Latanoprostene bunod ophthalmic solution

(Vyzulta®)

Vyzulta®

Drug updated on 9/4/2024

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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  • Vyzulta (latanoprostene bunod ophthalmic solution) is indicated for the reduction of intraocular pressure in patients with open-angle glaucoma or ocular hypertension.
  • This summary is based on the review of one systematic review(s)/meta-analysis(es). [1]
  • LBN vs. Unoprostone: Latanoprostene bunod (LBN) demonstrated a significant reduction in intraocular pressure (IOP) with a mean difference of -3.45 mmHg (95% CI: -4.77 to -2.12) compared to unoprostone.
  • LBN vs. Other Prostaglandin Analogues (PGAs): LBN showed a non-significant reduction in IOP compared to latanoprost (-0.70 mmHg; 95% CI: -1.83 to 0.43), tafluprost (-0.41 mmHg; 95% CI: -1.87 to 1.07), bimatoprost 0.01% (-0.02 mmHg; 95% CI: -1.59 to 1.55), and was slightly less effective than bimatoprost 0.03% (-0.17 mmHg; 95% CI: -1.42 to 1.07).
  • LBN vs. Beta-blockers: LBN was significantly more effective in lowering IOP compared to several beta-blockers, including apraclonidine, betaxolol, brimonidine, brinzolamide, carteolol, dorzolamide, and timolol.
  • There is no safety information available 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 ophthalmic solution) Prescribing Information.2019Bausch Health US, LLC., Bridgewater, NJ

Systematic Reviews / Meta-Analyses

Clinical Practice Guidelines

Document TitleYearSource
Primary open-angle glaucoma preferred practice pattern.2021Ophthalmology