drugset / Trial / NCT04658199

A Study to Test the Safety and Tolerability of Long-term UCB0107 Administration in Study Participants With Progressive Supranuclear Palsy

NCT04658199 ↗

Phase 1 Active not recruiting 19 enrolled UCB Biopharma SRL
NaSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to assess the long-term safety and tolerability of UCB0107 in study participants with progressive supranuclear palsy (PSP).

Timeline

Start
2020-11-16
Primary completion
2027-12-13
Completion
2027-12-13

Drugs

EvaluationDrugModalityDoseRoute
Subject bepranemab Monoclonal antibody — Intravenous