Campylobacter Jejuni Challenge Model Development: Assessment of Homologous Protection

NCT01048112 | Unknown Phase 1 DMC

• 2 other identifiers: CHRMS 10-086NMRC 2009.0017
• Study Type: interventional
• Target: 16
• Locations: 1 country
• Sites: 2

Brief Summary

The goal of this research is to continue to develop a model of infection with Campylobacter jejuni, a bacterium that causes food and water-borne disease (mainly diarrhea). The objectives are to 1) determine if healthy subjects develop short-term (\<6 month) protection to reinfection with C. jejuni; and 2) characterize the immune responses to C. jejuni infection. Information obtained will be used in development of a vaccine against Campylobacter infections. Volunteers will be screened for eligibility within 60 days prior to enrollment. Screening will include obtaining informed consent prior to any study procedure. This will be followed by medical history, physical examination, review of current medications, blood samples for safety labs (WBC, Hct, Hgb, platelet count; chemistry panel; screening for HIV, HLA-B27, HBV, and HCV); urine pregnancy testing for females. Stool will be tested for infection. Eligible volunteers will be enrolled in the study and admitted to the GCRC on Day -1. They will drink a measured dose of C. jejuni on Day 0, and followed for approximately 9 inpatient days, during which time the investigators expect at least 75% to develop a diarrheal illness, which will be promptly treated with replacement fluids (oral or IV, as indicated) and antibiotics. During the inpatient period, subjects will be assessed for any adverse events, and blood and stool specimens will be analyzed for markers of infection and markers of immune response. Subjects must have resolved or resolving symptoms and two negative stool cultures ≥12 hours apart to be eligible for discharge, and will be seen in outpatient follow-up at 21, 28, 35, 60, and 90 days for additional AE assessments and blood and stool analysis. Eight subjects will return for redosing approximately 98 days after the initial dose, with the same inpatient and outpatient follow-up as above. Few or none should develop a diarrheal illness. Four naïve (previously unexposed) subjects will also receive the dose on Day 98 to confirm a 75% illness rate with this dose. They will be followed as the initial group was. All participants will be assessed by phone 6 months after the final dose they received.

Conditions

Campylobacter Infections

Keywords

campylobacter; gastroenteritis; challenge models

Outcome Measures

Primary Outcomes (2)

• Development of campylobacteriosis in response to a dose of Campylobacter jejuni strain CG8421

  10 days

• Immunologic responses to dosing with Campylobacter jejuni strain CG8421

  9 months

Study Arms (2)

Repeated dose group

EXPERIMENTAL

Will receive one dose of Campylobacter jejuni strain CG8421 at day 0 and a second dose at approximately day 98.

Biological: Campylobacter jejuni strain CG8421

Single dose group

ACTIVE COMPARATOR

Will receive one dose of Campylobacter jejuni strain CG8421

Biological: Campylobacter jejuni strain CG8421

Interventions

Campylobacter jejuni strain CG8421 BIOLOGICAL

Single oral dose of Campylobacter jejuni strain CG8421 in sodium bicarbonate buffer

Repeated dose group; Single dose group

Eligibility Criteria

• Age: 18 Years - 50 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Male or female between 18 and 50 years of age, inclusive.
• General good health, without significant medical illness, abnormal physical examination findings or clinical laboratory abnormalities as determined by principal investigator or principal investigator in consultation with the medical monitor and sponsor.
• Demonstrate comprehension of the protocol procedures and knowledge of Campylobacter illness by passing a written examination (pass grade ≥ 70%)
• Willing to participate after informed consent obtained.
• Available for all planned follow-up visits, and remain available for medical interview/physical exam and monitoring for 90 days post-challenge (last challenge received), and a final telephone interview 180 days post-challenge.
• Negative urine pregnancy test at screening and a negative urine pregnancy test on the day of admittance to the inpatient phase for all female subjects. In addition, female subjects will be advised of the need for an effective means of birth control during the entire study period.

