A Prospective Non-interventional Observational Study to Observe Long-term Treatment and Outcomes in Pulmonary Arterial Hypertension (PAH) Patients
NCT06445673 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 110
Last updated 2024-08-07
Summary
The goal of this observational study is to learn about the long-term development and outcomes of different treatment patterns of patients who initially participated in the TripleTRE study.
The primary objective of this non-interventional follow-up study is to assess the long-term real-world clinical outcomes, including disease progression and survival rates, in patients who initially participated in and completed the randomized TripleTRE trial.
Planned observation duration per patient is a minimum of 3 years.
Conditions
Sponsors & Collaborators
-
AOP Orphan Pharmaceuticals AG
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-07-31
- Primary Completion
- 2030-06-30
- Completion
- 2030-06-30
Countries
- Austria
- Czechia
- France
- Germany
- Hungary
- Italy
- Poland
- Romania
- Spain
Study Locations
More Related Trials
-
Inhaled Treprostinil for PAH: Open-label Extension
NCT01557660 ·Status: WITHDRAWN ·Phase: PHASE3
-
Remodulin® to Oral Treprostinil Transition
NCT01588405 ·Status: COMPLETED ·Phase: PHASE2
-
FREEDOM DR: Oral Treprostinil in Combination With an Endothelin Receptor Antagonist (ERA) and/or a Phosphodiesterase-5 (PDE-5) Inhibitor or as Monotherapy for the Treatment of Pulmonary Arterial Hypertension (PAH)
NCT00760916 ·Status: WITHDRAWN ·Phase: PHASE3
-
Efficacy and Safety of Triple-targeted Drug Therapy in Treatment-naive Patients With Non-low-risk PAH: A Real-world, Multicenter Study
NCT06753981 ·Status: RECRUITING
-
Safety and Efficacy of Inhaled Treprostinil in Patients With PAH
NCT01557647 ·Status: WITHDRAWN ·Phase: PHASE3
-
Study to Compare Triple Therapy (Oral Treprostinil, Ambrisentan, and Tadalafil) With Dual Therapy (Ambrisentan, Tadalafil, and Placebo) in Subjects With Pulmonary Arterial Hypertension
NCT02999906 ·Status: WITHDRAWN ·Phase: PHASE3
-
A Study to Evaluate the Efficacy, Safety and Pharmacokinetics of Treprostinil Palmitil Inhalation Powder in Participants With Pulmonary Arterial Hypertension
NCT05147805 ·Status: COMPLETED ·Phase: PHASE2
-
Clinical Investigation Into Inhaled Treprostinil Sodium in Patients With Severe Pulmonary Arterial Hypertension (PAH)
NCT00147199 ·Status: COMPLETED ·Phase: PHASE3
-
Safety of Transition From Selexipag to Remodulin® Then Oral Treprostinil in Symptomatic Adult PAH
NCT03016468 ·Status: WITHDRAWN ·Phase: PHASE2
-
An Expanded Access Study to Assess Treprostinil Palmitil Inhalation Powder (TPIP) for Participants With Pulmonary Arterial Hypertension (PAH) and Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)
NCT06939647 ·Status: AVAILABLE
-
An Open-Label Extension Trial of UT-15C Sustained-release (SR) in Subjects With Pulmonary Arterial Hypertension
NCT01027949 ·Status: COMPLETED ·Phase: PHASE3
-
Extension Study of Efficacy and Safety of LTP001 in Pulmonary Arterial Hypertension Participants
NCT05764265 ·Status: TERMINATED ·Phase: PHASE2
-
Safety Evaluation of Inhaled Treprostinil Administration Following Transition From Inhaled Ventavis in Pulmonary Arterial Hypertension (PAH) Subjects
NCT00741819 ·Status: COMPLETED ·Phase: PHASE4
-
Post Marketing Observational Study in Patients With Pulmonary Arterial Hypertension
NCT01066845 ·Status: COMPLETED
-
Investigational Trial to Evaluate Safety and Tolerability of Treprostinil in Children Diagnosed With PAH
NCT06350032 ·Status: RECRUITING ·Phase: PHASE3
-
Efficacy and Safety of Treprostinil in Intermediate-Risk Pulmonary Arterial Hypertension
NCT07177703 ·Status: NOT_YET_RECRUITING ·Phase: PHASE2
-
Oral Treprostinil in Subjects With Pulmonary Hypertension Associated With Heart Failure With Preserved Ejection Fraction
NCT03037580 ·Status: TERMINATED ·Phase: PHASE3
-
An Extension Study of Treprostinil Palmitil Inhalation Powder (TPIP) for Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)
NCT05649722 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Oral Treprostinil in Subjects With Pulmonary Hypertension Associated With Pulmonary Fibrosis
NCT02603068 ·Status: WITHDRAWN ·Phase: PHASE2
-
Safety, Efficacy and Treatment Satisfaction in Patients With PAH Rapidly Switched From Epoprostenol to Remodulin
NCT00373360 ·Status: COMPLETED ·Phase: PHASE4
-
Effects of Treprostinil on Right Ventricular Structure and Function in Patients With Pulmonary Arterial Hypertension
NCT03835676 ·Status: RECRUITING ·Phase: PHASE4
-
Open-label Extension of Oral Treprostinil in Subjects With PH Associated With HFpEF
NCT03043651 ·Status: TERMINATED ·Phase: PHASE3
-
Study Of Right Ventricular Performance In PAH Patients Treated With Rapid Dose Treprostinil (Remodulin)
NCT02074449 ·Status: COMPLETED
-
A Study to Evaluate GSK1325760A - a Long-Term Extension Study
NCT00554619 ·Status: COMPLETED ·Phase: PHASE3
-
Observation Study With Implantable Medication Pump for Intravenous Treprostinil Therapy in Patients With Pulmonary Arterial Hypertension
NCT04309838 ·Status: UNKNOWN