Study of EC0489 for the Treatment of Refractory or Metastatic Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

65

Participants

Timeline

Start Date

April 30, 2009

Primary Completion Date

December 31, 2011

Study Completion Date

April 30, 2012

Conditions
Cancer
Interventions
DRUG

EC0489, Injection

PART A: Dose escalation from a starting dose of 1.0 mg/m2 IV bolus on Monday, Wednesday, and Friday Weeks 1 and 3 of a 4-week cycle to the Maximum Tolerated Dose (MTD)

DRUG

EC20

20-25 mCi 99mTc-EC20 administered IV bolus 1-2 hours prior to imaging and at end of study for subjects who received 1 cycle or more of EC0489.

DRUG

EC0489, Injection

PART B: Once PART A MTD is determined, PART B will begin. Dose escalation from a starting dose of 4.2 mg/m2 IV bolus once weekly in a 4-week cycle to the Maximum Tolerated Dose (MTD).

Trial Locations (6)

20817

Center for Cancer and Blood Disorders, Bethesda

21201

Greenebaum Cancer Center - University of Maryland, Baltimore

47905

Horizon Oncology Center, Lafayette

48075

Providence Cancer Institute, Southfield

48201

Barbara Ann Karmanos Cancer Institute - Wayne State University, Detroit

48910

Great Lakes Cancer Institute - Michigan State University, Lansing

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Endocyte

INDUSTRY

NCT00852189 - Study of EC0489 for the Treatment of Refractory or Metastatic Tumors | Biotech Hunter | Biotech Hunter