You may not qualify if:

• Presence of a significant medical condition (e.g., psychiatric conditions; gastrointestinal disease, such as peptic ulcer, symptoms or evidence of active gastritis, inflammatory bowel disease, irritable bowel syndrome; alcohol or illicit drug abuse/dependency), or other laboratory abnormalities which in the opinion of the investigator precludes participation in the study.
• Immunosuppressive illness, IgA deficiency (below the normal limits), or H2 antihistamine use within 48 h of admission or during inpatient period.
• Positive serology results for HIV, HBsAg, or HCV antibodies.
• Significant abnormalities in screening lab hematology, serum chemistry, as determined by PI or PI in consultation with the medical monitor and sponsor.
• Use of any medication known to affect the immune function (e.g., corticosteroids and others) within 30 days preceding receipt of the challenge inoculum or planned use during the active study period.
• Nursing mother on the day of admittance to the inpatient phase for all female subjects.
• Are not capable of fully informed consent (e.g., cannot read or write English)
• Personal or documented family history of an inflammatory arthritis such as reactive arthritis, Reiter's syndrome, ankylosing spondylitis, rheumatoid arthritis, or Guillain-Barré syndrome (would not include osteoarthritis or vague history of arthritis in a relative late in adulthood).
• Evidence of neurologic abnormalities (specifically extremity weakness, abnormal deep tendon reflexes, symmetric sensory abnormalities - vibratory, light touch, and proprioception).
• Evidence of inflammatory arthritis on exam and/or HLA-B27 positive (flow cytometry).
• Allergy or prior intolerance to any of the following antibiotics: azithromycin, fluoroquinolones, or penicillin.
• Fewer than 3 stools per week or more than 3 stools per day as the usual frequency, loose or liquid stools other than on an occasional basis.
• Regular use of laxatives or any agent that increases gastric pH (regular defined as at least weekly).
• Have household contacts who are \<2 years old or \>80 years old or infirmed or immunocompromised (for reasons including corticosteroid therapy, HIV infection, cancer chemotherapy, or other chronic debilitating disease).
• Employment as either a health care worker with direct patient care, in a daycare center (for children or the elderly), or working directly with food.

Sponsors & Collaborators

• University of Vermont: lead
• United States Army Medical Materiel Development Activity: collaborator
• Naval Medical Research Center: collaborator

Study Sites (2)

Navy Medical Research Center

Silver Spring, Maryland, 20910, United States

NOT YET RECRUITING

University of Vermont

Burlington, Vermont, 05401, United States

RECRUITING

Related Publications (1)

• Kirkpatrick BD, Lyon CE, Porter CK, Maue AC, Guerry P, Pierce KK, Carmolli MP, Riddle MS, Larsson CJ, Hawk D, Dill EA, Fingar A, Poly F, Fimlaid KA, Hoq F, Tribble DR. Lack of homologous protection against Campylobacter jejuni CG8421 in a human challenge model. Clin Infect Dis. 2013 Oct;57(8):1106-13. doi: 10.1093/cid/cit454. Epub 2013 Jul 9.

  PMID: 23840001 DERIVED

Related Links

• UVM Vaccine Testing Center

MeSH Terms

Conditions

Campylobacter Infections; Gastroenteritis

Condition Hierarchy (Ancestors)

Gram-Negative Bacterial Infections; Bacterial Infections; Bacterial Infections and Mycoses; Infections; Gastrointestinal Diseases; Digestive System Diseases

Study Officials

• Beth Kirkpatrick, MD

  University of Vermont

  PRINCIPAL INVESTIGATOR

• David Tribble, MD

  Navy Medical Research Center

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Cathy Larsson

CONTACT

802-656-9298; cathy.larsson@med.uvm.edu

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER

Study Record Dates

• First Submitted: January 12, 2010
• First Posted: January 13, 2010
• Study Start: January 1, 2010
• Primary Completion: December 1, 2010
• Study Completion: September 1, 2011
• Last Updated: January 13, 2010

Record last verified: 2010-01

Locations

US (2)