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Pharmacokinetics, Safety and Efficacy of BIIL 284 BS in Patients With Rheumatoid Arthritis (RA)

2014年9月23日 更新者:Boehringer Ingelheim

A Double-blind, Randomized, Three Parallel Group Placebo-controlled Study to Investigate Pharmacokinetics, Effect on Expression of CD11b/CD18 (Mac-1), as Well as Safety and Efficacy of Two Oral Doses of BIIL 284 BS (Dosage: 25 mg Daily, 150 mg Daily) in Patients With Rheumatoid Arthritis Over Two Weeks

Safety, pharmacokinetics, pharmacodynamics [CD11b/CD18 (Mac-1) expression] and efficacy.

研究概览

研究类型

介入性

注册 (实际的)

26

阶段

  • 阶段1

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 65年 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Male and female from 18 to 65 years of age
  • Patients suffering from active rheumatoid arthritis as defined by the ARA criteria revised 1987

    --- At least 4 of the following 7 criteria must have been present:

    • morning stiffness in and around the joints lasting at least 1 hour before maximal improvement for at least 6 weeks
    • arthritis (soft tissue thickening or fluid - not bony overgrowth alone) of at least 3 joint areas for at least 6 weeks
    • arthritis of hand joints (at least one area swollen in a wrist, metacarpophalangeal (MCP) or proximal interphalangeal (PIP) joint) for at least 6 weeks
    • symmetric arthritis (observed by a physician) with simultaneous involvement of the joints on both sides of the body for at least 6 weeks
    • rheumatoid nodules (observed by a physician) over bony prominences or extensor surfaces or in juxta-articular regions
    • serum rheumatoid factor positive
    • x-ray changes typical of rheumatoid arthritis (erosions or unequivocal bony decalcification localised in or most marked adjacent to the involved joints)
  • Patient belonging to the RA functional class I, II or III
  • Patient's written informed consent

Exclusion Criteria:

  • Pregnancy (to be excluded by pregnancy test) or breast feeding
  • Women of childbearing potential not using adequate contraception
  • Treatment with methotrexate in the previous month or intended use during the trial period
  • Treatment with slow acting antirheumatic drugs (SAARDs)/disease-modifying antirheumatic drugs (DMARDs) other than parenteral gold, D-penicillamine, sulfasalazine, chloroquine / hydroxychloroquine corticosteroid during the last 2 months prior to study entry
  • Treatment with more than one SAARD/DMARD and/or corticosteroid during the last 2 months prior to study entry
  • Change in treatment with SAARDs/DMARDs during the last 2 months prior to study entry or intended change during the trial duration
  • Change in treatment with corticosteroids during the last month prior to study entry or intended change during the trial duration
  • Systemic treatment with corticosteroids at a dose higher than 10 mg/day or 0.2 mg/kg/day (prednisone equivalent), respectively (whichever is lower) during the last month prior to study entry or their intended use during the trial treatment period
  • Change in treatment with non-steroidal anti-inflammatory drugs (NSAIDs) during the last month prior to study entry or intended change during the trial duration
  • Treatment with EnbrelTM (etanercept) or experimental therapies during the last 3 months prior to study entry
  • Synovectomy and/or surgical treatment for RA in the previous month or during the trial
  • Clinical evidence of known severe cardiovascular, hepatic, renal, respiratory, metabolic, haematological, immunological, gastro-intestinal, hormonal or mental disorders
  • Any other rheumatological or non-rheumatological disease that could interfere with the evaluation of efficacy and safety
  • Patients with active malignant disease
  • Patients with chronic or acute infections during the previous month
  • Patients with abnormal, clinically relevant laboratory values not related to RA
  • Participation in another clinical trial during this study or during the previous month
  • Previous participation in this trial (i.e. having been allocated a randomized treatment number)
  • Patient unable to comply with the protocol
  • Patient with known drug abuse
  • Patient with known alcohol abuse

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:安慰剂
实验性的:低剂量 BIIL 284 BS
实验性的:高剂量 BIIL 284 BS

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Changes from baseline in Mac-1 expression
大体时间:Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Plasma concentrations of BIIL 284 BS, BIIL 260 BS, BIIL 315 ZW and BIIL 304 ZW
大体时间:Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Maximum concentration of the analyte in plasma (Cmax)
大体时间:Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Trough concentration of the analyte in plasma shortly before drug administration in a steady state dosing interval (Cpre,ss)
大体时间:Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Time to reach the maximum concentration of the analyte in plasma (tmax)
大体时间:Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Area under the concentration-time curve of the analyte in plasma (AUC)
大体时间:Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Number of patients with adverse events
大体时间:Up to 4 weeks
Up to 4 weeks
Global assessment of tolerability by the patient on a 4-point scale
大体时间:Up to 14 days after start of treatment
Up to 14 days after start of treatment
Global assessment of tolerability by investigator on a 4-point scale
大体时间:Up to 14 days after start of treatment
Up to 14 days after start of treatment

次要结果测量

结果测量
措施说明
大体时间
Changes from baseline in tender joint count (TJC)
大体时间:Pre-dose, up to day 14 after start of treatment
Bilateral assessment of twenty-eight joints by e.g., pressure, joint manipulation etc.
Pre-dose, up to day 14 after start of treatment
Changes from baseline in swollen joint count (SJC)
大体时间:Pre-dose, up to day 14 after start of treatment
Twenty-eight joints were bilaterally assessed whether they are swollen or not
Pre-dose, up to day 14 after start of treatment
Changes from baseline in patient's current pain level assessment by visual analogue scale (VAS)
大体时间:Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Changes from baseline in patient's global assessment of disease activity by VAS
大体时间:Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Global assessment of disease activity by investigator on a 5-point scale
大体时间:Up to 14 days after start of treatment
Up to 14 days after start of treatment
Changes from baseline for patient's assessment of physical function
大体时间:Pre-dose, up to day 14 after start of treatment
Functional disability was measured using the disability section of the Health Assessment Questionnaire (HAQ)
Pre-dose, up to day 14 after start of treatment
Changes from baseline in erythrocyte sedimentation rate (ESR)
大体时间:Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Changes from baseline in C-reactive protein (CRP)
大体时间:Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Changes from baseline in american college of rheumatology (ACR) 20 score
大体时间:Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Changes from baseline in disease activity score (DAS)
大体时间:Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Global efficacy assessment by the patient on a 4-point scale
大体时间:Up to 14 days after start of treatment
Up to 14 days after start of treatment
Number of withdrawals due to adverse events
大体时间:Up to 4 weeks
Up to 4 weeks
Number of patients with clinically significant findings in laboratory adverse events
大体时间:Up to 4 weeks
Up to 4 weeks
Number of patients with clinically significant findings in vital signs (blood pressure, pulse rate)
大体时间:Up to 4 weeks
Up to 4 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

有用的网址

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2000年1月1日

初级完成 (实际的)

2000年5月1日

研究注册日期

首次提交

2014年9月19日

首先提交符合 QC 标准的

2014年9月23日

首次发布 (估计)

2014年9月25日

研究记录更新

最后更新发布 (估计)

2014年9月25日

上次提交的符合 QC 标准的更新

2014年9月23日

最后验证

2014年9月1日

更多信息

与本研究相关的术语

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安慰剂的临床试验

3
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