Induction of Immunity Against Measles in Pediatric Liver Transplant Recipients
Launched by KLARA M. PÓSFAY BARBE · Jan 15, 2013
Trial Information
Current as of July 22, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how to safely improve immunity against measles in children who have received a liver transplant. Measles is a serious illness that can be dangerous for children with weakened immune systems, like those who have undergone organ transplants. The trial aims to determine how the immune system responds to the measles vaccine in these children, especially those who were vaccinated before their transplant and are now at least a year post-surgery.
To participate in the study, children need to be at least 12 months old and have low levels of specific antibodies against measles. They must also be more than a year past their liver transplant and not currently receiving high doses of certain medications that suppress the immune system. Participants will receive the measles vaccine and will be monitored for their immune response. It’s important to know that children with certain recent illnesses or treatments may not be eligible for the trial. This study could help improve vaccination strategies for vulnerable children in the future.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age ≥ 12 months
- • Measles-specific IgG antibodies negative (\<0.2 IU/L), as detected by the routine ELISA assay
- • ≥ 12 months from the time of transplantation and ≥ 2 months from the time of an acute rejection episode
- • Steroids \< 2 mg/kg/day, tacrolimus \< 0.3mg/kg/day and tacrolimus level \< 8 ng/ml for \> 1 month.
- • Total lymphocyte count ≥ 750 cells/ul at time of immunization
- Exclusion Criteria:
- • Known wild-type measles exposure during the last four weeks
- • Measles-containing immunoglobulins administered within the 5 months preceding the measles vaccine. If the child receives measles-containing Ig before an additional dose of MMR vaccine, he/she will be withdrawn from the study
- • Antiviral agents administered during the last four weeks
- • Febrile illness (\>38.5°) in the 72 hours before vaccine administration
- • Chronic aspirin therapy
- • Any other immunization with a live-attenuated vaccine during the last four weeks
- • Pregnancy
About Klara M. Pósfay Barbe
Klara M. Pósfay Barbe is a dedicated clinical trial sponsor with a commitment to advancing medical research and improving patient outcomes. With a focus on innovative therapies and evidence-based practices, she leads a team that collaborates with healthcare professionals and research institutions to design and implement rigorous clinical trials. Her expertise spans various therapeutic areas, ensuring that each study adheres to the highest ethical standards and regulatory requirements. Klara's vision is to foster scientific progress through meticulous research, ultimately contributing to the development of new treatments that address unmet medical needs.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Geneva, Ge, Switzerland
Patients applied
Trial Officials
Klara M Posfay-Barbe, MD, MS
Principal Investigator
University Hospitals of Geneva
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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