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Generated: December 11, 2018

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CLINICAL TRIALS PROFILE FOR EPOPROSTENOL SODIUM

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Clinical Trials for Epoprostenol Sodium

Trial ID Title Status Sponsor Phase Summary
NCT00373360 Safety, Efficacy and Treatment Satisfaction in Patients With PAH Rapidly Switched From Epoprostenol to Remodulin Completed United Therapeutics Phase 4 The purpose of this 8-week study is to compare the effects of switching from therapy with epoprostenol or Flolan to IV Remodulin. This study will also assess the effect that changing to Remodulin will have on patient satisfaction with their treatment and impact on quality of life.
NCT00439946 Safety, Efficacy, and Treatment Satisfaction Switching From Flolan to Remodulin Using the Crono Five Ambulatory Pump in Patients With PAH Terminated United Therapeutics Phase 4 The purpose of this 8-week study is to compare the effects of switching from intravenous Flolan to intravenous Remodulin therapy. Remodulin (treprostinil sodium) is an approved therapy for pulmonary arterial hypertension (PAH). Unlike Flolan, Remodulin does not need to be mixed daily and is stable at room temperature, so there is no need for ice packs. In addition, Remodulin is changed every 48hrs, instead of every 12-24 (with ice packs) or every 8 hours (without ice packs) with Flolan. Flolan is given using a type of portable medication pump called the CADD Legacy infusion pump. In this study, Remodulin will be given using a smaller and lighter medication pump called the Crono Five infusion pump. This study will also assess the effect that changing to Remodulin will have on treatment satisfaction and patient quality of life.
NCT00643604 Rapid Switch From Flolan to Remodulin in the Outpatient Clinic Terminated United Therapeutics Phase 4 The purpose of this 8-week study is to compare the effects of switching from therapy with epoprostenol or Flolan to IV Remodulin. This study will also assess the effect that changing to Remodulin will have on patient satisfaction with their treatment and impact on quality of life.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Epoprostenol Sodium

Condition Name

Condition Name for Epoprostenol Sodium
Intervention Trials
Pulmonary Arterial Hypertension 3
Hypertension, Pulmonary 2
Pulmonary Hypertension 1
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Condition MeSH

Condition MeSH for Epoprostenol Sodium
Intervention Trials
Hypertension 6
Familial Primary Pulmonary Hypertension 4
Hypertension, Pulmonary 3
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Clinical Trial Locations for Epoprostenol Sodium

Trials by Country

Trials by Country for Epoprostenol Sodium
Location Trials
United States 23
Netherlands 2
Canada 1
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Trials by US State

Trials by US State for Epoprostenol Sodium
Location Trials
North Carolina 3
California 3
Texas 3
Colorado 2
Ohio 2
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Clinical Trial Progress for Epoprostenol Sodium

Clinical Trial Phase

Clinical Trial Phase for Epoprostenol Sodium
Clinical Trial Phase Trials
Phase 4 7
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Clinical Trial Status

Clinical Trial Status for Epoprostenol Sodium
Clinical Trial Phase Trials
Completed 5
Terminated 2
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Clinical Trial Sponsors for Epoprostenol Sodium

Sponsor Name

Sponsor Name for Epoprostenol Sodium
Sponsor Trials
United Therapeutics 3
Actelion 2
Free University Medical Center 1
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Sponsor Type

Sponsor Type for Epoprostenol Sodium
Sponsor Trials
Industry 6
Other 1
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