Published in Pharma Law Weekly, July 25th, 2006
This includes, formulation development, stability testing, metabolism, pharmacokinetics and toxicology studies. Drug substance manufacturing is being scaled to kilogram level to support GLP toxicology and phase I. The data from these studies will enable the company to submit an investigational new drug application (IND) and initiate phase I studies during 2007.
CF102, LIKE CF101, targets a specific cell surface receptor, the A3 adenosine receptor that is known to be over-expressed in tumor and inflammatory cells. CF102 has dual activity...
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Source: Pharma Law Weekly (2006-07-25)
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