Blarcamesine Deemed Safe and Effective in Phase 2 Extension Study by Anavex Life Sciences

AnavexLife Sciences, a leading biopharmaceutical company, has recently announced promising findings
from the 48-week, open-label extension of its phase 2 study involving
blarcamesine. Blarcamesine, also known as ANAVEX2-73, has shown significant
potential in the treatment of Parkinson disease dementia (PDD). 

Despite the challenges posed by the COVID-19 pandemic, the study demonstrated that patients
who continued treatment with blarcamesine experienced substantial improvements
in PDD symptoms for up to 48 weeks. This is an important development, as PDD
remains an urgent unmet need in the global healthcare landscape. 

During the extension phase, patients exhibited consistent longitudinal improvements in
their clinical symptoms while receiving active blarcamesine treatment. These
improvements were measured using various assessment tools, including the
Movement Disorder Society-Unified Parkinson’s Disease Rating Scale (MDS-UPDRS)
and the Clinical Global Impression-Improvement (CGI-I) scale. The results
showed positive changes in both the MDS-UPDRS scores and the CGI-I evaluations. 

Additionally, Anavex revealed that blarcamesine did not impair sleep and even had a positive
effect on rapid eye movement (REM) sleep behavior disorder, a common symptom in PDD patients. 

The primary and secondary objectives of the phase 2 extension study were successfully met,
indicating that blarcamesine is both safe and effective in treating PDD. These
findings are particularly encouraging as they suggest that blarcamesine has the
potential to not only slow down the progression of PDD but also reverse its
life-altering symptoms. 

It is important to note that while the results of the study are promising, they should be
interpreted with caution due to the small sample size and the nature of the study design. 

However, based on these positive outcomes, Anavex
Life Sciences plans to conduct a 6-month study
focusing on PDD, with MDS-UPDRS II + III and CGI-I as
the primary and key secondary endpoints. 

The developments surrounding blarcamesine and its potential as a treatment for PDD are exciting
for both patients and healthcare professionals. Further research and clinical
trials will be crucial in fully understanding the therapeutic benefits of this
investigational agent and its role in improving the lives of individuals with Parkinson disease dementia. 

Refer to this article, for related information. 

  

More about Anavex on https://www.globaldata.com/company-profile/anavex-life-sciences-corp/