In today's world, Latanoprostene bunod remains a topic of constant interest and debate. Over time, its relevance has increased and has impacted different sectors of society. From the personal level to the professional level, Latanoprostene bunod has proven to be a crucial point that cannot be ignored. Its influence has spread to all corners of the world, affecting people of all ages, cultures and conditions. In this article, we will explore in detail the various facets of Latanoprostene bunod and how it has shaped and continues to shape our reality.
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Clinical data | |
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Trade names | Vyzulta |
Other names | BOL-303259-X |
AHFS/Drugs.com | Monograph |
License data | |
Drug class | Prostaglandin analog |
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ECHA InfoCard | 100.251.571 |
Chemical and physical data | |
Formula | C27H41NO8 |
Molar mass | 507.624 g·mol−1 |
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Latanoprostene bunod, sold under the brand name Vyzulta, is an ophthalmic medication used for the reduction of intraocular pressure in people with open-angle glaucoma or ocular hypertension.[2][3] It is a prostaglandin analog[2] which, when broken down by esterases and other metabolism, produces latanoprost acid and eventually nitrous oxide. Latanoprost increases uveoscleral outflow while the nitrous oxide increases outflow via the trabecular meshwork.[3]
The most common side effects include conjunctival (eye) redness, eye irritation, and eye discomfort (pain).[4] Latanoprostene bunod may cause the iris (colored part of the eye) to become darker in color.[4]
Latanoprostene bunod was approved for medical use in the United States in November 2017.[2][4][5]
Latanoprostene bunod is indicated for the reduction of intraocular pressure in people with open-angle glaucoma or ocular hypertension.[2]
The US Food and Drug Administration (FDA) approved latanoprostene bunod based on evidence from two clinical trials that enrolled 840 participants with open angle glaucoma or ocular hypertension.[4] The trials evaluated the benefits and side effects of latanoprostene bunod.[4] In each trial, participants were randomly assigned to receive either latanoprostene bunod or an approved drug timolol (ophthalmic solution) every day for three months.[4] Neither the participants nor the health care providers knew which treatment was being given until after the trials were completed.[4] The trials were conducted in the United States, the United Kingdom, Germany, Italy, Bulgaria, the Czech Republic, and Japan.[4]