2016
DOI: 10.1016/j.ophtha.2016.06.043
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Results of the 2-Year Ocriplasmin for Treatment for Symptomatic Vitreomacular Adhesion Including Macular Hole (OASIS) Randomized Trial

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Cited by 88 publications
(139 citation statements)
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“…Ocriplasmin is a first-in-class drug and its safety profile is nowhere near completion. The primary endpoint of the first and main studies was changes on OCT, although these do not always go hand in hand with visual improvement or decline and thus more studies are needed focusing also on visual gain [7,8,10].…”
Section: Discussionmentioning
confidence: 99%
“…Ocriplasmin is a first-in-class drug and its safety profile is nowhere near completion. The primary endpoint of the first and main studies was changes on OCT, although these do not always go hand in hand with visual improvement or decline and thus more studies are needed focusing also on visual gain [7,8,10].…”
Section: Discussionmentioning
confidence: 99%
“…Macular Hole (OASIS) trial was designed by the drug manufacturer to evaluate the long-term efficacy and safety profile of ocriplasmin for the treatment of symptomatic VMA/VMT, including FTMH. 171 This trial demonstrated the long-term efficacy and safety of ocriplasmin, providing improved resolution of symptomatic VMA compared with previous phase III trials.…”
Section: The Ocriplasmin For Treatment For Symptomatic Vitreomacular mentioning
confidence: 70%
“…In the recent OASIS multicenter study, ocriplasmin was validated to be of benefit in the treatment of vitreomacular adhesion, including macular hole, even after 2 years of follow-up. The anatomical success of treatment was significantly higher in the treatment group [16] . In a phase III double-blinded trial [6] , there was a nonsurgical resolution of vitreomacular traction in 26.5% of the patients in the ocriplasmin group compared with 10.1% in the placebo group.…”
Section: Discussionmentioning
confidence: 84%