Intralink-Spine, Inc. Announces Continuation of CLBP Clinical Study

LEXINGTON, KY, January 7, 2020

 

Intralink-Spine, Inc. announces that it has received unanimous approval from the Data Safety Monitoring Board (DSMB) to proceed with the Réjuve® clinical safety study (GEM-SE) for chronic low back pain (CLBP). As a result, ILS will be adding new sites to broaden Principal Investigator (PI) and participant representation in Australia.

 

“After careful review of the patient data, the DSMB has unanimously decided to approve the continuation of the GEM-SE study”, states Dr. Harwant Singh, Orthopaedic Surgeon at Pantai Hospital and DSMB Chairman.

 

“This is a great way to begin the new year”, states Lyle Hawkins, CEO of Intralink-Spine, Inc. “The DSMB has reviewed the study participant data and unanimously recommended that the study continues. This is another important step for ILS, as we continue to move forward to commercialization of Réjuve.”

 

According to Tom Hedman, Ph.D., Founder and CSO of Intralink-Spine, Inc., “The unique ability of Réjuve to address the core issues contributing to CLBP and progressive and debilitating tissue degradation is even more important in view of the current opioid addiction crisis, where prescription of opioids following back surgery or as part of a treatment regimen for CLBP has played a role in this epidemic”.

 

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© 2018 by Intralink-Spine Inc.  Réjuveis a registered trademark of Intralink-Spine, Inc.

Attention: Réjuve™ is not available for sale in the US, Canada, or EU. Clinical studies are pending.