AR069729A1 - Uso de sustancias para el tratamiento de la perdida de vision ocular en humanos con glaucoma y otras enfermedades oculares degenerativas - Google Patents
Uso de sustancias para el tratamiento de la perdida de vision ocular en humanos con glaucoma y otras enfermedades oculares degenerativasInfo
- Publication number
- AR069729A1 AR069729A1 ARP080103650A ARP080103650A AR069729A1 AR 069729 A1 AR069729 A1 AR 069729A1 AR P080103650 A ARP080103650 A AR P080103650A AR P080103650 A ARP080103650 A AR P080103650A AR 069729 A1 AR069729 A1 AR 069729A1
- Authority
- AR
- Argentina
- Prior art keywords
- abeta
- treatment
- peptide
- amino acid
- prevention
- Prior art date
Links
- 208000030533 eye disease Diseases 0.000 title abstract 3
- 208000010412 Glaucoma Diseases 0.000 title abstract 2
- 230000003412 degenerative effect Effects 0.000 title 1
- 239000000126 substance Substances 0.000 title 1
- 108090000765 processed proteins & peptides Proteins 0.000 abstract 9
- 230000002265 prevention Effects 0.000 abstract 6
- 150000001413 amino acids Chemical group 0.000 abstract 5
- 230000003287 optical effect Effects 0.000 abstract 5
- 230000006974 Aβ toxicity Effects 0.000 abstract 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 abstract 4
- 230000015572 biosynthetic process Effects 0.000 abstract 4
- 239000008177 pharmaceutical agent Substances 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 3
- -1 aromatic amino acid Chemical group 0.000 abstract 3
- 239000003814 drug Substances 0.000 abstract 3
- 239000008194 pharmaceutical composition Substances 0.000 abstract 3
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 abstract 2
- ULGZDMOVFRHVEP-RWJQBGPGSA-N Erythromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 ULGZDMOVFRHVEP-RWJQBGPGSA-N 0.000 abstract 2
- 239000004471 Glycine Substances 0.000 abstract 2
- HUCJFAOMUPXHDK-UHFFFAOYSA-N Xylometazoline Chemical compound CC1=CC(C(C)(C)C)=CC(C)=C1CC1=NCCN1 HUCJFAOMUPXHDK-UHFFFAOYSA-N 0.000 abstract 2
- MYSWGUAQZAJSOK-UHFFFAOYSA-N ciprofloxacin Chemical compound C12=CC(N3CCNCC3)=C(F)C=C2C(=O)C(C(=O)O)=CN1C1CC1 MYSWGUAQZAJSOK-UHFFFAOYSA-N 0.000 abstract 2
- 239000003937 drug carrier Substances 0.000 abstract 2
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- 239000000546 pharmaceutical excipient Substances 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- QCHFTSOMWOSFHM-WPRPVWTQSA-N (+)-Pilocarpine Chemical compound C1OC(=O)[C@@H](CC)[C@H]1CC1=CN=CN1C QCHFTSOMWOSFHM-WPRPVWTQSA-N 0.000 abstract 1
- WCDDVEOXEIYWFB-VXORFPGASA-N (2s,3s,4r,5r,6r)-3-[(2s,3r,5s,6r)-3-acetamido-5-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5,6-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@@H]1C[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](C(O)=O)O[C@@H](O)[C@H](O)[C@H]1O WCDDVEOXEIYWFB-VXORFPGASA-N 0.000 abstract 1
- TWBNMYSKRDRHAT-RCWTXCDDSA-N (S)-timolol hemihydrate Chemical compound O.CC(C)(C)NC[C@H](O)COC1=NSN=C1N1CCOCC1.CC(C)(C)NC[C@H](O)COC1=NSN=C1N1CCOCC1 TWBNMYSKRDRHAT-RCWTXCDDSA-N 0.000 abstract 1
- CNIIGCLFLJGOGP-UHFFFAOYSA-N 2-(1-naphthalenylmethyl)-4,5-dihydro-1H-imidazole Chemical compound C=1C=CC2=CC=CC=C2C=1CC1=NCCN1 CNIIGCLFLJGOGP-UHFFFAOYSA-N 0.000 abstract 1
- GSDSWSVVBLHKDQ-UHFFFAOYSA-N 9-fluoro-3-methyl-10-(4-methylpiperazin-1-yl)-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid Chemical compound FC1=CC(C(C(C(O)=O)=C2)=O)=C3N2C(C)COC3=C1N1CCN(C)CC1 GSDSWSVVBLHKDQ-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
