Clinical trial

Safety/Tolerability Study of AV-412 in Subjects With Refractory or Relapsed…

NCT00381654 · AVEO Pharmaceuticals, Inc., Industry · Terminated

Key facts

NCT number NCT00381654
Title Safety/Tolerability Study of AV-412 in Subjects With Refractory or Relapsed Solid Tumor Malignancies
Official title A Phase 1, Sequential Cohort, Dose Escalation Trial to Determine the Safety, Tolerability, and Maximum Tolerated Dose of Daily Oral Administration of AV-412 in Patients With Refractory or Relapsed Solid Tumor Malignancies
Lead sponsor AVEO Pharmaceuticals, Inc., Industry
Status Terminated
Phase Phase 1
Study type Interventional
Conditions Tumor
Intervention type Drug
Interventions AV-412
Enrollment 27
Start date Oct 1, 2006
Primary completion Dec 1, 2009
Completion Feb 1, 2010
First posted Sep 28, 2006
Last update posted Oct 4, 2011
Countries Argentina, United States

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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