131-I-TM-601 Study in Adults With Recurrent High-Grade Glioma

PHASE2UnknownINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

November 30, 2004

Primary Completion Date

March 31, 2009

Study Completion Date

August 31, 2009

Conditions
Malignant GliomaGlioblastoma MultiformeGBMAnaplastic AstrocytomaOligo-AstrocytomaGliosarcoma
Interventions
DRUG

131-I-TM-601

131I-TM601, in solution, delivered intracavitarily following surgical resection 3 weekly administrations, 0.8 mg TM601 and 40mCi 131Iodine, per dose.

DRUG

131I-TM601

131I-TM601, in solution, delivered intracavitarily following surgical resection 6 weekly administrations, 0.8 mg TM601 and 40mCi 131Iodine, per dose.

Trial Locations (19)

10032

Columbia University Medical Center, New York

21287

Johns Hopkins Medical Center, Baltimore

28204

Carolina Neurosurgery and Spine, Charlotte

30322

Emory University, Atlanta

32804

Florida Hospital Cancer Institute, Orlando

33612

Moffitt Cancer Center, Tampa

48202

Henry Ford Hospital, Detroit

49503

Lacks Cancer Center at St. Mary's Health Care, Grand Rapids

60611

Northwestern University, Chicago

60637

University of Chicago, Chicago

63110

St. Louis Hospital, St Louis

Washington University Medical Center, St Louis

75246

Mary Crowley Medical Research Center, Dallas

84112

Huntsman Cancer Institute, Salt Lake City

90048

Cedars-Sinai Medical Center, Los Angeles

91010

City of Hope, Duarte

35294-3410

University of Alabama at Birmingham, Birmingham

02111

Tufts-New England Medical Center, Boston

98195-6470

University of Washington, Seattle

Sponsors

Lead Sponsor

All Listed Sponsors
lead

TransMolecular

INDUSTRY

NCT00114309 - 131-I-TM-601 Study in Adults With Recurrent High-Grade Glioma | Biotech Hunter | Biotech Hunter