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Conjugate Pneumococcal Vaccine in Ataxia Telangiectasia (AT)

Conjugate Pneumococcal Vaccine in Ataxia Telangiectasia (AT)

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00656409
Enrollment
30
Registered
2008-04-11
Start date
2006-06-30
Completion date
2008-03-31
Last updated
2008-04-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ataxia Telangiectasia (AT)

Keywords

Ataxia telangiectasia,, Conjugated pneumococcal,, Prevenar,, Immunogenicity ,, Vaccine

Brief summary

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.

Interventions

DRUGConjugated pneumococcal vaccine (Prevenar)

Sponsors

Great Ormond Street Hospital for Children NHS Foundation Trust
CollaboratorOTHER
Institute of Child Health
Lead SponsorOTHER

Study design

Primary purpose
BASIC_SCIENCE

Eligibility

Sex/Gender
ALL
Age
2 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Genetically confirmed diagnosis of AT

Design outcomes

Primary

MeasureTime frame
Immunogenicity of vaccine

Secondary

MeasureTime frame
Incidence of adverse reactions to vaccine

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026