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. 2022 Mar 3;140(4):363–371. doi: 10.1001/jamaophthalmol.2022.0059

Figure 1. Participant Disposition.

Figure 1.

The adverse events leading to study discontinuation were bradycardia (n = 1) and dyschromatopsia and bilateral visual field defect (n = 1) in the AGN-190584 group and corneal abrasion (n = 1) and headache and migraine (n = 1) in the vehicle group.

aParticipants could fail screening owing to multiple reasons.