Phase 1 of EC1169 In Patients With Recurrent MCRPC

PHASE1CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

May 31, 2014

Primary Completion Date

November 29, 2018

Study Completion Date

November 29, 2018

Conditions
Prostate Cancer
Interventions
DRUG

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."

OTHER

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.

Trial Locations (6)

10017

Memorial Sloan Kettering Cancer Center, New York

70112

Tulane Cancer Center, New Orleans

78229

South Texas Accelerated Research Therapeutics, San Antonio

85258

Scottsdale Healthcare Clinical Trials at the Virginia G. Piper Cancer Center, Scottsdale

89169

Comprehensive Cancer Centers of Nevada, Las Vegas

06520

Yale Cancer Center, New Haven

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Endocyte

INDUSTRY