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Improving the efficiency of clinical trials by standardizing processes for Investigator Initiated Trials

Contemp Clin Trials Commun. 2020-05-01; 
Dinesh Pal Mudaranthakam, Milind A Phadnis, Ron Krebill, Lauren Clark, Jo A Wick, Jeffrey Thompson, John Keighley, Byron J Gajewski, Devin C Koestler, Matthew S Mayo
Products/Services Used Details Operation
Gene Synthesis … BioMarin Pharmaceutical 2,293 0 22 15 Myriad Genetics 2,206 80 270 0 Vertex Pharmaceuticals 2,150 294 58 10 Alkermes 1,750 482 567 0 CK Life Sciences 1,747 0 0 0 GenScript Biotech 1,592 0 1 0 Amphastar Pharmaceuticals 1,541 0 0 0 Total 2,617 4,204 447 … Get A Quote

摘要

Early phase clinical trials are the first step in testing new medications and therapeutics developed by clinical and biomedical investigators. These trials aim to find a safe dose of a newly targeted drug (phase I) or find out more about the side effects and early signals of treatment efficacy (phase II). In a research institute, many biomedical investigators in oncology are encouraged to initiate such trials early in their careers as part of developing their research portfolio. These investigator-initiated trials (IITs) are funded internally by the University of Kansas Cancer Center or partially funded by pharmaceutical companies. As financial, administrative, and practical considerations play an essential rol... More

关键词

Clinical trial execution, Data driven approach, Investigator initiated trial, Trial optimization