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Latanoprostene bunod

Generic Name
Latanoprostene bunod
Brand Names
Vyzulta
Drug Type
Small Molecule
Chemical Formula
C27H41NO8
CAS Number
860005-21-6
Unique Ingredient Identifier
I6393O0922

Overview

Latanoprostene Bunod has been used in trials studying the treatment of Glaucoma, Ocular Hypertension, Open-Angle Glaucoma, Open Angle Glaucoma, and Intraocular Pressure. As of November 2, 2017 the FDA approved Bausch + Lomb's Vyzulta (latanoprostene bunod opthalmic solution), 0.024% for the indication of reducing intraocular pressure in patients with open-angle glaucoma or ocular hypertension. Latanoprostene bunod is the first prostaglandin analog with one of its metabolites being nitric oxide (NO). The novelty of this agent subsequently lies in the proposed dual mechanism of action that stems from both its prostaglandin F2-alpha analog latanoprost acid metabolite and its ability to donate NO for proposed tissue/cell relaxation effects. In comparison, both latanoprost and latanoprostene bunod contain a latanoprost acid backbone. Conversely however, latanoprostene bunod integrates an NO-donating moiety in lieu of the isopropyl ester typically found in latanoprost.

Background

Latanoprostene Bunod has been used in trials studying the treatment of Glaucoma, Ocular Hypertension, Open-Angle Glaucoma, Open Angle Glaucoma, and Intraocular Pressure. As of November 2, 2017 the FDA approved Bausch + Lomb's Vyzulta (latanoprostene bunod opthalmic solution), 0.024% for the indication of reducing intraocular pressure in patients with open-angle glaucoma or ocular hypertension. Latanoprostene bunod is the first prostaglandin analog with one of its metabolites being nitric oxide (NO). The novelty of this agent subsequently lies in the proposed dual mechanism of action that stems from both its prostaglandin F2-alpha analog latanoprost acid metabolite and its ability to donate NO for proposed tissue/cell relaxation effects. In comparison, both latanoprost and latanoprostene bunod contain a latanoprost acid backbone. Conversely however, latanoprostene bunod integrates an NO-donating moiety in lieu of the isopropyl ester typically found in latanoprost.

Indication

Latanoprostene bunod opthalmic solution is indicated for the reduction of intraocular pressure in patients with open-angle glaucoma or ocular hypertension .

Associated Conditions

  • Increased Intra Ocular Pressure (IOP)

FDA Approved Products

Vyzulta
Manufacturer:Bausch & Lomb Incorporated
Route:OPHTHALMIC
Strength:0.24 mg in 1 mL
Approved: 2024/02/27
NDC:24208-504
Latanoprostene Bunod Ophthalmic Solution, 0.024%
Manufacturer:Gland Pharma Limited
Route:OPHTHALMIC
Strength:0.24 mg in 1 mL
Approved: 2025/05/02
NDC:68083-564
Latanoprostene Bunod Ophthalmic Solution, 0.024%
Manufacturer:Gland Pharma Limited
Route:OPHTHALMIC
Strength:0.24 mg in 1 mL
Approved: 2025/05/02
NDC:68083-563

Singapore Approved Products

VYZULTA (LATANOPROSTENE BUNOD OPHTHALMIC SOLUTION) 0.024%
Manufacturer:Bausch & Lomb, Incorporated.
Form:SOLUTION, STERILE
Strength:0.24mg/ml
Online:Yes
Approved: 2021/06/01
Approval:SIN16214P

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