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COMPLETED Phase 3

Efficacy Study of Two Influenza Vaccines and Placebo in Healthy Adult Subjects

NCT00630331 · View on ClinicalTrials.gov ↗

Study Summary

The present study will evaluate clinical efficacy, safety, tolerability and immunogenicity of both Novartis Vaccines' cell-derived influenza vaccine and egg-derived influenza vaccine in healthy adults 18 to 49 years of age.

Conditions Studied

Interventions

  • BIOLOGICAL Placebo
  • BIOLOGICAL Cell culture-derived influenza vaccine
  • BIOLOGICAL Egg-derived influenza virus vaccine

Study Locations (20)

Other

  • Site 25 — Espoo
  • Site 26 — Helsinki
  • Site 27 — Helsinki

Florida

  • Site 15 — Pembroke Pines
  • Site 17 — South Miami

New York

  • Site 10 — Binghamton
  • Site 5 — Endwell

Texas

  • Site 9 — Austin
  • Site 8 — Dallas

Utah

  • Site 7 — Salt Lake City
  • Site 3 — Salt Lake City

Colorado

  • Site 14 — Denver

Kansas

  • Site 13 — Lenexa

Kentucky

  • Site 2 — Bardstown

Trial Details

FieldValue
Enrollment Target 11,404 participants
Start Date 2007-10
Est. Completion 2008-07
Phase Phase 3

Sponsor

Novartis Vaccines

7 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00630331

The ClinicalTrials.gov registry entry for NCT00630331 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 11,404 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novartis Vaccines, which has 7 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Influenza appearing as the primary indexed condition, and to 3 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00630331 reports 20 study locations spanning 14 distinct geographic areas — top geographies include Other, Florida, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00630331 about?

NCT00630331 is a clinical study titled "Efficacy Study of Two Influenza Vaccines and Placebo in Healthy Adult Subjects". The present study will evaluate clinical efficacy, safety, tolerability and immunogenicity of both Novartis Vaccines' cell-derived influenza vaccine and egg-derived influenza vaccine in healthy adults 18 to 49 years of age.

What is the current status of trial NCT00630331?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 11,404 participants. The study started on 2007-10. Estimated completion is 2008-07.

What conditions does trial NCT00630331 study?

This clinical trial studies the following conditions: Influenza. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00630331?

The interventions under investigation include: Placebo (BIOLOGICAL), Cell culture-derived influenza vaccine (BIOLOGICAL), Egg-derived influenza virus vaccine (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00630331?

This trial is sponsored by Novartis Vaccines, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00630331 being conducted?

This trial has 20 study locations across Colorado, Florida, Kansas, Kentucky, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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