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

This study has been withdrawn prior to enrollment.
(Sponsor preferred a better study design)
Information provided by (Responsible Party):
Mesoblast, Ltd. Identifier:
First received: December 17, 2008
Last updated: November 6, 2014
Last verified: October 2008
No Study Results Posted on for this Study
Study was withdrawn before participants were enrolled.
  Study Status: This study has been withdrawn prior to enrollment.
  Estimated Study Completion Date: November 2011
  Estimated Primary Completion Date: November 2011 (Final data collection date for primary outcome measure)