Study of a Candidate Clostridium Difficile Toxoid Vaccine in Subjects at Risk for C. Difficile Infection

Stopped early · Phase 3 · Has a placebo group

Conditions studied: Clostridium Difficile Infection

In brief

The aim of this study was to evaluate the efficacy of the Clostridium difficile vaccine to prevent primary symptomatic C. difficile infection (CDI) in participants at risk for CDI where there is a substantial unmet medical need. Primary objective: * To assess the efficacy of the C. difficile vaccine in preventing the onset of symptomatic primary CDI confirmed by polymerase chain reaction (PCR) in adult participants aged \>= 50 years who are at risk for CDI and have received at least 1 injection. Secondary Objectives: Efficacy: * To assess prevention of symptomatic PCR-confirmed primary CDI cases after 3 injections administered at 0, 7, and 30 days. * To assess prevention of symptomatic PCR-confirmed primary CDI cases after completion of at least 2 injections. Immunogenicity: * To describe the immunogenicity to toxin A and toxin B at specific time points in a subset of participant and in participants with CDI at Day 0 and Day 60. Safety: * To describe the safety profile of all participants who received at least 1 injection.

Key facts

Study ID

NCT01887912

Run by

Sanofi Pasteur, a Sanofi Company

People needed

9302

Starts

2013-07-30

Expected to finish

2018-06-12

Last updated by the study team

2022-03-28

Who can join

Age: 50 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Aged >= 50 years on the day of inclusion
• Informed consent form had been signed and dated.
• Attended all scheduled visits and complied with all trial procedures.
• Covered by health insurance (if required).
• Must fulfill at least 1 of the following criteria
• Risk Stratum 1:
• Had at least 2 hospital stays, each lasting at least >= 24 hours, in the 12 months before enrollment, and
• Had received systemic (not topical) antibiotics in the 12 months before enrollment, or
• Risk Stratum 2:
• Was anticipated to have an in-patient hospitalization for a planned surgical procedure within 60 days of enrollment. The impending hospital stay was planned to be >= 72 hours for a surgery involving 1 of the following:
• Kidney/bladder/urinary system
• Musculoskeletal system
• Respiratory system
• Circulatory system
• Central nervous system.

You may not qualify if…

• Participant was pregnant, or lactating, or of childbearing potential (to be considered of non-childbearing potential, a female must be post-menopausal for at least 1 year, surgically sterile, or using an effective method of contraception or abstinence from at least 4 weeks prior to the first vaccination and until at least 4 weeks after the last vaccination).
• Participation in the 4 weeks preceding the first trial vaccination or participation during the present trial period in another clinical trial investigating a vaccine, drug, medical device, or medical procedure.
• Receipt of any vaccine in the 4 weeks preceding the first trial vaccination except for influenza (seasonal or pandemic) and pneumococcal vaccines. This exception includes monovalent pandemic influenza vaccines and multivalent influenza vaccines.
• Previous vaccination against C. difficile with either the trial vaccine, another vaccine, or monoclonal antibodies.
• Diarrhea on day of enrollment.
• Self-reported current or prior CDI episode.
• Anticipated or current receipt of kidney dialysis treatment.
• History of gastrointestinal surgery for gastrointestinal malignancy (Note: Colonoscopy, polypectomy, and appendectomy are not exclusion criteria).
• History of inflammatory bowel disease, irritable bowel syndrome (must include diarrhea as a symptom), colostomy, or small or large intestine bowel surgery where resection was performed.
• Receiving enteral feeding (e.g., nasogastric, gastrostomy, and jejunostomy tube feeding).
• Known or suspected congenital or acquired immunodeficiency; or receipt of immunosuppressive therapy, such as anti-cancer chemotherapy or radiation therapy, within the preceding 6 months; or long-term systemic corticosteroid therapy (prednisone or equivalent for more than 2 consecutive weeks within the past 3 months).
• Known systemic hypersensitivity to any of the vaccine components, or history of a life-threatening reaction to the vaccine used in the trial or to a vaccine containing any of the same substances.
• Self-reported thrombocytopenia, contraindicating intramuscular vaccination.
• Deprived of freedom by an administrative or court order, or in an emergency setting, or hospitalized involuntarily.
• Current alcohol abuse or drug addiction that might interfere with the ability to comply with trial procedures in the opinion of the Investigator.
• Chronic illness that, in the opinion of the investigator, is at a stage where it might interfere with trial conduct or completion.
• Moderate or severe acute illness/infection (according to investigator judgment) on the day of vaccination or febrile illness (temperature >= 38.0 degree Celsius [>= 100.4°Fahrenheit]). A prospective participant should not be included in the study until the condition has resolved or the febrile event has subsided.
• Identified as an Investigator or employee of the Investigator or study center with direct involvement in the proposed study, or identified as an immediate family member (i.e., parent, spouse, natural or adopted child) of the Investigator or employee with direct involvement in the proposed study.

Where it is running

• Investigational Site 104 — Mobile, Alabama, United States
• Study site — Flagstaff, Arizona, United States
• Investigational Site 194 — Phoenix, Arizona, United States
• Investigational Site 503 — Surprise, Arizona, United States
• Study site — Little Rock, Arkansas, United States
• Study site — Bakersfield, California, United States
• Study site — Banning, California, United States
• Study site — Garden Grove, California, United States
• Study site — La Mesa, California, United States
• Investigational Site 534 — Los Angeles, California, United States
• Investigational Site 051 — Los Angeles, California, United States
• Study site — Modesto, California, United States
• Study site — Redding, California, United States
• Study site — Sacramento, California, United States
• Investigational Site 504 — Simi Valley, California, United States
• Investigational Site 057 — Stanford, California, United States
• Investigational Site 176 — Upland, California, United States
• Study site — Ventura, California, United States
• Investigational Site 546 — Wheat Ridge, Colorado, United States
• Study site — Bristol, Connecticut, United States
• Study site — Danbury, Connecticut, United States
• Investigational Site 143 — Bradenton, Florida, United States
• Investigational Site 187 — Brandon, Florida, United States
• Investigational Site 075 — Clearwater, Florida, United States
• Study site — Huntsville, Alabama, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.