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108 results about "Macula lutea degeneration" patented technology

Deterioration of the eye part called macula lutea of the retina

Compositions and methods for inhibiting drusen complement components C3a and C5a for the treatment of age-related macular degeneration

Activated C3 (C3a) and its receptor (C3aR) and activated C5 (C5a) and its receptor (C5aR) have been shown to induce vascular endothelial growth factor (VEGF) expression in vitro and in vivo. Compositions and methods for inhibiting C3a, C3aR, C5a and C5aR for the treatment and / or prevention of neovascular disease are provided. Also provided are Novel therapeutic targets and diagnostic markers for choroidal neovascularization.
Owner:KENTUCKY UNIVERISTY OF

Alphav integrin receptor antagonists

The present invention relates to novel alkanoic acid derivatives thereof, their synthesis, and their use as αv integrin receptor antagonists. More particularly, the compounds of the present invention are antagonists of the integrin receptors αvβ3 and / or αvβ5 and are useful for inhibiting bone resorption, treating and preventing osteoporosis, and inhibiting vascular restenosis, diabetic retinopathy, macular degeneration, angiogenesis, atherosclerosis, inflammatory arthritis, cancer, and metastatic tumor growth.
Owner:MERCK & CO INC

Anti-c5a antibodies and methods for using the antibodies

The present disclosure relates to, inter alia, antibodies, or antigen-binding fragments thereof, that bind to C5a and to use of the antibodies in methods for treating or preventing complement-associated disorders such as, but not limited to, atypical hemolytic uremic syndrome, age-related macular degeneration, rheumatoid arthritis, sepsis, severe burn, antiphospho lipid syndrome, asthma, lupus nephritis, Goodpasture's syndrome, and chronic obstructive pulmonary disease.
Owner:ALEXION PHARMA INC

Lipoxin A4 Protection for Retinal Cells

InactiveUS20100324138A1Inhibit apoptosisBiocideSenses disorderNeuroprotective factorsOxidative Stress Induction
Lipoxin A4 and its analogs have been found to be effective in inhibiting apoptosis of retinal pigment epithelial cells induced by oxidative stress. Thus lipoxin A4 and its analogs, for example, lipoxin A4 epimer 15, can be used to prevent and treat retinal diseases due to the progressive degeneration of photoreceptors and retinal pigment epithelial cells (RPE cells), e.g., the dry form of age-related macula degeneration. They can also be combined with other compounds known to prevent apoptosis in retinal pigment epithelial cells, e.g., docosahexaenoic acid and neuroprotectin D1.
Owner:BOARD OF SUPERVISORS OF LOUISIANA STATE UNIV & AGRI & MECHANICAL COLLEGE

Sunitinib formulations and methods for use thereof in treatment of ocular disorders

InactiveUS20170273901A1Avoid nerve damageIncreasing encapsulation and incorporationOrganic active ingredientsSenses disorderDiseaseCytotoxicity
Methods for increasing the encapsulation or incorporation of Sunitinib into polymeric matrices have been developed. The resulting formulations provide for more sustained controlled release of sunitinib or its analog or a pharmaceutically acceptable salt thereof. Increased loading is achieved using an alkaline solvent system. The pharmaceutical compositions can be administered to treat or prevent a disease or disorder in or on the eye of a patient associated with vascularization, such as corneal neovascularization and acute macular degeneration. Upon administration, the sunitinib or its analog or salt is released over an extended period of time at concentrations which are high enough to produce therapeutic benefit, but low enough to avoid unacceptable levels of cytotoxicity.
Owner:THE JOHN HOPKINS UNIV SCHOOL OF MEDICINE

Application of chloroxine in preparing anti-angiogenesis medicine

The invention relates to an application of chloroxine in preparing anti-angiogenesis medicine. Until now no relevant reports about the anti-angiogenesis activity of the chloroxine are available. The invention provides the application of chloroxine in preparing anti-angiogenesis medicines, anti-tumor medicines and medicines for preventing wet age-related macular degeneration. The in-vivo pharmacodynamic experiment using a zebra fish angiogenesis model shows that the chloroxine can remarkably suppress zebra fish angiogenesis, remarkably suppress the growth of transplanted human tumor cells and has a therapeutic effect to wet age-related macular degeneration. Therefore, the chloroxine can be used for preparing anti-angiogenesis medicines, anti-tumor medicines and medicines for preventing wet age-related macular degeneration.
Owner:HANGZHOU LEISUO PHARMA

