Clinical Trials Directory

Trials / Completed

CompletedNCT01412047

Paroxysmal Nocturnal Hemoglobinuria Human Anti-Human Antibodies Study

A Post Marketing, Multi-Center, Trial to Measure Human Anti-Human Antibodies (HAHA) to Soliris (Eculizumab) in Patients With Paroxysmal Nocturnal Hemoglobinuria

Status
Completed
Phase
Study type
Observational
Enrollment
75 (actual)
Sponsor
Alexion Pharmaceuticals, Inc. · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

How does long term treatment with Soliris affect HAHA in PNH patients?

Detailed description

To determine the long term effect of Soliris (eculizumab) treatment on the presence of human anti-human antibodies (HAHA) in Paroxysmal Nocturnal Hemoglobinuria (PNH) patients.

Conditions

Timeline

Start date
2012-03-01
Primary completion
2013-06-01
Completion
2013-06-30
First posted
2011-08-08
Last updated
2017-10-18

Locations

14 sites across 10 countries: United States, Australia, Belgium, France, Germany, Ireland, Italy, Netherlands, Switzerland, United Kingdom

Source: ClinicalTrials.gov record NCT01412047. Inclusion in this directory is not an endorsement.

Paroxysmal Nocturnal Hemoglobinuria Human Anti-Human Antibodies Study (NCT01412047) · Clinical Trials Directory