Clinical trial

Efficacy and Safety Study of StemEx®, to Treat Subjects With High Risk…

NCT00469729 · Gamida Cell -Teva Joint Venture Ltd., Other · Completed

Key facts

NCT number NCT00469729
Title Efficacy and Safety Study of StemEx®, to Treat Subjects With High Risk Hematologic Malignancies, Following Myeloablative Therapy
Official title A Multi-Center, Multi-National, Historical Cohort Controlled Study to Evaluate Efficacy and Safety of Transplantation of StemEx®, Umbilical Cord Blood Stem and Progenitor Cells Expanded Ex Vivo, in Subjects With Hematologic Malignancies Following Myeloablative Therapy
Acronym ExCell
Lead sponsor Gamida Cell -Teva Joint Venture Ltd., Other
Status Completed
Phase Phase 2/Phase 3
Study type Interventional
Conditions Hematologic Malignancies, Acute Myeloid Leukemia, Lymphoid Leukemia, Chronic Myeloid Leukemia, Hodgkin's Disease, Non-Hodgkin's Lymphoma, Myelodysplastic Syndromes
Intervention type Drug
Interventions StemEx®
Enrollment 101
Start date Oct 1, 2007
Primary completion Feb 1, 2013
Completion Jun 1, 2015
First posted May 4, 2007
Last update posted Jul 10, 2015
Countries Hungary, Israel, Italy, Spain, 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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