US2001023245A1PendingUtilityA1
Ophthalmic composition including a neurotrophic factor for treating optic nerve function disorders and method for treating optic nerve function disorders
Assignee: ADVANCED MEDICINE RES INSTPriority: Sep 13, 1996Filed: May 23, 2001Published: Sep 20, 2001
Est. expirySep 13, 2016(expired)· nominal 20-yr term from priority
Inventors:Shinseiro Okamoto
A61K 38/185A61K 9/0048A61K 38/18
44
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Claims
Abstract
According to the present invention, an ophthalmic composition which comprises a neurotrophic factor, an optic nerve functional disorder-treating agent which comprises a neurotrophic factor, and a method for treating an optic nerve functional disorder, which comprises administering an effective amount of a neurotrophic factor, particularly a glaucoma-treating agent and a method for treating the same are provided.
Claims
exact text as granted — not AI-modified1 . An ophthalmic composition which comprises a neurotrophic factor.
2 . The ophthalmic composition according to claim 1 , wherein the neurotrophic factor is one or two or more selected from a nerve growth factor (NGF), a brain-derived neurotrophic factor (BDNF), a ciliary neurotrophic factor (CNTF), neurotrophin-3 (NT-3), neurotrophin-4/5 (NT-4/5), neurotrophin-6 (NT-6), a gliacyte-derived neurotrophic factor (GDNF), an axogenesis factor (AF-1) and a glia growth factor (GGF2).
3 . The ophthalmic composition according to claim 2 , wherein the neurotrophic factor is one or two or more selected from NGF, BDNF, CNTF, NT-3, NT-4/5 and NT-6.
4 . The ophthalmic composition according to claim 3 , wherein the neurotrophic factor is BDNF.
5 . The ophthalmic composition according to any one of claims 1 to 4 , wherein the composition is an ophthalmic agent for external application.
6 . The ophthalmic composition according to claim 5 , wherein the ophthalmic agent for external application is an ophthalmic solution or an ophthalmic ointment.
7 . The ophthalmic composition according to claim 6 , wherein the composition contains an isotonicity-imparting agent.
8 . The ophthalmic composition according to claim 7 , wherein the concentration of the isotonicity-imparting agent is 0.6 to 2.0 in terms of an osmotic pressure ratio.
9 . The ophthalmic composition according to any one of claims 6 to 8 , wherein the composition contains a viscosity-imparting agent.
10 . The ophthalmic composition according to claim 9 , wherein the concentration of the viscosity-imparting agent is 0.001% to 10% (W/V).
11 . The ophthalmic composition according to any one of claims 6 to 8 and 10 , wherein the composition contains a suspending agent.
12 . The ophthalmic composition according to claim 11 , wherein the concentration of the suspending agent is 0.001 % to 10% (W/V).
13 . The ophthalmic composition according to any one of claims 6 to 8 , 10 and 12 , wherein the composition contains an emulsifier.
14 . The ophthalmic composition according to claim 13 , wherein the concentration of the emulsifier is 0.001% to 10% (W/V).
15 . The ophthalmic composition according to claims 6 to 8 , 10 , 12 and 14 , wherein the composition contains a preservative.
16 . The ophthalmic composition according to claim 15 , wherein the concentration of the preservative is 0.0001% to 10% (W/v).
17 . The ophthalmic composition according to any one of claims 6 to 8 , 10 , 12 , 14 and 16 , wherein the composition contains a pH adjuster.
18 . The ophthalmic composition according to claim 17 , wherein the composition contains a pH adjuster necessary for retaining pH at 3.0 to 8.0.
19 . The ophthalmic composition according to any one of claims 1 to 4 , 6 to 8 , 10 , 12 , 14 , 16 and 18 , wherein the concentration of the neurotrophic factor is 0.0001 to 0.5% (W/V).
20 . The ophthalmic composition according to any one of claims 1 to 4 , 6 to 8 , 10 , 12 , 14 , 16 and 18 , wherein the concentration of the neurotrophic factor is 10 −3 to 2×10 5 μg/l.
21 . The ophthalmic composition according to claim 19 or 20 , wherein the composition is formulated into a contact lens.
22 . An optic nerve functional disorder-treating agent which comprises a neurotrophic factor.
23 . The treatment agent according to claim 22 , wherein the optic nerve functional disorder is glaucoma.
24 . The treatment agent according to claim 23 , wherein the neurotrophic factor is one or two or more selected from a nerve growth factor (NGF), a brain-derived neurotrophic factor (BDNF), a ciliary neurotrophic factor (CNTF), neurotrophin-3 (NT-3), neurotrophin-4/5 (NT-4/5), neurotrophin-6 (NT-6), a gliacyte-derived neurotrophic factor (GDNF), an axogenesis factor (AF-1) and a glia growth factor (GGF2).
25 . The treatment agent according to claim 24 , wherein the neurotrophic factor is one or two or more selected from NGF, BDNF, CNTF, NT-3, NT-4/5 and NT-6.
26 . The treatment agent according to claim 25 , wherein the neurotrophic factor is BDNF.
27 . The treatment agent according to any one of claims 23 to 26 , wherein the treatment agent is an ophthalmic agent for external application.
28 . The treatment agent according to claim 27 , wherein the ophthalmic agent for external application is an ophthalmic solution or an ophthalmic ointment.
29 . The glaucoma-treating agent according to any one of claims 23 to 26 and 28 , wherein the treatment agent is formulated into a contact lens.
30 . A method for treating an optic nerve functional disorder, which comprises administering an effective amount of a neurotrophic factor.
31 . The treatment method according to claim 30 , wherein the optic nerve functional disorder is glaucoma.
32 . The treatment method according to claim 30 , wherein the neurotrophic factor is one or two or more selected from a nerve growth factor (NGF), a brain-derived neurotrophic factor (BDNF), a ciliary neurotrophic factor (CNTF), neurotrophin-3 (NT-3), neurotrophin-4/5 (NT-4/5), neurotrophin-6 (NT-6), a gliacyte-derived neurotrophic factor (GDNF), an axogenesis factor (AF-1) and a glia growth factor (GGF2).
33 . The treatment method according to claim 32 , wherein the neurotrophic factor is one or two or more selected from NGF, BDNF, CNTF, NT-3, NT-4/5 and NT-6.
34 . The treatment method according to claim 33 , wherein the neurotrophic factor is BDNF.
35 . The treatment method according to any one of claims 30 to 34 , wherein the neurotrophic factor is used in the form of an ophthalmic agent for external application.
36 . The treatment method according to claim 35 , wherein the ophthalmic agent for external application is used in the form of an ophthalmic solution or an ophthalmic ointment.
37 . The treatment method according to any one of claims 30 to 34 and 36 , wherein a contact lens into which a medicine is formulated is used.Join the waitlist — get patent alerts
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