A Dose Range Finding Study With Open-Label Extension to Evaluate the Safety of Oral LMI070/Branaplam in Early Manifest Huntington's Disease

PHASE2TerminatedINTERVENTIONAL
Enrollment

26

Participants

Timeline

Start Date

December 8, 2021

Primary Completion Date

October 27, 2023

Study Completion Date

October 27, 2023

Conditions
Early Manifest Huntington Disease
Interventions
DRUG

Branaplam

messenger ribonucleic acid (RNA) splicing modifier. Branaplam was administered as an oral solution once weekly.

DRUG

Placebo

Matching placebo oral solution once weekly

Trial Locations (12)

6720

Novartis Investigative Site, Szeged

28034

Novartis Investigative Site, Madrid

44791

Novartis Investigative Site, Bochum

48149

Novartis Investigative Site, Münster

49933

Novartis Investigative Site, Angers

59037

Novartis Investigative Site, Lille

89081

Novartis Investigative Site, Ulm

94010

Novartis Investigative Site, Créteil

H2W 1T8

Novartis Investigative Site, Montreal

H-1083

Novartis Investigative Site, Budapest

08036

Novartis Investigative Site, Barcelona

08041

Novartis Investigative Site, Barcelona

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY