Evaluate the Safety and Tolerability, for Nirsevimab in Immunocompromised Children

PHASE2CompletedINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

August 19, 2020

Primary Completion Date

February 17, 2023

Study Completion Date

February 17, 2023

Conditions
RSV Infection
Interventions
DRUG

Nirsevimab

Single fixed IM dose of nirsevimab 50 mg if body weight \< 5 kg or 100 mg if body weight ≥ 5 kg, and subjects entering their second RSV season will receive a single fixed IM dose of nirsevimab 200 mg

Trial Locations (28)

1200

Research Site, Brussels

2013

Research Site, Soweto

2193

Research Site, Parktown

4000

Research Site, Liège

8035

Research Site, Barcelona

13210

Research Site, Syracuse

18014

Research Site, Granada

28041

Research Site, Madrid

28046

Research Site, Madrid

29406

Research Site, North Charleston

33606

Research Site, Tampa

38105

Research Site, Memphis

49006

Research Site, Dnipro

61075

Research Site, Kharkiv

76104

Research Site, Fort Worth

90027

Research Site, Los Angeles

98405

Research Site, Tacoma

113-8519

Research Site, Bunkyō City

183-8561

Research Site, Fuchu-shi

216-8511

Research Site, Kawasaki-shi

830-0011

Research Site, Kurume-shi

606-8507

Research Site, Kyoto

852-8501

Research Site, Nagasaki

157-8535

Research Site, Setagaya-ku

305-8576

Research Site, Tsukuba

232 8555

Research Site, Yokohama

85-048

Research Site, Bydgoszcz

NG7 2UH

Research Site, Nottingham

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Iqvia Pty Ltd

INDUSTRY

lead

AstraZeneca

INDUSTRY