Conjugate Pneumococcal Vaccine in Ataxia Telangiectasia (AT)
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|ClinicalTrials.gov Identifier: NCT00656409|
Recruitment Status : Completed
First Posted : April 11, 2008
Last Update Posted : April 11, 2008
Ataxia Telangiectasia (AT) is an autosomal recessive inherited condition caused by mutations in the ATM gene1. Patients suffer from neuro-degenerative problems, usually commencing in the second year of life, and affecting predominantly the cerebellum. They also develop the characteristic superficial telangiectases. Between 60 and 80% of affected children are immunodeficient. This is associated with deficiency of immunoglobulin A (IgA ) 2, of IgG23 and of antibody responses to pneumococcal polysaccharides4. Patients suffer recurrent sino-pulmonary infections but a recent study suggests poor correlation between immune status and immunological parameters5. If uncontrolled, recurrent pulmonary infections can contribute to the development of chronic lung disease and bronchiectasis. Preventative management includes continuous prophylactic antibiotic treatment in some with the need for replacement immunoglobulin therapy in only a small proportion of cases. Antibiotics have been reasonably effective in this situation but the emergence of resistance amongst community acquired pneumococcal isolates is a cause for concern. Appropriate immunisation strategies may also have a role.
This study is designed to look at antibody responses in a one versus two dose regimen in a cohort of AT patients recruited through the AT Society a national charitable organisation involved in providing support to families with this condition and in fostering education and research in the field.
|Condition or disease||Intervention/treatment||Phase|
|Ataxia Telangiectasia (AT)||Drug: Conjugated pneumococcal vaccine (Prevenar)||Phase 3|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||30 participants|
|Primary Purpose:||Basic Science|
|Official Title:||Conjugate Pneumococcal Vaccine in Ataxia Telangiectasia (AT)|
|Study Start Date :||June 2006|
|Actual Study Completion Date :||March 2008|
Drug: Conjugated pneumococcal vaccine (Prevenar)
- Immunogenicity of vaccine
- Incidence of adverse reactions to vaccine
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00656409
|Great Ormond Street Hospital|
|London, United Kingdom, WC1N 3JH|