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Clinical trial

A Phase II, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of PROCHYMAL™ (ex Vivo Cultured Adult Human Mesenchymal Stem Cells) Intravenous Infusion for the Treatment of Subjects With Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)

NCT00683722 is registered in ClinicalTrials.gov with Mesoblast, Inc. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase II, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of PROCHYMAL™ (ex Vivo Cultured Adult Human Mesenchymal Stem Cells) Intravenous Infusion for the Treatment of Subjects With Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)
Lead sponsor
Mesoblast, Inc.
Phase
Phase 2
Overall status
Completed
Start date
March 20, 2008
Completion date
August 24, 2010
Enrollment
62 (actual)
Sites
6

Conditions

As the registry lists them; a condition with its own page is linked.