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Apellis Pharmaceuticals (APLS) Announces Publication of 24-Month Results from Phase 3 Studies of SYFOVRE

Apellis Pharmaceuticals (APLS) Announces Publication of 24-Month Results from Phase 3 Studies of SYFOVRE
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United statesUnited kingdomJeffrey heierCaroline baumalLissa pavlukCharles wykoffMeredith kayaExchange commission onResearch groupLancet glob healthExchange commissionApellis pharmaceuticals incApellis pharmaceuticalsRetina consultantsEleonora ladGeographic atrophy

LumiThera Inc : LumiThera Receives Notice of Award for National Eye Institute Grant to Support a 3rd Year Extension to LIGHTSITE III, the U S Multi-Center Clinical Trial for Treating Dry Age-Related Macular Degeneration

LumiThera Inc : LumiThera Receives Notice of Award for National Eye Institute Grant to Support a 3rd Year Extension to LIGHTSITE III, the U S Multi-Center Clinical Trial for Treating Dry Age-Related Macular Degeneration
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United statesBaden wübergLos angelesAllison dabneyClark tedfordDavid boyerNational institute of healthVitreous associates medical groupNational eye instituteFood drug administrationLumithera incCompany valedaNational instituteEleonora ladOphthalmology clinical researchDuke university school

Patients left BLIND after using Syfovre, an FDA-approved drug for vision loss – NaturalNews com

Patients left BLIND after using Syfovre, an FDA-approved drug for vision loss – NaturalNews com
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United statesAmerican society of retinal specialistsHealth rangerDrug administrationApellis pharmaceuticals incEleonora ladApellis pharmaceuticalsAmerican societyRetinal specialistsHealth ranger store

5 Patients Left Blind After Taking Newly Approved Drug Treating Vision Loss

5 Patients Left Blind After Taking Newly Approved Drug Treating Vision Loss
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United statesApellis pharmaceuticals incDuke university medical centerAmerican society of retinal specialistsDrug administrationEleonora ladApellis pharmaceuticalsAmerican societyRetinal specialistsBiopharma dive

Breakthrough Drug Gives Hope To Those Suffering From Macular Degeneration

A breakthrough drug aimed at slowing the progress of macular degeneration was approved by the Food and Drug Administration (FDA).

Wills eye hospitalUnited statesUnited kingdomSunir gargNational eye instituteDuke university medical centerDrug administrationNational eyeEleonora ladEye hospitalWills eye