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Clinical Trial Summary

The primary purpose of this study is to evaluate the efficacy of rexlemestrocel-L+HA compared to control in reducing low back pain at 12 months post-treatment and safety of a single injection of rexlemestrocel-L+HA injected into a lumbar intervertebral disc compared to control through 12 months post-treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06325566
Study type Interventional
Source Mesoblast, Ltd.
Contact David Nunez
Phone 512-826-8897
Email clinical@mesoblast.com
Status Not yet recruiting
Phase Phase 3
Start date May 2024
Completion date August 2027

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