight so that the aqueous eyedrops gel on contact with the eye, thus providing the advantages of a solid ophthalmic insert as described in U.S. Patent 4,861,760.
The formulation may also include a gum such as xanthan gum at a concentration of 0.1 to 2%, preferably 0.4 to 0.7%(w/w).
Particularly preferred is KELTROLTMT xanthan gum from Monsanto Performance Materials. The formulation of the instant invention employing xanthan gum will be a hypotonic solution, with a freezing point depression between about -0.28°C and -0.4°C, and preferably between about -0.31 °C and -0.37°C. Alternatively, the hypotonicity of the ophthalmic solutoins of the present invention employing xanthan gum will be between about 150 and 215 mOs/kg, and preferably between 170 and 200 mOs/kg. Coventional ophthalmic solutions are usually prepared as isotonic solutions using tonicity adjusting agents as potassium chloride, sodium chloride, mannitol, dextrose and glycerin.
An isotonic solution will have a freezing point depression of approximately -0.54 C. Tonicity may also be measured by the osmolality of the solution, an isotonic solution having an osmolality of about 290 milliosmoles per kilogram (mOs/kg).
The pharmaceutical preparation may also be in the form of a solid insert such as one which after dispensing the drug remains essentially intact as described in U.S. Patents 4,256,108; 4,160,452; and 4,265,874; or a bio-erodible insert that either is soluble in lacrimal fluids, or otherwise disintegrates as described in U.S. Patent 4,287,175 or EPO publication 0,077,261.
The pharmaceutical preparation may also be in the form of a suspension utilizing carbonic anhydrase inhibitors (CAI's) having aqueous solubilities greater than 10 ~.g/mL but less than 1000 p.g/mL at pH 7.4, octanol/water distribution coefficients (DC) measured at pH 7.4 of from 1.0 to 150 and dissociation constants (Ki) of 1.0 nM or lower.
The aqueous solubility is measured, for example, by mixing the CAI, in its neutral or salt form in 0.1 M phosphate buffer at a pH of 7.4. The mixture is then agitated for approximately 16 to 24 hours, while maintaining a pH of 7.4. If the mixture is a solution, a small amount of a seed crystal of the neutral CAI is added and the mixture is stirred for approximately 16 to 24 hours. The solid/liquid mixture is filtered throught a 0.45 p.m filter and the filtrated is assayed by HPLC against standards. The solubility as measured includes both the neutral and ionized forms of the CAI. Under these conditions, at pH 7.4, the CAI's employed for the suspension are predominantly unionized, with the possibility of 10 to 20% of the anionic sulfonamide present (depending on the pKa of the primary sulfonamide group). By way of an example, the suspension encompassed within the meaning of this invention is one which comprises 0.1-10.9 wt% of a carbonic anhydrase inhibitor and 0.01-10.0 wt.% of a polyethoxylated derivative of castor oil resulting WO 00/04898 PC'TNS99/16143 from the reaction of from 2-200 moles of ethylene oxide per 1 mole of castor oil, wherein the derivatives can be hydrogenated.
The measure of the dissociation constant is determined using the fluorescence competition assay which uses the fluorescent HCAII:dansylamide complex and is well known in the art, Chen et al., J.
Biol. Chem., 242, 5813 ( 1967) and Ponticello et al., J. Med. Chem., 30, 591 ( 1987). The relative Kis for the suspension are less than 3.3.
The following examples of ophthalmic formulations are given by way of illustration and are not limitative of the invention.
SOLUTION COMPOSITION I II III
(S,S)-(-}-5,6-dihydro-4-ethyl-amino-6-methyl-4H-thieno-[2,3bJthiopyran-2-sulfonamide-7,7-dioxide monohydrochloride 22.26 g 22.26 g 1.113 g {carbonic anhydrase inhibitor) 13,14-dihydro-15-keto-20-ethyl-PGF2. isopropyl ester (prostaglandin derivative) 10.0 g 1.0 g 1.U g (s)-(-)-1-(tert-butylamino)-3- 6.834 h 1.367 g 6.834 g [(4-morpholino-1,2,5-thiadiazol-3-yl)oxy]-2-propanol maleate Sodium citrate.2H20 2.940 g 2.940 g 2.940 g Benzalkonium Chloride 0.075 g 0.075 g 0.075 Hydroxyethylcellulose 5.00 g 5.00 g 5.00 g Sodium hydroxide q.s. pH = 6.0 pH = 6.0 pH = 6.0 Mannitol 16.00 g 21.00 g 35.90 g Water for injection q.s. ad. 1000 g 1000 g 1000 g The active compounds, phosphate buffer salts, benzalkonium chloride, and Polysorbate $0 are added to and suspended or dissolved in water. The pH of the composition is adjusted to 5.5-6.0 and diluted 30 to volume. The composition is rendered sterile by filtration through a sterilizing filter.
Following the procedures of Example l, solutions are prepared substituting the compounds below for the carbonic anhydrase inhibitors:
Compound Example No.
(S,S)-(-)-5,6-dihydro-4-ethylamino- 2 6-methyl-4H-thieno[2,3b]thiopyran-2-sulfonamide-7,7-dioxide (S,S)-(-)- 3,4-dihydro-4-ethylamino-2-methyl-2H-thieno[3,2-a]-1,2-thiazine-6-sulfon- 3 amide-1,1-dioxide hydrochloride R-(+)-3,4-dihydro-4-ethylamino-2-methyl-2H-thieno[3,2-a]-1,2- 4 thiazine-6-sulfonamide-l,l-dioxide hydrochloride R-(+)-3,4-dihydro-4-ethylamino-2-(2-methoxy)ethyl-2H-thieno[3,2-a]-1,2-thiazine-6-sulfonamide-1,1-dioxide hydrochloride (S,S)-(-)-5,6-dihydro-4-ethylamino- 6 6-propyl-4H-thieno[2,3b]thiopyran-2-sulfonamide-7,7-dioxide 2H-thieno[3,2-a]-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2- 7 (3-methoxypropyl)-l, l-dioxide EXAMPLE 8(Suspension,~
CONCENTRATION
WT/V%
R-(+)-4-ethylamino-3,4-dihydro-2-(3-methoxy) propyl-2H-thieno[3,2-a]-1,2-thiazine-6-sulfonamide l, l-dioxide 2%+2% xs (s)-(-)-1-(tert-butylamino)-3- 0.5%
[(4-morpholino-1,2,5-thiadiazol-3-yl)oxy]-2-propanol maleate ((3-adrenergic antagonist) 13,14-dihydro-15-keto-20-ethyl-PGF2a isopropyl ester (prostaglandin derivative) 0.5%
Hydroxypropylmethylcellulose 3%
Dibasic Sodium Phosphate 0.2%
This invention relates to novel ophthalmic compositions comprising a pharmaceutically acceptable carrier, a topical carbonic anhydrase inhibitor or an ophthamologically acceptable salt thereof, a !3-adrenergic antagonist or an ophthamologically acceptable salt thereof and a prostaglandin or prostaglandin derivative thereof such as a hypotensive lipid derived from PGF2a prostaglandins.
In one aspect of the invention a composition comprising 0.025 to 5% (w/w) of a compound of the structural formula II
Z
Q
~~-S02NH2 S (II) an individual diastereomer, an individual enantiomer or mixture thereof, or an ophthalmologically acceptable salt thereof, wherein:
I5 A is carbon or nitrogen, preferably carbon;
Z is -NHR or -OR, preferably -NHR;
R is C,_6alkyl, either straight or branched chain, preferably C~_4alkyl such as ethyl, propyl or isobutyl;
Q is {H, H), oxo or thioxo;
R' is (a) hydrogen, (b) C,_~alkyl, preferably methyl, ethyl or n-propyl, or (c) C,_4alkoxy-C,_4alkyl, preferably 3-methoxypropyl or ethoxymethyl; and X is -S(O)2- or -C(O)-, preferably -S(O)2-; 0.01 to 1.0% of a 13-adrenergic antagonist such as betaxolol, bufenolol, carteolol, levobunolol, metipranolol, timolol or an ophthalmologically acceptable salt thereof, preferably betaxolol or timolol, 0.005 to 2%
(w/w) of a prostaglandin such as 13,14-dihydro-15 (R)-17-phenyl-18,19,20-trinor-PGF2oc ester, or 13, 14-dihydro-15-keto-20-ethyl-PGF2a, or a prostaglandin derivative such as a hypotensive lipid derived from PGF2a prostaglandins and their traps and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material is disclosed. Said composition can optionally contain a gum belonging to the group consisting of gellan gum or xanthan gum.
