Edesa Biotech Announces FDA IND Clearance for Phase 2 Vitiligo Study
Edesa Biotech said the FDA cleared its IND application for a Phase 2 study of EB06 in vitiligo, allowing recruitment to expand to the United States. Recruitment is underway in Canada, and the company expects U.S. sites to begin enrolling next quarter, with topline data anticipated in fourth-quarter 2027.
Why it matters — The clearance enables U.S. participation in the study and marks a development milestone for Edesa’s EB06 program.