Viewing Study NCT06351592



Ignite Creation Date: 2024-05-06 @ 8:22 PM
Last Modification Date: 2024-10-26 @ 3:26 PM
Study NCT ID: NCT06351592
Status: RECRUITING
Last Update Posted: 2024-04-08
First Post: 2024-04-02

Brief Title: First in Human FIH Study of ALN-SOD in Adult Participants With Amyotrophic Lateral Sclerosis Associated With Mutation in the SOD1 Gene SOD1-ALS
Sponsor: Regeneron Pharmaceuticals
Organization: Regeneron Pharmaceuticals

Study Overview

Official Title: First in Human Study to Evaluate the Safety Tolerability Pharmacokinetics and Pharmacodynamics of Multiple Ascending Doses of Intrathecally Administered ALN-SOD in Participants With Amyotrophic Lateral Sclerosis and SOD1 Mutations
Status: RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study is researching an experimental drug called ALN-SOD called study drug This study is focused on people with amyotrophic lateral sclerosis ALS who have a mutation in a gene called the superoxide dismutase-1 SOD1 gene This type of ALS is known as SOD1-ALS This is the first time that ALN-SOD will be given to people The aim of the study is to see how safe and tolerable the study drug is

The study is looking at several other research questions including

The effect the study drug has on specific biomarkers which are molecules in the blood or in the fluid that surrounds the brain and spinal cord known as cerebrospinal fluid CSF
How much study drug is in the blood and in the CSF at different times
Whether the body makes antibodies against the study drug which could make the drug less effective or could lead to side effects
What effects the study drug has on ALS symptoms
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: True
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
2023-510344-20-00 REGISTRY EU CT Number None