Study Confirming A Human Challenge Model and Investigating The Safety Of VLA1701

Phase 2

Completed

Conditions: Enterotoxigenic Escherichia Coli Infection
Diarrhea

Interventions: Biological: VLA1701
Biological: Placebo
Other: Challenge Strain

Registration Number: NCT03576183

Lead Sponsor: Valneva Austria GmbH

Brief Summary: This is a single-center, double-blind, placebo-controlled, Phase II vaccination and challenge study designed to confirm a human challenge model with E. coli strain LSN03-016011/A.

Detailed Description: This is a single-center, double-blind, placebo-controlled, Phase II vaccination and challenge study designed to confirm a human challenge model with E. coli strain LSN03-016011/A (LT+ (Labile toxin), ST- (Stable toxin), CS17), as well as collect expanded safety and immunogenicity data.

The study will be carried out in two phases:

Vaccination phase: up to 34 subjects will be randomized 1:1 to receive 2 doses of either VLA1701 or placebo orally. The doses will be given 7 days apart and subjects will be followed as an outpatient for safety.

Challenge Phase: 30 Subjects, out of the 34 subjects, will be challenged.

After challenge, subjects will be monitored for diarrhea and other signs/symptoms of enteric illness by daily medical checks, vital sign determinations, grading and weighing of all stools.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 34

Inclusion Criteria

Healthy male and non-pregnant female subjects aged 18 to <50 years;
BMI of 19.0 to 35.0 kg/m2
Willingness to participate after informed consent has been obtained from the subject prior to any study related procedures.
Completion of a training session and demonstration of comprehension of the protocol procedures and knowledge of ETEC-associated illness by passing a written examination.
If subject is of childbearing potential:
1. Negative pregnancy test at screening with understanding to not become pregnant within 28 days after challenge;
2. Subject has practiced an effective method of contraception during the 30 days before screening (Visit 0);
3. Subject agrees to employ adequate birth control measures for the duration of the study.

Exclusion Criteria

Participated in research involving investigational product within 30 days before planned date of first vaccination or planned use through Day 44;
Any prior exposure to ETEC (including LSN03-016011/A) or cholera occupationally or received LT (Or any mutant forms of LT (e.g., LTR192G, LTR192GL211A), ETEC, or cholera vaccine);
Subjects with known abnormal stooling patterns (fewer than 3 per week or more than 3 per day);
Known allergies to any component of the vaccine;
Subjects with known allergies to more than 1 planned antibiotics:
History of diarrhea while traveling in a developing country within the last 3 years;
Subjects whose occupation involves handling of ETEC or cholera bacteria;
Women who are pregnant or breastfeeding;
Significant medical conditions including chronic, immunosuppressive, malignant, or gastrointestinal diseases (e.g. History of Irritable Bowel Syndrome (as defined by the Rome III criteria or medical diagnosis) or gastric ulcer disease) or enteric, pulmonary, cardiac, liver or renal disease. Some medical conditions which are adequately treated and stable may be acceptable in the study (e.g. hypertension);
Significant abnormalities in screening lab hematology or serum chemistries;
Use of any medication known to effect the immune system (e.g. systemic corticosteroids) within 30 days of vaccination or planned use during active study period (excluding inhaled steroids);
Evidence of confirmed infection with HIV, Hepatitis B or Hepatitis C;
Subjects with IgA (Immunoglobulin A) deficiency (serum IgA < 7 mg/dl or limit of detection of assay);
Regular use of antacids, antidiarrheal, loperamide, bismuth subsalicylate, diphenoxylate or similar medication less than 2 weeks prior to enrolling in the study and through the inpatient portion of the study;
Known or suspected alcohol abuse or illicit drug use within the last year, positive urine toxicology for drugs of abuse;
Persons who are committed to an institution (by virtue of an order issued either by the judicial or the administrative authorities);
Persons who are in a dependent relationship with the sponsor, an investigator or other study team members, or the study center.
Any other criteria which, in the investigator's opinion, would compromise the ability of the subject to participate in the study, the safety of the study, or the results of the study.

Exclusion Criteria

Not provided

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
VLA1701	VLA1701	VLA1701 is an investigational oral vaccine against LT-ETEC (Labile Toxin-Enterotoxigenic E coli) The vaccine is administered orally in 2 doses about 1 week apart.
VLA1701	Challenge Strain	VLA1701 is an investigational oral vaccine against LT-ETEC (Labile Toxin-Enterotoxigenic E coli) The vaccine is administered orally in 2 doses about 1 week apart.
Placebo	Placebo	The buffer component of VLA1701 will be used as Placebo. The vaccine is administered orally in 2 doses about 1 week apart.
Placebo	Challenge Strain	The buffer component of VLA1701 will be used as Placebo. The vaccine is administered orally in 2 doses about 1 week apart.

Primary Outcome Measures

Name	Time	Method
Percentage of Subjects With Moderate to Severe Diarrhea	5 days after challenge	within 120 hours of challenge with ETEC strain LSN03-016011/A.

Secondary Outcome Measures

Name	Time	Method
Percentage of Subjects With Any Adverse Events (AE)	until Month 6
Number of Subjects With Serious Adverse Events	until Month 6
Disease Severity Score After Challenge With ETEC Strain LSN03-016011/ A	7 days after challenge	ETEC diarrhea disease severity score with a score ranging from 0 (no disease) to 8 (most severe disease) utilizing objective signs, subjective Symptoms and stool output.
Percentage of Subjects With Any IMP (Investigational Medicinal Product) Related Adverse Events	up to Visit 4 (day of challenge, 23 days post first vaccination)	unsolicited events
Percentage of Subjects With Solicited Adverse Events	7days after each vaccination	adverse events covered by the subjects memory card
Percentage of Subjects With IMP-related Serious Adverse Events	up to Visit 4 (day of challenge, 23 days post first vaccination)