Another aspect of the invention is concerned with the use of the novel ophthalmic compositions in the treatment of ocular hypertension or glaucoma.
DETAILED DESCRIPTION OF THE INVENTION
This invention relates to novel ophthalmic combinations comprising a pharmaceutically acceptable carrier, a topical carbonic anhydrase inhibitor or an ophthamologically acceptable salt thereof, 13-adrenergic antagonist or an ophthamologically acceptable salt thereof and a prostaglandin or prostaglandin derivative thereof, which are used in the treatment of ocular hypertension and glaucoma.
Another aspect of this invention is realized when in the compounds of structural formula II A is carbon; and wherein R is -CH~CH~ and R' is -CH3; or R is -CH2CH2CH~ and R' is CHZCH~CHZOCH~; or R is -CHZCH; and R' is -CHZCH~CH3; or R is -CHZCH~(CH~)2 and R' is hydrogen; or R is -CH~CH~ and R' is -CH~OCH~CH~; and carbons 4 and 6 of the topical carbonic anhydrase inhibitor both have S absolute stereochemical configuration.
Another aspect of this invention is realized when in the compounds of structural formula II A is nitrogen; and wherein R is -CHzCH~ and R' is -CHI; or R is -CHZCHZCH~ and R' is -CHZCH2CH20CH~; or R is -CH~CH3 and R' is -CH2CHZCHj; or R is -CHZCH2(CH~)2 and R' is hydrogen; or R is -CH,CH~ and R' is -CH20CH2CH3.
A preferred topical carbonic anhydrase inhibitor for use in the novel compositions of the present invention is 5,6-dihydro-4-ethylamino-6-methyl-4H-thieno-[2,3-bJthiopyran-2-sulfonamide-7,7 dioxide hydrochloride or 2H-thieno[3,2-e)-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-l,l-dioxide and their trans and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material.
_ 'j _ The carbon atoms to which Z and R' are bonded may be chiral. When named according to absolute configuration, e.g., (R,S) or (S,S), the first letter represents the chirality the carbon atom to which Z
is bonded and the second letter represents the chirality of A when A is carbon. The carbonic anhydrase inhibitors of this invention accordingly may be used as diastereomeric mixtures or single enantiomers or as racemlc mixtures.
Still another aspect of this invention is realized when the prostaglandin isl l, 15-dipivaloyl PGF2a, 11-pivaloyl prostaglandin F2a hydroxyethyl ester, (+)-(Z)-sodium-7-[1R, 2R, 3R, 5S)-3,5-dihydroxy-2-[(E)-1-octenyl)cyclopentyl)-5-heptenoate sesquihydrate, [ 1 a,2(3,3a,5a]methyl-5-cis-2-(phenylethylsulfonamidomethyl)-3,5-dihydroxycyclopentyl heptenoate, (+-)-5-[6-(1-hydroxy)hexyl)-1,3-benzodioxol-5-yl)-pentanol, 15-pivaloyl PGFa, 7-[3a,5a dihydroxy-2-(3a-hydroxy-5--lE-pentenyl)cyclopentyl)-5Z-heptenoic acid, isopropyl (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl)cyclopentyl)-5-heptenoate, 13,14-dihydro-15(R)-17-phenyl-18,19,20-trinor-PGF2a esters, 13,14-dihydro-15-keto-20-ethyl-PGF2a isopropyl ester, (+)-isopropyl fluprostenol, [2R(lE, 3R),3S(4Z),4R)-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl)-4-heptanoate, 13,14-dihydro-PGF2p isoprpopyl esters, or 13,14-dihydro-15-keto-20-ethyl-PGFZa isopropyl ester trimethylphenol-l -acetate.
Another aspect of this invention is realized when hypotensive lipids derived from a prostaglandin or prostaglandin derivative such as lipids derived from PGFZa prostaglandins, in which the carboxylic acid group on the a-chain link of the basic prostaglandin _g_ structure is replaced with electrochemically neutral substituents, is used.
An example of a hypotensive lipid is that in which the carboxylic acid group is replaced with a C,_6 alkoxy group such as OCH~ (PGF2~ 1-OCH3), or a hydroxy group (PGF2~ 1-OH).
In another aspect of this invention, the novel ophthalmic compositions of this invention comprise a pharmaceuticallly acceptable carrier, a therapeutically effective amount of 7-[3a,5a dihydroxy-2-(3a-hydroxy-5--lE-pentenyl)cyclopentyl]-SZ-heptenoic acid;
isopropyl (Z)-7-[(1R,2R,3R,SS)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]-5-heptenoate;
(+)-(Z)-sodium-7-[1R, 2R, 3R, SS)-3,5-dihydroxy-2-[(E)-1-octenyl]cyclopentyl]-5-heptenoate sesquihydrate;
13,14-dihydro-15-keto-20-ethyl-PGF2a isopropyl ester trimethylphenol-1-acetate; (+)-isopropyl fluprostenol; 13,14-dihydro-PGF2p isoprpopyl esters; [2R(lE, 3R),3S(4Z),4R]-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate; or hypotensive lipids derived from a prostaglandin or prostaglandin derivative such as lipids derived from PGF2a prostaglandins wherein the COON is replaced with electrochemically neutral substituents like C,_6 alkoxy or hydroxy, 13-adrenergic antagonists such as betaxolol, bufenolol, carteolol, levobunolol, metipranolol, timolol or an ophthalmologically acceptable salt thereof and a topical carbonic anhydrase inhibitor belonging to the group consisting of 5,6-dihydro-4-ethylamino-6-methyl-4H-thieno-[2,3-b]thiopyran-2-sulfonamide-7,7 dioxide hydrochloride or 2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-1,1-dioxide and their traps and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material.
The term "prostaglandin or prostaglandin derivative", within this invention refers to those naturally occurring prostaglandins that are useful for lowering intraocular pressure, specifically prostaglandins A,B,C,D,E,F and J class as well as synthetically modified prostaglandins including but not limited to 15-keto (oxo group in place of OH at 15) 13,14-dihydro (single bond in place of double bond between positions 13 and 14), and esters thereof.
Prostaglandins of the F class, particularly PGF2«
derivatives are known to be particularly potent at lowering intraocular pressure. PGF2« prostaglandin derived hypotensive lipids, in which the carboxylic acid group on the a-chain link of the basic prostaglandin structure is replaced with electrochemically neutral substituents, are also known to be particularly potent at lowering intraocular pressure. In particular, the hypotensive lipids intended for the claimed invention are those compounds which increase aqueous humor outflow without any meaningful interaction with the FP prostaglandin receptor and little or no stimulation of the other prostanoid receptors (DP, EPl-4, IP, TP).
Examples of such lipids are taught in US Patent Nos. 4,494,274;
5,034,413; 5,656,635; 5,516,791, 5,385,945, 5,688,819, 5,352,708 and 5,607978 all incorporated herein by reference.
Although Formula I shows a basic skeleton having twenty carbon atoms, the prostaglandin compounds used in the present invention are not limited to those having the same number of carbon 10 atoms. The carbon atoms in Formula (I) are numbered 2 to 7 on the (a-chain starting from the a-carbon atom adjacent to the carboxylic carbon atom which is numbered I and towards the five membered ring 8 to 12 on the ring starting from the carbon atom on which the a-chain is attached, and 13 to 20 on the w-chain starting from the carbon atom adjacent to the ring. When the number of carbon atoms is decreased on the a-chain, the number is deleted in order starting from position 2 and when the number of carbon atoms is increased in the a-chain compounds are named as stbstituted derivatives having, substituents at position 1 in place of carboxy group at C-1. Similarly, when the number of carbon atoms is decreased in the w-chain, the number is deleted in order starting from position 20 and when the number of carbon atoms is increased on the co-chain, compounds are named as substituted derivatives having respective substituent at position 20.
