Safety and Immunogenicity of a Vi-DT Typhoid Conjugate Vaccine

Typhoid Clinical Trial

Official title:

A Randomized, Observer-Blinded, Phase I Study to Assess the Safety and Immunogenicity of Vi-DT Conjugate Vaccine Compared to Vi-Polysaccharide (Typhim Vi®, Sanofi Pasteur) Typhoid Vaccine in Healthy Filipino Adults and Children

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02645032
• Other study ID #: IVI T001
• Status: Completed
• Phase: Phase 1
• Start date: May 19, 2016
• Est. completion date: February 9, 2017

Study information

• Verified date: February 2018
• Source: International Vaccine Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase I, Randomized, observer-blinded, age de-escalating study.

The study objectives are:

1. To evaluate the safety of 25 μg of Vi-DT typhoid conjugate vaccine administered at 0 and 4 weeks.

2. To assess the immunogenicity of 25 μg of Vi-DT typhoid conjugate vaccine administered at 0 and 4 weeks.

3. To compare the safety and immunogenicity of Vi-DT and Vi-Polysaccharide typhoid vaccines.

Description:

This study will be carried out in healthy adults and children at a single site. Subjects will be stratified according to age.

The study procedure is as follows:

Visit 1 (day-1 to -7): Screen participants by medical history, physical examination and lab investigations. Collect blood for safety and immunogenicity assessments.

Visit 2 (day 0): Enroll, randomize and administer first dose of vaccine to eligible participants

Visit 3 (day 3): Assess participant safety by medical history and physical examination

Visit 4 (day 7): Record solicited adverse reaction 7 days post vaccination, and collect blood for safety lab assessments.

Visit 5 (day 28): Assess participant safety, collect blood for immunogenicity assessments, and administer second vaccine dose

Visit 6 (day 31): Participants safety will be assessed by medical history and physical examination

Visit 7 (day 35): Record solicited adverse reaction 7 days post second vaccination.

Visit 8 (day 56): Collect blood for immunogenicity assessments, assess participant safety, and fill in study completion form in the absence of any safety concern.

This study is observer-blind: vaccine administrator and vaccine safety evaluator will be two distinct persons to avoid bias of safety assessment. Trial staff other than the vaccine administrator.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 144
• Est. completion date: February 9, 2017
• Est. primary completion date: February 9, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 2 Years to 45 Years

Eligibility

Inclusion Criteria:

1. Healthy male and female individual 2-45 years of age

2. Participants/Parents who have voluntarily given informed consent and/or assent.

3. Participants/Parents willing to commit complying with the study procedures of the investigator and available for the entire duration of study

Exclusion Criteria:

1. Participants concomitantly enrolled or scheduled to be enrolled in another trial

2. Acute illness, in particular infectious diseases or fever (axillary temperature > 38°C), with in three days prior to enrollment and vaccination.

3. Known history of allergy to vaccines or other medications

4. Known history of allergy to egg, chiken protein, neomycin and formaldehyde.

5. History of uncontrolled coagulopathy or blood disorders

6. Known history of immune function disorders including immunodeficiency diseases, or chronic use of systemic steroids (> 20 mg/day prednisone equivalent for periods exceeding 10 days), cytotoxic or other immunosuppressive drugs

7. Any abnormality or chronic disease which in the opinion of the investigator might be detrimental for the safety of the participant and interfere with the assessment of the trial objectives

8. Pregnancy & Lactation (female adults)

9. Female with child-bearing potential during the study period. i.e., sexually active and not practicing effective acceptable contraceptive method

10. Individuals who have previously received any vaccines against typhoid fever

11. Individuals already immunized with any licensed vaccine within 4 weeks prior to enrolment/vaccination (day 0) and expected to receive other licensed vaccines within 60 days following the first dose (day 0), except for tetanus toxoid vaccine

12. Individuals who have a previously ascertained or suspected disease caused by S. typhi.

13. Individuals who have had household contact with/and or intimate exposure to an individual with laboratory-confirmed S. typhi

14. History of alcohol or substance abuse

15. Subject planning to move from the study area before the end of study period

Related Conditions & MeSH terms

• Typhoid
• Typhoid Fever

Intervention

Biological:
• Vi-DT
Manufacturer: SK Chemicals Co., Ltd. Ingredient: Purified Vi-polysaccharide conjugated to diphtheria toxoid Dose: 0.5 mL/Vial
• Typhim Vi®
Manufacturer: Sanofi Pasteur Ingredient: Purified Vi-polysaccharide Appearance: colourless liquid Dose: 0.5mL/vial
• VAXIGRIP®
Dose: Single injection, participants 6-35 months of age will receive 0.25 ml (half a dose), participants 36 months of age and older will receive 0.5ml (full dose) *Participants less than 9 years of age, who have not been vaccinated for flu before, will receive a second dose of flu-vaccine after the last follow-up visit of last participant in their age cohort.

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
International Vaccine Institute	SK Chemicals Co., Ltd.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety endpoints for solicited adverse events (reactogenicity) and serious adverse events	Proportion of participants with local and systemic solicited adverse events (reactogenicity) and Proportion of participant with Serious Adverse Events (SAEs)	4 weeks post first and second vaccination
Secondary	Proportion of participants with sero-conversion	Defined as a four-fold rise in anti-Vi antibody titers compared to baseline measured by anti-Vi IgG ELISA and Serum Bactericidal Assay	4 weeks post first and second injections of Vi-DT and one injection of Vipolysaccharide
Secondary	Geometric Mean Titers (GMT)	Measurement of the Geometric Mean Titers (GMT) following 4 weeks post first and second injections of Vi-DT and one injection of Vi-polysaccharide vaccine	4 weeks post first and second vaccination

External Links

•   Final Result