Overview

Study to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of MBF-015 in Huntington's Disease Patients

Status:
COMPLETED
Trial end date:
2024-12-04
Target enrollment:
Participant gender:
Summary
This is a Phase IIa (proof of concept), single center clinical trial to evaluate the safety and efficacy of daily MBF-015 oral treatment during 28 days in Huntington's Disease patients on top of standard of care.
Phase:
PHASE2
Details
Lead Sponsor:
Medibiofarma S.L.