Viewing Study NCT00185315



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Last Modification Date: 2024-10-26 @ 9:17 AM
Study NCT ID: NCT00185315
Status: COMPLETED
Last Update Posted: 2010-04-20
First Post: 2005-09-13

Brief Title: Safety Follow-up Study of Inhaled Iloprost in Patients With Pulmonary Hypertension
Sponsor: Bayer
Organization: Bayer

Study Overview

Official Title: Open-label Uncontrolled Long-term Surveillance Study of Iloprost Aerosol Inhalation Therapy in the Treatment of Patients With Primary or Secondary Pulmonary Hypertension Follow-up Program for Patients Who Completed 12 Weeks in Study ME97218300180
Status: COMPLETED
Status Verified Date: 2010-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of this study is to monitor long-term safety and tolerability of iloprost aerosol inhalation therapy in patients suffering from pulmonary hypertension
Detailed Description: This study has previously been posted by Schering AG Germany Schering AG has been renamed to Bayer Schering Pharma AG Germany

Bayer Schering Pharma AG Germany is the sponsor of the trial

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
Follow-up 90419-300180 None None None
303045 None None None