CKBR-12

CKBR-12 is a Natural Health Product (NHP) currently under evaluation as an anti-Parkinson medication. Developed by Genesis Parkinson’s Institute SA, a division of Genesis Research, Inc., CKBR-12 is manufactured under GMP conditions in a cGMP compliant facility.

CKBR-12 was employed in an experimental protocol in the treatment of non-motor and motor dysfunction symptoms of Parkinson disease (PD). 

The trial, which encompassed a holistic patient-driven view of care, demonstrated a rapid amelioration of both motor and non-motor symptoms of PD, leading to an overall improvement of patient health-related quality of life (HRQOL). 

These unexpected, promising and previously unreported results gave rise to the filing of a US and PCT provisional patent, Rapid Method for Reducing Motor and Non-Motor Symptoms of Parkinson’s disease.

Preliminary results indicate an amelioration of both non-motor symptoms and motor symptoms within two (2) weeks of the onset of the CKBR-12 treatment.

This has continued in patients monitored for eight years to date.

A tremendous reduced level of bradykinesia and rigidity was reported, which expressed itself in an improved postural stability gait, balance and speech. 

No excess saliva and drooling was also noted. 

The absence of depression along with anxiety and other psychological issues was one of the most promising findings during this 30 day treatment 

with CKBR-12.

Data was captured using Patient-Reported Outcome (PRO) tools and video to evaluate HRQOL

These observations provide support for the hypothesis that CKBR-12 represents a novel means of ameliorating non-motor and motor PD symptoms and improving the overall HRQOL of Parkinson patients.

The unexpected findings of CKBR-12 on the severity and occurrence of multiple NMS require FDA approval, as these observed effects could decrease the growing social disability of PD patients significantly and consequently ease the burden on the socio-economic costs for healthcare..