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- 239000004099 Chlortetracycline Substances 0.000 abstract 1
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- CEAZRRDELHUEMR-URQXQFDESA-N Gentamicin Chemical compound O1[C@H](C(C)NC)CC[C@@H](N)[C@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](NC)[C@@](C)(O)CO2)O)[C@H](N)C[C@@H]1N CEAZRRDELHUEMR-URQXQFDESA-N 0.000 abstract 1
- 229930182566 Gentamicin Natural products 0.000 abstract 1
- ZCVMWBYGMWKGHF-UHFFFAOYSA-N Ketotifene Chemical compound C1CN(C)CCC1=C1C2=CC=CC=C2CC(=O)C2=C1C=CS2 ZCVMWBYGMWKGHF-UHFFFAOYSA-N 0.000 abstract 1
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- QCHFTSOMWOSFHM-UHFFFAOYSA-N SJ000285536 Natural products C1OC(=O)C(CC)C1CC1=CN=CN1C QCHFTSOMWOSFHM-UHFFFAOYSA-N 0.000 abstract 1
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- 229960004150 aciclovir Drugs 0.000 abstract 1
- MKUXAQIIEYXACX-UHFFFAOYSA-N aciclovir Chemical compound N1C(N)=NC(=O)C2=C1N(COCCO)C=N2 MKUXAQIIEYXACX-UHFFFAOYSA-N 0.000 abstract 1
- 125000000539 amino acid group Chemical group 0.000 abstract 1
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- 230000001384 anti-glaucoma Effects 0.000 abstract 1
- 229940124599 anti-inflammatory drug Drugs 0.000 abstract 1
- 239000000043 antiallergic agent Substances 0.000 abstract 1
- 229960002610 apraclonidine Drugs 0.000 abstract 1
- IEJXVRYNEISIKR-UHFFFAOYSA-N apraclonidine Chemical compound ClC1=CC(N)=CC(Cl)=C1NC1=NCCN1 IEJXVRYNEISIKR-UHFFFAOYSA-N 0.000 abstract 1
- 239000000607 artificial tear Substances 0.000 abstract 1
- 229960004574 azelastine Drugs 0.000 abstract 1
- 229960002278 azidamfenicol Drugs 0.000 abstract 1
- SGRUZFCHLOFYHZ-MWLCHTKSSA-N azidamfenicol Chemical compound [N-]=[N+]=NCC(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 SGRUZFCHLOFYHZ-MWLCHTKSSA-N 0.000 abstract 1
- 229960002537 betamethasone Drugs 0.000 abstract 1
- UREBDLICKHMUKA-DVTGEIKXSA-N betamethasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)CO)(O)[C@@]1(C)C[C@@H]2O UREBDLICKHMUKA-DVTGEIKXSA-N 0.000 abstract 1
- 229960004324 betaxolol Drugs 0.000 abstract 1
- CHDPSNLJFOQTRK-UHFFFAOYSA-N betaxolol hydrochloride Chemical compound [Cl-].C1=CC(OCC(O)C[NH2+]C(C)C)=CC=C1CCOCC1CC1 CHDPSNLJFOQTRK-UHFFFAOYSA-N 0.000 abstract 1
- AQOKCDNYWBIDND-FTOWTWDKSA-N bimatoprost Chemical compound CCNC(=O)CCC\C=C/C[C@H]1[C@@H](O)C[C@@H](O)[C@@H]1\C=C\[C@@H](O)CCC1=CC=CC=C1 AQOKCDNYWBIDND-FTOWTWDKSA-N 0.000 abstract 1
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- 230000003115 biocidal effect Effects 0.000 abstract 1
- 230000000903 blocking effect Effects 0.000 abstract 1
- 229960003679 brimonidine Drugs 0.000 abstract 1
- 229960000722 brinzolamide Drugs 0.000 abstract 1
- HCRKCZRJWPKOAR-JTQLQIEISA-N brinzolamide Chemical compound CCN[C@H]1CN(CCCOC)S(=O)(=O)C2=C1C=C(S(N)(=O)=O)S2 HCRKCZRJWPKOAR-JTQLQIEISA-N 0.000 abstract 1
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- 229960001631 carbomer Drugs 0.000 abstract 1
- 229960001222 carteolol Drugs 0.000 abstract 1
- LWAFSWPYPHEXKX-UHFFFAOYSA-N carteolol Chemical compound N1C(=O)CCC2=C1C=CC=C2OCC(O)CNC(C)(C)C LWAFSWPYPHEXKX-UHFFFAOYSA-N 0.000 abstract 1
- 229960005091 chloramphenicol Drugs 0.000 abstract 1
- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 abstract 1
