Safety and efficacy of MIM-D3 ophthalmic solutions in a randomized, placebo-controlled Phase 2 clinical trial in patients with dry eye

被引:50
作者
Meerovitch, Karen [1 ]
Torkildsen, Gail [2 ]
Lonsdale, John [3 ]
Goldfarb, Heidi [4 ]
Lama, Teresa [1 ]
Cumberlidge, Garth [1 ]
Ousler, George W., III [5 ]
机构
[1] Mimetogen Pharmaceut Inc, 1000 La Gauchetiere St West,Suite 900, Montreal, PQ H3B 5H4, Canada
[2] Andover Eye Associates, Andover, MA USA
[3] Cent Maine Eye Care, Lewiston, ME USA
[4] SDC, Tempe, AZ USA
[5] Ora Inc, Andover, MA USA
关键词
nerve growth factor; controlled adverse environment; Mimetogen;
D O I
10.2147/OPTH.S44688
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 ophthalmic MIM-D3, a tyrosine kinase TrkA receptor agonist, in patients with dry eye. Design: A prospective, two-center, randomized, double-masked, placebo-controlled Phase 2 study. Methods: A total of 150 dry eye patients were randomized 1: 1: 1 to study medication (1% MIM-D3, 5% MIM-D3, or placebo) and dosed twice daily (BID) for 28 days. Key eligibility criteria included exacerbation in corneal staining and ocular discomfort in the Controlled Adverse Environment (CAE(SM)) on two visits, separated by 1 week of BID dosing with artificial tears. Safety and efficacy were evaluated at baseline, throughout treatment, and for 2 weeks post-treatment. The pre-specified primary outcome measures were fluorescein corneal staining post-CAE at day 28 and diary worst symptom scores over 28 days. Secondary outcomes included the pre-, post-, and the change from pre-to post-CAE fluorescein and lissamine green staining in both corneal and conjunctival regions, as well as individual diary symptoms. Results: The prespecified primary endpoints were not met. Compared with placebo, fluorescein corneal staining at day 28 was significantly improved (P < 0.05) in the 1% MIMD3 group for the assessment of change from pre-CAE to post-CAE. In addition, following CAE exposure, patients in the 1% MIM-D3 group showed significant improvements versus placebo (P < 0.05) in inferior fluorescein and lissamine green staining after 14 and 28 days. Compared with placebo, patients in the 5% MIM-D3 group reported significantly lower daily diary scores for ocular dryness (P < 0.05). In a subgroup defined by higher symptom scores during the run-in period, significant treatment effects (P < 0.05) were observed for diary symptoms for both MIM-D3 doses. Ocular adverse events were mild and not considered to be treatment-related. Conclusion: Treatment with topical ophthalmic MIM-D3 demonstrated protection against the effects of a CAE challenge on dry eye signs, reduced patient-reported diary symptoms, with a favorable safety profile.
引用
收藏
页码:1275 / 1285
页数:11
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