Clinical Trial SuccessCYB003's 71% remission rate at 12 months following two 16 mg doses, coupled with its FDA Breakthrough Therapy Designation, underscore meaningful registration potential.
Financial FlexibilityThe recent announcement of a US$500 million convertible debenture facility—with US$50 million now funded—provides additional capital flexibility and extends runway beyond 2026.
Regulatory ProgressCYB003’s durability signal and Breakthrough Therapy Designation, combined with CYB004’s short-acting profile, position Cybin to deliver differentiated, intermittent treatments across mood and anxiety disorders.