Complement 2: Blood Donations to Develop Vaccines Against Infectious Diseases

NCT ID: NCT01945307

Last Updated: 2023-04-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

101 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-10-31

Study Completion Date

2023-03-31

Brief Summary

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We need human blood to understand the immune response to infection and to test promising new vaccines against infectious diseases in the laboratory. One test is called the Serum Bactericidal Assay (or SBA), which is measure of how effective antibodies are at killing certain bacteria and can be an important measure of how effective a new vaccine may be.

The samples would be used in the laboratory analysis of clinical trials of vaccines used in adults and children, and some samples in pre-clinical (animal) experiments testing new vaccines before they enter human-stage testing. Most people have some form of protection against most bacteria already, so not everyone is a suitable blood donor for this laboratory test. We therefore start by taking a small blood sample and test this one before asking for more blood if we found yours suitable for the work we do.

Detailed Description

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Conditions

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Complement Mediated Bacterial Killing in Healthy Adults

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Healthy adults

Healthy adults aged 18 to 70 years

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Willing and able to give informed consent for participation in the study
* Aged between 18 and 70 years
* In good health as determined by medical history and clinical judgment of the Investigators
* Able to attend the scheduled visits and to comply with all study procedures
* If found to be a suitable complement that they are willing to be approached for further donations

Exclusion Criteria

* Body weight less than 50kgs
* Have any known or suspected impairment or alteration of immune function, resulting from, as examples:congenital or acquired immunodeficiency, receipt of immunosuppressive therapy such as anti-cancer chemotherapy or radiation therapy within the preceding 12 months or long-term systemic corticosteroid therapy, receipt of immunoglobulin or any blood product transfusion within the last 3 months
* Female participants who are pregnant
* Any chronic illness that could, in the opinion of the Investigators, interfere with immune function or with the donation of large volumes of blood (e.g. thrombocytopaenia or coagulopathy, malabsorption disorders, chronic anaemia)
* An individual who is on the delegation log for the study
* Planned blood donation within 4 months of undergoing testing to assess whether the individual is a suitable Complement donor
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Wellcome Trust

OTHER

Sponsor Role collaborator

University of Oxford

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Andrew Pollard, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Oxford

Locations

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Centre for Clinical Vaccinology and Tropical Medicine (CCVTM)

Oxford, Oxfordshire, United Kingdom

Site Status

Countries

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United Kingdom

Related Links

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Other Identifiers

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2012/11

Identifier Type: -

Identifier Source: org_study_id

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