- CYDMQBQPVICBEU-UHFFFAOYSA-N chlorotetracycline Natural products C1=CC(Cl)=C2C(O)(C)C3CC4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O CYDMQBQPVICBEU-UHFFFAOYSA-N 0.000 abstract 1
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- 235000019365 chlortetracycline Nutrition 0.000 abstract 1
- CYDMQBQPVICBEU-XRNKAMNCSA-N chlortetracycline Chemical compound C1=CC(Cl)=C2[C@](O)(C)[C@H]3C[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O CYDMQBQPVICBEU-XRNKAMNCSA-N 0.000 abstract 1
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- 239000006071 cream Substances 0.000 abstract 1
- 229940109248 cromoglycate Drugs 0.000 abstract 1
- IMZMKUWMOSJXDT-UHFFFAOYSA-N cromoglycic acid Chemical compound O1C(C(O)=O)=CC(=O)C2=C1C=CC=C2OCC(O)COC1=CC=CC2=C1C(=O)C=C(C(O)=O)O2 IMZMKUWMOSJXDT-UHFFFAOYSA-N 0.000 abstract 1
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- 229940079593 drug Drugs 0.000 abstract 1
- 229960000325 emedastine Drugs 0.000 abstract 1
- KBUZBQVCBVDWKX-UHFFFAOYSA-N emedastine Chemical compound N=1C2=CC=CC=C2N(CCOCC)C=1N1CCCN(C)CC1 KBUZBQVCBVDWKX-UHFFFAOYSA-N 0.000 abstract 1
- 229960003276 erythromycin Drugs 0.000 abstract 1
- 239000003889 eye drop Substances 0.000 abstract 1
- 229940012356 eye drops Drugs 0.000 abstract 1
- 239000012530 fluid Substances 0.000 abstract 1
- FAOZLTXFLGPHNG-KNAQIMQKSA-N fluorometholone Chemical compound C([C@@]12C)=CC(=O)C=C1[C@@H](C)C[C@@H]1[C@]2(F)[C@@H](O)C[C@]2(C)[C@@](O)(C(C)=O)CC[C@H]21 FAOZLTXFLGPHNG-KNAQIMQKSA-N 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- 229960002518 gentamicin Drugs 0.000 abstract 1
- 229940014041 hyaluronate Drugs 0.000 abstract 1
- 229960000890 hydrocortisone Drugs 0.000 abstract 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 abstract 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 abstract 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 abstract 1
- 229960003943 hypromellose Drugs 0.000 abstract 1
- 229960000318 kanamycin Drugs 0.000 abstract 1
- 229930027917 kanamycin Natural products 0.000 abstract 1
- SBUJHOSQTJFQJX-NOAMYHISSA-N kanamycin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N SBUJHOSQTJFQJX-NOAMYHISSA-N 0.000 abstract 1
- 229930182823 kanamycin A Natural products 0.000 abstract 1
- 229960004958 ketotifen Drugs 0.000 abstract 1
- GGXICVAJURFBLW-CEYXHVGTSA-N latanoprost Chemical compound CC(C)OC(=O)CCC\C=C/C[C@H]1[C@@H](O)C[C@@H](O)[C@@H]1CC[C@@H](O)CCC1=CC=CC=C1 GGXICVAJURFBLW-CEYXHVGTSA-N 0.000 abstract 1
- 229960001160 latanoprost Drugs 0.000 abstract 1
- 229960000831 levobunolol Drugs 0.000 abstract 1
- IXHBTMCLRNMKHZ-LBPRGKRZSA-N levobunolol Chemical compound O=C1CCCC2=C1C=CC=C2OC[C@@H](O)CNC(C)(C)C IXHBTMCLRNMKHZ-LBPRGKRZSA-N 0.000 abstract 1
- 229960001120 levocabastine Drugs 0.000 abstract 1
- ZCGOMHNNNFPNMX-KYTRFIICSA-N levocabastine Chemical compound C1([C@@]2(C(O)=O)CCN(C[C@H]2C)[C@@H]2CC[C@@](CC2)(C#N)C=2C=CC(F)=CC=2)=CC=CC=C1 ZCGOMHNNNFPNMX-KYTRFIICSA-N 0.000 abstract 1
- 229960003376 levofloxacin Drugs 0.000 abstract 1
- 229960004305 lodoxamide Drugs 0.000 abstract 1
- RVGLGHVJXCETIO-UHFFFAOYSA-N lodoxamide Chemical compound OC(=O)C(=O)NC1=CC(C#N)=CC(NC(=O)C(O)=O)=C1Cl RVGLGHVJXCETIO-UHFFFAOYSA-N 0.000 abstract 1
- 229960002422 lomefloxacin Drugs 0.000 abstract 1
- ZEKZLJVOYLTDKK-UHFFFAOYSA-N lomefloxacin Chemical compound FC1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC(F)=C1N1CCNC(C)C1 ZEKZLJVOYLTDKK-UHFFFAOYSA-N 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
