Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01129453 · ClinicalTrials.gov registry record · Phase 1

Safety and Immunogenicity of CVD 1902 Oral Attenuated Vaccine to Prevent S. Paratyphi A Infection

A Phase 1 study, sponsored by University of Maryland, Baltimore.

Completed
Registry status
Phase 1
Development phase
51
Enrollment target

NCT01129453 is a Phase 1 study that has completed, run by University of Maryland, Baltimore. The registered enrollment target is 51 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01129453, a Phase 1 study, has completed, sponsored by University of Maryland, Baltimore.

COMPLETED
Registry status
Phase 1
Development phase
51 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether CVD 1902 (a live, attenuated, oral vaccine) is safe and effective in the prevention of Salmonella enterica serovar paratyphi A infection.

Interventions

  • OTHER Placebo
  • BIOLOGICAL CVD 1902, a Salmonella enterica Serovar Paratyphi A live, oral vaccine

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2010-05
Est. Completion 2013-04
Phase Phase 1

Sponsor

University of Maryland, Baltimore

560 total trials

What the Registry Record Tells You About NCT01129453

The ClinicalTrials.gov registry entry for NCT01129453 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 51 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Maryland, Baltimore, which has 560 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT01129453 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01129453 about?

NCT01129453 is a clinical study titled "Safety and Immunogenicity of CVD 1902 Oral Attenuated Vaccine to Prevent S. Paratyphi A Infection". The purpose of this study is to determine whether CVD 1902 (a live, attenuated, oral vaccine) is safe and effective in the prevention of Salmonella enterica serovar paratyphi A infection.

What is the current status of trial NCT01129453?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 51 participants. The study started on 2010-05. Estimated completion is 2013-04.

What interventions are being tested in trial NCT01129453?

The interventions under investigation include: Placebo (OTHER), CVD 1902, a Salmonella enterica Serovar Paratyphi A live, oral vaccine (BIOLOGICAL).

Who is sponsoring clinical trial NCT01129453?

This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.