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Safety Evaluation of ART352-L in Subjects Undergoing Posterolateral Spinal 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. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04378543
Recruitment Status : Recruiting
First Posted : May 7, 2020
Last Update Posted : October 12, 2020
Sponsor:
Information provided by (Responsible Party):
Ankasa Regenerative Therapeutics, Inc.

No Study Results Posted on ClinicalTrials.gov for this Study
Recruitment Status : Recruiting
Estimated Primary Completion Date : April 2022
Estimated Study Completion Date : October 2023