Efficient process for the preparation of lycopene containing oleoresin and lycopene crystals for human consumption

InactiveUS20150004236A1Efficiently preparedEfficient processingPowder deliveryBiocideChemistryAntioxidant
The present invention provides a process for the preparation of lycopene containing oleoresin and lycopene crystals for human consumption. The present invention provides an efficient process for the preparation of lycopene crystals from lycopene containing oleoresin with at least 85% by weight lycopene, containing at least 90% by weight trans-lycopene and trace amounts of cis-lycopene and other carotenoids. The production of commercial grade lycopene crystals with high content of trans-lycopene makes it ideal and suitable for human consumption, use as an anti-oxidant, for applications in prevention of cancer and macular degenerative diseases, as an anti-oxidant, and as a food / feed colorant. The process is simple, convenient, economical and commercially feasible.
Owner:OMNIACTIVE HEALTH TECH

Amelioration of cataracts, macular degeneration and other ophthalmic diseases

InactiveCN101102770AImprovement of cataract developmentProtection from photooxidative damageSenses disorderOrganic chemistryPresbyopiaDisease
Ophthalmically acceptable compositions used in arresting the development of cataract, presbyopia, macular degeneration and other retinopathies, glaucoma, uveitis and various corneal disorders are disclosed. The compositions are also useful as a prophylactic treatment to prevent or delay development of age-related ocular disorders, which include cataracts, presbyopia, glaucoma and macular degeneration. The compositions comprise a pharmaceutically acceptable carrier or diluent and at least one compound having the formula where R1 and R2 are, independently, H or C1 to C3 alkyl ; R3 and R4 are, independently C1 to C3 alkyl; and where R1 and R2, taken together, or R3 and R4, taken together, or both may be cycloalkyl; R5 is H, OH, or C1 to C6 alkyl ; R6 is or C1 to C6 alkyl, alkenyl, alkynyl, or substituted alkyl or alkenyl ; R7 is C1 to C6 alkyl, alkenyl, alkynyl, or substituted alkyl or alkenyl or where R6 and R7, or R5, R6 and R7, taken together, form a carbocycle or heterocycle having from 3 to 7 atoms in the ring.
Owner:OTHERA HLDG

Complement factor B inhibitor as well as pharmaceutical composition, preparation method and application thereof

The invention provides a heterocyclic compound containing piperidine as shown in a formula (I). The compounds are used for treating diseases and diseases related to complement alternative pathway activation, such as paroxysmal nocturnal hemoglobinuria (PNH), IgA nephropathy (IgAN) including C3 glomerulopathy (C3G), membranous nephropathy (MN) and other glomerular diseases, atypical hemolytic uremic syndrome (aHUS), age-related macular degeneration (AMD), diabetic retinopathy (DR), and other diseases associated with abnormal activation of the alternative complement pathway by inhibiting / regulating a complement factor B.
Owner:SHANGHAI MEIYUE BIOTECH DEV

TREATMENT OF OCULAR DISEASES WITH FULLY-HUMAN POST-TRANSLATIONALLY MODIFIED ANTI-VEGF Fab

Compositions and methods are described for the delivery of a fully human post-translationally modified (HuPTM) monoclonal antibody (“mAb”) or the antigen-binding fragment of a mAb against human vascular endothelial growth factor (“hVEGF”)—such as, e.g., a fully human-glycosylated (HuGly) anti-hVEGF antigen-binding fragment—to the retina / vitreal humour in the eye(s) of human subjects diagnosed with ocular diseases caused by increased neovascularization, for example, neovascular age-related macular degeneration (“nAMD”), also known as “wet” age-related macular degeneration (“WAMD”), age-related macular degeneration (“AMD”), and diabetic retinopathy.
Owner:THE JOHN HOPKINS UNIV SCHOOL OF MEDICINE
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