Clinical trial

Evaluation of PROCHYMAL® Adult Human Stem Cells for Treatment-resistant…

NCT00482092 · Mesoblast, Inc., Industry · Completed

Key facts

NCT number NCT00482092
Title Evaluation of PROCHYMAL® Adult Human Stem Cells for Treatment-resistant Moderate-to-severe Crohn's Disease
Official title A Phase III, Multicenter, Placebo-controlled, Randomized, Double-blind Study to Evaluate the Safety and Efficacy of PROCHYMAL® (ex Vivo Cultured Adult Human Mesenchymal Stem Cells) Intravenous Infusion for the Induction of Remission in Subjects Experiencing Treatment-refractory Moderate-to-severe…
Lead sponsor Mesoblast, Inc., Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Crohn's Disease
Intervention type Drug
Interventions Prochymal®, Placebo
Enrollment 330
Start date Sep 17, 2007
Primary completion Sep 15, 2014
Completion Sep 15, 2014
First posted Jun 4, 2007
Last update posted Jan 13, 2022
Countries Australia, Canada, New Zealand, 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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