2
Participants
Start Date
November 30, 2013
Primary Completion Date
December 31, 2013
Study Completion Date
December 31, 2013
Administration of AZD6738
An oral formulation of AZD6738 will be used. The starting dose of 20 mg BD will be escalated to reach a maximum tolerated dose in patients as defined by dose-limiting toxicity. A '3 week on, 1 week off' schedule, as deemed optimal in modelling of data from non-clinical studies, will be used initially
Research Site, La Jolla
Lead Sponsor
CLL Consortium
UNKNOWN
AstraZeneca
INDUSTRY