Acumen Pharmaceuticals reported a net loss of $42.9 million for the year ended December 31, 2022, with cash, cash equivalents, and marketable securities totaling $193.4 million. The company completed enrollment in its Phase 1 INTERCEPT-AD trial and anticipates topline data in Q3 2023.
Completed enrollment in the Phase 1 INTERCEPT-AD clinical trial of ACU193 in patients with early Alzheimer’s disease.
Topline data from the INTERCEPT-AD trial expected in the third quarter of 2023.
Cash, cash equivalents, and marketable securities totaled $193.4 million as of December 31, 2022, expected to be sufficient to support clinical and operational goals through 2025.
Fast Track designation was granted by the FDA for ACU193 for the treatment of early Alzheimer’s disease in October 2022.
Acumen anticipates reporting topline results from the Phase 1 INTERCEPT-AD trial in the third quarter of 2023 and expects interaction with the FDA in the fourth quarter of 2023. The company believes its cash runway is sufficient through 2025.