A Double-blind, Randomised, Placebo-controlled (Within a Dose Group) Study to Evaluate Safety and Pharmacokinetics of Multiple Rising Doses of BIBF 1120 at 50 mg Bid (14 Days), 100 mg Bid (14 Days), and 150 mg Bid (28 Days) p.o., on Top of Standard Medical Care With Stratification According to Pirfenidone Use, in Japanese Patients With Idiopathic Pulmonary Fibrosis.
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 8
- 主要终点
- Drug-related Adverse Events
研究概览
简要总结
To investigate safety of BIBF 1120 in Japanese patients with idiopathic pulmonary fibrosis (IPF), with and without pirfenidone background treatment.
To assess pharmacokinetics of BIBF 1120 in Japanese patients, with and without pirfenidone background treatment.
To assess pharmacokinetics of pirfenidone in Japanese patients, alone and in combination with BIBF 1120 treatment.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 盲法
- Double
入排标准
- 年龄范围
- 40 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
研究组 & 干预措施
BIBF 1120 50 mg
Low dose for cohort 1
干预措施: BIBF 1120 (Drug)
BIBF 1120 100 mg
Middle dose for cohort 2
干预措施: BIBF 1120 (Drug)
BIBF 1120 150 mg
High dose for cohort 3
干预措施: BIBF 1120 (Drug)
Placebo
Placebo for cohort 1,2,3
干预措施: Placebo (Drug)
结局指标
主要结局
Drug-related Adverse Events
时间窗: after the first drug intake until 28 days from the last treatment administration, up to 60 days
The number of patients with drug-related adverse events stratified according to pirfenidone use in each group
次要结局
- AUCτ,ss After Multiple Doses of BIBF 1120 Without Pirfenidone(pre-dose, then 0.5 h, 1 h, 2 h, 3 h, 3.92 h, 6 h, 8 h, 12 h, 24 h, 48 h, 72 h after morning dose on days 14 to 17 (BIBF 1120 50 mg and 100 mg) or on days 28 to 31 (BIBF 1120 150 mg))
- Cmax,ss After Multiple Doses of BIBF 1120 Without Pirfenidone(pre-dose, then 0.5 h, 1 h, 2 h, 3 h, 3.92 h, 6 h, 8 h, 12 h, 24 h, 48 h, 72 h after morning dose on days 14 to 17 (BIBF 1120 50 mg and 100 mg) or on days 28 to 31 (BIBF 1120 150 mg))
- Cmax,ss After Multiple Doses of Pirfenidone 600 mg Without BIBF 1120 (After Lunch)(Day -1 at Visit 1: at pre-dose and 0.5 h, 1 h, 2 h, 3 h, 4 h, 6 h, 8 h after lunch dose)
- AUCτ,ss After Multiple Doses of BIBF 1120 With Pirfenidone(pre-dose, then 0.5 h, 1 h, 2 h, 3 h, 3.92 h, 6 h, 8 h, 12 h, 24 h, 48 h, 72 h after morning dose on days 14 to 17 (BIBF 1120 50 mg and 100 mg) or on days 28 to 31 (BIBF 1120 150 mg))
- AUC0-4,ss After Multiple Doses of Pirfenidone 600 mg Without BIBF 1120 (After Breakfast)(Day -1 at Visit 1: At pre-dose and 0.5 h, 1 h, 2 h, 3 h after morning dose and pre-dose after lunch dose)
- Cmax,ss After Multiple Doses of BIBF 1120 With Pirfenidone(pre-dose, then 0.5 h, 1 h, 2 h, 3 h, 3.92 h, 6 h, 8 h, 12 h, 24 h, 48 h, 72 h after morning dose on days 14 to 17 (BIBF 1120 50 mg and 100 mg) or on days 28 to 31 (BIBF 1120 150 mg))
- Cmax,ss After Multiple Doses of Pirfenidone 600 mg With BIBF 1120 (After Breakfast)(Day 14 at Visit 5 (BIBF 1120 50mg and 100mg) and day 28 (visit 7) (BIBF 1120 150mg): At pre-dose and 0.5 h, 1 h, 2 h, 3 h after morning dose and pre-dose after lunch dose)
- AUC0-8,ss After Multiple Doses of Pirfenidone 600 mg With BIBF 1120 (After Lunch)(Day 14 at Visit 5 (BIBF 1120 50mg and 100mg) and day 28 (visit 7) (BIBF 1120 150mg): at pre-dose and 0.5 h, 1 h, 2 h, 3 h, 4 h, 6 h, 8 h after lunch dose)
- Lung Function Measurement: Forced Expiratory Volume in 1 Second (FEV1)(baseline and day 35)
- Lung Function Measurement: Forced Vital Capacity (FVC)(baseline and day 35)
- Lung Function Measurement: Forced Vital Capacity Percent of Predicted (%FVC)(baseline and day 35)
- Cmax,ss After Multiple Doses of Pirfenidone 600 mg Without BIBF 1120 (After Breakfast)(Day -1 at Visit 1: At pre-dose and 0.5 h, 1 h, 2 h, 3 h after morning dose and pre-dose after lunch dose)
- AUC0-4,ss After Multiple Doses of Pirfenidone 600 mg With BIBF 1120 (After Breakfast)(Day 14 at Visit 5 (BIBF 1120 50mg and 100mg) and day 28 (visit 7) (BIBF 1120 150mg): At pre-dose and 0.5 h, 1 h, 2 h, 3 h after morning dose and pre-dose after lunch dose)
- Clinical Relevant Abnormalities in Laboratory Parameters- No Pirfenidone Background(after the first drug intake until 28 days from the last treatment administration, up to 60 days)
- Change From Baseline in Pulse Rate(baseline and day 35)
- Lung Function Measurement: Diffusing Capacity for Carbon Monoxide Percent of Predicted (%DLco)(baseline and day 35)
- AUC0-8,ss After Multiple Doses of Pirfenidone 600 mg Without BIBF 1120 (After Lunch)(Day -1 at Visit 1: at pre-dose and 0.5 h, 1 h, 2 h, 3 h, 4 h, 6 h, 8 h after lunch dose)
- Withdrawal Due to Adverse Event(after the first drug intake until 28 days from the last treatment administration, up to 60 days)
- Clinical Relevant Abnormalities in Laboratory Parameters- With Pirfenidone Background(after the first drug intake until 28 days from the last treatment administration, up to 60 days)
- Change From Baseline in Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP)(baseline and day 35)
- Lung Function Measurement: Diffusing Capacity for Carbon Monoxide (DLco)(baseline and day 35)
- Cmax,ss After Multiple Doses of Pirfenidone 600 mg With BIBF 1120 (After Lunch)(Day 14 at Visit 5 (BIBF 1120 50mg and 100mg) and day 28 (visit 7) (BIBF 1120 150mg): at pre-dose and 0.5 h, 1 h, 2 h, 3 h, 4 h, 6 h, 8 h after lunch dose)