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- 229960002704 metipranolol Drugs 0.000 abstract 1
- BLWNYSZZZWQCKO-UHFFFAOYSA-N metipranolol hydrochloride Chemical compound [Cl-].CC(C)[NH2+]CC(O)COC1=CC(C)=C(OC(C)=O)C(C)=C1C BLWNYSZZZWQCKO-UHFFFAOYSA-N 0.000 abstract 1
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- JBIMVDZLSHOPLA-LSCVHKIXSA-N olopatadine Chemical compound C1OC2=CC=C(CC(O)=O)C=C2C(=C/CCN(C)C)\C2=CC=CC=C21 JBIMVDZLSHOPLA-LSCVHKIXSA-N 0.000 abstract 1
- 229960000625 oxytetracycline Drugs 0.000 abstract 1
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- IWVCMVBTMGNXQD-PXOLEDIWSA-N oxytetracycline Chemical compound C1=CC=C2[C@](O)(C)[C@H]3[C@H](O)[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-PXOLEDIWSA-N 0.000 abstract 1
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- SONNWYBIRXJNDC-VIFPVBQESA-N phenylephrine Chemical compound CNC[C@H](O)C1=CC=CC(O)=C1 SONNWYBIRXJNDC-VIFPVBQESA-N 0.000 abstract 1
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- PHUTUTUABXHXLW-UHFFFAOYSA-N pindolol Chemical compound CC(C)NCC(O)COC1=CC=CC2=NC=C[C]12 PHUTUTUABXHXLW-UHFFFAOYSA-N 0.000 abstract 1
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- 229960005205 prednisolone Drugs 0.000 abstract 1
- OIGNJSKKLXVSLS-VWUMJDOOSA-N prednisolone Chemical compound O=C1C=C[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OIGNJSKKLXVSLS-VWUMJDOOSA-N 0.000 abstract 1
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- 150000003431 steroids Chemical class 0.000 abstract 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 abstract 1
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- NLVFBUXFDBBNBW-PBSUHMDJSA-N tobramycin Chemical compound N[C@@H]1C[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N NLVFBUXFDBBNBW-PBSUHMDJSA-N 0.000 abstract 1
- 231100000331 toxic Toxicity 0.000 abstract 1
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- QQJLHRRUATVHED-UHFFFAOYSA-N tramazoline Chemical compound N1CCN=C1NC1=CC=CC2=C1CCCC2 QQJLHRRUATVHED-UHFFFAOYSA-N 0.000 abstract 1
- MKPLKVHSHYCHOC-AHTXBMBWSA-N travoprost Chemical compound CC(C)OC(=O)CCC\C=C/C[C@H]1[C@@H](O)C[C@@H](O)[C@@H]1\C=C\[C@@H](O)COC1=CC=CC(C(F)(F)F)=C1 MKPLKVHSHYCHOC-AHTXBMBWSA-N 0.000 abstract 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/07—Tetrapeptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/06—Tripeptides
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- A—HUMAN NECESSITIES
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Abstract
Métodos para la prevencion y el tratamiento de trastornos oculares, en particular glaucoma, a través del bloqueo de los efectos toxicos de derivados de beta-amiloide (Abeta), y composiciones farmacéuticas para efectuar dicha prevencion y su tratamiento. Reivindicacion 1: El uso de un péptido, caracterizado porque comprende la secuencia de aminoácidos X-Y o Y-X, en donde X es un aminoácido aromático e Y es uno o más aminoácidos adicionales distintos de glicina, en donde el péptido tiene al menos 2 residuos de aminoácidos y menos de 15 residuos de aminoácidos, para la fabricacion de un medicamento para la prevencion y el tratamiento de una condicion optica asociada con toxicidad de beta-amiloide (Abeta) en donde se inhibe la formacion y/o aparicion de dicho Abeta. Reivindicacion 3: El