PMID- 35510270 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220716 IS - 1177-5467 (Print) IS - 1177-5483 (Electronic) IS - 1177-5467 (Linking) VI - 16 DP - 2022 TI - Efficacy and Patient Tolerability of Omidenepag Isopropyl in the Treatment of Glaucoma and Ocular Hypertension. PG - 1261-1279 LID - 10.2147/OPTH.S340386 [doi] AB - Current therapeutic approaches for glaucoma aim to reduce intraocular pressure (IOP), which is the only available and reliable strategy proven to control the risk of disease development and progression. Omidenepag isopropyl (OMDI) is a novel topical ocular hypotensive agent that was launched onto the market for the treatment of glaucoma and ocular hypertension (OHT). After topical instillation and during corneal penetration, OMDI is converted into the active metabolite omidenepag (OMD), which behaves as a non-prostaglandin, selective E-prostanoid subtype 2 (EP2) receptor agonist. The topical administration of 0.002% OMDI once-daily (QD) possesses a 20-35% IOP-lowering effect, comparable to that of prostaglandin analogs targeting F-prostanoid (FP) receptor QD, which are the current first-line for pharmaceutical reduction of IOP. However, the mechanism of action and adverse events (AEs) of OMDI are different from those of FP receptor agonists. OMDI reduces IOP by enhancing both conventional trabecular and uveoscleral outflow facilities without complications of prostaglandin-associated periorbitopathy (PAP) seen with FP receptor agonists. Moreover, OMDI was also effective and well-tolerated in non-/poor responders to latanoprost and showed a stable IOP-lowering effect for one year, and its concomitant use with timolol enhanced the IOP-lowering effect. OMDI demonstrated acceptable safety and tolerability with good adherence and can be used in almost every patient. However, OMDI has some AEs such as conjunctival hyperemia, corneal thickening, macular edema/cystoid macular edema and ocular inflammation. Moreover, OMDI is contraindicated in patients who are allergic to the product, in aphakic or pseudophakic eyes, and in combination with tafluprost eye drops. If used appropriately in the right patients, OMDI could be an effective treatment option for glaucoma and OHT as a first-line alternative to FP agonists. Here, we summarize the results of clinical studies of OMDI and discuss its efficacy and patient tolerability in glaucoma and OHT in this review. CI - (c) 2022 Matsuo et al. FAU - Matsuo, Masato AU - Matsuo M AUID- ORCID: 0000-0001-5261-669X AD - Department of Ophthalmology, Shimane University Faculty of Medicine, Izumo City, Shimane, 693-8501, Japan. FAU - Matsuoka, Yotaro AU - Matsuoka Y AD - Division of Ophthalmology, Matsue Red Cross Hospital, Matsue, Shimane, 690-8506, Japan. FAU - Tanito, Masaki AU - Tanito M AD - Department of Ophthalmology, Shimane University Faculty of Medicine, Izumo City, Shimane, 693-8501, Japan. LA - eng PT - Journal Article PT - Review DEP - 20220426 PL - New Zealand TA - Clin Ophthalmol JT - Clinical ophthalmology (Auckland, N.Z.) JID - 101321512 PMC - PMC9058248 OTO - NOTNLM OT - EP2 receptor OT - adverse event OT - glaucoma OT - intraocular pressure OT - omidenepag OT - prostaglandin COIS- Santen Pharmaceutical Co., Ltd. provided information on the status of latest clinical trials of OMDI and assisted us in the preparation of Figures 1 and 2. No involvement was made in the writing or reviewing. The authors report no conflicts of interest in this work. EDAT- 2022/05/06 06:00 MHDA- 2022/05/06 06:01 PMCR- 2022/04/26 CRDT- 2022/05/05 02:39 PHST- 2022/01/23 00:00 [received] PHST- 2022/04/14 00:00 [accepted] PHST- 2022/05/05 02:39 [entrez] PHST- 2022/05/06 06:00 [pubmed] PHST- 2022/05/06 06:01 [medline] PHST- 2022/04/26 00:00 [pmc-release] AID - 340386 [pii] AID - 10.2147/OPTH.S340386 [doi] PST - epublish SO - Clin Ophthalmol. 2022 Apr 26;16:1261-1279. doi: 10.2147/OPTH.S340386. eCollection 2022.