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dc.rights.licenseopenen_US
dc.contributor.authorSTALMANS, Ingeborg
dc.contributor.authorLIM, Kin Sheng
dc.contributor.authorODDONE, Francesco
dc.contributor.authorFICHTL, Marek
dc.contributor.authorBELDA, Jose I
dc.contributor.authorHOMMER, Anton
dc.contributor.authorLAGANOVSKA, Guna
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorSCHWEITZER, Cedric
ORCID: 0000-0002-2162-9479
IDREF: 133631583
dc.contributor.authorVOYKOV, Bogomil
dc.contributor.authorZARNOWSKI, Tomasz
dc.contributor.authorHOLLÓ, Gábor
dc.date.accessioned2024-11-28T10:06:15Z
dc.date.available2024-11-28T10:06:15Z
dc.date.issued2024-01-01
dc.identifier.issn1435-702Xen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/203516
dc.description.abstractEnPURPOSE   : To compare the efficacy and safety of the fixed-dose combination (FDC) of netarsudil 0.02%/latanoprost 0.005% ophthalmic solution (NET/LAT; Roclanda) with bimatoprost 0.03%/timolol maleate 0.5% (BIM/TIM; Ganfort) ophthalmic solution in the treatment of open-angle glaucoma (OAG) and ocular hypertension (OHT). MERCURY-3 was a 6-month prospective, double-masked, randomized, multicenter, active-controlled, parallel-group, non-inferiority study. Patients (≥ 18 years) with a diagnosis of OAG or OHT in both eyes that was insufficiently controlled with topical medication (IOP ≥ 17 mmHg in ≥ 1 eye and < 28 mmHg in both eyes) were included. Following washout, patients were randomized to once-daily NET/LAT or BIM/TIM for up to 6 months; efficacy was assessed at Week 2, Week 4, and Month 3; safety was evaluated for 6 months. Comparison of NET/LAT relative to BIM/TIM for mean IOP at 08:00, 10:00, and 16:00 h was assessed at Week 2, Week 6, and Month 3. Non-inferiority of NET/LAT to BIM/TIM was defined as a difference of ≤ 1.5 mmHg at all nine time points through Month 3 and ≤ 1.0 mmHg at five or more of nine time points through Month 3. Overall, 430 patients were randomized (NET/LAT, n = 218; BIM/TIM, n = 212), and all received at least one dose of study medication. Efficacy analyses were performed at Month 3 on 388 patients (NET/LAT, n = 184; BIM/TIM, n = 204). NET/LAT demonstrated non-inferiority to BIM/TIM, with a between-treatment difference in IOP of ≤ 1.5 mmHg achieved at all time points and ≤ 1.0 mmHg at the majority of time points (six of nine) through Month 3. Mean diurnal IOP during the study ranged from 15.4 to 15.6 mmHg and 15.2 to 15.6 mmHg in the NET/LAT and BIM/TIM groups respectively, with no between-group statistically significant difference. No significant differences were observed in key secondary endpoints. No serious, treatment-related adverse events (AEs) were observed, and AEs were typically mild/moderate in severity. The most common treatment-related AEs were conjunctival hyperemia (NET/LAT, 30.7%; BIM/TIM, 9.0%) and cornea verticillata (NET/LAT, 11.0%; BIM/TIM, 0%). Once-daily NET/LAT was non-inferior to BIM/TIM in IOP reduction in OAG and OHT, with AEs consistent with previous findings. NET/LAT offers a compelling alternative FDC treatment option for OAG and OHT.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enHumans
dc.subject.enGlaucoma
dc.subject.enOpen-Angle
dc.subject.enTimolol
dc.subject.enBimatoprost
dc.subject.enLatanoprost
dc.subject.enProspective Studies
dc.subject.enIntraocular Pressure
dc.subject.enAntihypertensive Agents
dc.subject.enTonometry
dc.subject.enOcular
dc.subject.enOcular Hypertension
dc.subject.enOphthalmic Solutions
dc.subject.enTreatment Outcome
dc.subject.enDouble-Blind Method
dc.subject.enBenzoates
dc.subject.enbeta-Alanine
dc.title.enMERCURY-3: a randomized comparison of netarsudil/latanoprost and bimatoprost/timolol in open-angle glaucoma and ocular hypertension
dc.title.alternativeGraefes Arch Clin Exp Ophthalmolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1007/s00417-023-06192-0en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed37615697en_US
bordeaux.journalGraefe's Archive for Clinical and Experimental Ophthalmologyen_US
bordeaux.page179-190en_US
bordeaux.volume262en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamLEHA_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDAerie Pharmaceuticalsen_US
bordeaux.identifier.funderIDSantenen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04808563
hal.version1
hal.date.transferred2024-11-28T10:06:18Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Graefe's%20Archive%20for%20Clinical%20and%20Experimental%20Ophthalmology&amp;rft.date=2024-01-01&amp;rft.volume=262&amp;rft.issue=1&amp;rft.spage=179-190&amp;rft.epage=179-190&amp;rft.eissn=1435-702X&amp;rft.issn=1435-702X&amp;rft.au=STALMANS,%20Ingeborg&amp;LIM,%20Kin%20Sheng&amp;ODDONE,%20Francesco&amp;FICHTL,%20Marek&amp;BELDA,%20Jose%20I&amp;rft.genre=article


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