Definitions
from Wiktionary, Creative Commons Attribution/Share-Alike License.
- noun organic chemistry Any
cyclic acetal derived fromacetone and adiol , especially from avicinal diol .
Etymologies
from Wiktionary, Creative Commons Attribution/Share-Alike License
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Examples
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Its advanced product candidate, ILUVIEN, is an investigational intravitreal insert containing fluocinolone acetonide FAc, a non-proprietary corticosteroid with demonstrated efficacy in the treatment of ocular disease.
unknown title 2011
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Each ILUVIEN insert is designed to provide a therapeutic effect of up to 36 months by delivering sustained sub-microgram levels of the corticosteroid fluocinolone acetonide FAc.
unknown title 2011
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Each ILUVIEN insert is designed to provide a therapeutic effect of up to 36 months by delivering sustained sub-microgram levels of fluocinolone acetonide FAc.
unknown title 2011
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The implant releases low daily doses of the steroid fluocinolone acetonide for as long as three years.
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Its advanced product candidate ILUVIEN is an intravitreal insert containing fluocinolone acetonide FAc, a non-proprietary corticosteroid with demonstrated efficacy in the treatment of ocular disease.
unknown title 2011
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Iluvien is a tiny tube implanted into the eyeball that releases low daily doses of the steroid fluocinolone acetonide for as long as three years.
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The Company's most advanced product candidate, ILUVIEN®, delivers the corticosteroid fluocinolone acetonide (FAc) for the treatment of diabetic macular edema (DME).
unknown title 2011
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The Company's most advanced product candidate, Iluvien(R), delivers fluocinolone acetonide (FA) for the treatment of diabetic macular edema.
unknown title 2011
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Its advanced product candidate, ILUVIEN, is an investigational intravitreal insert containing fluocinolone acetonide FAc, a non-proprietary corticosteroid with demonstrated efficacy in the treatment of ocular disease.
unknown title 2011
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These submissions were based on clinical trials that showed gouty arthritis patients treated with ACZ885 at the time of an attack experienced superior pain relief at 72 hours and a significant reduction in the risk of new attacks over six months, compared to patients treated with the injectable steroid, triamcinolone acetonide TA1.
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