The BACE1 inhibitor verubecestat (MK-8931) reduces CNS β-amyloid in animal models and in Alzheimer’s disease patients

Author:

Kennedy Matthew E.1,Stamford Andrew W.2,Chen Xia1,Cox Kathleen3,Cumming Jared N.2,Dockendorf Marissa F.3,Egan Michael4,Ereshefsky Larry5,Hodgson Robert A.1,Hyde Lynn A.1,Jhee Stanford5,Kleijn Huub J.3,Kuvelkar Reshma1,Li Wei2,Mattson Britta A.6,Mei Hong3,Palcza John7,Scott Jack D.2,Tanen Michael8,Troyer Matthew D.9,Tseng Jack L.9,Stone Julie A.3,Parker Eric M.1,Forman Mark S.9

Affiliation:

1. Department of Neuroscience, Merck Research Laboratories, Kenilworth, NJ 07033, USA.

2. Department of Global Chemistry, Merck Research Laboratories, Kenilworth, NJ 07033, USA.

3. Department of Pharmacokinetics, Pharmacodynamics and Drug Metabolism, Merck Research Laboratories, Kenilworth, NJ 07033, USA.

4. Department of Clinical Research, Merck Research Laboratories, Kenilworth, NJ 07033, USA.

5. PAREXEL, Glendale, CA 91206, USA.

6. Department of Safety Assessment, Merck Research Laboratories, West Point, PA 19446, USA.

7. Department of Biostatistics, Merck Research Laboratories, Kenilworth, NJ 07033, USA.

8. Translational Biomarkers Department, Merck Research Laboratories, Kenilworth, NJ 07033, USA.

9. Department of Translational Medicine, Merck Research Laboratories, Kenilworth, NJ 07033, USA.

Abstract

The BACE1 inhibitor verubecestat safely reduces β-amyloid deposition in rats, monkeys, healthy human subjects, and patients with Alzheimer’s disease.

Funder

Merck & Co. Inc.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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