Thus, 13,14-dihydro-15-keto-PG compounds having 10 carbon atoms in the c~-chain are 13,14-dihydro-15-keto-20-ethyl PGs. The term prostaglandin derivative also includes esters of the C-1 carboxyl group, such as the C1-5 alkyl esters.
The hypotensive lipids contemplated by the claimed invention include PGFZa lipid analogs which, unlike PGF2a" exhibit no meaningful interaction with recombinant or constitutively expressed FP
receptors (human, moust, cat). Further the PGFZa lipid analogs exhibit only either minimal or absent interaction with other prostanoid receptors (DP, EP,_4, TP). Even with their inability to interact with with prostanoid receptors the subject PGFZa lipid analogs, having electrochemically neutral substituents, are potent and efficacious at lowering elevated intraocular pressure (IOP). Examples of such lipids are taught in US Patent Nos. 4,494,274; 5,034,413; 5,656,635;
5,385,945, 5,688,819, 5,352,708 and 5,607978 all incorporated herein by reference. A particular ocular hypotensive agent is referred to as I5 AGN 192024, disclosed in VanDenburgh et al., Investigative Oph. and Vis. Sci. March 15, 1998, Vol. 39, No.4. p. S258 abstract 1177 and at the May 10-15, 1998 Association for Research in Vision and Ophthalmology (ARVO) meeting by Allergan of Irvine, California.
The novel ophthalmic formulations of this invention comprise about 0.025 to 5% (w/w), usually about 0.5 to 3% (w/w) and more preferably about 0.7 to about 2% (w/w) of the carbonic anhydrase inhibitors discussed herein, preferably 5,6-dihydro-4-ethylamino-6-methyl-4H-thieno-[2,3-b]thiopyran-2-sulfonamide-7,7 dioxide hydrochloride or 2H-thieno[3,2-a]-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-1,1-dioxide and their trans and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material, 0.01 to 1.0%, preferably about 0.1 to 0.5% {w/w) of a f3-adrenergic antagonist such as betaxolol, bufenolol, carteolol, levobunolol, metipranolol, timolol or an ophthalmologically acceptable salt thereof, and about 0.001 to 2.0% (w/w), preferably about 0.1 to 1 % (w/w) of the prostaglandin or prostaglandin derivatives discussed herein, preferably 13,14-dihydro-15(R)-17-phenyl-18,19,20-trinor-PGF2a esters or 13, 14-dihydro-15-keto-20-ethyl-PGF2a isopropryl esters, and more preferably isopropyl 7-[3a,5a dihydroxy-2-(3a-hydroxy-5--lE-pentenyl)cyclopentylJ-SZ-heptenoic acid;
isopropyl (Z)-7-[(1R,2R,3R,SS)-3,S-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]-5-heptenoate;
(+)-(Z)-sodium-7-[1R, 2R, 3R, SS)-3,5-dihydroxy-2-[(E)-1-octenyl]cyclopentyl]-5-heptenoate sesquihydrate;
13,14-dihydro-15-keto-20-ethyl-PGF2a isopropyl ester trimethylphenol-1-acetate, (+)-isopropyl fluprostenol; 13,14-dihydro-PGF~p isoprpopyl esters; [2R(lE, 3R),3S(4Z),4R]-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanylJ-4-heptanoate; or a hypotensive lipid derived from a prostaglandin or prostaglandin derivative such as lipids derived from PGF2~, prostaglandins, in which the carboxylic acid on the a-chain has been replaced by an electrochemically neutral substituent, to be administered on a 1 to 2 times a day schedule.
A novel method of this invention comprises the topical ocular administration of about 0.025 to about 5 mg per day, preferably about 0.25 to about 3 mg per day of a carbonic anhydrase inhibitor, concomitant, prior or previous administration of about 0.005 to about 1 mg per day, preferably about 0.05 to about 0.5 mg per day of (3-adrenergic antagonist and concomitant, prior, or previous administration of about 0.001 to 2 mg per day, preferably about 0.1 to 1.0 mg per day, of prostaglandin or prostaglandin derivative to each eye.
Suitable subjects for the administration of the formulation of the present invention include mammals, primates, man, and other animals, particularly man and domesticated animals such as cats and dogs. For topical ocular administration the novel formulations of this invention may take the form of solutions, gels, ointments, suspensions or solid inserts, formulated so that a unit dosage comprises a therapeutically effective amount of each active component or some submultiple thereof.
Typical ophthalmologically acceptable carriers for the novel formulations are, for example, water, mixtures of water and water-miscible solvents such as lower alkanols or aralkanols, vegetable oils, polyalkylene glycols, petroleum based jelly, ethyl cellulose, ethyl oleate, carboxymethylcellulose, polyvinylpyrrolidone, isopropyl myristate and other conventionally employed acceptable carriers. The pharmaceutical preparation may also contain non-toxic auxiliary substances such as emulsifying, preserving, wetting agents, bodying agents and the like, as for example, polyethylene glycols 200, 300, 400 and 600, carbowaxes 1,000, 1,500, 4,000, 6,000 and 10,000, antibacterial components such as quaternary ammonium compounds, phenylmercuric salts known to have cold sterilizing properties and which are non-injurious in use, thimerosal, benzalkonium chloride, methyl and propyl paraben, benzyldodecinium bromide, benzyl alcohol, phenylethanol, buffering ingredients such as sodium chloride, sodium borate, sodium acetate, or gluconate buffers, and other conventional ingredients such as sorbitan monolaurate, triethanolamine, polyoxyethylene sorbitan monopalmitylate, dioctyl sodium sulfosuccinate, monothioglycerol, thiosorbitol, ethylenediamine tetra acetic acid, and the like. Additionally, suitable ophthalmic vehicles can be used as carrier media for the present purpose including conventional phosphate buffer vehicle systems, isotonic boric acid vehicles, isotonic sodium chloride vehicles, isotonic sodium borate vehhicles and the like.
The formulation may also include a gum such as gellan gum at a concentration of 0.1 % to 2% by weight so that the aqueous eyedrops gel on contact with the eye, thus providing the advantages of a solid ophthalmic insert as described in U.S. Patent 4,861,760.
The formulation may also include a gum such as xanthan gum at a concentration of 0.1 to 2%, preferably 0.4 to 0.7%(w/w).
Particularly preferred is KELTROLTMT xanthan gum from Monsanto Performance Materials. The formulation of the instant invention employing xanthan gum will be a hypotonic solution, with a freezing point depression between about -0.28°C and -0.4°C, and preferably between about -0.31 °C and -0.37°C. Alternatively, the hypotonicity of the ophthalmic solutoins of the present invention employing xanthan gum will be between about 150 and 215 mOs/kg, and preferably between 170 and 200 mOs/kg. Coventional ophthalmic solutions are usually prepared as isotonic solutions using tonicity adjusting agents as potassium chloride, sodium chloride, mannitol, dextrose and glycerin.
An isotonic solution will have a freezing point depression of approximately -0.54 C. Tonicity may also be measured by the osmolality of the solution, an isotonic solution having an osmolality of about 290 milliosmoles per kilogram (mOs/kg).
The pharmaceutical preparation may also be in the form of a solid insert such as one which after dispensing the drug remains essentially intact as described in U.S. Patents 4,256,108; 4,160,452; and 4,265,874; or a bio-erodible insert that either is soluble in lacrimal fluids, or otherwise disintegrates as described in U.S. Patent 4,287,175 or EPO publication 0,077,261.
The pharmaceutical preparation may also be in the form of a suspension utilizing carbonic anhydrase inhibitors (CAI's) having aqueous solubilities greater than 10 ~.g/mL but less than 1000 p.g/mL at pH 7.4, octanol/water distribution coefficients (DC) measured at pH 7.4 of from 1.0 to 150 and dissociation constants (Ki) of 1.0 nM or lower.
