To determine NCX 470 (0.1%) and Lumigan (bimatoprost ophthalmic solution, 0.01%-LUM) intraocular pressure (IOP)-lowering activity after single or repeated (5 days) dosing along with changes in aqueous humor (AH) dynamics. Ocular hypotensive activity of NCX 470 and LUM was compared with vehicle (VEH) in Beagle dogs using TonoVet. Non-human primates (NHP) and bioengineered three-dimensional (3D) human Trabecular Meshwork/Schlemm's Canal (HTM/HSC™) constructs exposed to transforming growth factor-2 (TGF2) were used to monitor NCX 470 and LUM-induced changes in AH dynamics. NCX 470 (30 μL/eye) showed greater IOP reduction compared with LUM (30 μL/eye) following single AM dosing [maximum change from baseline (CFB) = -1.39 ± 0.52, -6.33 ± 0.73, and -3.89 ± 0.66 mmHg (mean ± standard error of the mean) for VEH, NCX 470, and LUM, respectively]. Likewise, repeated 5 days daily dosing of NCX 470 resulted in lower IOP than LUM across the duration of the study (average IOP decrease across tests was -0.45 ± 0.22, -6.06 ± 0.15, and -3.60 ± 0.22 mmHg for VEH, NCX 470, and LUM, respectively). NCX 470 increased outflow facility (Cfl) in NHP (Cfl = 0.37 ± 0.09 μL/min/mmHg and Cfl = 0.64 ± 0.17 μL/min/mmHg) as well as (C) in HTM/HSC constructs (C_ = 0.47 ± 0.02 μL/min/mm/mmHg and C_ = 0.76 ± 0.03 μL/min/mm/mmHg). In addition, NCX 470 increased uveoscleral outflow (Fu = 0.62 ± 0.26 μL/min and Fu = 1.53 ± 0.39 μL/min with episcleral venous pressure of 15 mmHg) leaving unaltered aqueous flow (AHF = 2.03 ± 0.22 μL/min and AHF = 1.93 ± 0.31 μL/min) in NHP. NCX 470 elicits greater IOP reduction than LUM following single or repeated dosing. Data in NHP and 3D-HTM/HSC constructs suggest that changes in Cfl and Fu account for the robust IOP-lowering effect of NCX 470.

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