Clinical trial

A Human Experimental Medicine Study to Assess Whether the Gut Microbiota Regulates Specific and Non-specific Immune Responses to Vaccination

Name
2023/HREC00066
Description
The goal of this clinical trial is to examine immune responses to the BCG vaccine in healthy adults who have, or who have not, taken antibiotics to deplete their gut bacteria prior to vaccination. The main question it aims to answer is: does depletion of the gut microbiota lead to impaired BCG-induced protection against specific and non-specific to challenges to the immune system?
Trial arms
Trial start
2023-11-23
Estimated PCD
2027-10-01
Trial end
2028-10-01
Status
Recruiting
Phase
Early phase I
Treatment
BCG vaccine
0.1ml injected intradermally over the distal insertion of the deltoid muscle onto the humerus
Arms:
Substudy 1 - BCG vaccine, antibiotics and 2nd BCG vaccine, Substudy 1 - BCG vaccine, antibiotics and placebo vaccine, Substudy 1 - BCG vaccine, no antibiotics and 2nd BCG vaccine, Substudy 1 - BCG vaccine, no antibiotics and placebo vaccine, Substudy 2 - Yellow Fever vaccine, antibiotics and BCG vaccine, Substudy 2 - Yellow Fever vaccine, no antibiotics and BCG vaccine
Yellow Fever vaccine
0.5ml injected subcutaneously
Arms:
Substudy 2 - Yellow Fever vaccine, antibiotics and BCG vaccine, Substudy 2 - Yellow Fever vaccine, antibiotics and placebo vaccine, Substudy 2 - Yellow Fever vaccine, no antibiotics and BCG vaccine, Substudy 2 - Yellow Fever vaccine, no antibiotics and placebo vaccine
Vancomycin Oral Capsule
500mg every 6 hours for 3 days
Arms:
Substudy 1 - BCG vaccine, antibiotics and 2nd BCG vaccine, Substudy 1 - BCG vaccine, antibiotics and placebo vaccine, Substudy 2 - Yellow Fever vaccine, antibiotics and BCG vaccine, Substudy 2 - Yellow Fever vaccine, antibiotics and placebo vaccine
Other names:
Firvanq, Vancocin HCl Pulvules
Neomycin Oral Product
1000mg every 6 hours for 3 days
Arms:
Substudy 1 - BCG vaccine, antibiotics and 2nd BCG vaccine, Substudy 1 - BCG vaccine, antibiotics and placebo vaccine, Substudy 2 - Yellow Fever vaccine, antibiotics and BCG vaccine, Substudy 2 - Yellow Fever vaccine, antibiotics and placebo vaccine
Other names:
Neo-Fradin
Size
348
Primary endpoint
Sub-study 1 BCG re-challenge
5 years
Sub-study 2 Yellow Fever vaccine
5 years
Eligibility criteria
Inclusion Criteria: * 18-35 years old * Provided a signed and dated informed consent form * BCG naïve (Arm 1) and BCG and YF vaccine naïve (Arm 2) * Willing to take short antibiotic course * Willing to undergo a punch biopsy (Arm 1) * Willing to have up to 7 blood samples and 3 stool samples collected over 5-7 months * Not pregnant or intending to get pregnant for the duration of the study (a pregnancy test will be offered to females) Exclusion Criteria: * Previous BCG or YF vaccination * Previous YF infection * Evidence of latent TB infection (LTBI) (assessed through a questionnaire) (IGRA to confirm if needed) * People with contraindications for BCG vaccination: * malignancies involving bone marrow or lymphoid systems, primary or secondary immunodeficiencies, HIV infection * moderate/severe skin disease including eczema, dermatitis or psoriasis * requiring immunosuppressive drugs or other immune modifying drugs e.g. corticosteroids, non-biological immunosuppressants, biological agents (such as monoclonal antibodies against tumour necrosis factor (TNF)-alpha) * People with contraindications to YF vaccination: * History of thymus disease, including myasthenia gravis, thymoma, thymectomy, DiGeorge syndrome, thymic damage from chemoradiotherapy or graft-versus-host disease * YF vaccination is contraindicated in immunocompromised individuals, including individuals who have HIV infection, primary immunodeficiencies (including inherited IFNAR1 deficiency), or are taking corticosteroids or other immunosuppressive agents and haematopoietic stem cell transplant recipients * People who have had a haematopoietic stem cell transplant * Individuals with history of severe allergic reactions to egg or chicken proteins * Pregnant or breastfeeding or planning to become pregnant * History of renal disease/insufficiency * Tattoo obscuring BCG vaccination site(s) * Any history of severe allergic reaction or anaphylaxis to vaccination * People with chronic serious underlying illness * Have received any prescribed oral or intravenous antibiotic in the 28 days prior to study visits 1 and 4 (including isoniazid, rifampicin, streptomycin and ethambutol as these particular antibiotics have activity against M. bovis)
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'Participants are allocated to Substudy 1 (BCG re-challenge) or Substudy 2 (Yellow Fever vaccine) Participants are randomised to receive\n\n* antibiotics or comparator (unblinded) and\n* BCG vaccine or placebo (blinded)\n* BCG vaccine or Yellow Fever vaccine (unblinded)', 'primaryPurpose': 'BASIC_SCIENCE', 'maskingInfo': {'masking': 'DOUBLE', 'maskingDescription': 'Participants and Investigator are blinded to BCG vaccine or placebo.', 'whoMasked': ['PARTICIPANT', 'INVESTIGATOR']}}, 'enrollmentInfo': {'count': 348, 'type': 'ESTIMATED'}}
Updated at
2024-04-04

1 organization

4 products

1 indication

Product
BCG
Product
Vancomycin
Product
Neomycin