drugset / Trial / NCT06461026

Summary

The purpose of this study is to assess the safety, tolerability, and pharmacokinetics of L9LS in infants in Mali and to evaluate the impact of L9LS on subsequent R21/Matrix-MTM vaccine immunogenicity.

Timeline

Start
2024-08-19
Primary completion
2025-06-27
Completion
2026-06

Drugs

EvaluationDrugModalityDoseRoute
Subject L9LS Monoclonal antibody 150 mg Intramuscular

Indications