Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Massive study tracks rare blood disease in over 6,000 patients

NCT ID NCT01374360

Summary

This study collected health information from over 6,000 people with paroxysmal nocturnal hemoglobinuria (PNH), a rare blood disease. The goal was to track how the disease progresses over time and monitor the safety of treatments like Soliris and Ultomiris. It was an observational registry, meaning it collected data but did not test a new treatment.

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes NO responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for PAROXYSMAL NOCTURNAL HEMOGLOBINURIA are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Contacts and locations

Locations

  • Contact the PNH Registry at Alexion Pharmaceuticals, Inc. for worldwide locations.

    Boston, Massachusetts, 02210, United States

Conditions

Explore the condition pages connected to this study.