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Withdrawn Phase 2 Interventional

Assessment of Efficacy of CR8020 and CR6261, Monoclonal Antibodies, Against Influenza Infection

ClinicalTrials.gov ID: NCT01992276

Public ClinicalTrials.gov record NCT01992276. 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 Sep 5, 2026, 7:55 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

Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Effect of CR8020 and CR6261 in Hospitalized Patients With Influenza A Infection

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the rate of decline in quantitative viral load measured in hospitalized patients with Influenza A infection

Study identification

NCT ID
NCT01992276
Recruitment status
Withdrawn
Study type
Interventional
Phase
Phase 2
Lead sponsor
Crucell Holland BV
Industry
Enrollment
Not listed

Conditions and interventions

Conditions

Interventions

Biological

Eligibility (public fields only)

Age range
18 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
Nov 30, 2013
Primary completion
Sep 30, 2014
Completion
Jan 31, 2015
Last update posted
Mar 3, 2014

2013 – 2015

United States locations

U.S. sites
21
U.S. states
15
U.S. cities
21
Facility City State ZIP Site status
Not listed Fresno California
Not listed Stanford California
Not listed Washington D.C. District of Columbia
Not listed Tampa Florida
Not listed Chicago Illinois
Not listed Maywood Illinois
Not listed Baltimore Maryland
Not listed Detroit Michigan
Not listed Royal Oak Michigan
Not listed Troy Michigan
Not listed Minneapolis Minnesota
Not listed St Louis Missouri
Not listed Hackensack New Jersey
Not listed Somers Point New Jersey
Not listed New York New York
Not listed Rochester New York
Not listed Winston-Salem North Carolina
Not listed Dayton Ohio
Not listed Wilkes-Barre Pennsylvania
Not listed Nashville Tennessee
Not listed Houston Texas

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 47 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01992276, 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 Mar 3, 2014 · Synced Sep 5, 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 NCT01992276 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →