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Idiopathic Pulmonary Fibrosis clinical trials

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NCT ID: NCT01321996 Terminated - Clinical trials for Idiopathic Pulmonary Fibrosis

68Ga-DOTA-NOC PET/CT in Patients With Idiopathic Pulmonary Fibrosis

Start date: February 2009
Phase: Phase 4
Study type: Interventional

The investigators aim to evaluate the role of 68Ga-DOTA-NOC PET/CT in patients with idiopathic pulmonary fibrosis, in particular in patients with a diagnosis of IPF/UIP (idiopathic pulmonary fibrosis, diagnosed based in the American Thoracic Society and European Respiratory Society criteria) and in forms of NSIP (non-specific interstitial pneumonia). PET/CT imaging data will be compared with HRCT (high-resolution computed tomography) findings to assess disease extension, early disease detection and to non-invasively detect somatostatin receptors expression at lung level in these patients, with potential therapeutic implications.

NCT ID: NCT01266135 Terminated - Clinical trials for Idiopathic Pulmonary Fibrosis

Safety and Efficacy of QAX576 in Patients With Idiopathic Pulmonary Fibrosis (IPF)

Start date: December 2010
Phase: Phase 2
Study type: Interventional

This study is designed to evaluate the safety, tolerability, pharmacokinetics and efficacy of QAX576 in patients with idiopathic pulmonary fibrosis.

NCT ID: NCT01203943 Terminated - Clinical trials for Idiopathic Pulmonary Fibrosis

A Study to Characterize the Safety, PK and Biological Activity of CC-930 in Idiopathic Pulmonary Fibrosis (IPF)

Start date: January 1, 2011
Phase: Phase 2
Study type: Interventional

The primary purpose of the study is to evaluate the safety and PK profile of CC-930 in idiopathic pulmonary fibrosis patients.

NCT ID: NCT01151527 Terminated - Clinical trials for Idiopathic Interstitial Pneumonias

Peripheral Blood Biomarkers in Idiopathic Interstitial Pneumonias

Start date: April 2010
Phase: N/A
Study type: Observational

We hypothesize that a peripheral blood biomarker or biological signature (gene or protein expression pattern) of idiopathic interstitial pneumonias (IIPs) will simplify and improve the accuracy of diagnosis of IIP and diagnose individuals at an earlier, more treatable, stage of their disease.

NCT ID: NCT00981747 Terminated - Clinical trials for Idiopathic Pulmonary Fibrosis

Targeting Vascular Reactivity in Idiopathic Pulmonary Fibrosis

Start date: September 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether combination therapy with sildenafil and losartan can improve function and exercise tolerance in patients with idiopathic pulmonary fibrosis.

NCT ID: NCT00957242 Terminated - Clinical trials for Idiopathic Pulmonary Fibrosis

AntiCoagulant Effectiveness in Idiopathic Pulmonary Fibrosis

ACE-IPF
Start date: October 2009
Phase: Phase 3
Study type: Interventional

This study will test the effectiveness of warfarin in patients with IPF. Approximately 256 patients will be randomized 1:1 to either warfarin or placebo. Patients will return at week 1 for a safety review and every 16 weeks for 48 weeks. The primary endpoint in the study is the time to either death, non-bleeding/non-elective hospitalization, or a drop of greater than 10% in forced vital capacity (FVC) from baseline.

NCT ID: NCT00879229 Terminated - Clinical trials for Pulmonary Hypertension

ARTEMIS-PH - Study of Ambrisentan in Subjects With Pulmonary Hypertension Associated With Idiopathic Pulmonary Fibrosis

ARTEMIS-PH
Start date: July 2009
Phase: Phase 3
Study type: Interventional

Ambrisentan is an endothelin receptor antagonist used for the treatment of pulmonary hypertension (PH). Based on research suggesting a role for endothelin-1 in the pathogenesis of idiopathic pulmonary fibrosis (IPF) and the poor prognosis for patients with IPF who are also diagnosed with PH, this study was designed to evaluate the effectiveness and safety of ambrisentan in that patient population.

NCT ID: NCT00768300 Terminated - Clinical trials for Idiopathic Pulmonary Fibrosis

(ARTEMIS-IPF) Randomized, Placebo-Controlled Study to Evaluate Safety and Effectiveness of Ambrisentan in IPF

ARTEMIS-IPF
Start date: December 2008
Phase: Phase 3
Study type: Interventional

The ARTEMIS-IPF study was conducted to determine if ambrisentan was effective in delaying disease progression and death in participants with idiopathic pulmonary fibrosis (IPF), to evaluate its safety, and to evaluate its effect on development of pulmonary hypertension, quality of life, and dyspnea (shortness of breath) symptoms in this participant population. Participants were randomized in a 2:1 ratio to receive ambrisentan or placebo, respectively. Participation in the study was to be up to 4 years, depending on how long it would take to enroll participants and observe study events. After randomization, visits to the clinic took place every 3 months, and laboratory procedures were performed every month.

NCT ID: NCT00703339 Terminated - Clinical trials for Pulmonary Hypertension

Effects of Inhaled Treprostinil Sodium for the Treatment of Pulmonary Hypertension Associated With Idiopathic Pulmonary Fibrosis

Start date: June 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to establish single-dose tolerability of inhaled treprostinil sodium in idiopathic pulmonary fibrosis (IPF) patients with pulmonary hypertension, and to explore the acute hemodynamic effects over a range of tolerable doses. The safety and pharmacodynamic information obtained from this study will inform the design and conduct of future studies in inhaled treprostinil sodium in this population.

NCT ID: NCT00690885 Terminated - Clinical trials for Pulmonary Disease, Chronic Obstructive

Interferon-alpha Treatment of Chronic Cough in Chronic Obstructive Pulmonary Disease and Idiopathic Pulmonary Fibrosis

Start date: June 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether lozenges containing interferon-alpha can reduce the frequency and severity of coughing in patients with chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF).