drugset / Trial / NCT06469853

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

NCT06469853 ↗

Phase 2 Completed 10 enrolled Medibiofarma S.L.
Non-randomizedSingle-groupOpen-labelTreatment

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.

Timeline

Start
2024-02-01
Primary completion
2024-12-04
Completion
2024-12-04

Drugs

EvaluationDrugModalityDoseRoute
Subject MBF-015 Unknown 16 mg Oral
Subject MBF-015 Unknown 32 mg Oral

Indications