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Sep 30, 2022

MindMed Q3 2022 Earnings Report

Reported financial results for the quarter ended September 30, 2022, and provided a business update.

Key Takeaways

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.

EPS
-$0.56
Previous year: -$0.9
-37.8%
R&D Expenses
$7.77M
Previous year: $9.02M
-13.8%
G&A Expenses
$9.21M
Previous year: $8.21M
+12.2%
Cash and Equivalents
$155M
Total Assets
$181M

MindMed

MindMed

Forward Guidance

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.

Positive Outlook

  • Topline results from MM-120 Phase 2b trial for GAD expected in the second half of 2023.
  • Topline results from MM-120 Phase 2a trial for ADHD expected in the second half of 2023.
  • Planned initiation of a Phase 1 clinical trial of MM-402 in 2023.
  • Ongoing collaboration with the University Hospital Basel in Switzerland for a Phase 1 trial of R(-)-MDMA, S(+)-MDMA and R/S-MDMA.
  • Prioritizing and focusing development efforts on MM-120 in psychiatric indications.

Challenges Ahead

  • History of negative cash flows.
  • Limited operating history.
  • Incurrence of future losses.
  • Dependence on availability of additional capital.
  • Early stage product development.