drugset / Trial / NCT00733798

A Safety and Efficacy Study of Intravenous 131I-TM601 in Adult Patients With Malignant Melanoma

NCT00733798 ↗

Phase 1/2 Terminated 58 enrolled TransMolecular
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and effectiveness of 131I-TM601 in the treatment of adult patients with progressive and/or recurrent malignant melanoma.

Timeline

Start
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Primary completion
—
Completion
—

Outcome

Outcome not reported

Stopped (Business): “For Strategic Reasons”

Drugs

EvaluationDrugModalityDoseRoute
Subject 131I-TM601 Peptide 0.4 mg Intravenous
Subject 131I-TM601 Peptide 44.4 mbq/kg Intravenous
Subject 131I-TM601 Peptide 740 mbq Intravenous

Indications