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Withdrawn Phase 2 Interventional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 Oct 20, 2026, 3:03 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

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Withdrawn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
Dec 2013 (Type not available)
Primary completion
Oct 2014 (Estimated)
Completion
Feb 2015 (Estimated)
Last update posted
Mar 4, 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 4, 2014 · Synced Oct 20, 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 public registry record, listed eligibility criteria, and available contact information for NCT01992276 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →