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

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