drugset / Trial / NCT04470167

Phase 1/2 Clinical Study of TPX-115 in Patients With Partial-Thickness Rotator Cuff Tear

NCT04470167 ↗

Phase 1/2 Completed 49 enrolled Tego Science, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

Rotator cuff tear is one of the most common shoulder diseases and conservative treatment is commonly used for tears involving ≤50% of tendon thickness. Since conventional conservative treatments are not fundamental to repair tendon tissue, there is a growing need of new therapy to improve structural outcome. This study assesses the safety and efficacy of allogeneic fibroblasts on partial-thickness rotator cuff tear. The primary outcome is change in American Shoulder and Elbow Surgeons (ASES) score at 24 weeks after TPX-115 injection. Secondary outcomes include changes from baseline in Visual Analogue Score (VAS) pain score, functional evaluations including Range of Motion (ROM), Constant Score (CS), ASES score and Simple Shoulder Test (SST) at 4, 12 and 24 weeks after administration and structural evaluation using MRI at 24 weeks after injection.

Timeline

Start
2020-10-26
Primary completion
2022-02-17
Completion
2022-02-17

Drugs

EvaluationDrugModalityDoseRoute
Subject TPX-115 Cell therapy — Other

Indications