Acceleration dating clinical trial
That the substitution of CMF by Capecitabine will not be detrimental to patient outcome but will offer advantages in Quality of Life and/or toxicity.Protocol TACT2: Version 1d approved on the 23/09/2005, UK Ethics Committee MREC ref: 04/MRE00/88Version 3 approved on the 13/05/2008.Study Design: Randomised phase II screening/ "pick-the-winner " design to select a single regimen to go forward for phase III testing.
validating cluster resource analysis services
No concomitant medical, psychiatric or geographic problems that might prevent completion of treatment or follow-up Patient Adult Both 4400 patients (both male and female) 1. Locally advanced breast cancer (T4 and/or N3 disease)5.
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