MindMed reported its Q3 2022 financial results, highlighting the initiation of patient dosing in the Phase 2b dose-optimization study of MM-120 for GAD and advancements in IND-enabling studies for MM-402. The company's cash and cash equivalents of $154.5 million are expected to fund operations into the first half of 2025.
Initiated patient dosing in Phase 2b dose-optimization study of MM-120 for the treatment of Generalized Anxiety Disorder (GAD), with key clinical readout expected in late 2023.
Advanced IND-enabling studies for MM-402 and initiated a Phase 1 investigator-initiated trial in Q3 2022.
Enhanced financial resources with approximately $60.0 million in gross proceeds from an at-the-market selling program and a public offering.
Cash and cash equivalents totaled $154.5 million, expected to fund the current operating plan into the first half of 2025.
MindMed expects topline results from the Phase 2b dose-optimization study of MM-120 for GAD and the Phase 2a proof-of-concept trial for ADHD in the second half of 2023. Initiation of a Phase 1 clinical trial of MM-402 is planned in 2023.