AUGEN & HAUT Zentrum-Praxis Dr. Jacobi, Nürnberg, Germany.
Novaliq GmbH, Heidelberg, Germany.
J Ocul Pharmacol Ther. 2022 Jun;38(5):348-353. doi: 10.1089/jop.2021.0102. Epub 2022 May 4.
NovaTears+Omega-3 is a water-free eye drop solution with non-animal-derived omega-3 fatty acids. It allows to supplement omega-3 fatty acids directly in the tear film of patients with dry eye disease (DED). This post-market clinical follow-up (PMCF) study evaluated for the first time the effects on clinical signs and patient symptoms of DED, and safety and tolerability of NovaTears+Omega-3 (0.2%) eye drops, when used in accordance with its approved label. A prospective, multicenter, single-arm, uncontrolled, open-label observational cohort study was performed in patients suffering from symptoms of evaporative DED. Patients were treated 4 times daily bilaterally according to the instructions for use for 8 weeks, and standard of care clinical end points were assessed at baseline and follow-up. The trial was conducted at 2 investigational sites in Germany, Europe. Thirty-six patients were included and 33 completed the study. NovaTears+Omega-3 (0.2%) showed clinically and statistically significant improvements in various clinical signs, such as total corneal staining, tear film break-up time, and Meibomian gland dysfunction (MGD) score, as well as in symptoms measured by Ocular Surface Disease Index (OSDI) and visual analog scales over the 8-week treatment period with change from baseline values all <0.0001. No worsening of any safety parameter (intraocular pressure, slit-lamp examination, visual acuity) was observed, and no adverse event was reported throughout the study. In this observational PMCF study, NovaTears+Omega-3 was safe and well tolerated. Treatment over an 8-week period resulted in significantly improved clinical signs and subjective symptoms in patients with evaporative dry eye. The study was registered at www.clinicaltrials.gov (NCT04521465).
NovaTears+Omega-3 是一种不含水的滴眼液,含有非动物源性的欧米伽-3 脂肪酸。它可以补充干眼症 (DED) 患者泪膜中的欧米伽-3 脂肪酸。这项上市后临床随访 (PMCF) 研究首次评估了 NovaTears+Omega-3(0.2%)滴眼液在按照批准标签使用时对 DED 的临床体征和患者症状的影响,以及安全性和耐受性。 一项前瞻性、多中心、单臂、非对照、开放性观察队列研究在患有蒸发型 DED 症状的患者中进行。患者按照使用说明每天双侧治疗 4 次,共 8 周,并在基线和随访时评估标准护理临床终点。该试验在欧洲德国的 2 个研究地点进行。 共纳入 36 例患者,其中 33 例完成了研究。NovaTears+Omega-3(0.2%)在各种临床体征方面显示出临床和统计学上的显著改善,例如总角膜染色、泪膜破裂时间和睑板腺功能障碍 (MGD) 评分,以及通过眼表面疾病指数 (OSDI) 和视觉模拟量表测量的症状,在 8 周治疗期间,与基线值相比,所有变化均<0.0001。未观察到任何安全参数(眼压、裂隙灯检查、视力)恶化,整个研究过程中未报告任何不良事件。 在这项观察性 PMCF 研究中,NovaTears+Omega-3 安全且耐受良好。治疗 8 周后,可显著改善蒸发性干眼症患者的临床体征和主观症状。该研究在 www.clinicaltrials.gov 上注册(NCT04521465)。