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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT01557660
Date of registration: 14/03/2012
Prospective Registration: Yes
Primary sponsor: United Therapeutics
Public title: Inhaled Treprostinil for PAH: Open-label Extension INTREPID - OL
Scientific title: Inhaled Treprostinil in Subjects With Pulmonary Arterial Hypertension: An Open-Label, Phase III, International, Multi-Center Study
Date of first enrolment: June 2012
Target sample size: 0
Recruitment status: Withdrawn
URL:  http://clinicaltrials.gov/show/NCT01557660
Study type:  Interventional
Study design:  Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment  
Phase:  Phase 3
Countries of recruitment
Contacts
Key inclusion & exclusion criteria

Participation and completion of all required visits for study RIN-PH-302.



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Pulmonary Arterial Hypertension
Intervention(s)
Drug: inhaled treprostinil
Primary Outcome(s)
Long term safety of inhaled treprostinil [Time Frame: up to 5 years]
Secondary Outcome(s)
Six-minute walk distance [Time Frame: up to 5 years]
Secondary ID(s)
RIN-PH-303
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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