Acumen Pharmaceuticals reported a net loss of $10.7 million for the third quarter of 2022, compared to a net loss of $3.9 million for the same period in 2021. As of September 30, 2022, cash, cash equivalents and marketable securities totaled $200.2 million.
INTERCEPT-AD, a Phase 1 clinical trial of ACU193 in patients with early Alzheimer’s disease continues to progress.
Acumen anticipates completing enrollment in the first quarter of 2023 and reporting topline data from this trial in the second half of 2023.
ACU193 was granted Fast Track designation from the U.S. FDA for the treatment of early Alzheimer’s disease.
Cash, cash equivalents and marketable securities of $200.2 million as of Sept. 30, 2022 expected to be sufficient to support clinical and operational goals through 2025.
Acumen anticipates completing enrollment in the first quarter of 2023 and reporting topline data from the INTERCEPT-AD trial in the second half of 2023.