39
Participants
Start Date
July 31, 2011
Primary Completion Date
October 31, 2011
Study Completion Date
January 31, 2012
PX-866
Volunteers in part 1 of the study will receive two single dose 8 mg treatments of PX-866 (one each of crystalline PX-866 tablets and amorphous PX-866 capsules) in Periods A and B, separated by at least seven days. Volunteers in part 2 of the study will receive two single dose 6 mg treatments of PX-866 (crystalline PX-866 tablets administered in either fed or fasted state), in Periods C and D, separated by at least seven days.
Comprehensive Clinical Development NW, Tacoma
Lead Sponsor
Cascadian Therapeutics Inc.
INDUSTRY