ClinicalTrials.gg
RecruitingNCT07562061TITREUpdated May 1, 2026

mulTiplex Immunoassay qualiTy assuRance Panel

An observational study in Group B Strep Infection, sponsored by St George's, University of London. Recruiting at 1 site in Uganda. Open to female participants. Per ClinicalTrials.gov, last updated 2026-05-01.

Sponsored by St George's, University of London · Observational

From the registry’s dates

  • Primary completion was expected by May 2026, 6 months ago, but the record still lists the study as recruiting.
  • Started Mar 2026; still recruiting 7 months later.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
50
Sex
Female
01

Study summary

Collection of serum from women not living with HIV, who received the GBS6 vaccine in the "a placebo-controlled clinical trial investigating the safety and immunogenicity of GBS6 in pregnant women with and without human immunodeficiency virus (HIV) infection and their infants" (GBS6) Clinical Trial in Kampala, Uganda, for the Development of Group B Streptococcus quality assurance panel for the GASTON multiplex anti-CPS IgG immunoassay

Read the detailed description

This is a single-visit study designed to collect serum samples from women who previously participated in the GBS6 clinical trial, "A placebo-controlled clinical trial investigating the safety and immunogenicity of GBS6 in pregnant women with and without human immunodeficiency virus (HIV) infection and their infants" (GBS6 trial). The purpose of this follow-up study is to obtain serum samples for the development of Quality Control Sera (QCS) and Assay Bridging (AB) panels to support long-term quality control and performance monitoring of the GASTON immunoassay.

The GBS6 trial enrolled 300 pregnant women between October 2022 and July 2023 at Kawempe National Referral Hospital and Kisenyi Health Centre IV. The last participant completed follow-up on 23 October 2024. Of these, 150 participants (75 living with HIV and 75 not living with HIV) were randomized to receive either the GBS6 vaccine or placebo (normal saline). The GBS6 vaccine is a capsular polysaccharide conjugate vaccine targeting the six most common disease-causing GBS serotypes.

For this follow-up study, only participants who received the GBS6 vaccine and are not living with HIV (n=75) will be contacted via telephone using the contact details provided in the GBS6 trial records. Each consenting participant will attend a single study visit for serum collection. Collected samples will be shipped to the City, St George's laboratory for antibody screening. The GASTON assay will measure IgG concentrations for serotypes Ia, Ib, II, III, IV, and V. Based on these results, samples will be ranked by IgG values, and an appropriate pooling strategy will be developed to generate the QCS and AB panels.

02

Conditions studied

  • Group B Strep Infection
03

In context

Streptococcal Infections

146 studies on the registry are indexed under Streptococcal Infections; 14 are open to participants now.

This study's planned enrollment of 50 is below the median of 400 across 31 observational studies indexed under Streptococcal Infections.

Browse Streptococcal Infections studies →

Lead sponsor

St George's, University of London is the lead sponsor of 106 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Women not living with HIV, who received the GBS6 vaccine in the "a placebo-controlled clinical trial investigating the safety and immunogenicity of GBS6 in pregnant women with and without human immunodeficiency virus (HIV) infection and their infants" (GBS6) Clinical Trial in Kampala, Uganda.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • -uninfected women who received the GBS6 vaccine during pregnancy and completed the whole period of study participation.
  • Reachable by phone
  • Willing and able to provide consent.
  • Willingness to provide a blood sample.

Exclusion criteria

Exclusion Criteria:

  • Receipt of blood/plasma transfusion in the last 3 months
  • Participants who receive treatment with therapy, including cytotoxic agents or systemic .
  • Women who will test positive for Syphilis or at screening
  • Current alcohol abuse or illicit drug use, or with a psychiatric condition
  • Major illness of the mother that, in the investigator's judgment, will substantially increase the risk associated with the participant's participation in the study, including but not limited to the following:

I. heart disease II. severe anaemia ( level less than 7.0g/dL)

Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
50 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Women not living with HIV, who received the GBS6 vaccine GBS6 Clinical Trial in Kampala, Uganda

    Women not living with HIV, who received the GBS6 vaccine in the "a placebo-controlled clinical trial investigating the safety and immunogenicity of GBS6 in pregnant women with and without human immunodeficiency virus (HIV) infection and their infants" (GBS6) Clinical Trial in Kampala, Uganda. The GBS6 trial enrolled 300 pregnant women between October 2022 and July 2023. Of these, 150 participants (75 living with HIV and 75 not living with HIV) were randomized to receive either the GBS6 vaccine (a capsular polysaccharide conjugate vaccine targeting the six most common disease-causing GBS serotypes) or placebo (normal saline). For this follow-up study, only participants who received the GBS6 vaccine and are not living with HIV (n=75) will be contacted via telephone using the contact details provided in the GBS6 trial records. Each consenting participant will attend a single study visit for serum collection.

    Other: Collection of 50mls of blood

Interventions

  • OtherCollection of 50mls of blood

    50mls of blood will be collected from all participants who give consent.

06

What researchers measure

Primary outcomes

  1. Creation of a quality control and bridging panels for the GBS multiplex immunoassay (GASTON assay)

    Approx 50mL of blood will be collected from each study participant and will be used only for the development of QCS and AB panels. Blood samples will be processed and serum stored at -20C in Kampala, Uganda. The serum will be transferred to the City St George's, University of London laboratory, in the United Kingdom (UK), where the serum will be assayed for GBS6 serotype-specific anti-capsular antibodies using the GASTON multiplex anti-CPS IgG immunoassay. Concentrations of anti-capsular IgG for the 6 serotypes (Ia, Ib, II, III, IV, and V) will be determined and a serum pooling strategy developed to produce a QCS panel consisting of three samples that span high, medium and low IgG values for each serotype and a 22- member bridging panel that will span the range of the assay for all serotypes. The QC panels will be distributed to members of the GASTON consortium for the purpose of assay performance monitoring until they are depleted.

    Time frame: 1 year

07

Study locations

1 of 1 sites recruiting
  • MUJHU Care Ltd, Kampala
    Kampala, Uganda
    Recruiting
    • Zakaria Mukasa, Dr · Contactzmukasa@mujhu.org · +256 782 201308
    • Robert Mboizi · Principal investigator
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07562061
Responsible party
Sponsor
First posted
May 1, 2026
Start date
Mar 27, 2026
Primary completion
May 2026 (estimated)
Completion
Jan 2027 (estimated)
Last update
May 1, 2026

Study contacts

Mary Kyohere
Contact
mkyohere@sgul.ac.uk
+447490390327
Madeleine Cochet
Contact
mcochet@sgul.ac.uk
+442087255214
Kirsty Le Doare
principal investigator · City St George's, University of London

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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