2016
DOI: 10.1136/bjophthalmol-2015-308319
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Three-month outcome of ziv-aflibercept for exudative age-related macular degeneration

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Cited by 32 publications
(16 citation statements)
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“…In August 2012, US Food and Drug Administration approved ziv-aflibercept for the treatment of advanced colorectal carcinoma 9 12. Ziv-aflibercept is packaged at the same concentration of 1.25 mg/0.05 mL as 4 and 8 mL vials.…”
Section: Discussionmentioning
confidence: 99%
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“…In August 2012, US Food and Drug Administration approved ziv-aflibercept for the treatment of advanced colorectal carcinoma 9 12. Ziv-aflibercept is packaged at the same concentration of 1.25 mg/0.05 mL as 4 and 8 mL vials.…”
Section: Discussionmentioning
confidence: 99%
“…The dose of ziv-aflibercept used was 1.25 mg, which is 62.5% of the standard dose of 2 mg aflibercept used in VIEW, VIVID and VISTA protocols;9 12 however, in the VIEW trials, 0.5 and 2.0 mg produced quite comparable outcomes 6 9 12…”
Section: Discussionmentioning
confidence: 99%
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“…Clinical trial conducted by Malik et al [3] to address the safety issue of ziv-aflibercept in vivo and in vitro and concluded that there is non-significant RPE toxicity where, Mansour et al [4] has studied the safety of intravitreal Ziv-aflibercept in six patients and all patients, and the results didn't show any signs of retinal, ocular toxicity or inflammation and suggested that the 0.05 ml Ziv-aflibercept is diluted in 4 ml of vitreous when intravitreally injected, thus it is 80 times diluted which means the final osmolarity of 312 mOsm/kg after intravitreal injection of 0.05 ml Ziv-aflibercept, Masnour et al [5] also studied the safety and efficacy of intravitreal ziv-aflibercept in wet age related macular degeneration and concluded that intravitreal ziv-aflibercept can be safe and effective without causing any ocular toxicity. …”
Section: Discussionmentioning
confidence: 99%