Condition: Partial Thickness Rotator Cuff Tears · Sponsor: Tego Science, Inc.
The goal of this study is to evaluate the efficacy and safety of allogeneic dermal fibroblasts (TPX-115) compared to placebo in patients with Partial-Thickness Rotator Cuff Tear(PTRCT). Primary endpoint is to evaluate the efficacy of TPX-115 compared to placebo, as measured by improvement in the Constant-Murley Score (CMS) in patients with PTRCT. Secondary endpoints are: * To evaluate functional (including shoulder pain) and structural improvements in the affected shoulder after administration of TPX-115 compared to placebo in patients with PTRCT * To evaluate the safety and tolerability of TPX-115 in patients with PTRCT * To assess the immunogenicity of TPX-115
This description comes directly from the study's public registry record.
Contact details are listed per location below or on the registry record.
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| BioSolutions Clinical Research Center | La Mesa, California, United States | Recruiting |
| Sports & Orthopedic Center - Advanced Research | Deerfield Beach, Florida, United States | Active Not Recruiting |
| Rush University Medical Center | Chicago, Illinois, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07219654