Bhagat Purvi, Singhania Mukesh, Navare Sujata, Mazumdar Mohua, Paul Chandrima, Shet Satish, Vks Kalyani, Nicholsan Anjali, Bansal Nitesh, Jain Prachi
Ophthalmology, Civil Hospital Campus, Ahmedabad, IND.
Ophthalmology, Anand Multispeciality Hospital, Ahmedabad, IND.
Cureus. 2024 Nov 13;16(11):e73599. doi: 10.7759/cureus.73599. eCollection 2024 Nov.
Introduction Fixed-dose combinations (FDCs) have the potential in glaucoma management to improve efficacy due to the complementary mechanism of action of the drugs as well as compliance while reducing adverse effects by minimizing exposure to preservatives and the financial burden on the patients. FDC of brinzolamide/timolol has demonstrated efficacy and safety in multinational phase 3 studies in primary open-angle glaucoma (POAG) and ocular hypertension. However, efficacy and safety in the Indian population are not known. This study compared the efficacy and safety of FDC brinzolamide 1%/timolol 0.5% with FDC dorzolamide 2%/timolol 0.5% in Indian patients with POAG or ocular hypertension. Material and methods This 12-week randomized, phase 3, open-label, comparative, multicentric study was conducted on 221 subjects at nine sites in India, with assessments done at baseline and weeks 4, 8, and 12. Patients with intraocular pressure (IOP) of 24-36 mmHg of the affected eye(s), either newly diagnosed or inadequately controlled on mono-therapy of carbonic anhydrase inhibitor, beta-blocker, or any other IOP-lowering therapy, were included. Patients were randomly assigned to receive either FDC of brinzolamide 1%/timolol 0.5% (n = 111) or FDC of dorzolamide 2%/timolol 0.5% (n = 110). Primary efficacy was a noninferiority comparison of mean change in two-hour IOP and zero-hour IOP at the end of treatment compared to the respective baseline IOP. Safety was analyzed by comparing the frequency of the observed adverse events (AEs) between the two groups. Results FDC brinzolamide/timolol produced comparable and non-inferior IOP-lowering efficacy to FDC dorzolamide/timolol. The IOP reductions ranged from 6.55 to 8.36 mmHg in FDC brinzolamide/timolol group and from 5.37 to 7.55 mmHg in FDC dorzolamide/timolol group. Fewer subjects in FDC brinzolamide/timolol group experienced ocular AEs as compared with FDC dorzolamide/timolol group (9.9% vs. 26.4%), especially ocular hyperemia (2.7% vs. 22.7%). Conclusion FDC of brinzolamide 1%/timolol 0.5% affords an ocular comfort advantage with a clinically meaningful reduction in IOP that was non-inferior to FDC of dorzolamide 2%/timolol 0.5% in Indian patients with POAG and ocular hypertension.
引言
固定剂量复方制剂(FDCs)在青光眼治疗中具有提高疗效的潜力,因为药物的作用机制具有互补性,可提高患者的依从性,同时通过减少防腐剂暴露降低不良反应,并减轻患者的经济负担。布林佐胺/噻吗洛尔固定剂量复方制剂已在原发性开角型青光眼(POAG)和高眼压症的多国3期研究中证明了其有效性和安全性。然而,其在印度人群中的有效性和安全性尚不清楚。本研究比较了1%布林佐胺/0.5%噻吗洛尔固定剂量复方制剂与2%多佐胺/0.5%噻吗洛尔固定剂量复方制剂在印度POAG或高眼压症患者中的有效性和安全性。
材料与方法
本为期12周的随机、3期、开放标签、对照、多中心研究在印度9个地点的221名受试者中进行,在基线以及第4、8和12周进行评估。纳入患眼眼压(IOP)为24 - 36 mmHg的患者,这些患者要么是新诊断的,要么在碳酸酐酶抑制剂、β受体阻滞剂或任何其他降低眼压治疗的单药治疗中控制不佳。患者被随机分配接受1%布林佐胺/0.5%噻吗洛尔固定剂量复方制剂(n = 111)或2%多佐胺/0.5%噻吗洛尔固定剂量复方制剂(n = 110)。主要疗效指标是治疗结束时两小时眼压和零时眼压的平均变化与各自基线眼压的非劣效性比较。通过比较两组观察到的不良事件(AE)发生率来分析安全性。
结果
布林佐胺/噻吗洛尔固定剂量复方制剂产生了与多佐胺/噻吗洛尔固定剂量复方制剂相当且非劣效的降眼压效果。布林佐胺/噻吗洛尔固定剂量复方制剂组眼压降低范围为6.55至8.36 mmHg,多佐胺/噻吗洛尔固定剂量复方制剂组眼压降低范围为5.37至7.55 mmHg。与多佐胺/噻吗洛尔固定剂量复方制剂组相比,布林佐胺/噻吗洛尔固定剂量复方制剂组发生眼部不良事件的受试者更少(9.9%对26.4%),尤其是眼部充血(2.7%对22.7%)。
结论
1%布林佐胺/0.5%噻吗洛尔固定剂量复方制剂在印度POAG和高眼压症患者中具有眼部舒适度优势,眼压降低具有临床意义且不劣于2%多佐胺/0.5%噻吗洛尔固定剂量复方制剂。