A phase Ib study to investigate the safety and effect of BR-003

Status

Completed

Phases

Phase 1

Study type

Interventional

Source

EU CTIS

Registry ID

CTIS2024-516338-37-00

Acronym

STX-102

Enrollment

Registered

2024-08-09

Start date

2023-05-11

Completion date

2025-02-18

Last updated

2024-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

and posterior decompression., intervertebral body fusion devices, osteotomies, Patients planned for open or percutaneous posterior spinal stabilisation with 4 or 6 pedicle screws with a diameter of 5 to 7.5 mm (inclusive), vertebral augmentation, with or without concomitant posterolateral fusion

Interventions

None listed

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Countries

Netherlands

Outcome results