A 48-week Study of the Effect of Dual Therapy (Inhaled Treprostinil and Tadafafil) Versus Monotherapy (Tadalafil).

Not Recruiting

Trial ID: NCT01305252

Purpose

The Study Hypothesis: Aggressive, upfront, dual therapy for treatment-naïve NYHA I/II/III PAH is superior to a traditional "step-up" approach. The study will evaluate: 1. Impact of dual, upfront, therapy on cardiovascular parameters in PAH as gauged by cardiac magnetic resonance imaging (cMRI) at 24 weeks and event free survival at outcome at 48 weeks. 2. Value of novel biomarkers (NT-pro BNP, Mts1/S100A4, and insulin resistance) and cutting-edge imaging technologies (cardiac MRI) as newer endpoints for clinical trials in PAH. 3. Utility of longer clinical trial design with the use of combined clinical events as time to clinical worsening surrogate

Official Title

CombinatiON Up-FRON t Therapy for PAH - A Phase 4, Randomized, Multicenter Study of Inhaled Treprostinil in Treatment naïve Pulmonary Arterial Hypertension Patients Starting on Tadalafil

Eligibility


Inclusion criteria:

   1. Age 18 and < 75 years at baseline visit.

   2. Diagnosis of Idiopathic PAH, Heritable PAH (including Hereditary Hemorrhagic
   Telangiectasia), Associated PAH (including collagen vascular disorders, drug+toxin
   exposure, repaired congenital heart disease repaired > 5 years, portopulmonary
   disease, and human immunodeficiency virus (HIV) infection not on protease inhibitor).

   3. PAH treatment naïve including any prostacycline, endothelin receptor antagonist, or
   phosphodiesterase inhibitors within 12 months prior to enrollment.

   4. Previous Right Heart Catheterization that documented:

      1. Mean PAP; 25 mmHg.

      2. Pulmonary capillary wedge pressure < 15 mmHg.

      3. Pulmonary Vascular Resistance; 3.0 Wood units or 240 dynes/sec/cm5 5.6MW
      distances; 150 m and < 450 meters.

6. WHO functional class II or III as judged by principal investigators.

Exclusion Criteria:

Exclusion criteria:

   1. Group II - V pulmonary hypertension.

   2. PAH with unrepaired congenital heart defect.

   3. Current or prior PAH treatments within the last 6-12 months including experimental PAH
   therapies (including but not limited to tyrosine kinase inhibitors, rho-kinase
   inhibitors, phosphodiesterase inhibitors, prostacycline, or cGMP modulators).

   4. TLC < 60% predicted; if TLC b/w 60 and 70% predicted, high resolution computed
   tomography must be available to exclude significant interstitial lung disease.

   5. FEV1 / FVC < 70% predicted and FEV1 < 60% predicted

   6. Significant left-sided heart disease (based on pre-trial Echocardiogram):

      1. Significant aortic or mitral valve disease

      2. Diastolic dysfunction ; Grade II C.LV systolic function < 45%

   d. Pericardial constriction e. Restrictive cardiomyopathy f. Significant coronary
   disease with demonstrable ischemia

   7. Chronic renal insufficiency defined as an estimated creatinine clearance < 30 ml/min
   (by MDRD equation)

   8. Current atrial arrhythmias

   9. Uncontrolled systemic hypertension: SBP > 160 mm or DBP > 100mm

10. Severe hypotension: SBP < 80 mmHg.

11. Pregnant or breast-feeding

12. Psychiatric, addictive, or other disorder that compromises patient's ability to
   provide informed consent, follow study protocol, and adhere to treatment instructions

13. Co-morbid conditions that would impair a patient's exercise performance and ability to
   assess WHO functional class, including but not limited to chronic low-back pain or
   peripheral musculoskeletal problems.

14. Contraindications for magnetic resonance imaging, including significant
   claustrophobia, implanted metallic objects, or others as per Appendix X).

15. Known allergy to treprostinil or tadalafil.

16. Active oral nitrate use.

17. Diabetes mellitus.

18. Planned initiation of cardiac or pulmonary rehabilitation during period of study.

Intervention(s):

drug: tadalafil

drug: treprostinil inhalations

Not Recruiting

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
val scott
650-725-8082