U.S., July 24 -- ClinicalTrials.gov registry received information related to the study (NCT07722962) titled 'Additional Phase 3 Study of KP-100IT in Subjects With Acute Spinal Cord Injury' on July 20.
Brief Summary: This is a Phase 3, multicenter, open-label, single-arm additional study to evaluate the efficacy of intrathecal KP-100IT in patients with acute spinal cord injury. Eligible patients will receive KP-100 0.6 mg/body by intrathecal administration once per week for a total of 5 doses and will be followed for approximately 24 weeks after the first dose.
Study Start Date: July 31
Study Type: INTERVENTIONAL
Condition:
Acute Spinal Cord Injury (SCI)
Intervention:
DRUG: KP-100IT
The contents of each vial were dissolved in the dis...