The Lancet Regional Health. Western Pacific (Apr 2024)

Varenicline solution nasal spray for dry eye disease in Chinese patients: a randomized phase 3 trialResearch in context

  • Lei Tian,
  • Xiuming Jin,
  • Jibing Wang,
  • Yonggen Xu,
  • Chengwei Lu,
  • Shaozhen Zhao,
  • Qian Zhu,
  • Hong Dai,
  • Hao Gu,
  • Mingchang Zhang,
  • Linnong Wang,
  • Xiaohe Lu,
  • Lixiao Ma,
  • Lei Zhu,
  • Qingyan Zeng,
  • Hong Zhang,
  • Yao Fu,
  • Suxia Li,
  • Liming Tao,
  • Qian Ren,
  • Faming Ding,
  • Shenglin Zhang,
  • Shaopin Zhu,
  • Zhiping Li,
  • Ying Jie

Journal volume & issue
Vol. 45
p. 101032

Abstract

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Summary: Background: Dry eye disease has a high prevalence and exerts a significant negative effect on quality of life. In China, there are currently no available nasal sprays to promote natural tear production in patients with dry eye disease. We therefore evaluated the efficacy and safety of OC-01 (varenicline solution) nasal spray versus vehicle in Chinese patients with dry eye disease. Methods: This was a randomized, multicenter, double-masked, vehicle-controlled, phase 3 clinical trial conducted at ophthalmology departments in 20 hospitals across China (NCT05378945). Eligible patients had a diagnosis of dry eye disease based on patient symptoms, Eye Dryness Score (EDS), Schirmer's Test (with topical anesthesia) Score (STS), and corneal fluorescein staining (CFS) score. Participants were randomly assigned 1:1 using an Interactive Web Response System (IWRS) to receive OC-01 0.6 mg/mL twice daily (BID) or vehicle nasal spray. Participants, investigators, and sponsor were all masked to treatment assignment. The primary endpoint was the percentage of subjects in the intention-to-treat population achieving ≥10 mm improvement in STS from baseline at week 4. Findings: In total, 340 patients were randomized from 21 July 2022 to 04 April 2023, 78.8% were female. Patients in the OC-01 group (n = 176) had significantly higher achievement of ≥10 mm improvement in STS (35.8% [n = 63] versus 17.7% [n = 29], stratified odds ratio: 2.67, 95% CI: 1.570–4.533, p = 0.0002) and a significantly greater increase from baseline STS (least-squares mean difference [SE]: 3.87 [0.794], p < 0.0001) at week 4 versus the vehicle group (n = 164). In addition, OC-01 led to a numerically greater reduction in mean EDS from baseline at week 4 compared to the vehicle group (LS mean [SE] difference: −1.3 [2.20]; 95% CI: −5.64 to 2.99, p = 0.5467). The most common adverse event was mild, transient sneezing (78% of OC-01 administrations). No serious adverse events related to nasal administration occurred. Interpretation: OC-01 (varenicline solution) nasal spray BID has clinically meaningful efficacy for reducing the signs (as measured by STS) and may improve the symptoms (as measured by EDS) of dry eye disease, with an excellent safety and tolerability profile, in the Chinese population. Funding: Jixing Pharmaceutical Co. Ltd.

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