At a glance
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A Multi-center, Randomized, Double-blind, Placebo-controlled, Parallel Design, Prospective, Phase IIa Exploratory Clinical Trial to Evaluate the Efficacy and Safety of SC Administration of GV1001 0.56 or 1.12 mg/Day in Patients With PSP
In Brief
A Phase 2 clinical trial evaluating GV1001 Placebo, GV1001 0.56mg, and 1 other intervention for Progressive Supranuclear Palsy. Completed, enrolled 78 participants across 5 sites.
Detailed Summary
The study will be conducted by the Sponsor to evaluate the efficacy and safety of GV1001 (0.56 mg and 1.12 mg) administered subcutaneously as a treatment for Progressive Supranuclear Palsy, (PSP). In 75 patients diagnosed with PSPR Richardson(PSP-RS) or PSP-Parkinsonism (PSP-P) at five hospitals in Korea, subcutaneous administration of GV1001 0.56 or 1.12 mg/day will be conducted with multicenter, randomized, double-blind, placebo-controlled, parallel design, prospective phase 2a.
Study Details
Timeline
Interventions
0.9% normal saline
Lyophilized peptide from hTERT
Lyophilized peptide from hTERT