CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed
Drug / intervention
RSV Polyclonal Immunoglobulindrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00001903
NCT00001903Phase 4Completed

Prevention of RSV Infections in Bone Marrow Transplant Recipients

National Institute of Allergy and Infectious Diseases (NIAID)·interventional·Posted Dec 10, 2002·Updated Mar 4, 2008

In Brief

A Phase 4 clinical trial evaluating RSV Polyclonal Immunoglobulin for Respiratory Syncytial Virus Infection. Completed, across 1 site.

Detailed Summary

Respiratory Syncytial Virus (RSV) infections are very common and widespread. By age 5, virtually everyone has been infected and developed antibodies against some strain of the virus. RSV infections happen during adulthood, leading to common cold syndromes. In Bone Marrow Transplant recipients the disease is much more severe, usually progressing to pneumonia. This phenomenon is associated with mortality rates around 60-80%. RSV Polyclonal Immunoglobulin (Respigam® (Registered Trademark)) has been approved by the Food and Drug Administration and recommended by the American Academy of Pediatrics for prophylaxis of RSV disease in premature babies and children born with bronchopulmonary dysplasia. Furthermore, it has been used to treat RSV pneumonia in children and Bone Marrow Transplant recipients with encouraging results and no complications. Currently, no preventive strategies are available when approaching this infection among bone marrow transplant patients. We intend to prevent our bone marrow transplant patients from developing RSV pneumonia by employing the strategy already used in premature babies, i.e., by passive immunization with Respigam® (Registered Trademark). Our goal to evaluate the efficacy and safety of this strategy in such immunocompromised population. We believe that this will be a more reasonable approach than waiting for the infection to settle in and only then treating it, because optimal therapy is not currently available.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 4CompletedFinished
19992000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedDec 10, 2002
Enrollment StartApr 1, 1999
Study CompletionMay 1, 2001
TodayJul 2, 2026
Posted 23.6 years ago

Interventions

RSV Polyclonal Immunoglobulindrug