Study of Efficacy and Safety of Secukinumab in Participants With Moderate-severe Rotator Cuff Tendinopathy

Summary

The purpose of the present study was to assess the efficacy of secukinumab 300 mg s.c. (subcutaneous) compared to placebo, each in combination with standard of care, in improving signs, symptoms and physical function in participants with moderate to severe rotator cuff tendinopathy (RCT), using a randomized, double-blind, placebo controlled, parallel group design to minimize bias.

Timeline

Start

2023-08-10

Primary completion

2024-10-17

Completion

2024-12-13

Outcome

Outcome not reported

Stopped (Business): “Project discontinued to prioritize other key programs in portfolio”

Drugs

Indications