Study of Palivizumab in Children With High Risk of Severe Respiratory Syncytial Virus (RSV) Disease

NCT ID: NCT06851806

Last Updated: 2025-11-17

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 138 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-11-30
• Study Completion Date: 2027-02-28

Brief Summary

This is a Phase IV, prospective, open-label, multicentre study to evaluate the safety of palivizumab IM injection for the prevention of severe LRTD in Indian infants and children who are at high-risk of RSV disease. All enrolled participants will receive palivizumab 15 mg/kg IM injection once a month for up to 5 injections during the study. Children who undergo cardiac surgery with cardiopulmonary bypass during the study should receive an additional dose of study intervention immediately after surgery, when medically stable for IM injection as determined by the physician. Prior to each study intervention administration, all participants will undergo safety assessments. A follow-up visit will be performed telephonically with the parent(s) or legal guardian(s) of all participants 30 days after their last injection of palivizumab.

Conditions

Respiratory Syncytial Virus (RSV)

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Study Arm

All the eligible participants will receive palivizumab 15 mg/kg on Days 1, 31, 61, 91, and 121.

Group Type: EXPERIMENTAL

Palivizumab 15 mg/kg

Intervention Type: DRUG

Single-dose liquid solution vials, 50 mg/0.5 mL, IM injection

Interventions

Palivizumab 15 mg/kg

Single-dose liquid solution vials, 50 mg/0.5 mL, IM injection

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Participants at risk of severe RSV disease defined as fulfilling at least one of the following:

1. Infants born ≤ 35 wGA and are < 6 months of age at enrolment.

2. Children < 24 months of age at enrolment and requiring treatment for BPD within the last 6 months.

3. Children < 24 months of age and with haemodynamically significant CHD.

2. Written informed consent obtained from the participant's parent(s)/legal guardian and the participant's parent(s)/legal guardian is able to understand and comply with the requirements of the protocol including follow-up visits as judged by the investigator.

Exclusion Criteria

Participants are excluded from the study if any of the following criteria apply:

1. Hospitalisation at the time of enrolment, unless the discharge is expected within 30 days of the time of enrolment

2. Required mechanical ventilation (including continuous positive airway pressure) or other mechanical respiratory or cardiac support at the time of enrolment.

3. Anticipated cardiac surgery within 2 weeks after enrolment.

4. Anticipated survival of < 6 months after enrolment in the trial.

5. Active LRTD, including RSV infection at the time of enrolment and/or study intervention administration.

6. Any fever (≥ 38.0°C) or acute illness within 7 days prior to investigational product administration.

7. Known history of evolving or unstable neurologic disorder.

8. Known history of unstable cardiac or respiratory status, including cardiac defects so severe that survival is not expected or for which cardiac transplantation is planned or anticipated.

9. Known allergy, including to immunoglobulin products, or history of allergic reaction.

10. Receipt of palivizumab or other RSV monoclonal antibodies or any RSV vaccine, including maternal RSV vaccination.

11. Receipt of any monoclonal or polyclonal antibody (for example, hepatitis B immune globulin, intravenous immunoglobulin) or anticipated use during the study.

12. Concurrent enrolment in another interventional study.

13. Children of employees of the sponsor, clinical study site, or any other individuals involved with the conduct of the study, or immediate family members of such individuals.

14. Judgment by the investigator that the participant should not participate in the study if the participant or the participant's parent/legal guardian is unlikely to comply with study procedures, restrictions, and requirements.

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

AstraZeneca

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Central Contacts

AstraZeneca Clinical Study Information Center

Role: CONTACT

information.center@astrazeneca.com

1-877-240-9479

Other Identifiers

2025-000041-13

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

D4800L00014

Identifier Type: -

Identifier Source: org_study_id