Kringle Pharma, Inc. announced that the last patient has now completed the treatment and follow-up in the Phase 3 clinical trial of KP-100IT, the intrathecal formulation of recombinant human HGF, in patients with acute spinal cord injury. This Phase 3 trial is a nonrandomized, multicenter, confirmatory trial in 25 subjects with severe cervical spinal cord injury. KRINGLE plans to collect and fix all clinical data from this trial for further analysis and evaluation of efficacy and safety.

The top-line results are expected to be released in the first half of 2024.