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| ID | Type | Description | Link |
|---|---|---|---|
| BB013742 |
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| Name | Class |
|---|---|
| SNBL Clinical Pharmacology Center, Inc. | INDUSTRY |
| Johns Hopkins University | OTHER |
| University of Vermont | OTHER |
| SGS U.S. Testing Company Inc. |
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The purpose of this study is to determine whether ACE393 vaccination can protect against Campylobacteriosis in a challenge model.
This study is a randomized, double blind, parallel group, placebo controlled study, in which subjects, with no evidence of prior C.jejuni infections or immunity, will be vaccinated with ACE393, a protein sub-unit vaccine, or placebo, and then subsequently challenged with C.jejuni. The study will include vaccination of approximately 72 subjects, with the aim of challenging a total of 60 subjects. ACE393 or placebo will be administered twice by intramuscular injection on an outpatient basis, three weeks apart and then the subjects will be challenged three weeks later with C.jejuni. During the inpatient monitoring period, volunteers will be evaluated daily for safety, clinical signs and symptoms of disease and stool microbiology). Criteria for early institution of oral hydration, intravenous fluids, serum electrolyte monitoring, blood cultures, and/or antibiotics are predefined. All volunteers will receive antibiotic therapy 6 days after challenge (unless treated early). Discharge criteria are predefined. Post-discharge follow-up will further monitor safety, confirm C .jejuni eradication after antibiotic therapy, and assess immunologic response.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | vaccination with ACE393 followed by challenge with campylobacter jejuni |
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| 2 | Placebo Comparator | Placebo vaccination followed by challenge with campylobacter jejuni |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ACE393 | Biological | ACE393 250 micrograms as intra muscular injection at day 0 and day 21 |
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| Measure | Description | Time Frame |
|---|---|---|
| Incidence of Moderate or Severe Diarrhea | 20 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Median Total (individual) stool number (grade 3-5 stools, diarrheal episodes only) | 20 Weeks | |
| Median Total (individual) stool volume (grade 3-5 stools, diarrheal episodes only) | 20 weeks | |
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Inclusion criteria (selected):
Exclusion Criteria (selected):
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| Name | Affiliation | Role |
|---|---|---|
| Mohamed Al-Ibrahim, MD | Shin Nippon Biomedical Laboratories | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Shin Nippon Biomedical Laboratories | Baltimore | Maryland | 21201 | United States |
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| ID | Term |
|---|---|
| D002169 | Campylobacter Infections |
| D003967 | Diarrhea |
| ID | Term |
|---|---|
| D016905 | Gram-Negative Bacterial Infections |
| D001424 | Bacterial Infections |
| D001423 | Bacterial Infections and Mycoses |
| D007239 | Infections |
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| INDUSTRY |
| Fulcrum Pharma (Europe) Ltd | UNKNOWN |
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| Placebo vaccine | Biological | Placebo 500 micrograms Alhydrogel as intra muscular injection at day 0 and day 21 |
|
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| Maximum stool number and volume in a 24 hr period (grade 3-5 stools, diarrheal episodes only) |
| 20 weeks |
| Incidence of severe diarrhea | 20 weeks |
| D012817 | Signs and Symptoms, Digestive |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |