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Completed Phase 4 Interventional Results available

A Study of Oseltamivir (Tamiflu) for the Seasonal Prophylaxis of Influenza in Immunocompromised Participants

ClinicalTrials.gov ID: NCT00412737

Public ClinicalTrials.gov record NCT00412737. 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 24, 2026, 5:53 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 Double-blind, Randomized, Placebo Controlled, Multi-center Trial of Oseltamivir for the Seasonal Prophylaxis of Influenza in Immunocompromised Patients

Study identification

NCT ID
NCT00412737
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
477 participants

Conditions and interventions

Conditions

Interventions

  • Oseltamivir Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
1 Year 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
Dec 31, 2006
Primary completion
Apr 30, 2008
Completion
Apr 30, 2008
Last update posted
Jun 9, 2016

2007 – 2008

United States locations

U.S. sites
34
U.S. states
20
U.S. cities
31
Facility City State ZIP Site status
Not listed Birmingham Alabama 35233
Not listed Little Rock Arkansas 72202
Not listed Stanford California 94305
Not listed Denver Colorado 80262
Not listed Hartford Connecticut 06106-3316
Not listed Newark Delaware 19718
Not listed St. Petersburg Florida 33701
Not listed Atlanta Georgia 30309
Not listed Augusta Georgia 30912
Not listed Chicago Illinois 60611
Not listed Chicago Illinois 60612
Not listed New Orleans Louisiana 70121
Not listed Detroit Michigan 48201
Not listed Detroit Michigan 48202-2689
Not listed Brooklyn Center Minnesota 55430
Not listed Missoula Montana 59802
Not listed Camden New Jersey 08103
Not listed Hackensack New Jersey 07601
Not listed Livingston New Jersey 07039
Not listed Newark New Jersey 07112
Not listed Buffalo New York 14263
Not listed New York New York 10023
Not listed New York New York 10032
Not listed Chapel Hill North Carolina 27599-7211
Not listed Charlotte North Carolina 28207
Not listed Durham North Carolina 27705
Not listed Cincinnati Ohio 45267
Not listed Cleveland Ohio 44195
Not listed Oklahoma City Oklahoma 73112-44A1
Not listed Hershey Pennsylvania 17033
Not listed Philadelphia Pennsylvania 19104
Not listed Pittsburgh Pennsylvania 15213
Not listed Dallas Texas 75203
Not listed Houston Texas 77030

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 44 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00412737, 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 Jun 9, 2016 · Synced Jul 24, 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 NCT00412737 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →