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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00656409
Other study ID # 04MI07
Secondary ID
Status Completed
Phase Phase 3
First received April 7, 2008
Last updated April 10, 2008
Start date June 2006
Est. completion date March 2008

Study information

Verified date April 2008
Source Institute of Child Health
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date March 2008
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 2 Years and older
Eligibility Inclusion Criteria:

- Genetically confirmed diagnosis of AT

Study Design

Primary Purpose: Basic Science


Intervention

Drug:
Conjugated pneumococcal vaccine (Prevenar)


Locations

Country Name City State
United Kingdom Great Ormond Street Hospital London

Sponsors (2)

Lead Sponsor Collaborator
Institute of Child Health Great Ormond Street Hospital for Children NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Immunogenicity of vaccine
Secondary Incidence of adverse reactions to vaccine