FDA Approves IND for Hallux Subungual Gel 42%
A New Approach Enabling Physicians to Treat Toenail Fungus at the Point-of-Care
Hallux CEO Mark Taylor said, “My deep appreciation goes to the small and dedicated Hallux team that ran the rigorous 47 subject, multicenter phase 2a pilot that was followed by a productive Type B meeting with the agency and the filing of this new IND enabling HSG 42 to proceed into its first well controlled study." HSG 42 is highly differentiated. It is the first subungual-topical treatment for toenail fungus administered by physicians in-clinic. It is the first antifungal agent to be evaluated against dermatophytoma in a controlled study. Pending statistically significant clinical outcomes, it could be the first terbinafine topical approved by the FDA for onychomycosis.
About Hallux Inc.
Hallux is a clinical stage pharmaceutical company determined to bring to market a novel subungual-topical form of terbinafine that is applied by physicians to treat nail fungus at the point-of-care. Hallux’s goal is to provide chronic sufferers of onychomycosis with a highly effective topical therapy that is quick, safe and administered by physician that kills fungi and reliably facilitates the regrowth of disease-free nail.
Mark Taylor
Hallux Inc.
+1 949-637-4656
Mark@Halluxinc.com
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