Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Ester doai
Reexamination Certificate
2001-08-13
2003-10-28
Spivack, Phyllis G. (Department: 1614)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Ester doai
C514S534000, C514S561000, C514S562000, C514S563000, C514S564000, C514S617000, C514S618000, C514S619000
Reexamination Certificate
active
06638976
ABSTRACT:
FIELD OF THE INVENTION
This invention relates to the treatment of retinopathy. In particular, this invention relates to the use of certain 3-benzoylphenylacetic acids and derivatives to treat or prevent neurodegenerative disorders of the retina and optic nerve head.
BACKGROUND OF THE INVENTION
3-benzoylphenylacetic acid and certain of its derivatives are known to possess anti-inflammatory activity. U.S. Pat. Nos. 4,254,146, 4,045,576, 4,126,635, and 4,503,073, and U.K. Patent Application Nos. 2,071,086A and 2,093,027A disclose various 3-benzoylphenylacetic acids, salts and esters, and hydrates thereof, having anti-inflammatory activity. U.S. Pat. No. 4,568,695 discloses 2-amino-3-benzoylphenylethyl alcohols having anti-inflammatory activity. U.S. Pat. No. 4,313,949 discloses 2-amino-3-benzoyl-phenylacetamides having anti-inflammatory activity.
Certain derivatives of 2-amino-3-benzoylbenzeneacetic acid (amfenac) and 2-amino-3-(4-chloro-benzoyl)benzeneacetic acid have also been evaluated by Walsh et al., J. Med Chem., 33:2296-2304 (1990), in an attempt to discover nonsteroidal anti-inflammatory prodrugs with minimal or no gastrointestinal side effects upon oral administration.
U.S. Pat. No. 4,683,242 teaches the transdermal administration of 2-amino-3-benzoylphenylacetic acids, salts, and esters, and hydrates and alcoholates thereof to control inflammation and alleviate pain.
U.S. Pat. No. 4,910,225 teaches certain benzoylphenylacetic acids for local administration to control ophthalmic, nasal or otic inflammation. Only acetic acids are disclosed in the '225 patent; no esters or amides are mentioned or taught as anti-inflammatory agents for local administration to the eyes, nose and ears.
U.S. Pat. No. 5,475,034 discloses topically administrable compositions containing certain amide and ester derivatives of 3-benzyolphenylacetic acid, including nepafenac, useful for treating ophthalmic inflammatory disorders and ocular pain. According to the '035 patent at Col. 15, lines 35-39, “[s]uch disorders include, but are not limited to uveitis, scleritis, episcleritis, keratitis, surgically-induced inflammation and endophthalmitis.”
U.S. Pat. No. 6,066,671 discloses the topical use of certain amide and ester derivatives of 3-benzoylphenylacetic acid, including nepafenac, for treating GLC1A glaucoma.
SUMMARY OF THE INVENTION
It has now been found that certain 3-benzoylphenylacetic acids and derivatives, including nepafenac (2-amino,3-benzoyl-phenylacetamide), are useful in treating neurodegenerative disorders of the retina and optic nerve head.
DETAILED DESCRIPTION OF THE INVENTION
The 3-benzoylphenylacetic acids and derivatives useful in the methods of the present invention are those of formula (I) below.
R=H, C
1-4
(un)branched alkyl, CF
3
, SR
4
Y=OR′, NR″R′;
R′=H, C
1-10
(un)branched alkyl, (un)substituted aryl (substitution as defined by X below), (un)substituted heterocycle (substitution as defined by X below), —(CH
2
)
n
Z(CH
2
)
n′
A;
n=2-6;
n′=1-6;
Z=nothing, O, C═O, OC(═O), C(═O)O, C(═O)NR
3
, NR
3
C(═O), S(O)
n
2
, CHOR
3
, NR
3
;
n
2
=0-2;
R
3
=H, C
1-6
(un)branched alkyl, (un)substituted aryl (substitution as defined by X below), (un)substituted heterocycle (substitution as defined by X below)
A=H, OH, optionally (un)substituted aryl (substitution as defined by X below), (un)substituted heterocycle (substitution as defined by X below), —(CH
2
)
n
OR
3
;
R″=H, OH, OR′
X and X′ independently=H, F, Cl, Br, I, OR′, CN, OH, S(O)
n
2
R
4
, CF
3
, R
4
, NO
2
;
R
4
=C
1-6
(un)branched alkyl;
m=0-3;
m′=0-5;
W=O, H.
