Clinical Trial ProgressThe DRAGON study's prior data demonstrated a 50% reduction in lesion growth, significantly exceeding the clinically meaningful threshold, suggesting favorable odds for approval.
Financial PositionThe company closed a public offering, raising $125M, which could support a future commercial launch of tinlarebant in the U.S.
Regulatory ApprovalTinlarebant has been granted several designations in the U.S., including Breakthrough Therapy and Orphan Drug, which are favorable for regulatory approval.