ClinicalTrials.gov record
Completed Phase 2 Interventional Accepts healthy volunteers Results available

A Study To Investigate Two 3-dose Schedules Of A Clostridium Difficile Vaccine In Healthy Adults Aged 65 to 85 Years

ClinicalTrials.gov ID: NCT02561195

Public ClinicalTrials.gov record NCT02561195. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 18, 2026, 10:47 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A PHASE 2, PLACEBO-CONTROLLED, RANDOMIZED, OBSERVER-BLINDED STUDY TO EVALUATE THE SAFETY, TOLERABILITY, AND IMMUNOGENICITY OF TWO 3-DOSE REGIMENS OF A CLOSTRIDIUM DIFFICILE VACCINE IN HEALTHY ADULTS AGED 65 TO 85 YEARS

Study identification

NCT ID
NCT02561195
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
300 participants

Conditions and interventions

Interventions

  • Clostridium difficile Vaccine Biological
  • Placebo Biological

Biological

Eligibility (public fields only)

Age range
65 Years to 85 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 15, 2015
Primary completion
Mar 6, 2017
Completion
Feb 12, 2020
Last update posted
Mar 7, 2021

2015 – 2020

United States locations

U.S. sites
17
U.S. states
9
U.S. cities
14
Facility City State ZIP Site status
Avail Clinical Research, LLC DeLand Florida 32720
QPS-MRA, LLC (Broward Research Group) Hollywood Florida 33024
QPS-MRA, LLC (Miami Research Associates) South Miami Florida 33143
East-West Medical Research Institute Honolulu Hawaii 96814
Vince & Associates Clinical Research, Inc. Overland Park Kansas 66212
Vince & Associates Clinical Research, Inc Overland Park Kansas 66212
Meridian Clinical Research, LLC Omaha Nebraska 68134
Clinical Research Center of Nevada LLC Las Vegas Nevada 89104
Wake Research Associates, LLC Raleigh North Carolina 27612
PMG Research of Wilmington, LLC Wilmington North Carolina 28401
Cincinnati Childrens Hospital Medical Center Cincinnati Ohio 45206
Cincinnati Childrens Hospital Medical Center Cincinnati Ohio 45229
Benchmark Research Austin Texas 78705
Texas Center For Drug Development, Inc. Houston Texas 77081
Clinical Trials of Texas, Inc. San Antonio Texas 78229
J. Lewis Research, Inc. / Foothill Family Clinic Salt Lake City Utah 84109
J. Lewis Research, Inc. / Foothill Family Clinic South Salt Lake City Utah 84121

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02561195, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 7, 2021 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02561195 live on ClinicalTrials.gov.

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