uso del péptido de acuerdo con la reivindicacion 1 en combinacion con al menos un agente farmacéutico adicional que es efectivo en el tratamiento de la condicion optica, caracterizado porque la combinacion del péptido de acuerdo con la reivindicacion 1 y el al menos un agente farmacéutico adicional es efectivo para tratar la condicion, Reivindicacion 4: El uso de acuerdo con la reivindicacion 3, caracterizado porque el al menos un agente farmacéutico adicional se selecciona de medicaciones administrados para tratar enfermedades oculares que contienen fármacos antiglaucoma, antibioticos, fármacos antiinflamatorios, esteroides, fármacos antialérgicos y fluido de lágrimas artificiales. Reivindicacion 5: El uso reivindicado de acuerdo con la reivindicacion 3, caracterizado porque el al menos un agente farmacéutico adicional se selecciona de acetazolamida, diclofenamida, carteolol, timolol, metipranolol, betaxolol, pindolol, levobunolol, brimonidina, clonidina, pilocarpina, carbacol, dipivefrina, apraclonidina, brinzolamida, dorzolaminida, bimatoprost, travaprost, latanoprost, clortetraciclina, ciprofloxacina, ofloxacina, ácido fusidínico, gentamicina, canamicina, levofloxacina, lomefloxacina, oxitetraciclina, natamicina, azidamfenicol, cloranfenicol, tobramicina, eritromicina, polimixina-B, aciclovir, trifluridina, betametasona, dexametasona, fluorometolona, hidrocortisona, prednisolona, rimexolona, cromoglicato, azelastina, lodoxamida, emedastina, nedocromilo, levocabastina, olopatadina, ketotifeno, hipromelosa, carbomero, hialuronato, carmelosa, hipromelosa, povidona, hietelosa, alcohol polivinílico, dexpantenol, tetrizolina, troxerutina, tramazolina, nafazolina, xilometazolina, fenilefrina y antazolina. Reivindicacion 8: El uso reivindicado de acuerdo con la reivindicacion 1, caracterizado porque el medicamento es fabricado para proporcionar el péptido en la forma de gotas oculares, cremas oculares y formulaciones intraoculares de deposito. Reivindicacion 12: Una composicion farmacéutica para la prevencion y el tratamiento de una condicion optica asociada con toxicidad de beta-amiloide (Abeta), caracterizada porque la formacion de Abeta y/o la aparicion de dicho Abeta es inhibida al comprender un péptido de acuerdo con la reivindicacion 1, o una de sus sales por adicion de ácido farmacéuticamente aceptable, solo o en combinacion con uno o más portadores y/o excipientes farmacéuticamente aceptables. Reivindicacion 13: Una composicion farmacéutica para la prevencion y el tratamiento de una condicion optica asociada con toxicidad de beta-amiloide (Abeta), caracterizada porque la formacion de Abeta y/o la aparicion de dicho Abeta es inhibida al comprender un péptido de acuerdo con la reivindicacion 3, o una de sus sales por adicion de ácido farmacéuticamente aceptable, solo o en combinacion con uno o más portadores y/o excipientes farmacéuticamente aceptables. Reivindicacion 14: Un péptido que comprende la secuencia de aminoácidos X-Y o Y-X, en donde X es un aminoácido aromático e Y es uno o más aminoácido adicionales distinto de glicina, caracterizado porque el péptido tiene al menos 2 residuos de aminoácidos y menos de 15 residuos de aminoácidos, para la prevencion y el tratamiento de una condicion optica asociada con toxicidad de beta-amiloide (Abeta) en donde a formacion de Abeta y/o la aparicion de dicho Abeta está inhibida.
