BENITIONSClinical Trial Intelligence

Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT

第2相 完了 NCT02036970

対象疾患Pulmonary Arterial Hypertension, Pulmonary Hypertension, Interstitial Lung Disease, Idiopathic Interstitial Pneumonia
第2相
スポンサーBiogen
ステータス完了
参加者数166 名
介入(薬剤)Bardoxolone methyl
開始日2014年5月31日
完了日2018年1月19日
結果公開日2021年7月23日

概要

This study assesses the safety and efficacy of bardoxolone methyl relative to placebo in patients with pulmonary hypertension to determine the recommended dose range, evaluate the change from baseline in 6-minute walk distance (6MWD) and determine the effect of Bardoxolone methyl in pulmonary hypertension associated with connective tissue disease, interstitial lung disease, and idiopathic etiologies, including subsets of patients with WHO Group III or WHO Group V PH following 16 weeks of study participation.

Change From Baseline Though Week 16 in 6-Minute Walk Distance (6MWD) for Bardoxolone Methyl Compared to Placebo

Baseline through Week 16 · meters

Part 1: Dose-Ranging Bardoxolone Methyl 2.5 mg/Part 2: Open-Label32.5 ± 29.14 meters
Part 1: Dose-Ranging Bardoxolone Methyl 5 mg/Part 2: Open-Label24 ± 30.08 meters
Part 1: Dose-Ranging Bardoxolone Methyl 10 mg/Part 2: Open-Label3.4 ± 31.28 meters
Part 1: Dose-Ranging Bardoxolone Methyl 20 mg/Part 2: Open-Label-3.2 ± 39.53 meters
Part 1: Dose-Ranging Placebo 2.5 mg/Part 2: Bardoxolone Methyl 2.5 mg20.3 ± 13.08 meters
Part 1: Dose-Ranging Placebo 5 mg/Part 2: Bardoxolone Methyl 5 mg24.6 ± 59.4 meters
p-value0.8133
Mean Difference (Net)-1.74 (95% CI -16.22–12.74)

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