Preservative-Free versus Benzalkonium Chloride-Preserved Latanoprost Ophthalmic Solution in Patients with Primary Open-Angle Glaucoma or Ocular Hypertension: A Phase 3 US Clinical Trial

被引:0
|
作者
Bacharach, Jason [1 ]
Ahmed, Iqbal Ike K. [2 ]
Sharpe, Elizabeth [3 ]
Korenfeld, Michael S. [4 ]
Zhang, Steven [5 ]
Baudouin, Christophe [6 ,7 ]
机构
[1] North Bay Eye Associates, Sonoma, CA 95476 USA
[2] Univ Utah, John Moran Eye Ctr, Salt Lake City, UT USA
[3] Glaucoma Consultants & Ctr Eye Res, Mt Pleasant, SC USA
[4] Comprehens Eye Care, Washington, MO USA
[5] Thea Pharm Inc, Lexington, MA USA
[6] Paris Saclay Versailles St Quentin Univ, Quinze Vingts Natl Ophthalmol Hosp, Versailles, Paris, France
[7] Paris Saclay Versailles St Quentin Univ, Vision Inst, IHU Foresight, Paris, France
来源
CLINICAL OPHTHALMOLOGY | 2023年 / 17卷
关键词
glaucoma; ocular hypertension; intraocular pressure; benzalkonium chloride; latanoprost; preservative; QUALITY-OF-LIFE; SURFACE DISEASE; EYE DROPS; MULTICENTER; PROGRESSION; PREVALENCE; EFFICACY; SAFETY;
D O I
10.2147/OPTH.S414015
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To evaluate the safety and efficacy of a preservative-free latanoprost 0.005% formulation (T2345) in patients with primary open-angle glaucoma (POAG) or ocular hypertension (OHT) compared to benzalkonium chloride-preserved latanoprost 0.005% Patients and Methods: A prospective, randomized, multicenter, observer-masked, parallel-group study enrolled 335 patients diagnosed with POAG or OHT from 31 US sites who had adequately controlled intraocular pressure (IOP; & LE;18 mm Hg) with latanoprost monotherapy. After a & GE;72-hour washout period, patients were randomized to T2345 (n=165) or BPL (n=170) groups. Study drugs were dosed once-daily from Day 0 to Day 84 in one or both eyes. The study eye was the eye with lower IOP at baseline. The primary efficacy measure was the between-group comparison of the mean IOP values in the study eye at each time point (8 AM, 10 AM, and 4 PM on Days 15, 42, and 84). Safety measurements included ocular and systemic treatment-emergent adverse eventsResults: Both T2345 and BPL adequately controlled IOP with 95% CIs within 1.5 mm Hg in the study eye at all assessed time points. The percentages of patients with diurnal IOP <18 mm Hg at Day 84 were 73.1% vs 78.7% for the T2345 and BPL groups, respectively. Adverse events were generally mild-to-moderate and primarily ocular. Fewer patients in the T2345 group experienced ocular TEAEs (13.9% vs 22.5%, respectively) and TEAEs with a suspected relationship to the study medication compared with the BPL group (5.5% vs 11.8%, respectively). The most common ocular TEAEs were instillation site pain and conjunctival hyperemia.Conclusion: In patients with POAG or OHT, both T2345 and BPL maintained IOP at or below clinically meaningful values for the duration of the study. T2345 showed a favorable safety profile, with numerically lower incidences of ocular TEAEs than BPL.
引用
收藏
页码:2575 / 2588
页数:14
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