Immune Response Elicited by Concomitant Administration of Oral Typhoid Fever (Vivotif®) and Cholera (Dukoral®) Vaccines

Cholera Clinical Trial

Official title:

Immune Response Elicited by Concomitant Administration of Oral Typhoid Fever (Vivotif®) and Cholera (Dukoral®) Vaccines

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06104345
• Other study ID #: Dukoral+Vivotif
• Status: Recruiting
• Phase: Phase 4
• Start date: October 2023
• Est. completion date: December 2025

Study information

• Verified date: October 2023
• Source: Helsinki University Central Hospital
• Contact: Anu Kantele, MD, PhD
• Phone: +358503097640
• Email: anu.kantele[@]hus.fi
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this clinical trial is to explore the coadministration of oral typhoid fever (Vivotif®) and cholera (Dukoral®) vaccines in healthy volunteers aged 18-65 years. The main question it aims to answer is: • Does coadministration impact the immune responses to Vivotif® and Dukoral® vaccines Participants will: - receive either oral typhoid fever (Vivotif®) or oral cholera (Dukoral®) vaccines or both simultaneously - give blood samples for immunogenicity analyses - participate in adverse event follow up Researchers will compare those receiving only one of the vaccines to those receiving both simultaneously to see if coadministration has an impact on antigen-specific responses measured with: - ELISPOT (plasmablast responses specific to Salmonella typhi, Vibrio Cholerae and Enterotoxigenic Escherichia coli) - ELISA (antibodies in lymphocyte supernatants (ALS) and serum antibodies specific to vaccine antigens)

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: December 2025
• Est. primary completion date: December 2025
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Male or female subjects aged =18 to =65 years.

2. General good health as established by medical history and physical examination.

3. Written informed consent.

4. Females of childbearing potential must agree to use an efficacious hormonal or barrier method of birth control during the study (14 days before immunization to day 28 ± 3). Abstinence is acceptable.

5. Available for all visits scheduled in this study.

Exclusion Criteria:

1. Vaccination against typhoid fever or cholera within 5 years before dosing.

2. History of clinical typhoid fever or cholera.

3. Immunization with any other vaccine (oral or parenteral) within 4 weeks prior to study period or vaccination planned during it.

4. Current intake of antibiotics or end of antibiotic therapy <8 days before first IMP administration.

5. Chronic (longer than 14 days) administration of immunosuppressants or other immunemodifying drugs within 6 months before the first dose of IMP; oral corticosteroids in dosages of =0.5 mg/kg/d prednisolone or equivalent are excluded; inhaled or topical steroids allowed.

6. Acute or chronic clinically significant gastrointestinal disease.

7. Any confirmed or suspected immunosuppressive or immunodeficient condition, including human immunodeficiency virus (HIV) infection.

8. Pregnancy or lactation.

9. Acute disease at the time of enrolment (defined as the presence of a moderate or severe illness with or without fever (fever defined as body temperature of =38 °C).

10. Alcohol or drug abuse.

11. Suspected non-compliance.

12. Use of any investigational drug or vaccine within 30 days preceding the first dose of study vaccine, or planned use during the study period.

13. Any clinically significant history of known or suspected anaphylaxis or hypersensitivity reaction based on the judgement of the investigator.

14. Employee at the investigational site or relative or spouse of the investigator.

15. Any other criteria which, in the investigator's opinion, would compromise the ability of a subject to participate in the study, a subject's well-being, or the outcome of the study.

Related Conditions & MeSH terms

• Cholera
• Fever
• Typhoid Fever

Intervention

Biological:
• Oral typhoid fever vaccine
Oral typhoid fever vaccine (Vivotif®) on Days 0, 2 and 4.
• Oral cholera vaccine
Oral cholera vaccine (Dukoral®) on Days 0 and 7.

Locations

Country	Name	City	State
Finland	Meilahti Vaccine Research Center, Helsinki University Hospital	Helsinki

Sponsors (2)

Lead Sponsor	Collaborator
Helsinki University Central Hospital	University of Helsinki

Country where clinical trial is conducted

Finland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Titer of antigen-specific serum antibodies to oral typhoid fever (Vivotif®) and cholera (Dukoral®) vaccines.	Measurement of anti-salmonella, anti-cholera and anti-ETEC antibodies in serum (ELISA)	Blood samples on Days 0 and 28 ± 3 for all participants.
Primary	Magnitude of antigen-specific plasmablast responses to oral typhoid fever (Vivotif®) and cholera (Dukoral®) vaccines (ASCs/million PBMCs)	Measurement of IgA -, IgG- and IgM-secreting antibody cells (ASC ELISPOT) specific to Salmonella typhi (whole cell), Vibrio cholerae (whole cell and CTB-toxin) and Enterotoxigenic Escherichia coli (ETEC whole cell and LTB-toxin).	Blood samples on Days 0-7 for all participants and Days 12-14 for participants in Dukoral and Dukoral+Vivotif arms.
Secondary	Titer of antigen-specific antibodies in lymphocyte supernatants (ALS) to oral typhoid fever (Vivotif®) and cholera (Dukoral®) vaccines.	Measurement of anti-salmonella, anti-cholera and anti-ETEC antibodies in ALS samples (ELISA)	Blood samples on Days 0-7 for all participants and Days 12-14 for participants in Dukoral and Dukoral+Vivotif arms.