STOCKHOLM, Oct. 28, 2020 /PRNewswire/ -- BioArctic AB (publ) (Nasdaq Stockholm: BIOA B) announced today that the company's partner Eisai will conduct four oral presentations related to the drug candidate BAN2401 (lecanemab) at the 13th Clinical Trials on Alzheimer's Disease Conference (CTAD) on November 4-7. Presentations will include the latest data on BAN2401, as well as the study design and initial screening results from the Phase 3 program AHEAD 3-45 and baseline characteristics of currently enrolled Alzheimer's disease patients in the Phase 3 study Clarity AD.
During the conference, Eisai will hold four presentations and present new information from all three on-going clinical studies with the investigational anti-amyloid beta (A?) protofibril antibody BAN2401;
Asset in Development, Session Number | Topic/Planned Date and Time(Eastern Standard Time) |
BAN2401 OC2 | The AHEAD 3-45 Study of BAN2401 in Preclinical Alzheimer's Disease: Study Design and Initial Screening Results November 4 (Wednesday) 10:00 - 10:15AM (live session) 11:25 - 11:40 AM, Live Q&A of oral communications |
BAN2401 OC10 | Baseline Characteristics for Clarity AD: A Phase 3 Placebo-Controlled, Double-Blind, Parallel-Group, 18-Month Study Evaluating BAN2401 in Early Alzheimer's Disease November 4 (Wednesday) 1:00 PM (on demand) |
BAN2401 OC14 | BAN2401 and ARIA-E in Early Alzheimer's Disease: Pharmacokinetic/Pharmacodynamic Time-to-Event Analysis from the Phase 2 Study in Early Alzheimer's Disease November 5 (Thursday) 9:45 - 10:00 AM (live session) 11:15 - 11:30 AM, Live Q&A of oral communications |
BAN2401 LB24 | Preliminary Analysis of BAN2401 Effects on Brain Amyloid and ARIA-E Findings Over 12 Months of Treatment in the Open-Label Extension of the Phase2b Study BAN2401-G000-201 in Subjects with Early Alzheimer's Disease November 7 (Saturday) 12:10 AM - 12:25 PM (live session) 12:25 - 12:50 PM, Live Q&A of late breakers |
This release discusses investigational uses of an agent in development and is not intended to convey conclusions about efficacy or safety. There is no guarantee that any investigational uses of such product will successfully complete clinical development or gain health authority approval.
This information was submitted for publication at 08:00 am CET on October 28, 2020.
CONTACT:
Gunilla Osswald, CEO, BioArctic AB
E-mail: [email protected]
Phone: +46-8-695-69-30
Oskar Bosson
Vice President Communications and Investor Relations, BioArctic AB
E-mail: [email protected]
Phone: +46-70-410-71 80
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SOURCE BioArctic
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