Phase 1a/b Study on Safety of IMX101 in H. Pylori-negative and H. Pylori-infected Healthy Volunteers (IMX-02)

ImevaX

Status and phase

Completed

Phase 1

Conditions

Helicobacter Pylori Infected Subjects

Helicobacter Pylori Naive Subjects

Treatments

Biological: CTA control

Biological: IMX101 vaccine

Study type

Interventional

Funder types

Industry

Identifiers

NCT03270800

2015-004761-82

Details and patient eligibility

About

A Phase 1, multi-center, randomised, double-blind and adjuvant-controlled study to evaluate the safety, tolerability, and efficacy of IMX101 in H. pylori-negative and H. pylori-infected healthy volunteers.

The study will be conducted in 2 phases. Phase A: Study design contains 6 cohorts, each containing 8 subjects. Three cohorts (24 subjects) will be H. pylori-negative and 3 cohorts will be H. pylori-infected. Subjects fulfilling the inclusion criteria will be assigned to one of 3 sequential dose cohorts with a 3:1 randomisation to IMX101 or to CTA within each cohort.

Phase B: Two cohorts with H. pylori-infected subjects can be expanded up to 20 subjects in each cohort. The decision whether to expand the cohorts will be taken by the Sponsor and the DSMB, as soon as the results of the safety and efficacy analyses are available.

Up to 72 subjects collectively in Phases A & B will be recruited. depending on immunogenicity status.

Enrollment

72 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

H. pylori-infected subjects: Confirmed H. pylori infection by urea breath test and serology.

H. pylori-negative subjects: Presenting no H. pylori infection by urea breath test and serology.

Men and women aged ≥18 years and ≤ 50 years.
Female subjects must either be of non-childbearing potential or use highly effective methods of contraception for at least 1 month prior to Screening and 1 month after end of study participation (see section pregnancy and contraceptives).
Women with a negative serum test at Screening (V2) and women of childbearing potential additionally with a negative urine pregnancy test at each visit (except V1 and FU V10/V12).
Have given written informed consent prior to admission to the study in accordance with ICH-GCP and local legislation.
Ability to comply with the requirements of the study protocol.

Exclusion criteria

History of successful treatment for H. pylori infection.
Regular use (once a week or more) of diclofenac, other non-steroidal anti-inflammatory drugs (NSAIDs), e.g. acetylsalicylic acid (Aspirin®), or proton pump inhibitor (PPI). Additionally, PPI is used within 2 weeks prior to V1 and V11.
Use of anticoagulants (i.e. heparin, coumarin derivatives, e.g. Marcumar®).
Use of antibiotics employed in H. pylori therapy within the month prior to study entry (V1) as well as 1 month prior to each endoscopy (V3 and V9/V11).
Recent or current (within the last 6 months) systemic corticosteroid use including inhaled corticosteroids. Topical corticosteroid medication is allowed.
Current or previous gastric ulcer diseases or preneoplastic changes in the stomach mucosa according to medical records or endoscopy findings confirmed by histological assessment at Baseline (V3).
Current or previous medically significant gastroduodenal disease.
Preceding cholera immunisation or disease.
Uncontrolled hypertension or orthostatic hypotension.
Body mass index (BMI) ≤ 18 or ≥ 30.
Poorly-controlled type I or type II diabetes mellitus (glycosylated haemoglobin [HbA1c] ≥ 7.5% within the last 6 weeks) and subjects requiring insulin treatment.
History, evidence or suspicion of tumour burden.
Epilepsy or seizure disorder.
Bleeding diathesis.
Positive viral serology screening result for hepatitis B surface antigen (HBS Ag), antibodies to hepatitis C virus (HCV Ab), or human immunodeficiency virus (HIV) type 1 and 2.
Known significant allergic reaction to any drug as determined by the investigator, such as anaphylaxis requiring hospitalisation.
A history of active alcohol abuse or drug addiction.
Administration of a live vaccine within 90 days prior to the first study immunisation (V4) and throughout the study.
Receipt of blood, blood products or plasma derivatives 30 days prior to study entry (V1).
Pregnancy or lactation.
Participation in a clinical study within 30 days prior to admission to the study if investigational or marketed drug were employed. Any disease or condition which in the Investigator's opinion would exclude the subject from the study.