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Completed Phase 3 Interventional Results available

A Study of Intravenous Zanamivir Versus Oral Oseltamivir in Adults and Adolescents Hospitalized With Influenza

ClinicalTrials.gov ID: NCT01231620

Public ClinicalTrials.gov record NCT01231620. 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 Jul 22, 2026, 2:46 PM 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 III International, Randomized, Double-blind, Double-dummy Study to Evaluate the Efficacy and Safety of 300 mg or 600 mg of Intravenous Zanamivir Twice Daily Compared to 75 mg of Oral Oseltamivir Twice Daily in the Treatment of Hospitalized Adults and Adolescents With Influenza

Study identification

NCT ID
NCT01231620
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
626 participants

Conditions and interventions

Interventions

  • Zanamivir Drug
  • Placebo to match zanamivir Drug
  • Oseltamivir Drug
  • Placebo to match oseltamivir Drug

Drug

Eligibility (public fields only)

Age range
16 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Jan 14, 2011
Primary completion
Mar 17, 2015
Completion
Mar 17, 2015
Last update posted
Oct 14, 2018

2011 – 2015

United States locations

U.S. sites
40
U.S. states
25
U.S. cities
40
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35249
GSK Investigational Site Phoenix Arizona 85023
GSK Investigational Site Chula Vista California 91911
GSK Investigational Site Escondido California 92025
GSK Investigational Site Fullerton California 92835
GSK Investigational Site La Jolla California 92037
GSK Investigational Site La Mesa California 91942
GSK Investigational Site Oceanside California 92056
GSK Investigational Site Aurora Colorado 80045
GSK Investigational Site Stamford Connecticut 06902
GSK Investigational Site Orlando Florida 32806
GSK Investigational Site Sarasota Florida 34239
GSK Investigational Site Sunrise Florida 33323
GSK Investigational Site Atlanta Georgia 30342
GSK Investigational Site Augusta Georgia 30912
GSK Investigational Site Idaho Falls Idaho 83404
GSK Investigational Site Chicago Illinois 60611
GSK Investigational Site Oak Park Illinois 60302
GSK Investigational Site Peoria Illinois 61637
GSK Investigational Site Council Bluffs Iowa 51503
GSK Investigational Site Topeka Kansas 66604
GSK Investigational Site Louisville Kentucky 40241
GSK Investigational Site Boston Massachusetts 02115
GSK Investigational Site Royal Oak Michigan 48073
GSK Investigational Site Troy Michigan 48085
GSK Investigational Site St Louis Missouri 63110-1093
GSK Investigational Site Missoula Montana 59802
GSK Investigational Site Las Vegas Nevada 89109
GSK Investigational Site Valhalla New York 10595
GSK Investigational Site Asheville North Carolina 28801
GSK Investigational Site Chapel Hill North Carolina 27599-7215
GSK Investigational Site Bismarck North Dakota 58504
GSK Investigational Site Cleveland Ohio 44195
GSK Investigational Site Columbus Ohio 43215
GSK Investigational Site Toledo Ohio 43608
GSK Investigational Site Bethlehem Pennsylvania 18105
GSK Investigational Site Philadelphia Pennsylvania 19107
GSK Investigational Site Houston Texas 77030
GSK Investigational Site Roanoke Virginia 24013
GSK Investigational Site Marshfield Wisconsin 54449

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 130 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01231620, 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 Oct 14, 2018 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01231620 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →