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CompletedNCT01329783

EuroSIDA As An External Comparator To MOTIVATE Trials

Incidence And Risk Factors For Acquired Immune Deficiency Syndrome (AIDS) Defining And Non-AIDS Defining Malignancies, And Other AIDS Defining Illnesses In The EuroSIDA Study

Status
Completed
Phase
Study type
Observational
Enrollment
1,181 (actual)
Sponsor
ViiV Healthcare · Industry
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

Human Immunodeficiency Virus (HIV) infected patients who meet the entry criteria for the maraviroc pivotal trials (Maraviroc versus Optimized Therapy in Viremic Antiretroviral Treatment-Experienced Patients, MOTIVATE) will be identified from the EuroSIDA HIV cohort. The rates of specific clinical adverse events in this identified patient population will be compared with the rates of these events in the participants of the MOTIVATE trials.

Detailed description

All patients in EuroSIDA cohort that meet the entry criteria of MOTIVATE trials are included without any sampling.

Conditions

Interventions

TypeNameDescription
OTHERmaravirocNo intervention is distributed during this trial.

Timeline

Start date
2007-04-01
Primary completion
2011-03-01
Completion
2011-03-01
First posted
2011-04-06
Last updated
2011-05-16

Source: ClinicalTrials.gov record NCT01329783. Inclusion in this directory is not an endorsement.

EuroSIDA As An External Comparator To MOTIVATE Trials (NCT01329783) · Clinical Trials Directory