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A Phase 1/2, Multi-Center, Safety and Efficacy Study Evaluating Intravenously Administered 131I-TM601 in Patients With Progressive and/or Recurrent Malignant Melanoma.

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Trial Profile

A Phase 1/2, Multi-Center, Safety and Efficacy Study Evaluating Intravenously Administered 131I-TM601 in Patients With Progressive and/or Recurrent Malignant Melanoma.

Status: Discontinued
Phase of Trial: Phase I/II

Latest Information Update: 22 May 2009

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At a glance

  • Drugs TM 601 I-131 (Primary)
  • Indications Malignant melanoma
  • Focus Adverse reactions; Therapeutic Use

Most Recent Events

  • 13 May 2009 Status changed from recruiting to discontinued as reported by ClinicalTrials.gov.
  • 30 Sep 2008 Planned end date (Sep 2010) added as reported by CT.gov
  • 30 Sep 2008 Planned initiation date changed from 1 Oct 2008 to 1 Nov 2008 as reported by CT.gov

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