- Presents Positive Topline Results from First-in-Human Phase 1 Study of ACU193 for Early Alzheimer's Disease at the Alzheimer's Association International Conference (AAIC) 2023
The drug, ACI193, was well tolerated in the first trial testing it in people, the company said. Results of the randomized, placebo-controlled study of 62 patients with early Alzheimer's disease were presented at the Alzheimer's Association's International Conference in Amsterdam.
Acumen's drug targets and binds to amyloid beta oligimers, a toxic, soluble version of the amyloid protein that forms brain plaques associated with the memory-robbing disease, Dr. Eric Siemers, chief medical officer of Acumen, said in an interview.
The target is similar to that of Biogen and Eisai's recently-approved Leqembi, which hits another soluble, toxic form of the protein in the brain. Leqembi won standard U.S. approval earlier this month after showing it could remove amyloid plaques and slow the advance of Alzheimer's in early-stage patients.
In the Acumen trial, 10.4% of treated participants (5 people) developed a brain swelling condition known as ARIA-E associated with amyloid-targeting treatments. Of these, only one had symptoms, which resolved after the drug was stopped.
Another 8.3% developed bleeding in the brain associated with treatment, known as ARIA-H.
Acumen Pharmaceuticals announces $100 million proposed public offering of common stock
Acumen intends to use its net proceeds from the public offering primarily to fund the Phase 2 portion of a future, potential Phase 2/3 adaptable trial of ACU193, to fund chemistry, manufacturing and other research and development activities, and for working capital and other general corporate purposes. |
No comments:
Post a Comment