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Clinical Trial Summary

Overview of Study Design: This is a phase 1, multicenter, open-label, multiple-dose, dose-escalation study designed to evaluate the safety, tolerability, pharmacokinetics (PK), and antitumor activity of TAK-960 in patients with advanced nonhematologic malignancies. This study will be the first to administer TAK-960 to humans. The patient population will consist of adults with a nonhematologic malignancy for which standard treatment is no longer effective or does not offer curative or life-prolonging potential, or for which no standard treatment is available.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Advanced Nonhematological Malignancies
  • Neoplasms

NCT number NCT01179399
Study type Interventional
Source Millennium Pharmaceuticals, Inc.
Contact
Status Terminated
Phase Phase 1
Start date September 2010
Completion date January 2013

See also
  Status Clinical Trial Phase
Completed NCT01045421 - MLN8237 in Adults With Nonhematological Malignancies, Followed by MLN8237 in Lung, Breast, Head and Neck or Gastroesophageal Malignancies Phase 1/Phase 2