The aqueous solubility is measured, for example, by mixing the CAI, in its neutral or salt form in 0.1 M phosphate buffer at a pH of 7.4. The mixture is then agitated for approximately 16 to 24 hours, while maintaining a pH of 7.4. If the mixture is a solution, a small amount of a seed crystal of the neutral CAI is added and the mixture is stirred for approximately 16 to 24 hours. The solid/liquid mixture is filtered throught a 0.45 p.m filter and the filtrated is assayed by HPLC against standards. The solubility as measured includes both the neutral and ionized forms of the CAI. Under these conditions, at pH 7.4, the CAI's employed for the suspension are predominantly unionized, with the possibility of 10 to 20% of the anionic sulfonamide present (depending on the pKa of the primary sulfonamide group). By way of an example, the suspension encompassed within the meaning of this invention is one which comprises 0.1-10.9 wt% of a carbonic anhydrase inhibitor and 0.01-10.0 wt.% of a polyethoxylated derivative of castor oil resulting WO 00/04898 PC'TNS99/16143 from the reaction of from 2-200 moles of ethylene oxide per 1 mole of castor oil, wherein the derivatives can be hydrogenated.
The measure of the dissociation constant is determined using the fluorescence competition assay which uses the fluorescent HCAII:dansylamide complex and is well known in the art, Chen et al., J.
Biol. Chem., 242, 5813 ( 1967) and Ponticello et al., J. Med. Chem., 30, 591 ( 1987). The relative Kis for the suspension are less than 3.3.
The following examples of ophthalmic formulations are given by way of illustration and are not limitative of the invention.
SOLUTION COMPOSITION I II III
(S,S)-(-}-5,6-dihydro-4-ethyl-amino-6-methyl-4H-thieno-[2,3bJthiopyran-2-sulfonamide-7,7-dioxide monohydrochloride 22.26 g 22.26 g 1.113 g {carbonic anhydrase inhibitor) 13,14-dihydro-15-keto-20-ethyl-PGF2. isopropyl ester (prostaglandin derivative) 10.0 g 1.0 g 1.U g (s)-(-)-1-(tert-butylamino)-3- 6.834 h 1.367 g 6.834 g [(4-morpholino-1,2,5-thiadiazol-3-yl)oxy]-2-propanol maleate Sodium citrate.2H20 2.940 g 2.940 g 2.940 g Benzalkonium Chloride 0.075 g 0.075 g 0.075 Hydroxyethylcellulose 5.00 g 5.00 g 5.00 g Sodium hydroxide q.s. pH = 6.0 pH = 6.0 pH = 6.0 Mannitol 16.00 g 21.00 g 35.90 g Water for injection q.s. ad. 1000 g 1000 g 1000 g The active compounds, phosphate buffer salts, benzalkonium chloride, and Polysorbate $0 are added to and suspended or dissolved in water. The pH of the composition is adjusted to 5.5-6.0 and diluted 30 to volume. The composition is rendered sterile by filtration through a sterilizing filter.
Following the procedures of Example l, solutions are prepared substituting the compounds below for the carbonic anhydrase inhibitors:
Compound Example No.
(S,S)-(-)-5,6-dihydro-4-ethylamino- 2 6-methyl-4H-thieno[2,3b]thiopyran-2-sulfonamide-7,7-dioxide (S,S)-(-)- 3,4-dihydro-4-ethylamino-2-methyl-2H-thieno[3,2-a]-1,2-thiazine-6-sulfon- 3 amide-1,1-dioxide hydrochloride R-(+)-3,4-dihydro-4-ethylamino-2-methyl-2H-thieno[3,2-a]-1,2- 4 thiazine-6-sulfonamide-l,l-dioxide hydrochloride R-(+)-3,4-dihydro-4-ethylamino-2-(2-methoxy)ethyl-2H-thieno[3,2-a]-1,2-thiazine-6-sulfonamide-1,1-dioxide hydrochloride (S,S)-(-)-5,6-dihydro-4-ethylamino- 6 6-propyl-4H-thieno[2,3b]thiopyran-2-sulfonamide-7,7-dioxide 2H-thieno[3,2-a]-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2- 7 (3-methoxypropyl)-l, l-dioxide EXAMPLE 8(Suspension,~
CONCENTRATION
WT/V%
R-(+)-4-ethylamino-3,4-dihydro-2-(3-methoxy) propyl-2H-thieno[3,2-a]-1,2-thiazine-6-sulfonamide l, l-dioxide 2%+2% xs (s)-(-)-1-(tert-butylamino)-3- 0.5%
[(4-morpholino-1,2,5-thiadiazol-3-yl)oxy]-2-propanol maleate ((3-adrenergic antagonist) 13,14-dihydro-15-keto-20-ethyl-PGF2a isopropyl ester (prostaglandin derivative) 0.5%
Hydroxypropylmethylcellulose 3%
Dibasic Sodium Phosphate 0.2%
Sodium Chloride 0.7%
Disodium Edetate 0.01 %
Polysorbate 80 0.05%
Benzalkonium Chloride 0.01 %
NaOH/HCl pH adjust Purified Water q.s. 100%
The suspension may be prepared by heating 400 mL of purified water to boiling. HPMC (30.Og) is added and the mixture stirred vigorously until homegeneous. To this is added a solution consisting of sodium chloride (7.0 g), dibasic sodium phosphate (2.Og), disodium edta (O.lg), polysorbate 80 (O.Sg) and benzalkonium chloride ( 10.5 mL of a 1 % solution) and purified water is added to a final volume of 900 mL. The mixture is stirred and cooled in an ice bath to room temperature and the pH is adjusted to 7.2 employing HCl (3.5 mL
of a 1 N solution. The mixture is q.s. to the final weight with purified water (total lOlOg) and filtered through a 10 micron filter. The formulation is prepared by the addition of the above HPMC vehicle ( 15.014 g) to the above TCAI (0.3074 g) and prostaglandin ( 1.0 g) and the mixture ias ball milled with 3 mm glass beads (5 g) for approximately 45 hours.
Following the procedures of Example 1, solutions are prepared substituting the compounds below for the prostaglandin derivative - 1$ -Compound Example No.
PGF2a,-1-isopropyl ester g 13,14-dihydro-15-keto-PGE2 11 methyl ester 15-keto-PGF2a 12 PGF2a tromethamine salt 13 PGF2a derived hypotensive lipid 15 (+)-isopropyl fluprostenol 16 [2R(lE, 3R),3S(4Z),4RJ-isopropyl- 1'7 7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate;
3o SOLUTION COMPOSITION I II
5,6-dihydro-4-ethylamino 6-methyl-4H-thieno[2,3b]thiopyran-2-sulfonamide-7,7-dioxide monohydrochloride 2.0 mg 0.2 mg (carbonic anhydrase inhibitor) (s)-(-)-1-(tert-butylamino)-3-[(4-morpholino-1,2,5-thiadiazol-3-yl)oxy]-2-propanol maleate 0.6 mg 0.1 mg ((3-adrenergic antagonist) 13,14-dihydro-15-keto-20-ethyl-PGF2a isopropyl ester trimethylphenol-1-acetate 0.1 mg 1.0 mg GelriteTM gellan gum 6.0 mg 6.0 mg Monobasic sodium phosphate Quantity sufficient to give .2H20 Dibasic sodium phosphate final pH 5.5 - 6.0 .12H20 Benzyldodecinium bromide 0.10 mg 0.10 mg Polysorbate 80 0.2 mg 0.2 mg Water for injection q.s. ad. 1.0 mL 1.0 mL
The active compounds, Gelrite' gellan gum, phosphate buffer salts, benzyldodecinium bromide and Polysorbate 80 are added to and suspended or dissolved in water. The pH of the composition is adjusted to 5.5-6.0 and diluted to volume. The composition is rendered sterile by ionizing radiation.
Following the procedures of Example 16, solutions are prepared substituting the compounds below for the carbonic anhydrase inhibitors:
Compound Example No.
(S,S)-(-)-5,6-dihydro-4-ethylamino-6-methyl-4H-thien6[2,3b]thiopyran- 19 2-sulfonamide-7,7-dioxide 3,4-dihydro-4-ethylamino-2-methyl-2H-thieno(3,2-a]-1,2-thiazine-6-sulfon- 20 amide-1,1 dioxide hydrochloride R-(+)-3,4-dihydro-4-ethylamino-2-methyl-2H-thieno[3,2-a]-1,2- 21 thiazine-6-sulfonamide-1,1-dioxide hydrochloride R-(+)-3,4-dihydro-4-ethylamino-2- 22 (2-methoxy)ethyl-2H-thieno[3,2-a]-1,2-thiazine-6-sulfonamide-1,1-dioxide hydrochloride (S,S)-trans-5,6-dihidro-4-ethylamino- 23 6-propyl-4H-thieno[2,3b]thiopyran-2-sulfonamide-7,7- dioxide 2H-thieno[3,2-e)-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2- 24 (3-methoxypropyl)-1,1-dioxide Following the procedures of Example 16, solutions are prepared substitutiilg the compounds below for the prostaglandin derivative.
