Overview

Evaluate the Safety and Tolerability, for Nirsevimab in Immunocompromised Children

Status:
Recruiting
Trial end date:
2023-01-26
Target enrollment:
Participant gender:
Summary
Study D5290C00008 is a Phase 2, open-label, uncontrolled, single-dose study to evaluate the safety and tolerability, PK, occurrence of ADA, and efficacy of nirsevimab in immunocompromised children who are ≤ 24 months of age at the time of dose administration. Approximately 100 subjects will be enrolled. Subjects will be followed for approximately 1 year after dose administration.
Phase:
Phase 2
Details
Lead Sponsor:
AstraZeneca
MedImmune LLC
Collaborators:
Iqvia Pty Ltd
IQVIA Services Japan K.K.