Could There Be a Vaccine for Alzheimer’s? A New Drug Shows Promise in Trials


Alzheimer’s is an irreversible and progressive brain disorder that affects memory and thinking skills, eventually rendering most patients unable to perform everyday tasks. But a leading clinical-stage biotech company has published completed phase II results of AADvac1, its tau vaccine against Alzheimer’s disease, with positive results. ADAMANT, a 24-month randomised, placebo-controlled, trial, was conducted to assess the safety and efficacy of AADvac1 vaccine in patients with mild Alzheimer’s. While the primary objective was to evaluate the safety and tolerability of long-term AADvac1 treatment, the secondary objectives included the evaluation of immunogenicity and vaccine efficacy in slowing cognitive and functional decline. The vaccine was found to be most effective on the subgroup of patients with confirmed Alzheimer’s disease biomarker profiles.

Axion Neuroscience, a clinical-stage biotech company at the forefront of treating and preventing Alzheimer’s disease, conducted the study. For it, the company recruited 196 patients from eight European countries.

The results of its completed Phase II study were published in the journal Nature Aging. The abstract of the report stated: “Alzheimer’s disease (AD) pathology is partly characterised by accumulation of aberrant forms of tau protein. Here, we report the results of ADAMANT, a 24-month double-blinded, parallel-arm, randomised phase 2 multi-center placebo-controlled trial of AADvac1.”


According to the published results, AADvac1 was safe and well-tolerated. Not just that, the vaccine reduced, significantly, the accumulation of Neurofilament Light Chain (NFL), an important biomarker of neurodegeneration, in the blood by 58 percent.

In the subgroup of patients with confirmed Alzheimer’s disease biomarker profile, according to the study, AADvac1 slowed the clinical decline by 27 percent as measured by CDR-SB and functional decline by 30 percent, as measured by ADCS-MCI-ADL.

In further comparison to the placebo, the vaccine considerably reduced the NFL blood levels by 62 per cent (p value=0.010).


“The vaccine induced high levels of IgG antibodies. No significant effects were found in cognitive and functional tests on the whole study sample (Clinical Dementia Rating-Sum of the Boxes scale adjusted mean point difference −0.360 (95% CI −1.306, 0.589)), custom cognitive battery adjusted mean z-score difference of 0.0008 (95% CI −0.169, 0.172),” read the abstract of the paper.

In a press release, Michal Fresser, CEO of Axon Neuroscience, said, “Our Phase II trial successfully demonstrated the strengths of our lead asset AADvac1, a tau vaccine on track to prevent and treat Alzheimer’s disease,” and added, “The results confirm the disease-modifying effect of AADvac1”.

The website also has a quote from Fresser saying that “the very positive results from our landmark Phase II clinical trial underpin our confidence, and strengthen our motivation to get a treatment to patients as soon as possible”.


Stay connected with us on social media platform for instant update click here to join our  Twitter, & Facebook

We are now on Telegram. Click here to join our channel (@TechiUpdate) and stay updated with the latest Technology headlines.

For all the latest Technology News Click Here 


 For the latest news and updates, follow us on Google News

Read original article here

Denial of responsibility! TechAzi is an automatic aggregator around the global media. All the content are available free on Internet. We have just arranged it in one platform for educational purpose only. In each content, the hyperlink to the primary source is specified. All trademarks belong to their rightful owners, all materials to their authors. If you are the owner of the content and do not want us to publish your materials on our website, please contact us by email – [email protected]. The content will be deleted within 24 hours.


This website uses cookies to improve your experience. We'll assume you're ok with this, but you can opt-out if you wish. Accept Read More