Latanoprostene bunod

(Vyzulta®)

Vyzulta®

Drug updated on 12/11/2024

Dosage FormSolution (topical ophthalmic; 0.24 mg/mL [0.024%])
Drug ClassProstaglandin analogs
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the reduction of intraocular pressure in patients with open-angle glaucoma or ocular hypertension.

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Summary
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  • This summary is based on the review of two systematic review(s)/meta-analysis(es). [1-2]
  • Latanoprostene bunod (LBN) demonstrated significant reductions in intraocular pressure (IOP), outperforming unoprostone by -3.45 mm Hg and numerically exceeding latanoprost (-0.70 mm Hg) and tafluprost (-0.41 mm Hg). It was similar to bimatoprost 0.01% (-0.02 mm Hg) and slightly less effective than bimatoprost 0.03% (-0.17 mm Hg).
  • LBN was significantly more effective in reducing IOP compared to beta-blockers, including apraclonidine, betaxolol, brimonidine, brinzolamide, carteolol, dorzolamide, and timolol.
  • There was no difference between medical therapies, including LBN, and placebo or no treatment in terms of visual acuity, quality of life, or functional outcomes.
  • Recently approved glaucoma therapies, including LBN, were associated with an increased risk of adverse events compared to older therapies, though no specific numerical data for LBN alone were provided.
  • There is no further safety information specific to LBN detailed in the reviewed studies.
  • There is no population types or subgroups information available in the reviewed studies.

Product Monograph / Prescribing Information

Document TitleYearSource
Vyzulta (latanoprostene bunod) Prescribing Information.2024Bausch Health US, LLC., Bridgewater, NJ

Systematic Reviews / Meta-Analyses

Clinical Practice Guidelines

Document TitleYearSource
Primary Open-Angle Glaucoma Preferred Practice Pattern2021Ophthalmology