A Study of 131I-TM601 in Adults With Recurrent Malignant Glioma

PHASE1/PHASE2UnknownINTERVENTIONAL
Enrollment

64

Participants

Timeline

Start Date

August 31, 2008

Primary Completion Date

February 28, 2010

Study Completion Date

April 30, 2010

Conditions
Malignant GliomaGlioblastoma MultiformeGBMAstrocytomaOligodendroglioma
Interventions
DRUG

131I-TM601

In the first study phase (Dose Escalation), patients will be assigned to treatment to between 2-5 doses of 131I-TM601 treatment at a treatment dose of 1.2 mCi/kg of lean body mass (in scaled dosing, this will amount to 0.024 mg TM601 peptide/kg of lean body mass), once weekly (for between 2-5 weeks, depending upon dose cohort). The maximum amount of administered radioactivity per infusion is 100 mCi.

Trial Locations (4)

21287

Johns Hopkins University, Baltimore

49503

St. Mary's Health Care, Grand Rapids

60637

University of Chicago, Chicago

22908-0394

University of Virginia, Charlottesville

Sponsors

Lead Sponsor

All Listed Sponsors
lead

TransMolecular

INDUSTRY

NCT00683761 - A Study of 131I-TM601 in Adults With Recurrent Malignant Glioma | Biotech Hunter | Biotech Hunter