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

NCT00777790 · ClinicalTrials.gov registry record · Phase 2

Study of a Booster Dose of Meningococcal Diphtheria Toxoid Conjugate Vaccine in Adolescents

A Phase 2 study, sponsored by Sanofi Pasteur, a Sanofi Company.

Completed
Registry status
Phase 2
Development phase
241
Enrollment target

NCT00777790: Completed Phase 2 study, sponsored by Sanofi Pasteur, a Sanofi Company.

NCT00777790 is a Phase 2 study that has completed, run by Sanofi Pasteur, a Sanofi Company. The registered enrollment target is 241 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (81% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00777790, a Phase 2 study, has completed, sponsored by Sanofi Pasteur, a Sanofi Company.

COMPLETED
Registry status
Phase 2
Development phase
241 participants
Enrollment target

Study Summary

This study was designed to evaluate the antibody response to a Menactra® booster dose in participants who previously received one dose of Menactra® or Menomune® as adolescents 3 years earlier in Study MTA02. Primary Objective: To evaluate the antibody responses to a booster dose of a tetravalent meningococcal diphtheria toxoid conjugate vaccine (Menactra®) in participants who had previously received Menactra® or Menomune® as adolescents in the MTA02 Study and antibody responses to a dose of Menactra® in naive adolescents.

Primary Outcome

Geometric mean titers and their 95% confidence interval of serum bactericidal activity for the 4 vaccine serogroups before vaccination, at 8 days post- and 28 days post-booster dose of Menactra vaccine or a primary dose of Menactra vaccine in the meningococcal vaccine-naïve Control group.

Interventions

  • BIOLOGICAL Meningococcal Polysaccharide Diphtheria Toxoid Conjugate

Trial Details

FieldValue
Enrollment Target 241 participants
Start Date 2004-02
Est. Completion 2005-04
Phase Phase 2
Sanofi Pasteur, a Sanofi Company

153 total trials

What the finished NCT00777790 record still lists

NCT00777790 is an interventional study that assigns participants to a tested intervention. The registered 241 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (81% higher).

The record links to 0 conditions, and to 1 intervention - of which Meningococcal Polysaccharide Diphtheria Toxoid Conjugate is the first listed.

NCT00777790 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00777790 about?

NCT00777790 is a clinical study titled "Study of a Booster Dose of Meningococcal Diphtheria Toxoid Conjugate Vaccine in Adolescents". This study was designed to evaluate the antibody response to a Menactra® booster dose in participants who previously received one dose of Menactra® or Menomune® as adolescents 3 years earlier in Study MTA02. Primary Objective: To evaluate the antibody responses to a booster dose of a tetravalent m...

What is the current status of trial NCT00777790?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 241 participants. The study started on 2004-02. Estimated completion is 2005-04.

What interventions are being tested in trial NCT00777790?

The interventions under investigation include: Meningococcal Polysaccharide Diphtheria Toxoid Conjugate (BIOLOGICAL).

Who is sponsoring clinical trial NCT00777790?

This trial is sponsored by Sanofi Pasteur, a Sanofi Company, which has 153 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00777790's enrollment target sits among peer trials

241 239th of 2000 higher than 1,762 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01189786 · 241 participants · NA

    Ex Vivo T-Cell Depletion of Mobilized Peripheral Blood Stem Cells Via CD34-Selection

  • NCT05050383 · 241 participants · NA

    DISE: Phenotyping Obstruction Patterns

  • NCT05683418 · 241 participants · Phase 1

    A Study to Evaluate the Safety and Tolerability of TOS-358 in Adults With HR+ Breast Cancer and Other Select Solid Tumors

  • NCT07213791 · 241 participants · Phase 1

    A Study of LY4337713 in Participants With FAP-Positive Solid Tumors

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00777790, the US trial registry maintained by the National Library of Medicine. NCT00777790 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.