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. 2012 Jun 16;32(5):507–517. doi: 10.1007/s10792-012-9589-2

Table 2.

Studies demonstrating the efficacy and safety of rimexolone 1 % for postoperative inflammation

Study parameters Bron et al. [39] Assil et al. [7] Kavuncu et al. [40] Yaylali et al. [41] Hirneiss et al. [42]
Comparator Placebo Placebo PA PA PA and ketorolac
No. of patients 182 197 80 48 45
Treatment duration (weeks) 2 Up to 2 2 2 4
Patients with resolution of ACIa at final visit ( %) Rimexolone—60 % Rimexolone—60 % Not reportedb Not reportedb Not reportedb
Vehicle—28 % Placebo—32 %
Mean IOP at final visit No perceptible changes in IOP Mean decrease in IOP in both treatment groups compared to baseline Rimexolone—13.0 ± 3.2 mmHg Rimexolone—11.6 ± 1.4 mmHg Rimexolone—13.25 mmHg
PA group—14.60 mmHg
PA group—11.7 ± 2.9 mmHg PA group—10.8 ± 1.3 mmHg Ketorolac group—13.73 mmHg
Clinically significant increases in IOP (≥ 10 mmHg) Not reported n = 2 for rimexolone; Not reported Not reported Not reported
n = 2 for placebo

ACI anterior chamber inflammation, IOP intraocular pressure, PA prednisolone acetate

aResolution of ACI defined as anterior chamber cell count <5 and flare Grade 0 (none)

bThe study did not report the percentages of patients with resolution of ACI; instead, mean cell and flare at study visits were reported