40
Participants
Start Date
May 31, 2014
Primary Completion Date
November 29, 2018
Study Completion Date
November 29, 2018
EC1169
"PART A: EC1169 - Dose dependent on cohort, IV (in the vein) on days 1 and 8 of each 21 day cycle for the QW schedule.~PART B: EC1169 cohort 1 - taxane naive - Recommended Phase 2 dose, IV (in the vein) on days 1 and 8 of each 21 day cycle for the QW schedule.~PART B: EC1169 cohort 2 - taxane exposed - Recommended Phase 2 dose, IV (in the vein) on days 1 and 8 of each 21 day cycle for the QW schedule."
EC0652
PART A AND B: EC0652 is in development as a radioimaging agent for PSMA-expressing tumors. All patients receive a baseline 99mTc-EC0652 SPECT/CT scan for PSMA expression prior to Cycle 1 Day 1.
Memorial Sloan Kettering Cancer Center, New York
Tulane Cancer Center, New Orleans
South Texas Accelerated Research Therapeutics, San Antonio
Scottsdale Healthcare Clinical Trials at the Virginia G. Piper Cancer Center, Scottsdale
Comprehensive Cancer Centers of Nevada, Las Vegas
Yale Cancer Center, New Haven
Lead Sponsor
Endocyte
INDUSTRY