Alzheimer's drugs don't slow cognitive decline in inherited disease trial

Publicly released:
Australia; NSW; VIC; WA

Two drugs, Gantenerumab and solanezumab, that are being developed for the prevention of Alzheimer’s disease have shown no significant impact on cognitive decline in people with an inherited form of Alzheimer’s disease, according to a phase 2/3 clinical trial. The two drugs are both designed to stimulate the immune system to attack the beta-amyloid plaques that are believed to form in the brain of Alzheimer's patients. The study looked at this inherited form of Alzheimer's because it is a predictable form of the disease, allowing researchers to examine patients before they become symptomatic. Neither drug showed a beneficial effect on cognitive measures compared to placebo, however the authors say one of the drugs, gantenerumab, did show some effect on other biological features of Alzheimer's, which may be worth pursuing. 

News release

From: Springer Nature

Medical research: Investigational drugs for prevention of Alzheimer’s disease do not significantly affect cognitive decline

Gantenerumab and solanezumab — investigational drugs for prevention of Alzheimer’s disease — demonstrated no significant impact on cognitive decline in people with dominantly inherited Alzheimer’s disease (DIAD) in a phase 2/3 clinical trial published in Nature Medicine.

DIAD is a rare form of Alzheimer's disease (AD) — estimated to represent less than 1% of cases — in which patients carry genes that predispose them to the disease. Those with DIAD exhibit characteristics that facilitate the investigation of interventions in both the asymptomatic stages of AD and its symptomatic stages, to delay or slow disease progression. These include the development of Alzheimer’s dementia at a predictable age, the presentation of pathological signs of the disease years before symptom onset, and the low likelihood of experiencing other conditions that contribute to cognitive decline.

Randall Bateman and colleagues assigned 144 people with DIAD to treatment with either gantenerumab or solanezumab or a placebo control for up to seven years. Although both drugs engaged their targets, neither was shown to significantly slow or prevent AD compared with results obtained with the placebo. The therapeutic potential of these treatments, however, remain unclear, given that the asymptomatic placebo group showed no cognitive decline. Furthermore, although the observed absence of cognitive or clinical benefit is a potential roadblock in the journey toward the development of effective drugs against AD, significant reductions in many biological features of AD in patients treated with gantenerumab suggest potential utility in the early treatment of DIAD.

The authors conclude that this trial has emphasized the need for improved and more-sensitive cognitive measures in asymptomatic populations, and the use of higher doses over longer timescales to augment drug-target engagement.

Attachments

Note: Not all attachments are visible to the general public. Research URLs will go live after the embargo ends.

Research Springer Nature, Web page Please link to the article in online versions of your report (the URL will go live after the embargo ends).
Journal/
conference:
Nature Medicine
Research:Paper
Organisation/s: Neuroscience Research Australia (NeuRA), The University of New South Wales, The University of Melbourne, The University of Western Australia, Washington University School of Medicine, USA
Funder: See paper for extensive funding and conflict of interest information
Media Contact/s
Contact details are only visible to registered journalists.