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Tag Archives: toxicology
Therapeutics for Rare and Neglected Diseases – How Rare is Rare?
The U.S. National Institutes of Health (NIH) classifies a rare disease as affecting less than 200,000 individuals in the United States. As insignificant as this classification may sound, collectively there are more than 25 million people in the United States … Continue reading
Posted in Clinical Trials, Regulatory Strategy
Tagged analytical testing, biomarker, clinical trials, dos, exclusivity, FDA, IND, NIH, novel therapeutic, Orphan Drug Designations, tax credit, toxicology
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New Book – Principles of Anticancer Drug Development
Recently, Humana Press/Springer published a new book, Principles of Anticancer Drug Development. Neil Clendeninn M.D., Ph.D., a Senior Clinical Research Physician for Cato Research, served as an editor for the book, which has been described as a practical guide to the design, conduction, analysis and reporting of clinical trials with anticancer drugs. Continue reading
Posted in Publications
Tagged anticancer, cancer vaccine, Cato Research, clinical trials, drug development, FDA, pediatric, pharmacokinetics, preclinical, statistical analysis, toxicology, vaccines
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Cato at the SOT 2010 Annual Meeting
The Society of Toxicology (SOT) will hold its 49th Annual Meeting from March 7-11, 2010 in Salt Lake City, UT. The SOT Annual Meeting is the largest toxicology meeting and exhibition in the world, attracting over 6,000 scientists from industry, … Continue reading
Posted in Conferences and Meetings
Tagged nonclinical research, salt lake city, SOT, toxicology
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