Clinical trial

Safety and Efficacy Study of an Anti-CD20 Monoclonal Antibody (AME-133v) to…

NCT00354926 · Applied Molecular Evolution, Industry · Completed

Key facts

NCT number NCT00354926
Title Safety and Efficacy Study of an Anti-CD20 Monoclonal Antibody (AME-133v) to Treat Non-Hodgkin's Lymphoma
Official title Open-Label, Multicenter, Phase 1/2 Dose-Escalation Study of AME-133v (LY 2469298), Administered Intravenously in Four Weekly Doses, in Subjects With CD20+ Follicular Relapsed or Refractory Non-Hodgkin's Lymphoma
Lead sponsor Applied Molecular Evolution, Industry
Status Completed
Phase Phase 1
Study type Interventional
Conditions Non-Hodgkin's Lymphoma
Intervention type Biological
Interventions AME-133v (LY2469298)
Enrollment 67
Start date Jul 1, 2006
Primary completion Jan 1, 2009
Completion Jan 1, 2009
First posted Jul 20, 2006
Last update posted Jan 7, 2016
Countries United States

At a glance

  • 10–99 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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