Clinical Trials Directory

Trials / Completed

CompletedNCT01727232

Efficacy and Safety of Rituximab Given at Fixed Dose (1000 mg on Days 1 and 15) Compared to the Standard Regimen in Adult's Immune Thrombocytopenia

Status
Completed
Phase
Study type
Observational
Enrollment
107 (actual)
Sponsor
Henri Mondor University Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this large French multicentric retrospective study was to compare the efficacy and safety of two (the standard and the Rheumatoid arthritis) rituximab regimens in adult's immune thrombocytopenia .

Detailed description

Every adult (age ≥ 18 years) seen in one of the 3 participating centre (dijon, Marseille, Mondor) over a 7-year period (2005-2012) with a definite diagnosis of primary ITP according to the American Society Hematology guidelines who received RTX regardless the regimen could be included.

Conditions

Timeline

Start date
2007-01-01
Primary completion
2012-06-01
Completion
2012-10-01
First posted
2012-11-15
Last updated
2012-11-15

Source: ClinicalTrials.gov record NCT01727232. Inclusion in this directory is not an endorsement.

Efficacy and Safety of Rituximab Given at Fixed Dose (1000 mg on Days 1 and 15) Compared to the Standard Regimen in Adul (NCT01727232) · Clinical Trials Directory