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. 2024 Oct 28;32(4):101360. doi: 10.1016/j.omtm.2024.101360

Table 1.

Clinical adverse events observations

Horse Dose Adverse event Days identifieda
1. Saline control not applicable none not applicable
2. LD AAV-eqIL-10 (LD 1) 3.75e−11 vgs none not applicable
3. LD AAV-eqIL-10 (LD 2) 3.75e−11 vgs conjunctival hyperemia OD aqueous flare (scores 0.5–1)b OD 35–49
4. HD AAV-eqIL-10 (HD 1) 3.75e−12 vgs keratic precipitates OU 77–86
5. HD AAV-eqIL-10 (HD 2) 3.75e−12 vgs peripapillary depigmentation OD
conjunctival hyperemia OS
keratic precipitates OU
21–86
35
70–86

OD, right eye; OS, left eye; OU, both eyes; vg, viral genome.

a

Ocular examinations were performed on days 0, 1, 3, and 7, and then weekly until day 86.

b

Modified SPOTs (semiquantitative preclinical ocular toxicology) scoring system was used to generate numerical scores.