Efficacy, Safety, Tolerability and Pharmacokinetics (PK) of Nilotinib (AMN107) in Pulmonary Arterial Hypertension (PAH)
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Purpose
The purpose of this trial is to establish the safety, tolerability and PK of nilotinib in this population and to test the hypothesis that 6 months treatment with nilotinib will significantly reduce pulmonary artery resistance.
| Condition | Intervention | Phase |
|---|---|---|
|
Pulmonary Arterial Hypertension |
Drug: Nilotinib 50 mg Drug: Nilotinib 150mg Drug: Nilotinib 300mg Drug: Nilotinib placebo |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment |
| Official Title: | A 24 Week, Randomized, Double Blind, Multicenter, Placebocontrolled Efficacy, Safety, Tolerability and PK Trial of Nilotinib (Tasigna®, AMN107) in Pulmonary Arterial Hypertension (PAH) |
- Change in pulmonary vascular resistance (PVR) [ Time Frame: 168 days ] [ Designated as safety issue: No ]
- Change in Six-Minute Walk Distance (6MWD) from baseline [ Time Frame: Baseline, 168 ] [ Designated as safety issue: No ]
- Reporting of adverse events (AEs) [ Time Frame: 168 days ] [ Designated as safety issue: Yes ]
All study emergent adverse events (AEs) will be summarized and listed.
AEs starting on or after the time of the first use of study drug but not later than 7 days (30 days in case of an SAE) after the last dose of study drug will be classified as a treatment emergent AE. AEs that started during the study but before the time of the first use of study drug will be classified as a prior AE and not summarized, but included in AE listings. The same will be done for AEs that started more as a post-treatment AE.
| Enrollment: | 31 |
| Study Start Date: | July 2010 |
| Study Completion Date: | January 2013 |
| Primary Completion Date: | January 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Nilotinib |
Drug: Nilotinib 50 mg
capsules for oral administration
Drug: Nilotinib 150mg
capsules for oral administration
Drug: Nilotinib 300mg
capsules for oral administration
|
| Experimental: Nilotinib Placebo |
Drug: Nilotinib placebo
capsules for oral administration
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- World Health Organization (WHO) Functional Class II or III
- 6MWD ≥ 150 m and ≤ 450 m at screening
- Current diagnosis of PAH according to Dana Point 2008 Meeting
- Inadequate clinical response on one or more class(es) of PAH drug
- Stabilization of pulmonary hypertension medications for ≥ 2 months on approved therapeutic dose of at least one PAH drug and still symptomatic with WHO functional Class II or III performance.
Exclusion Criteria:
- Women of child-bearing potential not practicing birth control
- In treatment with chronic nitric oxide therapy
- Pre-existing lung disease
- Use of drugs prolonging the QT interval or strong CYP3A4 inhibitors
- Long QT syndrome or QTc > 450 ms males; > 470 ms females.
- WHO Class IV
- Pulmonary capillary wedge pressure > 15 mm Hg
- Other diagnosis of PAH in WHO Diagnostic Group 1
- PAH associated with: venous hypertension (WHO Diagnostic Group II), hypoxia (WHO Diagnostic Group III), chronic pulmonary thromboembolic disease (WHO Diagnostic Group IV) or other miscellaneous causes (WHO Diagnostic Class V, which includes sarcoidosis, histiocytosis X, lymphangiomatosis, compression of pulmonary vessels)
- Thrombocytopenia < 50 x109/L (50 x 103/µL)
- Uncontrolled systemic arterial hypertension, systolic > 160 mm Hg or diastolic >90 mm Hg
- Any advanced, severe, or unstable disease of any type that may interfere with the primary and secondary endpoint evaluations.
Other protocol-defined inclusion/exclusion criteria may apply
Contacts and Locations| United States, Massachusetts | |
| Novartis Investigative Site | |
| Boston, Massachusetts, United States, 02118 | |
| United States, Michigan | |
| Novartis Investigative Site | |
| Ann Arbor, Michigan, United States, 48109-0391 | |
| United States, North Carolina | |
| Novartis Investigative Site | |
| Chapel Hill, North Carolina, United States, 27599 | |
| United States, Ohio | |
| Novartis Investigative Site | |
| Cleveland, Ohio, United States, 44195 | |
| United States, Tennessee | |
| Novartis Investigative Site | |
| Nashville, Tennessee, United States, 37232-2573 | |
| Canada, Alberta | |
| Novartis Investigative Site | |
| Calgary, Alberta, Canada, T6G 2B7 | |
| Germany | |
| Novartis Investigative Site | |
| Hamburg, Germany, 20246 | |
| Novartis Investigative Site | |
| Heidelberg, Germany, 69120 | |
| Novartis Investigative Site | |
| Marburg, Germany, 35039 | |
| Korea, Republic of | |
| Novartis Investigative Site | |
| Seoul, Korea, Korea, Republic of, 120-752 | |
| Singapore | |
| Novartis Investigative Site | |
| Singapore, Singapore, 119074 | |
| Switzerland | |
| Novartis Investigative Site | |
| Zurich, Switzerland, 8091 | |
| Study Director: | Novartis Pharmaceuticals | Novartis Pharmaceuticals |
More Information
No publications provided
| Responsible Party: | Novartis ( Novartis Pharmaceuticals ) |
| ClinicalTrials.gov Identifier: | NCT01179737 History of Changes |
| Other Study ID Numbers: | CAMN107X2201, 2010-019883-36 |
| Study First Received: | August 3, 2010 |
| Last Updated: | March 25, 2013 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Novartis:
|
Pulmonary Arterial Hypertension Nilotinib 6MWD Pulmonary Hypertension |
Additional relevant MeSH terms:
|
Hypertension, Pulmonary Hypertension Lung Diseases |
Respiratory Tract Diseases Vascular Diseases Cardiovascular Diseases |
ClinicalTrials.gov processed this record on May 16, 2013