Rapid Switch From Flolan to Remodulin in the Outpatient Clinic

• Status: Terminated
• Trial end date: 2012-02-01
• Target enrollment: 0
• Participant gender: All

Summary

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.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: United Therapeutics
• Treatments: Epoprostenol; Treprostinil

Criteria

Inclusion Criteria:

• Be between 18 years and 70 years of age

• Be male or if female, be physiologically incapable of childbearing or practicing an acceptable method of birth control (women of childbearing potential must have a negative pregnancy test).

• Have a current World Health Organization (WHO) functional classification of II-III status

• Diagnosis of one of the following WHO Classifications of pulmonary hypertension: Group 1 pulmonary arterial hypertension (IPAH, FPAH, APAH);Group 3 pulmonary hypertension associated with lung disease (Mild interstitial lung disease associated with predominant features of right heart failure as seen in Group 1 PAH patients); Group 4 pulmonary hypertension due to chronic thromboembolic pulmonary hypertension (CTEPH)

• In the opinion of the investigator, be hemodynamically stable with no signs or symptoms of disease progression

• Be receiving intravenous epoprostenol therapy for at least three months and a stable dose for at least one month prior to Baseline.

• Have a central intravenous catheter in place.

• Have a baseline six-minute walk distance of at least 150 meters.

• Be optimally treated with conventional pulmonary hypertension therapy and clinically stable for at least one month prior to baseline assessments.

• Be mentally and physically capable of learning to administer Remodulin using an intravenous infusion pump.

Exclusion Criteria:

• Be a nursing or pregnant woman

• Have had a new type of chronic therapy (including but not limited to oxygen, a different category of vasodilator, a diuretic, digoxin, bosentan, sildenafil) for pulmonary hypertension added within the last month.

• Have any PAH medication discontinued within the week prior to study entry.

• Received any prostacyclin or prostacyclin analog except epoprostenol in the past 3 months.

• Have an on-going central venous line infection within the past 30 days.

• Have evidence of predominant left-sided heart disease

• Have any other disease that is associated with pulmonary hypertension (e.g. sickle cell anemia, schistosomiasis).

• Have a musculoskeletal disorder (e.g. arthritis, artificial leg, etc.) or any other disease, which is thought to limit ambulation, or be connected to a machine, which is not portable.

• Have uncontrolled systemic hypertension as evidenced by a systolic blood pressure greater than 160 mmHg or diastolic blood pressure greater than 100 mmHg.

• Be receiving an investigational drug, have in place an investigational device, or have participated in an investigational drug study within the past 30 days.

• Have the presence of any physiological or psychological condition that contraindicates the administration of Remodulin.