PharmAbcine Receives Safety Review Committee Approval to Advance to Dose Level 2 of Clinical Trial of PMC-403 with Neovascular Age-related Macular Degeneration following Dose Level 1 Safety Data
Safety Review Committee evaluated dose level 1 safety data of PMC-403 and approved advancing to the higher dose treatment.
- Safety Review Committee evaluated dose level 1 safety data of PMC-403 and approved advancing to the higher dose treatment.
- The starting dose (0.7mg) of PMC-403 showed potential in improving eyesight for neovascular age-related macular degeneration patients with suboptimal response to currently available therapies.
- In this clinical study, a maximum of 36 patients with neovascular age-related macular degeneration with suboptimal response to currently available therapy will be evaluated for safety and maximum tolerated dose (MTD) of PMC-403.
- The SRC reviewed the clinical data for dose level 1, and all of the SRC members agreed to advance to the dose level 2.