A Phase 2, multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of SAR443820 in adult participants with amyotrophic lateral sclerosis, followed by an open-label extension
Recruiting
18 years - 80 years
All
Phase
2
7 participants needed
1 Location
Brief description of study
SAR443820 is a selective, orally bioavailable, central nervous system (CNS)-penetrant, receptor-interacting serine/threonine-protein kinase 1 (RIPK1) inhibitor. The aim of this Phase 2 study is to determine the efficacy, safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of SAR443820 in treating adult participants with amyotrophic lateral sclerosis (ALS).
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Amyotrophic Lateral Sclerosis,ALS
-
Age: 18 years - 80 years
-
Gender: All
Male and Female patients between 18 and 80 years of age; confirmed ALS diagnosis; less than 2 years since symptom onset; no history of seizures/epilepsy; no significant cognitive impairment; no PICC or port-a-cath lines.
Updated on
04 Aug 2024.
Study ID: 850960