A Study to Assess the Safety and Effectiveness of Palivizumab Administered to Children at High Risk of Severe Respiratory Syncytial Virus (RSV) Infection in the Russian Federation and the Republic of Belarus

Last updated: February 9, 2018
Sponsor: AbbVie
Overall Status: Completed

Phase

3

Condition

Respiratory Syncytial Virus (Rsv)

Treatment

N/A

Clinical Study ID

NCT02968173
M15-539
2016-000221-39
  • Ages < 24
  • All Genders

Study Summary

This is a Phase 3b, prospective, multicenter, open-label, non-controlled study to assess the safety and effectiveness of immunoprophylaxis with the intramuscular (IM) administration of the liquid formulation of palivizumab for the prevention of RSV hospitalizations in infants at high risk (infants born at less than or equal to 35 weeks gestational age and less than or equal to 6 months of age at enrollment; or infants less than or equal to 24 months of age with a diagnosis of chronic lung disease [CLD] of prematurity requiring on-going medical treatment within the previous 6 months or infants less than or equal to 24 months of age with hemodynamically significant congenital heart disease [CHD]).

Eligibility Criteria

Inclusion

Inclusion Criteria:

Infants at high risk of severe RSV infection defined as fulfilling at least one of the following:

  • Infants born ≤ 35 weeks gestational age AND are ≤ 6 months of age at enrollment

  • Infants ≤ 24 months of age at enrollment AND with a diagnosis of bronchopulmonary dysplasia (BPD) (defined as oxygen requirement at a corrected gestational age of 36 weeks) requiring intervention/management (i.e., oxygen, diuretics, bronchodilators, corticosteroids, etc.) anytime within 6 months prior to enrollment

  • Infants ≤ 24 months of age at enrollment with hemodynamically significant CHD, either cyanotic or acyanotic, unoperated or partially corrected. Children with acyanotic cardiac lesions must have pulmonary hypertension (≥ 40 mmHg measured pressure in the pulmonary artery [ultrasound acceptable]) or the need for daily medication to manage hemodynamically significant CHD

Exclusion Criteria (main exclusion criteria):

  • Hospitalization at the time of enrollment (unless discharge is anticipated within 14 days)

  • Mechanical ventilation (including continuous positive airway pressure, CPAP) at the time of enrollment

  • Life expectancy less than 6 months

  • Unstable cardiac or respiratory status, including cardiac defects so severe that survival is not expected or for which cardiac transplantation is planned or anticipated

  • Active respiratory illness, or other acute infection

Study Design

Total Participants: 50
Study Start date:
November 09, 2016
Estimated Completion Date:
July 13, 2017

Study Description

Participants will receive palivizumab solution for injection at 15 mg/kg by IM injection every 30 days for a minimum of 3 and a maximum of 5 injections given during anticipated periods of RSV risk in the community; the number of doses will depend on the time of enrollment during the RSV season.

Connect with a study center

  • Mother and Child National Research Center /ID# 150143

    Minsk, 220043
    Belarus

    Site Not Available

  • UZ "Vitebsk Regional Children Clinical Center" /ID# 151242

    Vitebsk, 210022
    Belarus

    Site Not Available

  • Kazan State University /ID# 149848

    Kazan, 42012
    Russian Federation

    Site Not Available

  • Russian National Research Medical University n.a. N.I. Pirog /ID# 150734

    Moscow, 117997
    Russian Federation

    Site Not Available

  • State Institution of Healthcare Childrens City Hospital #22 /ID# 149822

    Saint-Petersburg, 196657
    Russian Federation

    Site Not Available

  • St. Petersburg State Pediatric Medical Academy /ID# 149820

    St. Petersburg, 194100
    Russian Federation

    Site Not Available

  • Federal state budget educational Institution /ID# 150732

    Tomsk, 634050
    Russian Federation

    Site Not Available

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