This is a Phase 2b/3 study. The purpose of a 2b/3 study is to learn more about the safety and effects of VX-210 in patients with acute traumatic cervical SCI. VX-210 is an investigational drug; “investigational” means the drug is not approved by Health Canada or the US Food and Drug Administration (FDA) and is still being tested for safety and effectiveness.
VX-210 will be combined with a commonly used fibrin sealant during your surgery. Fibrin sealants are approved, marketed products used for tissue sealing or to stop bleeding. They are often used during surgery after spinal cord injury.
This multicenter study will evaluate effect of VX-210 on the recovery of muscle strength and sensation following SCI. This study will also assess the impact of VX-210 on the ability to perform activities of daily living (ADLs) and the need for attendant care following injury.
Study Coordinators and Research Nurses cannot give medical advice over the phone. Telephone numbers and email addresses are provided for obtaining additional information on specific research studies only. If you have specific questions which require clinical expertise, please call your primary care physician.