Strong Phase III Enrollment Progress
MindMed is on track with enrollment in three pivotal Phase III trials for MM120 ODT, targeting Generalized Anxiety Disorder (GAD) and Major Depressive Disorder (MDD).
Breakthrough Therapy Designation
MM120 was granted breakthrough therapy designation by the FDA based on Phase IIb trial results in GAD, showcasing an effect size of 0.81 in the 100-microgram cohort.
Financial Stability
MindMed ended the quarter with $237.9 million in cash, cash equivalents, and investments, projected to fund operations into 2027.
Strategic Leadership Additions
Brandi Roberts, with over 25 years of life sciences financial experience, has joined as CFO, bringing expertise from a prior successful IPO and acquisition.
Commercial Preparation
The company is actively preparing for commercial readiness, including strategic hires and market research indicating strong provider interest in psychedelic therapies.