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TWI486162B (zh) * | 2010-06-16 | 2015-06-01 | Sinphar Pharmaceutical Co Ltd | 異類葉升麻苷或其醫藥學上可接受之鹽於抑制澱粉樣β肽生成、累積或聚集、以及製備預防或治療澱粉樣β肽相關疾病或狀況的藥物之用途 |
EP2632897B1 (en) | 2010-10-29 | 2014-10-01 | Merz Pharma GmbH & Co. KGaA | Indole derivatives and process for their preparation |
EP2640737B1 (en) | 2010-11-15 | 2018-08-29 | Ramot at Tel-Aviv University Ltd. | Dipeptide analogs for treating conditions associated with amyloid fibril formation |
TW201412325A (zh) * | 2012-06-20 | 2014-04-01 | 梅茲製藥有限兩合公司 | 用於治療患有青光眼及其他退化性眼疾之人類視力喪失的間隔醫療 |
-
2007
- 2007-10-02 EP EP07253904A patent/EP2044951A1/en not_active Withdrawn
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2008
- 2008-08-18 TW TW097131444A patent/TWI400080B/zh not_active IP Right Cessation
- 2008-08-21 US US12/733,270 patent/US20100204137A1/en not_active Abandoned
- 2008-08-21 AU AU2008290825A patent/AU2008290825B2/en not_active Ceased
- 2008-08-21 WO PCT/EP2008/006888 patent/WO2009024346A2/en active Application Filing
- 2008-08-21 EP EP08785661A patent/EP2180898A2/en not_active Withdrawn
- 2008-08-21 CA CA002688215A patent/CA2688215A1/en not_active Abandoned
- 2008-08-21 RU RU2010110544/15A patent/RU2481120C2/ru not_active IP Right Cessation
- 2008-08-21 JP JP2010519389A patent/JP2010535728A/ja active Pending
- 2008-08-21 MX MX2009013604A patent/MX2009013604A/es unknown
- 2008-08-21 CN CN200880021418A patent/CN101743015A/zh active Pending
- 2008-08-21 AR ARP080103650A patent/AR069729A1/es unknown
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2016
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2019
- 2019-12-01 US US16/699,662 patent/US10987400B2/en active Active
Also Published As
Publication number | Publication date |
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JP2010535728A (ja) | 2010-11-25 |
AU2008290825A1 (en) | 2009-02-26 |
MX2009013604A (es) | 2010-01-26 |
WO2009024346A2 (en) | 2009-02-26 |
RU2481120C2 (ru) | 2013-05-10 |
TWI400080B (zh) | 2013-07-01 |
EP2044951A1 (en) | 2009-04-08 |
CN101743015A (zh) | 2010-06-16 |
CA2688215A1 (en) | 2009-02-26 |
US20200085906A1 (en) | 2020-03-19 |
WO2009024346A3 (en) | 2009-06-04 |
US10987400B2 (en) | 2021-04-27 |
US20170065664A1 (en) | 2017-03-09 |
TW200916112A (en) | 2009-04-16 |
US10525097B2 (en) | 2020-01-07 |
US20100204137A1 (en) | 2010-08-12 |
AU2008290825B2 (en) | 2012-07-12 |
RU2010110544A (ru) | 2011-09-27 |
EP2180898A2 (en) | 2010-05-05 |
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