SentryX is pleased to announce that in November, a Clinical Trial Application (CTA) has been submitted to Swissmedic, the Swiss surveillance authority for medicines and medical devices, and ethics committee for a first-in-human Phase 1b clinical trial for its lead candidate, BR-003. The trial will take place at the Orthopädie Sonnenhof Clinic in Bern and two hospitals in the Netherlands, and will enroll patients undergoing elective lumbar spine surgery with pedicle screw instrumentation.

The CTA submission builds on several years of research and development resulting in strong preclinical safety data as well as compelling in-vivo evidence of the local performance of the candidate product. SentryX is well-prepared and excited to be entering the clinical development phase.