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Safety and Efficacy Study of NeoFuse in Subjects Requiring Posterolateral Lumbar Fusion

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00810212
Recruitment Status : Withdrawn (Sponsor preferred a better study design)
First Posted : December 18, 2008
Last Update Posted : November 7, 2014
Sponsor:
Information provided by (Responsible Party):
Mesoblast, Ltd.

No Study Results Posted on ClinicalTrials.gov for this Study
Study was withdrawn before participants were enrolled.
  Recruitment Status : Withdrawn
  Estimated Primary Completion Date : November 2011
  Estimated Study Completion Date : November 2011