Crossover Randomized Study of Pharmacologic Effects of Ripasudil-Brimonidine Fixed-Dose Combination Versus Ripasudil or Brimonidine

被引:7
|
作者
Tanihara, Hidenobu [1 ]
Yamamoto, Tetsuya [2 ]
Aihara, Makoto [3 ]
Koizumi, Noriko [4 ]
Minami, Hiroomi [5 ]
Kojima, Satoshi [5 ]
Isobe, Tomoyuki [6 ]
Kanazawa, Mizuho [7 ]
Suganami, Hideki [8 ]
机构
[1] Biei Municipal Hosp, Dept Ophthalmol, 3-8-35 Naka Machi, Biei, Hokkaido 0710207, Japan
[2] Kaiya Eye Clin, Prof Kazuo Iwata Mem Kaijin Glaucoma Ctr, Shizuoka, Japan
[3] Univ Tokyo, Dept Ophthalmol, Tokyo, Japan
[4] Doshisha Univ, Fac Life & Med Sci, Dept Biomed Engn, Kyoto, Japan
[5] Kowa Co Ltd, Pharmaceut Clin Dev Management Dept, Tokyo, Japan
[6] Kowa Co Ltd, Tokyo New Drug Res Labs, Tokyo, Japan
[7] Kowa Co Ltd, Med Affairs Dept, Tokyo, Japan
[8] Kowa Co Ltd, Data Sci Ctr, Tokyo, Japan
关键词
Conjunctival hyperemia; Corneal endothelial cell; Intraocular pressure; Pupil diameter; Ripasudil-brimonidine fixed-dose combination; RHO-KINASE INHIBITOR; OPEN-ANGLE GLAUCOMA; VISUAL-FIELD PROGRESSION; INTRAOCULAR-PRESSURE; OCULAR HYPERTENSION; PROTEIN-KINASE; K-115; INSTILLATION; LATANOPROST; REDUCTION;
D O I
10.1007/s12325-023-02534-w
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
IntroductionMultidrug regimens for glaucoma treatment often result in adherence issues due to inconvenience; these issues may be improved with fixed-dose combination drugs. The ophthalmic solution of ripasudil-brimonidine fixed-dose combination (RBFC; K-232) is the first treatment combining a Rho kinase inhibitor and an alpha(2)-adrenoceptor agonist, and has demonstrated ability to lower intraocular pressure (IOP) and have various effects on conjunctival hyperemia and corneal endothelial cell morphology. This study evaluates the pharmacologic effects of RBFC treatment versus its separate components-ripasudil or brimonidine.MethodsThis single-center, prospective, randomized, open-label, blinded endpoint study with 3 x 3 crossover design randomly assigned healthy adult men to three groups (1:1:1) to undergo consecutive 8-day administration phases (with drug-free intervals of at least 5 days). Subjects received twice-daily instillation of RBFC -> ripasudil -> brimonidine (group A), ripasudil -> brimonidine -> RBFC (group B), or brimonidine -> RBFC -> ripasudil (group C). Endpoints included change in IOP, severity of conjunctival hyperemia, corneal endothelial cell morphology, pupil diameter, and pharmacokinetics.ResultsEighteen subjects were assigned in total (six to each group). RBFC significantly reduced IOP from baseline at 1 h post-instillation on days 1 and 8 (12.7 vs. 9.1 and 9.0 mmHg, respectively; both P < 0.001), and provided significantly greater IOP reductions than ripasudil or brimonidine at several time points. The most common adverse drug reaction with all three treatments was mild conjunctival hyperemia, which transiently increased in severity with RBFC or ripasudil, peaking at 15 min post-instillation. In post hoc analyses, conjunctival hyperemia scores were lower with RBFC than with ripasudil at several time points. Transient morphologic changes in corneal endothelial cells occurred for up to several hours with RBFC or ripasudil, but not with brimonidine. Pupil diameter did not change with RBFC.ConclusionRBFC significantly reduced IOP compared with each agent alone. A combination of each agent's pharmacologic profile was observed in that of RBFC.
引用
收藏
页码:3559 / 3573
页数:15
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