A week after Aldeyra’s drug candidate was rejected by the FDA for a rare eye cancer, the biotech touted data on the asset in a small, open-label study in a degenerative retinal disease that leads to blindness.
The biotech said its intravitreally-injected ADX-2191, a formulation of the chemo drug methotrexate, met the primary goal of safety in a Phase II trial in patients with retinitis pigmentosa, who currently have no approved treatment option. ADX-2191 led to statistically significant improvements in retinal function as compared to patients’ visual acuity headed into the study.
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