https://doi.org/10.55788/5923d1bf
TRAILBLAZER-ALZ 4 (NCT05108922) is the first study to directly compare disease-modifying therapies in patients with early AD, said Prof. Stephen Salloway (Warren Alpert Medical School of Brown University, RI, USA) [1]. The phase 3 trial was a randomised, open-label, parallel-group study performed in 31 centres across the USA. Participants were 50–85 years old with early symptomatic AD. They were stratified on APOEε4 status and amyloid burden at baseline. Participants randomised to donanemab could discontinue treatment on meeting predefined brain amyloid clearance criteria.
After 7 weeks of screening, 148 participants were included and 74 were assigned to each group. For aducanumab, US-approved label dosing was used; for donanemab, the following clinical trial protocol was applied: 3 doses of IV 700 mg donanemab every 4 weeks, followed by 1400 mg every 4 weeks. The co-primary endpoint was amyloid clearance (to <24.1 cl) at 6 months in the full-analysis set and in the intermediate tau-subpopulation.
Upon assessing florbetapir (18F) PET scans at 6 months, the researchers found that 37.9% of participants in the donanemab group met the co-primary endpoint in the full-analysis set, compared with 1.6% in the aducanumab group (P<0.001). In the intermediate tau subpopulation, these percentages were 38.5 and 3.8, respectively (P=0.008). Donanemab was also superior in reducing plasma phosphor-tau (P-tau217).
The safety profiles of both treatments were consistent with previous study data. “Despite the greater clearance of amyloid in the donanemab group, there was no difference in the incidence of amyloid-related imaging abnormalities (ARIA) characterised by either oedema and effusion (ARIA-E) or cerebral micro-haemorrhages (ARIA-H),” finished Prof. Salloway. The TRAILBLAZER-ALZ 4 study is ongoing; analyses at 12 and 18 months are underway.
- Salloway SP, et al. Direct comparison of donanemab to aducanumab on amyloid lowering in early, symptomatic AD: TRAILBLAZER-ALZ 4 topline study results. S26.009, AAN 2023 Annual Meeting, 22–27 April, Boston, USA.
Copyright ©2023 Medicom Medical Publishers
Posted on
Previous Article
« Original antigenic sin influences humoral immune response to SARS-CoV-2 Next Article
Lecanemab may slow decline of cognition and function in Alzheimer’s Disease »
« Original antigenic sin influences humoral immune response to SARS-CoV-2 Next Article
Lecanemab may slow decline of cognition and function in Alzheimer’s Disease »
Table of Contents: AAN 2023
Featured articles
Letter from the Editor
Positive results for hereditary transthyretin-mediated amyloid polyneuropathy
Infectious Diseases
Allogenic T-cell-based immunotherapy for PML in development
Cognitive Impairment and Dementia
Lecanemab may slow decline of cognition and function in Alzheimer’s Disease
Donanemab shows rapid and deep plaque clearance in early Alzheimer’s Disease
Epilepsy
Seizure forecasting and detection with wearable devices are feasible
Encouraging first results of GABAergic interneurons implants for focal epilepsy
Headache and Migraine
Lecture on migraine: from the prodromal phase to future paradigm shifts
Zavegepant nasal spray exhibits good efficacy and safety in acute migraine
A vaccine as a potentially safe and effective immunotherapy against CGRP
Multiple Sclerosis
Teriflunomide prevents conversion to MS in patients with RIS
Gold nanocrystals may be effective as adjunctive MS therapy
Muscle and Neuro-Muscular Disorders
First-ever ALS platform trial reports on outcomes of 4 treatments
Pridopidine for Huntington’s disease fails to meet the primary endpoint
Parkinson's Disease
Continuous levodopa/carbidopa infusion shows favourable safety and efficacy
Unilateral right STN-DBS improves verbal fluency
Stroke
Harnessing the microbiome as a possible stroke treatment
Patients with a large core infarct benefit from thrombectomy
Miscellaneous
Artificial intelligence applications in neurology: seize the moment
Spinal cord stimulation eases painful diabetic neuropathy
EVT improves functional outcomes in Chinese patients with BAO
Severe sleep apnoea associated with white matter hyperintensities
Related Articles
October 29, 2020
Physical activity improves AHI in sleep apnoea patients
July 5, 2021
OSA: A risk factor for earlier cognitive decline
© 2024 Medicom Medical Publishers. All rights reserved. Terms and Conditions | Privacy Policy
HEAD OFFICE
Laarderhoogtweg 25
1101 EB Amsterdam
The Netherlands
T: +31 85 4012 560
E: publishers@medicom-publishers.com