| Literature DB >> 34079215 |
James A Katz1, Paul M Karpecki2, Alexandra Dorca3, Sima Chiva-Razavi4, Heather Floyd4, Elizabeth Barnes4, Mark Wuttke4, Eric Donnenfeld5.
Abstract
Presbyopia is a common age-related vision disorder characterized by a progressive inability to focus on near objects. If uncorrected or under-corrected, presbyopia can significantly impact patients' quality of life. Presbyopia represents an area of considerable unmet need due to its rising prevalence worldwide as the population ages, the high proportion of under-treated individuals in some parts of the world, and the limitations of currently available corrective methods. Progressive or bifocal spectacles are associated with peripheral blur, a restricted visual field and impaired depth perception, which have been linked to an increased risk of falls in the elderly. Contact lens options can be difficult to maintain due to the development of age-related dry eye symptoms and reduced manual dexterity. Other corrective methods involve surgical interventions that modify the optics of the cornea, replace the crystalline lens, or attempt to restore active accommodation. While patients undergoing surgery report satisfactory outcomes post-operatively, many of them eventually require reading glasses. Non-invasive therapies with novel mechanisms of action are currently being investigated; these include miotic agents and UNR844, a lipoic acid choline ester. In this narrative review, available evidence on presbyopia prevalence, quality of life impact and risk factors are described, with a focus on observational studies in non-clinical settings. The diagnosis pathway and patient journey in presbyopia are outlined, and various treatment options are analyzed. The data reviewed herein reveals significant gaps in the provision of vision correction for this common condition, with a paucity of effective, non-invasive treatment options broadly accessible to presbyopic individuals.Entities:
Keywords: epidemiology; patient characterization; pharmacological therapies; presbyopia; vision correction
Year: 2021 PMID: 34079215 PMCID: PMC8163965 DOI: 10.2147/OPTH.S259011
Source DB: PubMed Journal: Clin Ophthalmol ISSN: 1177-5467
Current Surgical Options for Presbyopia
| Site | Surgical Options |
|---|---|
| Cornea | Monovision (LASIK) |
Presbyopic LASIK* (multifocal laser ablation) | |
Photorefractive keratectomy (PRK) | |
Intracor Femtosecond Laser (LASIK) | |
KAMRATM Corneal Inlay | |
Conductive keratoplasty | |
| Lens: refractive lens exchange | Monovision (monofocal IOL) |
Multifocal IOL | |
Accommodative IOL | |
Light adjustable lens | |
| Sclera* | VisAbility Micro-Insert scleral implant (Refocus Group, Dallas, TX, USA) |
Scleral laser anterior ciliary excision (LaserACE, Ace Vision Group, Newark, CA, USA) | |
Scleral laser micro-excision |
Note: *Not FDA-approved
Abbreviations: IOL, intraocular lens; LASIK, laser-assisted in situ keratomileusis.
Topical Pharmacological Options Currently Under Investigation, Defined as Those Working via Pupil Modulation or Aiming to Restore Accommodation
| Compound Name and Formulation | Mechanism of Action | Clinical Development Status | Key Findings | Manufacturer/ClinicalTrials.gov |
|---|---|---|---|---|
| Pupil modulation | ||||
| Carbachol/brimonidine | Miotic | Phase 2 | Statistically significant improvement in NVA over placebo; effect was maintained over 3 months (N=48) | Therapeutics press release 2020 |
| FOV Tears (pilocarpine/phenylephrine/polyethyleneglycol/nepafenac/pheniramine/naphazoline) | Miotic | Phase 1; currently available in Columbia, with Phase 2 studies ongoing | Pupil size initially decreased and NVA improved up to 5 h (N=14) | Renna et al, 2016 |
| AGN-190584 ophthalmic solution (pilocarpine) | Miotic | Phase 3 complete FDA registration | A statistically significant greater proportion of participants treated with AGN-190584 gained 3 lines or more in mesopic, high contrast, binocular DCNVA (N=327) | Allergan press release 2020 |
| AGN-199201 ophthalmic solution (pilocarpine/oxymetazoline) | Miotic | Phase 2 | Up to 70% of patients had at least a 2-line improvement in uncorrected NVA (N=151) | NCT02780115 |
| PRX ophthalmic solution (aceclidine/tropicamide) | Miotic | Phase 2b | Primary endpoint vs placebo was met; duration of effect was approximately 7 hrs | Presbyopia Therapies press release 2018 |
| Nyxol (phentolamine ophthalmic solution)/pilocarpine | Miotic | Phase 2 | Primary endpoint is percentage of subjects with ≥ 15 letters of improvement in photopic binocular DCNVA | Ocuphire |
| CSF-1 | Miotic | Phase 2b complete | Statistically significant improvement in DCNVA of a 3-line or greater gain. | Orasis Pharmaceuticals press release |
| VISION-1 (pilocarpine) | Miotic | Phase 3 | Primary outcome is the proportion of subjects gaining ≥ 15 letters in mesopic, high contrast, binocular distance corrected near visual acuity (DCNVA) [Time Frame: 120 minutes post-dosing] | Eyenovia |
| Treatments for the underlying cause of presbyopia | ||||
| UNR844 | Lipoic acid choline ester | Phase 1/2 | Bilateral DCNVA improved, with 53.1% UNR844 vs 21.7% placebo subjects gaining ≥10 letters. Improvements in DCNVA were sustained at 5 and 7 months after UNR844 dosing ceased. | Novartis NCT02516306 |
| UNR844 | Lipoic acid choline ester | Phase 2a | Bilateral DCNVA improved, with a four-letter median difference between UNR844 vs placebo groups (p = 0.0924), and no meaningful differences in side effects | Novartis |
Notes: ≥, greater than or equal to; (DC)NVA, (distance-corrected) near vision acuity; N, study population sample size; P, statistically significance; vs, versus. This table only includes products for which clinical data is available.