Viaskin Pertussis Vaccine Trial

Phase 1

Completed

• Conditions: Whooping Cough
• Interventions: Biological: Viaskin PT 25 mcg; Biological: Viaskin PT 50 mcg; Biological: Viaskin PT Placebo; Biological: Boostrix™

• Registration Number: NCT03035370
• Lead Sponsor: DBV Technologies

Brief Summary

The study is a Phase I, first in human, monocenter study, aiming at assessing the safety and immunogenicity of a genetically detoxified pertussis toxin (PT) when administered via the cutaneous route with Viaskin patches to healthy volunteers at 2 different doses of 25 mcg or 50 mcg PT protein compared to Viaskin placebo.

Two cohorts of 30 subjects will be successively enrolled. Safety of the product will be assessed throughout the 10-week study and its immunogenicity will be assessed at regular intervals with collection of blood samples for immunological analyses.

Four weeks after the second Viaskin application (at Day 42 of the study), all subjects will receive a dose of diphtheria-tetanus-pertussis vaccine (Boostrix® dTpa) to ensure the optimal recall of their immunity against pertussis.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2016-03-15
• Study Start: 2016-09-05
• Study First Submitted QC: 2017-01-25
• Study First Posted: 2017-01-30
• Primary Completion: 2018-04-25
• Study Completion: 2018-04-25
• Status Verified: 2020-02
• Last Update Submitted: 2020-02-28
• Last Update Posted: 2020-03-02

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 102

Inclusion Criteria

• Has provided written informed consent before enrollment;
• Adult male or female, ages 18 to 40 years (inclusive) at the time of enrollment;
• Non-pregnant, non-lactating female;
• Free of clinically significant health problems, as determined by pertinent medical history and clinical examination at study screening;
• With documented history of pertussis immunization (at least 4 doses);
• Women of childbearing potential with a negative pregnancy test at entry;
• Females of childbearing potential who are willing to use an effective method of contraception.

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Exclusion Criteria

• Prior dTpa immunization within the last 10 years or prior dT immunization within the last 2 years, or any other investigational vaccine likely to impact on interpretation of the trial data;
• Suspected or confirmed pertussis infection within the last 10 years or documented pertussis infection in a household member within the last 10 years;
• Receipt of licensed vaccines within 14 days of planned study immunization (30 days for live vaccines) or ongoing participation in another clinical interventional trial.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Viaskin PT 25 mcg	Viaskin PT 25 mcg	Viaskin PT 25 mcg
Viaskin PT 50 mcg	Viaskin PT 50 mcg	Viaskin PT 50 mcg
Viaskin PT 25 mcg	Boostrix™	Viaskin PT 25 mcg
Viaskin PT 50 mcg	Boostrix™	Viaskin PT 50 mcg
Viaskin PT Placebo	Viaskin PT Placebo	Viaskin PT Placebo
Viaskin PT Placebo	Boostrix™	Viaskin PT Placebo

Primary Outcome Measures

Name	Time	Method
Incidence of Treatment-Emergent Adverse Events (AE).	From Day 0 to Day 70.	* Solicited AEs occurring from the time of each application through 14 days following Viaskin PT application; * Unsolicited AEs from the time of application through 28 days following the 1st application; * Serious Adverse Events from the time of the inform consent form signature through the final study visit of subject.

Secondary Outcome Measures

Name	Time	Method
PT-specific antibody response (anti-PT IgG antibodies and PT-specific neutralizing antibodies).	Day 14, Day 28, Day 42, Day 70.

Trial Locations

Locations (1)

Center for Vaccinology Medical faculty UNIGE and University of Geneva (HUG); 🇨🇭 Geneva, Switzerland