Compound Example PGF2a,-1-isopropyl ester 25 l0 PGA2 26 13,14-dihydro-15-keto-PGE2 2~
methyl ester 15-keto-PGF2a 2g PGF2a tromethamine salt 29 PGF2a derived hypotensive lipid 31 (+)-isopropyl fluprostenol 32 [2R(lE, 3R),3S(4Z),4R]-isopropyl- 33 7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate;
SOLUTION COMPOSITION I II
5,6-dihydro-4-ethylamino 6-methyl-4H-thieno[2,3b]thiopyran-2-sulfonamide-7,7-dioxide monohydrochloride ~ 2% 2%
(carbonic anhydrase inhibitor) 4-[2-hydroxy-3-(1-methylethyl)-amino]-propoxyl]-2,3,6-trimethylphenol-L-acetate 0.6% 0.6%
13,14-dihydro-15-keto-20-ethyl-PGF2a isopropyl ester trimethylphenol-1-acetate 0.1 % 1.0 %
Xanthan gum 0.5 % 0.7 %
Sodium Chloride 0.2% 0.2%
Benzalkonium Chloride 0.0075% 0.0075%
Sodium Hydroxide qs pH5.6 pH 5.6 Water qs 100% 100%
The active compounds, sodium chloride and benzalkonium chloride are dissolved in water for injection. The pH of the composition is adjusted to 5.6 by addition of 0.2N sodium hydroxide solution, and water for injection is added until the weight of the composition is equal to 75 parts of the final weight (I) or 65 parts of the final weight (II).
The composition is sterilized by filtration, and the solution flushed with sterile nitrogen. Then a clarified, steam sterilized concentrate of 2%
xanthan gum is added to the solution of drug and the resulting solution is homogenized by stirring. The solution is aseptically subdivided into sterile vials and sealed.
Following the procedures of Example 30, solutions are prepared substituting the compounds below for the carbonic anhydrase inhibitors:
Compound Example No.
(S,S)-(-)-5,6-dihydro-4-ethylamino-6-methyl-4H-thien6[2,3b]thiopyran- 35 2-sulfonamide-7,7-dioxide 3,4-dihydro-4-ethylamino-2-methyl-2H-thieno[3,2-a]-1,2-thiazine-6-sulfon- 36 amide-1,1 dioxide hydrochloride R-(+)-3,4-dihydro-4-ethylamino-2-methyl-2H-thieno[3,2-a]-1,2- 37 thiazine-6-sulfonamide-l,l-dioxide hydrochloride R-(+)-3,4-dihydro-4-ethylamino-2- 3g (2-methoxy)ethyl-2H-thieno[3,2-a]-1,2-thiazine-6-sulfonamide-l,l-dioxide hydrochloride (S,S)-trans-5,6-dihidro-4-ethylamino- 39 6-propyl-4H-thieno[2,3b]thiopyran-2-sulfonamide-7,7- dioxide WO 00/04898 PCT/US99/Ib143 2H-thieno[3,2-e)-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2- 40 (3-methoxypropyl)-l, l-dioxide Following the procedures of Example 30, solutions are prepared substituting the compounds below for the prostaglandin derivative.
Compound Example PGF2a-1-isopropyl ester 41 13,14-dihydro-15-keto-PGE2 43 methyl ester 15-keto-PGF2« 44 PGFz« tromethamine salt 45 PGF2« derived hypotensive lipid 47 (+)-isopropyl fluprostenol 4g [2R{lE, 3R),3S(4Z),4R]-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate;
Disodium Edetate 0.01 %
Polysorbate 80 0.05%
Benzalkonium Chloride 0.01 %
NaOH/HCl pH adjust Purified Water q.s. 100%
The suspension may be prepared by heating 400 mL of purified water to boiling. HPMC (30.Og) is added and the mixture stirred vigorously until homegeneous. To this is added a solution consisting of sodium chloride (7.0 g), dibasic sodium phosphate (2.Og), disodium edta (O.lg), polysorbate 80 (O.Sg) and benzalkonium chloride ( 10.5 mL of a 1 % solution) and purified water is added to a final volume of 900 mL. The mixture is stirred and cooled in an ice bath to room temperature and the pH is adjusted to 7.2 employing HCl (3.5 mL
of a 1 N solution. The mixture is q.s. to the final weight with purified water (total lOlOg) and filtered through a 10 micron filter. The formulation is prepared by the addition of the above HPMC vehicle ( 15.014 g) to the above TCAI (0.3074 g) and prostaglandin ( 1.0 g) and the mixture ias ball milled with 3 mm glass beads (5 g) for approximately 45 hours.
Following the procedures of Example 1, solutions are prepared substituting the compounds below for the prostaglandin derivative - 1$ -Compound Example No.
PGF2a,-1-isopropyl ester g 13,14-dihydro-15-keto-PGE2 11 methyl ester 15-keto-PGF2a 12 PGF2a tromethamine salt 13 PGF2a derived hypotensive lipid 15 (+)-isopropyl fluprostenol 16 [2R(lE, 3R),3S(4Z),4RJ-isopropyl- 1'7 7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate;
3o SOLUTION COMPOSITION I II
5,6-dihydro-4-ethylamino 6-methyl-4H-thieno[2,3b]thiopyran-2-sulfonamide-7,7-dioxide monohydrochloride 2.0 mg 0.2 mg (carbonic anhydrase inhibitor) (s)-(-)-1-(tert-butylamino)-3-[(4-morpholino-1,2,5-thiadiazol-3-yl)oxy]-2-propanol maleate 0.6 mg 0.1 mg ((3-adrenergic antagonist) 13,14-dihydro-15-keto-20-ethyl-PGF2a isopropyl ester trimethylphenol-1-acetate 0.1 mg 1.0 mg GelriteTM gellan gum 6.0 mg 6.0 mg Monobasic sodium phosphate Quantity sufficient to give .2H20 Dibasic sodium phosphate final pH 5.5 - 6.0 .12H20 Benzyldodecinium bromide 0.10 mg 0.10 mg Polysorbate 80 0.2 mg 0.2 mg Water for injection q.s. ad. 1.0 mL 1.0 mL
The active compounds, Gelrite' gellan gum, phosphate buffer salts, benzyldodecinium bromide and Polysorbate 80 are added to and suspended or dissolved in water. The pH of the composition is adjusted to 5.5-6.0 and diluted to volume. The composition is rendered sterile by ionizing radiation.
Following the procedures of Example 16, solutions are prepared substituting the compounds below for the carbonic anhydrase inhibitors:
Compound Example No.
(S,S)-(-)-5,6-dihydro-4-ethylamino-6-methyl-4H-thien6[2,3b]thiopyran- 19 2-sulfonamide-7,7-dioxide 3,4-dihydro-4-ethylamino-2-methyl-2H-thieno(3,2-a]-1,2-thiazine-6-sulfon- 20 amide-1,1 dioxide hydrochloride R-(+)-3,4-dihydro-4-ethylamino-2-methyl-2H-thieno[3,2-a]-1,2- 21 thiazine-6-sulfonamide-1,1-dioxide hydrochloride R-(+)-3,4-dihydro-4-ethylamino-2- 22 (2-methoxy)ethyl-2H-thieno[3,2-a]-1,2-thiazine-6-sulfonamide-1,1-dioxide hydrochloride (S,S)-trans-5,6-dihidro-4-ethylamino- 23 6-propyl-4H-thieno[2,3b]thiopyran-2-sulfonamide-7,7- dioxide 2H-thieno[3,2-e)-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2- 24 (3-methoxypropyl)-1,1-dioxide Following the procedures of Example 16, solutions are prepared substitutiilg the compounds below for the prostaglandin derivative.
