drugset / Trial / NCT04322149

Multiple Doses of AT-1501-A201 in Adults With ALS

NCT04322149

Phase 2 Completed 54 enrolled Anelixis Therapeutics, LLC
NaSequentialOpen-labelTreatment

Summary

This is a Phase 2a, multi-center, open label, multiple dose study of AT-1501, a humanized monoclonal antibody antagonist to CD40 ligand (CD40L). Approximately 54 adults with Amyotrophic Lateral Sclerosis (ALS) will be enrolled into the study in the United States and Canada at approximately 13 ALS treatment sites. Participants will be enrolled into one of four ascending doses.

Timeline

Start
2020-10-16
Primary completion
2022-03-24
Completion
2022-03-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Tegoprubart Monoclonal antibody 1 mg/kg Intravenous
Subject Tegoprubart Monoclonal antibody 2 mg/kg Intravenous
Subject Tegoprubart Monoclonal antibody 4 mg/kg Intravenous
Subject Tegoprubart Monoclonal antibody 8 mg/kg Intravenous