A Study to Evaluate the Safety and Efficacy of MEDI8897 for the Prevention of Medically Attended Lower Respiratory Tract Infection Due to Respiratory Syncytial Virus in Healthy Late Preterm and Term Infants (MELODY)

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE 3 RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE SAFETY AND EFFICACY OF MEDI 8897, A MONOCLONAL ANTIBODY WITH AN EXTENDED HALF-LIFE AGAINST RESPIRATORY SYNCYTIAL VIRUS, IN HEALTHY LATE PRETERM AND TERM INFANTS (MELODY)

Intervention/treatment:
MEDI8897 (NIRSEVIMAB)
Medical condition:
RESPIRATORY SYNCYTIAL VIRUS
Protocol code:
D5290C00004
Control number:
228805
Status:
Closed
Approved:
July 18, 2019
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT03979313
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
0 Years to 1 Year
Accepts healthy volunteers: Yes

Contacts and locations

Contact
Name
Global Clinical Lead
Organization
Astrazeneca
Phone:
+1 877-240-9479
Sponsor
MEDIMMUNE LIMITED

Locations

Alberta

Research Site
Calgary, Alberta, T3B 6A8

British Columbia

Research Site
Vancouver, British Columbia, V6H 3V4

Quebec

Research Site
Pierrefonds, Quebec, H9H 4Y6

Results

See the results from the trial NCT03979313. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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