Compound Example PGF2a,-1-isopropyl ester 25 l0 PGA2 26 13,14-dihydro-15-keto-PGE2 2~
methyl ester 15-keto-PGF2a 2g PGF2a tromethamine salt 29 PGF2a derived hypotensive lipid 31 (+)-isopropyl fluprostenol 32 [2R(lE, 3R),3S(4Z),4R]-isopropyl- 33 7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate;
SOLUTION COMPOSITION I II
5,6-dihydro-4-ethylamino 6-methyl-4H-thieno[2,3b]thiopyran-2-sulfonamide-7,7-dioxide monohydrochloride ~ 2% 2%
(carbonic anhydrase inhibitor) 4-[2-hydroxy-3-(1-methylethyl)-amino]-propoxyl]-2,3,6-trimethylphenol-L-acetate 0.6% 0.6%
13,14-dihydro-15-keto-20-ethyl-PGF2a isopropyl ester trimethylphenol-1-acetate 0.1 % 1.0 %
Xanthan gum 0.5 % 0.7 %
Sodium Chloride 0.2% 0.2%
Benzalkonium Chloride 0.0075% 0.0075%
Sodium Hydroxide qs pH5.6 pH 5.6 Water qs 100% 100%
The active compounds, sodium chloride and benzalkonium chloride are dissolved in water for injection. The pH of the composition is adjusted to 5.6 by addition of 0.2N sodium hydroxide solution, and water for injection is added until the weight of the composition is equal to 75 parts of the final weight (I) or 65 parts of the final weight (II).
The composition is sterilized by filtration, and the solution flushed with sterile nitrogen. Then a clarified, steam sterilized concentrate of 2%
xanthan gum is added to the solution of drug and the resulting solution is homogenized by stirring. The solution is aseptically subdivided into sterile vials and sealed.
Following the procedures of Example 30, solutions are prepared substituting the compounds below for the carbonic anhydrase inhibitors:
Compound Example No.
(S,S)-(-)-5,6-dihydro-4-ethylamino-6-methyl-4H-thien6[2,3b]thiopyran- 35 2-sulfonamide-7,7-dioxide 3,4-dihydro-4-ethylamino-2-methyl-2H-thieno[3,2-a]-1,2-thiazine-6-sulfon- 36 amide-1,1 dioxide hydrochloride R-(+)-3,4-dihydro-4-ethylamino-2-methyl-2H-thieno[3,2-a]-1,2- 37 thiazine-6-sulfonamide-l,l-dioxide hydrochloride R-(+)-3,4-dihydro-4-ethylamino-2- 3g (2-methoxy)ethyl-2H-thieno[3,2-a]-1,2-thiazine-6-sulfonamide-l,l-dioxide hydrochloride (S,S)-trans-5,6-dihidro-4-ethylamino- 39 6-propyl-4H-thieno[2,3b]thiopyran-2-sulfonamide-7,7- dioxide WO 00/04898 PCT/US99/Ib143 2H-thieno[3,2-e)-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2- 40 (3-methoxypropyl)-l, l-dioxide Following the procedures of Example 30, solutions are prepared substituting the compounds below for the prostaglandin derivative.
Compound Example PGF2a-1-isopropyl ester 41 13,14-dihydro-15-keto-PGE2 43 methyl ester 15-keto-PGF2« 44 PGFz« tromethamine salt 45 PGF2« derived hypotensive lipid 47 (+)-isopropyl fluprostenol 4g [2R{lE, 3R),3S(4Z),4R]-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate;
Claims (26)
1. An ophthalmic formulation for the treatment of ocular hypertension and glaucoma in a subject in need thereof, comprising a pharmaceutically acceptable carrier, a topical carbonic anhydrase inhibitor or an ophthamologically acceptable salt thereof, a .beta.-adrenergic antagonist or an ophthamologically acceptable salt thereof, and a prostaglandin or prostaglandin derivative thereof or a hypotensive lipid derived from a prostaglandin or prostaglandin derivative.
2. An ophthalmic formulation for the treatment of ocular hypertension and glaucoma in a subject in need thereof comprising 0.025 to 5% (w/w) of a compound of the structural formula II
(II) an individual diastereomer, an individual enantiomer or mixture thereof, or an ophthalmologically acceptable salt thereof, wherein:
A is carbon or nitrogen;
Z is -NHR or -OR;
R is C1-6alkyl, either straight or branched chain, preferably C2-4alkyl such as ethyl, propyl or isobutyl;
Q is (H,H), oxo or thioxo;
R1 is (a) hydrogen, (b) C1-3alkyl or (c) C1-4alkoxy-C1-4alkyl; and X is -S(O)2- or -C(O)-; 0.01 to 1.0% of a .beta.-adrenergic antagonist such as betaxolol, bufenolol, carteolol, levobunolol, metipranolol, timolol or an ophthalmologically acceptable salt thereof, 0.001 to 2% (w/w) of a prostaglandin such as 13,14-dihydro-15(R)-17-phenyl-18,19,20-trinor-PGF2.alpha. ester, 13,14-dihydro-15-keto-20-ethyl-PGF2.alpha. or prostaglandin derivative such as a hypotensive lipid derived from PGF2.alpha. prostaglandins and their trans and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material.
(II) an individual diastereomer, an individual enantiomer or mixture thereof, or an ophthalmologically acceptable salt thereof, wherein:
A is carbon or nitrogen;
Z is -NHR or -OR;
R is C1-6alkyl, either straight or branched chain, preferably C2-4alkyl such as ethyl, propyl or isobutyl;
Q is (H,H), oxo or thioxo;
R1 is (a) hydrogen, (b) C1-3alkyl or (c) C1-4alkoxy-C1-4alkyl; and X is -S(O)2- or -C(O)-; 0.01 to 1.0% of a .beta.-adrenergic antagonist such as betaxolol, bufenolol, carteolol, levobunolol, metipranolol, timolol or an ophthalmologically acceptable salt thereof, 0.001 to 2% (w/w) of a prostaglandin such as 13,14-dihydro-15(R)-17-phenyl-18,19,20-trinor-PGF2.alpha. ester, 13,14-dihydro-15-keto-20-ethyl-PGF2.alpha. or prostaglandin derivative such as a hypotensive lipid derived from PGF2.alpha. prostaglandins and their trans and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material.
3. A formulation according to claim 2 wherein A is carbon; and wherein R is -CH2CH3 and R1 is -CH3; or R is -CH2CH2CH3 and R1 is -CH2CH2CH2OCH3; or R is -CH2CH3 and R1 is -CH2CH2CH3; or R is -CH2CH2(CH3)2 and R1 is hydrogen; or R is -CH2CH3 and R1 is -CH2OCH2CH3; and carbons 4 and 6 of the topical carbonic anhydrase inhibitor both have S absolute stereochemical configuration.
4. A formulation according to claim 2 wherein A is nitrogen; and wherein R is -CH2CH3 and R1 is -CH3; or R is -CH2CH3CH3 and R1 is -CH2CH2CH2OCH3; or R is -CH2CH3 and R1 is -CH2CH2CH3; or R is -CH2CH2(CH3)2 and R1 is hydrogen; or R is -CH2CH3 and R1 is -CH2OCH2CH3.
5. A formulation according to claim 2 wherein the carbonic anhydrase inhibitor is 5,6-dihydro-4-ethylamino-6-methyl-4H-thieno-[2,3-b]thiopyran-2-sulfonamide-7,7 dioxide hydrochloride or 2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-1,1-dioxide and their trans and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material.
6. A formulation according to claim 2 wherein the prostaglandin is 11, 15-dipivaloyl PGF2.alpha., 11-pivaloyl prostaglandin F2.alpha. hydroxyethyl ester, (+)-(Z)-sodium-7-[1R, 2R, 3R, 5S)-3,5-dihydroxy-2-[(E)-1-octenyl]cyclopentyl]-5-heptenoate sesquihydrate, (1.alpha.,2.beta.,3.alpha.,5.alpha.]methyl-5-cis-2-(phenylethylsulfonamidomethyl)-3,5-dihydroxycyclopentyl heptenoate, (+-)-5-[6-(1-hydroxy)hexyl)-1,3-benzodioxol-5-yl]-pentanol, 15-pivaloyl PGF.alpha., 7-[3.alpha.,5.alpha. dihydroxy-2-(3a-hydroxy-5--1E-pentenyl)cyclopentyl]-5Z-heptenoic acid, isopropyl (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]-5-heptenoate, 13,14-dihydro-15(R)-17-phenyl-18,19,20-trinor-PGF2.alpha. esters, 13,14-dihydro-15-keto-20-ethyl-PGF2.alpha. isopropyl ester, (+)-isopropyl fluprostenol;
13,14-dihydro-PGF2.beta. isoprpopyl esters;
[2R(1E,3R),3S(4Z),4R]-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate, or 13,14-dihydro-15-keto-20-ethyl-PGF2.alpha. isopropyl ester trimethylphenol-1-acetate.
