Treprostinil Combined With Tadalafil for Pulmonary Hypertension

Stopped early · Phase 4 · Has a placebo group

Conditions studied: Pulmonary Arterial Hypertension

In brief

Objectives: To test whether the combined administration of the medications treprostinil(a prostacycline therapy), and tadalafil(a PDE-5 \[ phosphodiesterase type 5\]Inhibitor therapy) is better than the administration of treprostinil alone. This treatment would be offered to newly diagnosed patients with pulmonary arterial hypertension who are on no treatment for this disease and are deemed candidates for the medication treprostinil by their physician. The combination therapy will be compared to single therapy with only treprostinil in a double-blind manner. Current therapy is to begin one treatment, either a PDE5 inhibitor or a prostacycline, depending on the severity of the patient's PAH (pulmonary arterial hypertension) disease and add additional therapies as deterioration occurs. This treatment could add two agents initially. Secondary objectives are: To improve pulmonary arterial pressures as measured through a cardiac echocardiogram, improve the subject's 6minute walk distance, delaying the time to clinical worsening, and lowering plasma BNP levels. Research Procedures: To begin the administration of both treatments at the same time. Time period is 16 weeks with a one- year follow-up. Cardiac Echocardiograms, clinic physician exams, and lab work will be followed. Subjects will be between the ages of 18 - 75.

Key facts

Study ID

NCT01302444

Run by

Rhode Island Hospital

People needed

1

Starts

2011-03-01

Expected to finish

2012-03-01

Last updated by the study team

2013-07-26

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult patients 18-80 years of age
• World Health Organization Group 1 PAH
• Idiopathic PAH
• Heritable PAH
• PAH associated with connective tissue disease
• PAH associated with surgical repair of congenital left to right shunt
• PAH associated with anorectic drug use
• WHO functional Class III-IV
• 6 minute walking distance > 150-meters and < 450 meters
• Right heart catheterization showing mean PAP (pulmonary arterial pressure)> 25 mmHg and PCWP (pulmonary capillary wedge pressure) < 15 mmHg within 6 months of study entry.

You may not qualify if…

• Pulmonary hypertension associated with
• a. Portal hypertension b. HIV infection c. Pulmonary venous hypertension defined as PCWP > 15 mmHg d. Chronic lung disease defined as i. FEV1(forced expiratory volume at one second
• )/FVC (forced vital capacity) less than 0.65 ii. TLC < 0.70 iii. Untreated Sleep Apnea with AHI (apnea-hypopnea index )> 20 or hemoglobin oxygen saturation nadir < 87% e. Chronic Thromboembolic Disease f. Sarcoidosis g. Pulmonary veno occlusive disease (PVOD)
• Concomitant use of nitrates (any form) either regularly or intermittently.
• Concomitant use of potent CYP3A inhibitors (e.g., ritonavir, ketoconazole, itraconazole)
• Vascular disease of the retina including retinitis pigmentosa, any sudden vision loss, including any damage to the optic nerve or NAION
• low blood pressure or high blood pressure that is not controlled
• Postural hypotension
• Inability to manage home infusion therapy
• Pulmonary vasodilator therapy with any phosphodiesterase inhibitor or endothelin receptor antagonist within 30 days of study entry
• Participation in a clinical investigational study within previous 30 days
• Renal failure defined as:
• estimated creatinine clearance < 30 ml/min
• serum creatinine > 2.5 mg/dl
• Subjects with liver function abnormalities (ALT [Alanine Aminotransferase or AST (Alanine Aminotransferase ) > 3 times the upper limit of normal at screening or at baseline) or chronic liver disease
• History of hypersensitivity reaction or adverse effect related to tadalafil
• Life expectancy < 12 months
• History of deformed penis shape, an erection that lasted more than 4 hours, or Peyronie's disease.
• Blood cell problems such as sickle cell anemia, multiple myeloma, or leukemia
• Pregnant or planning to become pregnant or breast feed.

Where it is running

• Maine Medical Center — Portland, Maine, United States
• Tuft's New England Medical Center — Boston, Massachusetts, United States
• Brigham & Womens Hospital — Boston, Massachusetts, United States
• Saint Barnabas Health Care System, Newark Beth Israel Medical Center — Newark, New Jersey, United States
• Beth Israel Medical Center — New York, New York, United States
• Weill Cornell Medical Center — New York, New York, United States
• University of Rochester Medical Center — Rochester, New York, United States
• Rhode Island Hospital — Providence, Rhode Island, United States
• Inova Fairfax Hospital — Falls Church, Virginia, United States

Full record on ClinicalTrials.gov

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