As used herein, the acid (Y=OH) includes pharmaceutically acceptable salts as well.
Preferred compounds for use in the methods of the present invention are those of Formula I wherein:
R=H, C
1-2
alkyl;
Y=NR′R″;
R′=H, C
1-6
(un)branched alkyl, —(CH
2
)
n
Z(CH
2
)
n′
A;
Z=nothing, O, CHOR
3
, NR
3
;
R
3
=H;
A=H, OH, (un)substituted aryl (substitution as defined by X below);
X and X′ independently=H, F, Cl, Br, CN, CF
3
, OR′, SR
4
, R
4
;
R″=H;
R
4
=C
1-4
(un)branched alkyl;
m=0-2;
m′=0-2;
W=H;
n=2-4;
n′=0-3.
The most preferred compounds for use in the compositions or method of the present invention are 2-Amino-3-(4-fluorobenzoyl)-phenylacetamide; 2-Amino-3-benzoyl-phenylacetamide (nepafenac); and 2-Amino-3-(4-chlorobenzoyl)-phenylacetamide.
According to the present invention, a therapeutically effective amount of a compound of formula (I) is administered topically, locally or systemically to treat or prevent neurodegenerative disorders of the retina and optic nerve head. Such disorders include, but are not limited to atrophic macular degeneration; retinitis pigmentosa; iatrogenic retinopathy; retinal tears and holes; diabetic retinopathy; sickle cell retinopathy; retinal vein and artery occlusion; and optic neuropathy. Certain ophthalmic disorders, such as sickle cell retinopathy and retinal vein or artery occlusion, can be characterized by both angiogenesis and neurodegenerative components. According to the present invention, a compound of formula (I) is administered to treat or prevent disorders characterized, at least in part, by neurodegeneration.
The compounds of formula (I) can be administered in a variety of ways, including all forms of local delivery to the eye, such as subconjunctival injections or implants, intravitreal injections or implants, sub-Tenon's injections or implants, incorporation in surgical irrigating solutions, etc. Additionally, the compounds of formula (I) can be administered systemically, such as orally or intravenously. Suitable pharmaceutical vehicles or dosage forms for injectable compositions, implants, and systemic administration are known. The compounds of formula (I) and especially those wherein Y=NR′R″, however, are preferably administered topically to the eye and can be formulated into a variety of topically administrable ophthalmic compositions, such as solutions, suspensions, gels or ointments.
Pharmaceutical compositions comprising a compound of formula (I) in aqueous solution or suspension, optionally containing a preservative for multidose use and other conventionally employed ophthalmic adjuvants, can be topically administered to the eye. The most preferred form of delivery is by aqueous eye drops, but gels or ointments can also be used. Aqueous eye drops, gels and ointments can be formulated according to conventional technology and would include one or more excipients. For example, topically administrable compositions may contain tonicity-adjusting agents, such as mannitol or sodium chloride; preservatives such as chlorobutanol, benzalkonium chloride, polyquaternium-1, or chlorhexidine; buffering agents, such as phosphates, borates, carbonates and citrates; and thickening agents, such as high molecular weight carboxy vinyl polymers, including those known as carbomers, hydroxyethylcellulose, or polyvinyl alcohol.
The doses of the compounds of formula (I) used in the treatment or prevention of neurodegenerative disorders of the retina and optic nerve head will depend on the type of disorder to be prevented or treated, the age and body weight of the patient, and the form of preparation/route of administration. Compositions intended for topical ophthalmic administration will typically contain a compound of formula (I) in an amount of from about 0.001 to about 4.0% (w/v), preferably from about 0.01 to about 0.5% (w/v), with 1-2 drops once to several times a day. Likewise, representative doses for other forms of preparations are approximately 1-100 mg/day/adult for injections and approximately 10-1000 mg/adult for oral preparations, each administered once to several times a day.
Additional therapeutic agents may be added to supplement t
Gamache Daniel A.
Graff Gustav
Kapin Michael A.
Yanni John M.
Alcon Inc.
Schultz Teresa J.
Spivack Phyllis G.
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