Clinical Trials Directory

Trials / Completed

CompletedNCT02158169

Biosimilar Retacrit® in the Treatment of Chemotherapy-induced Anaemia in Oncology and Haematology

Pharmaco-epidemiological Study on the Effect of Retacrit® on Chemotherapy Induced Anaemia in Standard Oncology and Haematology Practice: Impact of Concomitant Iron Supplementation

Status
Completed
Phase
Study type
Observational
Enrollment
2,167 (actual)
Sponsor
Hospira, now a wholly owned subsidiary of Pfizer · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to describe, in a real-life context, the impact of an epoetin alpha biosimilar, Retacrit®, on anaemia in patients receiving chemotherapy, according to concomitant iron supplementation.

Detailed description

This is a longitudinal, observational, prospective, multicentre, cohort study, conducted on a representative sample of public and/or private hospital-based oncologists and haematologists practicing in Metropolitan France.

Conditions

Timeline

Start date
2012-06-01
Primary completion
2014-12-01
Completion
2014-12-01
First posted
2014-06-06
Last updated
2015-07-28

Locations

69 sites across 1 country: France

Source: ClinicalTrials.gov record NCT02158169. Inclusion in this directory is not an endorsement.

Biosimilar Retacrit® in the Treatment of Chemotherapy-induced Anaemia in Oncology and Haematology (NCT02158169) · Clinical Trials Directory