Evaluate the Safety of Neuronata-R® Inj. Suspended With HypoTHermosol® FRS (HTS-FRS) in Patients With ALS

PHASE1CompletedINTERVENTIONAL
Enrollment

8

Participants

Timeline

Start Date

November 9, 2022

Primary Completion Date

November 27, 2023

Study Completion Date

November 27, 2023

Conditions
Amyotrophic Lateral Sclerosis
Interventions
BIOLOGICAL

Lenzumestrocel

1.0 ⅹ 10\^6 cells/kg of Neuronata-R mixed with HTS-FRS suspension are administered twice in the cerebrospinal fluid at intervals of 26 days

DRUG

Riluzole

In the case of a subject who is not taking Riluzole at the time of screening (visit 1), Riluzole should be taken except when discontinued due to Adverse events. The dose can be changed within the authorization according to the medical expert's judgement

Trial Locations (1)

04763

Hanyang university hospital, Seoul

Sponsors
All Listed Sponsors
lead

Corestemchemon, Inc.

INDUSTRY

NCT06676423 - Evaluate the Safety of Neuronata-R® Inj. Suspended With HypoTHermosol® FRS (HTS-FRS) in Patients With ALS | Biotech Hunter | Biotech Hunter