A Study Evaluating the Safety and Tolerability of QRL-201 in ALS

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

64

Participants

Timeline

Start Date

December 16, 2022

Primary Completion Date

October 8, 2026

Study Completion Date

October 8, 2026

Conditions
Amyotrophic Lateral Sclerosis
Interventions
DRUG

Multiple ascending doses of QRL-201

Multiple ascending doses of QRL-201 will be intrathecally administered to individuals with sporadic ALS.

DRUG

Multiple ascending doses of Placebo

Multiple ascending doses of placebo comparator will be intrathecally administered to individuals with sporadic ALS.

DRUG

QRL-201

QRL-201 will be intrathecally administered to individuals with C9orf72 ALS.

DRUG

Placebo

Placebo comparator will be intrathecally administered to individuals with C9orf72 ALS.

Trial Locations (15)

10117

Charité Research Organisation, Berlin

53127

Deutsches Zentrum für Neurodegenerative Erkrankungen e. V. (DZNE), Bonn

89081

Universitätsklinikum Ulm, Ulm

B-3000

Universitaire Ziekenhuizen Leuven (UZ Leuven), Leuven

T2N 1N4

University of Calgary, Calgary

T6G 2G3

University of Alberta, Edmonton

M4N 3M5

Sunnybrook Health Science Centre, Toronto

H2L 4M1

CHUM - Hopital Notre-Dame, Montreal

H3A 2B4

Montreal Neurological Institute-Hospital, Montreal

Unknown

University Hospital Schleswig-Holstein (UKSH) Campus Lübeck, Department for Neurology/ Precision Neurology, Lübeck

Universitair Medisch Centrum Utrecht, Utrecht

D08 A978

St James's Hospital, Dublin

S10 2JF

The University of Sheffield, Royal Hallamshire Hospital, Sheffield

SE5 9RS

Kings College Hospital NHS Foundation Trust, London

WC1N 3BG

National Hospital for Neurology and Neurosurgery, London

All Listed Sponsors
lead

QurAlis Corporation

INDUSTRY