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  Coressence Product Pipeline
   
 

Our product pipeline covers functional food ingredients, cosmetics and topically applied products, candidate compounds for Type II diabetes, anti-cancer products for colon cancer and skin cancer and candidate compounds for animal health.

 

 

The Coressence pipeline currently has 9 product lines each at a different stage:

Functional Food

 

 Mode of Action  

Novel Food Status

Pre-clinical Studies

Clinical Studies

Placed on Market

Evesse® Juice

eNOS dependent vasodilator

Approved 2006

 2007

 2008

 2007

Evesse® Granules

eNOS dependent vasodilator

Approved 2006

 2007

 2008

 2007

Evesse® Fructose

eNOS dependent vasodilator 

Approved 2006

2007

2008

2007

 Evesse® Red  Natural Food Colour

Not Required

Licensed

2009

2010

 Evesse® EPC  eNOS dependent vasodilator

 Awaiting Clearance

Licensed

2009

 2010

             
Pharma /OTC

Mode of Action

Pre-clinical

Phase I

Phase II

Phase III

 Topical Cremes

Anti-skin cancer / anti-aging

2009

Out-Licensing

Cooperation

Cooperation

Type II Diabetes Glucose AbsorptionBlocker 2010 Out-Licensing Cooperation Cooperation
Equine Health Glucose Absorption Blocker /Vasodilator 2010 Out-Licensing Cooperation Cooperation

Colon Cancer

Angiogenisis Blocker 2010 Out-Licensing Cooperation Cooperation

 1) Evesse Juice - Completed pre-clinical trials in 2007, clinical trials 2008 and placed on the market

 2) Evesse Granules - Completed pre-clinical trials in 2007, clinical trials 2008 and placed on the market

 3) Evesse Fructose - Now a stable intermediate for enzyme activated post-processing

 4) Evesse Red - Clinical trials 2009

 5) Evesse EPC - Clinical trials 2009

 6) Co-EPC3 - Early stage candidate for topical cosmetics applications

 7) EPCO3E - Early stage candidate for Type II diabetic glucose absorption blocker

 8) Co-EPCO3E - Early stage Equine candidate

 9) Candidate colon, skin and prostate cancer molecules

 

Our candidate molecules are:

 1) manufactured to the highest levels of a cGMP (Good Manufacturing Practice) at a site regularly inspected by authorities such as FDA and MHRA

 2) accompanied by a comprehensive pre-clinical animal toxicology package

 3) being used in numerous ongoing human clinical studies, and

 4) Can be tested in human clinical studies with a short lead time

 

 

 
 
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