Donanemab (LY3002813) dose-escalation study in Alzheimer's disease.

Alzheimer's disease dementia donanemab mild to moderate tolerability

Journal

Alzheimer's & dementia (New York, N. Y.)
ISSN: 2352-8737
Titre abrégé: Alzheimers Dement (N Y)
Pays: United States
ID NLM: 101650118

Informations de publication

Date de publication:
2021
Historique:
received: 14 10 2020
accepted: 15 10 2020
entrez: 22 2 2021
pubmed: 23 2 2021
medline: 23 2 2021
Statut: epublish

Résumé

This study explored the safety and tolerability features of donanemab (LY3002813) in patients with mild cognitive impairment due to Alzheimer's disease (AD) or mild to moderate AD dementia. Patients with AD were enrolled into the single-ascending dose phase and were administered a single, intravenous (IV) dose of donanemab (five dosing cohorts from 0.1 to 10 mg/kg) or placebo followed by a 12-week follow-up period for each dose level. After the follow-up period, the same patients proceeded into the multiple-ascending dose (MAD) phase (five cohorts) and were administered IV doses of donanemab (0.3 to 10 mg/kg) or placebo approximately once per month for up to four doses depending on the initial doses (only cohort 1 went from 0.1 mg/kg to a higher dose of 0.3 mg/kg during the MAD phase). This phase concluded with a 12-week follow-up period. The relative exposure assessment of an unblinded, single, subcutaneous 3-mg/kg dose of donanemab in patients with AD was also performed, followed by a 12-week follow-up period. One cohort of healthy subjects received an unblinded, single, IV 1-mg/kg dose of donanemab. These two cohorts did not continue to the MAD phase. Donanemab was generally well tolerated up to 10 mg/kg. After single-dose administration from 0.1 to 3.0 mg/kg, the mean terminal elimination half-life was ≈4 days, increasing to ≈10 days at 10 mg/kg. Only the 10-mg/kg dose showed changes in amyloid positron emission tomography. Amyloid reduction of 40% to 50% was achieved. Approximately 90% of subjects developed anti-drug antibodies at 3 months after a single intravenous dose. Intravenous donanemab 10 mg/kg can reduce amyloid deposits in AD despite having a shorter than expected half-life.

Identifiants

pubmed: 33614890
doi: 10.1002/trc2.12112
pii: TRC212112
pmc: PMC7882532
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e12112

Informations de copyright

© 2020 The Authors. Alzheimer's & Dementia: Translational Research & Clinical Interventions published by Wiley Periodicals, Inc. on behalf of Alzheimer's Association.

Déclaration de conflit d'intérêts

Authors are employees and minor stockholders of Eli Lilly and Company. Anne Hawdon is a former employee of Eli Lilly and Company.

Références

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Auteurs

Stephen Loucian Lowe (SL)

Eli Lilly and Company Lilly Centre for Clinical Pharmacology Singapore Singapore.

Brian A Willis (BA)

Eli Lilly and Company Lilly Corporate Center DC 1532 Indianapolis Indiana USA.

Anne Hawdon (A)

Eli Lilly and Company Limited Erl Wood Manor, Windlesham United Kingdom.

Fanni Natanegara (F)

Eli Lilly and Company Lilly Corporate Center DC 1532 Indianapolis Indiana USA.

Laiyi Chua (L)

Eli Lilly and Company Lilly Corporate Center DC 1532 Indianapolis Indiana USA.

Joanne Foster (J)

Eli Lilly and Company Limited Erl Wood Manor, Windlesham United Kingdom.

Sergey Shcherbinin (S)

Eli Lilly and Company Lilly Corporate Center DC 1532 Indianapolis Indiana USA.

Paul Ardayfio (P)

Eli Lilly and Company Lilly Corporate Center DC 1532 Indianapolis Indiana USA.

John R Sims (JR)

Eli Lilly and Company Lilly Corporate Center DC 1532 Indianapolis Indiana USA.

Classifications MeSH