Akesis Pharmaceuticals has announced plans to begin a 13-week preclinical safety program for AKP-020, a novel vanadium compound that has shown considerable potential as a treatment for Type 2 diabetes.
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The studies will be conducted by Charles River Laboratories, and follows a recently completed 28-day preclinical safety program, also performed by Charles River.
AKP-020 is the product designation for a novel vanadium compound otherwise known as bis(ethylmaltolato)oxovanadium (IV), or BEOV.
Jay Lichter, president and CEO of Akesis, said: “The initial results from the earlier trial are encouraging, and we believe warrant this additional research.”
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