13,14-dihydro-PGF2.beta. isoprpopyl esters;
[2R(1E,3R),3S(4Z),4R]-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate, or 13,14-dihydro-15-keto-20-ethyl-PGF2.alpha. isopropyl ester trimethylphenol-1-acetate.
7. A formulation according to claim 2 in which the prostaglandin derivative is a hypotensive lipid derived from PGF2.alpha.
prostaglandins wherein the carboxylic acid group on the .alpha.-chain link of the basic prostaglandin structure is replaced with electrochemically neutral substituents.
prostaglandins wherein the carboxylic acid group on the .alpha.-chain link of the basic prostaglandin structure is replaced with electrochemically neutral substituents.
8. A formulation according to claim 2 which comprises a pharmaceuticallly acceptable carrier, a therapeutically effective amount of a prostaglandin which is 7-[3.alpha.,5.alpha. dihydroxy-2-(3a-hydroxy-5--1E-pentenyl)cyclopentyl]-5Z-heptenoic acid;
isopropyl (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]-5-heptenoate;
(+)-(Z)-sodium-7-[1R, 2R, 3R, 5S)-3,5-dihydroxy-2-[(E)-1-octenyl]cyclopentyl)-5-heptenoate sesquihydrate;
13,14-dihydro-15-keto-20-ethyl-PGF2.alpha. isopropyl ester trimethylphenol-1-acetate; (+)-isopropyl fluprostenol; 13,14-dihydro-PGF2.beta. isoprpopyl esters; [2R(1E,3R),3S(4Z),4R]-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate; or a hypotensive lipid derived from PGF2.alpha. prostaglandins, a .beta.-adrenergic antagonist such as betaxolol, bufenolol, carteolol, levobunolol, metipranolol, timolol or an ophthalmologically acceptable salt thereof and a topical carbonic anhydrase inhibitor belonging to the group consisting of 5,6-dihydro-4-ethylamino-6-methyl-4H-thieno-[2,3-b]thiopyran-2-sulfonamide-7,7 dioxide hydrochloride or 2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-1,1-dioxide and their trans and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material.
isopropyl (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]-5-heptenoate;
(+)-(Z)-sodium-7-[1R, 2R, 3R, 5S)-3,5-dihydroxy-2-[(E)-1-octenyl]cyclopentyl)-5-heptenoate sesquihydrate;
13,14-dihydro-15-keto-20-ethyl-PGF2.alpha. isopropyl ester trimethylphenol-1-acetate; (+)-isopropyl fluprostenol; 13,14-dihydro-PGF2.beta. isoprpopyl esters; [2R(1E,3R),3S(4Z),4R]-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate; or a hypotensive lipid derived from PGF2.alpha. prostaglandins, a .beta.-adrenergic antagonist such as betaxolol, bufenolol, carteolol, levobunolol, metipranolol, timolol or an ophthalmologically acceptable salt thereof and a topical carbonic anhydrase inhibitor belonging to the group consisting of 5,6-dihydro-4-ethylamino-6-methyl-4H-thieno-[2,3-b]thiopyran-2-sulfonamide-7,7 dioxide hydrochloride or 2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-1,1-dioxide and their trans and cis enantiomers, or an ophthalmologically acceptable salt thereof, including racemic material.
9. The formulation of Claim 2 wherein the concentration of carbonic anhydrase inhibitor is 0.5 % to 3 %, the concentration of .beta.-adrenergic antagonist is 0.1 to 0.5% and the concentration of the prostaglandin or prostaglandin derivative is 0.03%
to 1.0%.
to 1.0%.
10. The formulation of claim 2 wherein the carbonic anhydrase inhibitor has an aqueous solubility greater than 10 ug/mL but less than 1000 ug/mL at pH 7.4, and a Ki of 1.0 nM or lower.
11. The formulation of claim 10 which is a suspension.
12. The formulation of claim 2 which optionally contains from about 0.1 % to about 2% of gellan gum.
13. The formulation of claim 2 which optionally contains from about 0.1 % to about 2% (w/w) of xanthan gum.
14. The formulation of claim 13 which contains from about 0.4 to about 0.7%(w/w) of xanthan gum, said xanthan gum being a hypotonic solution, with a freezing point depression between about -0.28°C and -0.4°C.
15. The formulation of claim 13 wherein the gum is KELTROLTMT xanthan gum in a hypotonic solution with a freezing point from about -0.31 °C to about -0.37°C.
16. A method of treating ocular hypertension and glaucoma which comprises the topical ocular administration to a patient in need of such treatment of a unit dose of the formulation of Claim 1.
17. A method of treating ocular hypertension and glaucoma which comprises the topical ocular administration to a patient in need of such treatment of a unit dose of the formulation of Claim 2.
18. A method of treating ocular hypertension and glaucoma which comprises the topical ocular administration to a patient in need of such treatment of a unit dose of the formulation of Claim 11.
19. A method of treating ocular hypertension and glaucoma which comprises the topical ocular administration to a patient in need of such treatment of a unit dose of the formulation of Claim 12.
20. A method of treating ocular hypertension and glaucoma which comprises the topical ocular administration to a patient in need of such treatment of a unit dose of the formulation of Claim 13.
21. A formulation which comprises a pharmaceutically acceptable carrier, a topical carbonic anhydrase inhibitor 5,6-dihydro-4-ethylamino-6-methyl-4H-thieno-[2,3-b]thiopyran-2-sulfonamide-7,7 dioxide hydrochloride, a prostaglandin which is 7-[3.alpha.,5.alpha. dihydroxy-(3a-hydroxy-5-1E-pentenyl)cyclopentyl]-5Z-heptenoic acid; isopropyl (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]-5-heptenoate; (+)-(Z)-sodium-7-[1R,2R,3R, 5S)-3,5-dihydroxy-2-((E)-1-octenyl]cyclopentyl]-5-heptenoate sesquihydrate; (+)-isopropyl fluprostenol; 13,14-dihydro-PGF2.beta.
isoprpopyl esters; [2R(1E,3R),3S(4Z),4R)-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate; or13,14-dihydro-15-keto-20-ethyl-PGF2.alpha. isopropyl ester trimethylphenol-1-acetate and a .beta.-adrenergic antagonist (s)-(-)-1-(tert-butylamino)-3-[(4-inorpholino-1,2,5-thiadiazol-3-yl)oxy]-2-propanol maleate.
isoprpopyl esters; [2R(1E,3R),3S(4Z),4R)-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate; or13,14-dihydro-15-keto-20-ethyl-PGF2.alpha. isopropyl ester trimethylphenol-1-acetate and a .beta.-adrenergic antagonist (s)-(-)-1-(tert-butylamino)-3-[(4-inorpholino-1,2,5-thiadiazol-3-yl)oxy]-2-propanol maleate.
22. A formulation according to claim 21 which optionally contains gellan gum or xanthan gum.
23. A formulation which comprises a pharmaceutically acceptable carrier, a topical carbonic anhydrase inhibitor 2H-thieno(3,2-e]-1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-1, 1-dioxide, a prostaglandin comprising 7-[3.alpha.,5.alpha.
dihydroxy-2-(3a-hydroxy-5--1E-pentenyl)cyclopentyl]-5Z-heptenoic acid;isopropyl (Z)-7-((1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]-5-heptenoate;
(+)-(Z)-sodium-7-[1R, 2R, 3R, 5S)-3,5-dihydroxy-2-[(E)-1-octenyl]cyclopentyl]-5-heptenoate sesquihydrate;
13, 14-dihydro-15-keto-20-ethyl-PGF2.alpha. isopropyl ester trimethylphenol-1-acetate, (+)-isopropyl fluprostenol; 13,14-dihydro-PGF2.beta. isoprpopyl esters; [2R(1E,3R),3S(4Z),4R]-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate; and a .beta.-adrenergic antagonist (s)-(-)-1-(tert-butylamino)-3-[(4-morpholino-1,2,5-thiadiazol-3-yl)oxy]-2-propanol maleate.
dihydroxy-2-(3a-hydroxy-5--1E-pentenyl)cyclopentyl]-5Z-heptenoic acid;isopropyl (Z)-7-((1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]-5-heptenoate;
(+)-(Z)-sodium-7-[1R, 2R, 3R, 5S)-3,5-dihydroxy-2-[(E)-1-octenyl]cyclopentyl]-5-heptenoate sesquihydrate;
13, 14-dihydro-15-keto-20-ethyl-PGF2.alpha. isopropyl ester trimethylphenol-1-acetate, (+)-isopropyl fluprostenol; 13,14-dihydro-PGF2.beta. isoprpopyl esters; [2R(1E,3R),3S(4Z),4R]-isopropyl-7-(tetrahydro-2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl)-4-hydroxy-3-furanyl]-4-heptanoate; and a .beta.-adrenergic antagonist (s)-(-)-1-(tert-butylamino)-3-[(4-morpholino-1,2,5-thiadiazol-3-yl)oxy]-2-propanol maleate.
24. A formulation according to claim 23 which optionally contains gellan gum or xanthan gum.
25. A formulation which comprises a pharmaceutically acceptable carrier, a topical carbonic anhydrase inhibitor 2H-thieno[3,2-e]- 1,2-thiazine-6-sulfonamide-4-(ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-1,1-dioxide, a hypotensive lipid derived from PGF2.alpha.
prostaglandins, in which the carboxylic acid group on the .alpha.-chain link of the basic prostaglandin structure is replaced with electrochemically neutral substituents and a .beta.-adrenergic antagonist (s)-(-)-1-(tert-butylamino)-3-[(4-morpholino-1,2,5-thiadiazol-3-yl)oxy)-2-propanol maleate.
prostaglandins, in which the carboxylic acid group on the .alpha.-chain link of the basic prostaglandin structure is replaced with electrochemically neutral substituents and a .beta.-adrenergic antagonist (s)-(-)-1-(tert-butylamino)-3-[(4-morpholino-1,2,5-thiadiazol-3-yl)oxy)-2-propanol maleate.
26. A formulation according to claim 25 which optionally contains gellan gum or xanthan gum.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9359498P | 1998-07-21 | 1998-07-21 | |
| US60/093,594 | 1998-07-21 | ||
| PCT/US1999/016143 WO2000004898A1 (en) | 1998-07-21 | 1999-07-16 | Ophthalmic compositions for treating ocular hypertension |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2337399A1 true CA2337399A1 (en) | 2000-02-03 |
Family
ID=22239789
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002337399A Abandoned CA2337399A1 (en) | 1998-07-21 | 1999-07-16 | Ophthalmic compositions for treating ocular hypertension |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1109546A1 (en) |
| JP (1) | JP2002521332A (en) |
| AU (1) | AU5001199A (en) |
| CA (1) | CA2337399A1 (en) |
| WO (1) | WO2000004898A1 (en) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL350917A1 (en) | 1999-03-05 | 2003-02-10 | Procter & Gamble | C16 unsaturated fp-selective prostaglandins analogs |
| US20020013294A1 (en) | 2000-03-31 | 2002-01-31 | Delong Mitchell Anthony | Cosmetic and pharmaceutical compositions and methods using 2-decarboxy-2-phosphinico derivatives |
| US20020172693A1 (en) | 2000-03-31 | 2002-11-21 | Delong Michell Anthony | Compositions and methods for treating hair loss using non-naturally occurring prostaglandins |
| WO2001085152A2 (en) * | 2000-05-10 | 2001-11-15 | Alcon, Inc. | R-eliprodil for treating glaucoma |
| US6414021B1 (en) * | 2000-08-25 | 2002-07-02 | Sucampo Ag | Control of intraocular pressure during surgery |
| TWI298257B (en) | 2001-05-31 | 2008-07-01 | Allergan Inc | Hypotensive lipid and timolol compositions and methods of using same |
| US20040058313A1 (en) * | 2002-04-24 | 2004-03-25 | Abreu Marcio Marc | Compositions, targets, methods and devices for the therapy of ocular and periocular disorders |
| KR101182496B1 (en) | 2002-09-09 | 2012-09-12 | 산텐 세이야꾸 가부시키가이샤 | Transparent eye drops containing latanoprost |
| US7993634B2 (en) | 2004-04-30 | 2011-08-09 | Allergan, Inc. | Oil-in-oil emulsified polymeric implants containing a hypotensive lipid and related methods |
| US7799336B2 (en) | 2004-04-30 | 2010-09-21 | Allergan, Inc. | Hypotensive lipid-containing biodegradable intraocular implants and related methods |
| US8722097B2 (en) | 2004-04-30 | 2014-05-13 | Allergan, Inc. | Oil-in-water method for making polymeric implants containing a hypotensive lipid |
| US9498457B2 (en) | 2004-04-30 | 2016-11-22 | Allergan, Inc. | Hypotensive prostamide-containing biodegradable intraocular implants and related implants |
| CN101031310B (en) | 2004-09-28 | 2010-10-27 | 千寿制药株式会社 | Ophthalmic composition containing xanthan gum and amino acid |
| US20060135609A1 (en) | 2004-10-21 | 2006-06-22 | Duke University | Ophthamological drugs |
| ES2337501T3 (en) | 2005-07-11 | 2010-04-26 | Senju Pharmaceutical Co., Ltd. | OPHTHALMIC PREPARATION THAT INCLUDES XANTAN AND TERPENOID RUBBER. |
| KR101381035B1 (en) | 2006-03-23 | 2014-04-04 | 센주 세이야꾸 가부시키가이샤 | Ophthalmic composition comprising xanthan gum and glucose |
| US20070254920A1 (en) * | 2006-04-26 | 2007-11-01 | Aerie Pharmaceuticals, Inc. | Prodrug derivatives of acids using alcohols with homotopic hydroxy groups and methods for their preparation and use |
| DE102009021372A1 (en) * | 2009-05-14 | 2010-11-18 | Ursapharm Arzneimittel Gmbh | Phosphate-free pharmaceutical composition for glaucoma treatment |
| US20110136872A1 (en) * | 2009-12-09 | 2011-06-09 | Burk Robert M | Stable aqueous compositions of prostglandin agonist prodrugs and methods for use thereof |
| MX2012012941A (en) * | 2010-05-07 | 2013-07-29 | Sun Pharma Advanced Res Co Ltd | Novel ophthalmic compositions. |
| SI2598118T1 (en) | 2010-07-29 | 2018-12-31 | Allergan, Inc. | Preservative free bimatoprost and timolol solutions |
| US9061034B2 (en) | 2010-07-29 | 2015-06-23 | Allergan, Inc. | Preservative free bimatoprost and timolol solutions |
| US10046001B2 (en) | 2013-12-05 | 2018-08-14 | University Of Miami | Compositions and methods for reducing intraocular pressure |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4599353A (en) * | 1982-05-03 | 1986-07-08 | The Trustees Of Columbia University In The City Of New York | Use of eicosanoids and their derivatives for treatment of ocular hypertension and glaucoma |
-
1999
- 1999-07-16 WO PCT/US1999/016143 patent/WO2000004898A1/en not_active Application Discontinuation
- 1999-07-16 CA CA002337399A patent/CA2337399A1/en not_active Abandoned
- 1999-07-16 AU AU50011/99A patent/AU5001199A/en not_active Abandoned
- 1999-07-16 JP JP2000560891A patent/JP2002521332A/en not_active Withdrawn
- 1999-07-16 EP EP99934101A patent/EP1109546A1/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| AU5001199A (en) | 2000-02-14 |
| JP2002521332A (en) | 2002-07-16 |
| EP1109546A1 (en) | 2001-06-27 |
| WO2000004898A1 (en) | 2000-02-03 |
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