Interleukin-6 Inhibitors and Drug-drug Interactions in Patients With Rheumatoid Arthritis
试验速览
- 阶段
- 1 期
- 状态
- 终止
- 入组人数
- 3
- 试验地点
- 3
- 主要终点
- Short-term change in CYP3A4 activity assessed by midazolam metabolic ratio.
研究概览
简要总结
With this study the investigators aim to assess if drug metabolism changes in patients with rheumatoid arthritis when an interleukin (IL)-6 inhibitor is initiated.
Patients with rheumatoid arthritis have an increased level of inflammation in the body which can lead to decreased expression and activity of drug metabolizing enzymes in the liver. This will lead to a decreased metabolism and excretion of drugs. The inflammation is driven by a number of proinflammatory cytokines e.g., IL-6. The investigators hypothesize that patients with rheumatoid arthritis initiating treatment with an IL-6-receptor inhibitor (anti-IL-6R) will obtain a normalization of the activated IL-6-pathway resulting in increased expression and activity of drug metabolizing enzymes and hence increased metabolism. Ultimately, this normalization of drug metabolism could lead to insufficient efficacy of a wide variety of drugs.
The investigators will perform a clinical pharmacokinetic trial. The study will include patients with active rheumatoid arthritis and a need to initiate treatment with an IL-6 receptor antibody. Patients will ingest a 6-drug cocktail consisting of probes for specific CYP enzymes. Plasma and urine will be drawn over 6 hours to determine concentrations of the drugs and their metabolites. Patients will then initiate IL-6 receptor antibody treatment and to assess both short- and long-term impact of altered inflammation, the same 6-drug cocktail will be ingested, and concentrations measured, after three weeks and three months. To help understand the mechanism and the putative involvement of inflammation, markers of inflammation such as cytokines, transcription factors, etc. will also be assesses.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Active rheumatoid arthritis
- •Age 18-75 years
- •eGFR > 30 mL/min
- •absolute neutrophil count (ANC) ≥ 2 x 109 /L
- •Platelet count > 150 x 103 /μL (corresponding to >150 x 109 /L)
- •ALAT in the normal range or within 1.5x the upper limit of normal.
- •Use of effective contraception (only woman of childbearing potential)
- •Negative test for hepatitis and tuberculosis
排除标准
- •Known sensitivity to any of the medications used.
- •Active severe infections
- •Malignancy
- •Diverticulitis
- •Intake of medications which can influence the safety of the patient or the results of the study. Can include prescription medications, over-the-counter medications, herbal medicines or dietary supplements. Will be assessed by the investigators.
- •Participation in other clinical intervention trials.
- •Pregnancy or breastfeeding
研究组 & 干预措施
Interleukin 6 receptor antibody
Tocilizumab, 162 mg subcutaneous, once every week OR Sarilumab, 200 mg subcutaneous, once every two weeks.
干预措施: Tocilizumab (Drug)
Interleukin 6 receptor antibody
Tocilizumab, 162 mg subcutaneous, once every week OR Sarilumab, 200 mg subcutaneous, once every two weeks.
干预措施: Sarilumab (Drug)
结局指标
主要结局
Short-term change in CYP3A4 activity assessed by midazolam metabolic ratio.
时间窗: 3 weeks
A change in metabolic ratio of midazolam after 3 weeks of treatment with an IL-6Ra as compared to baseline. The metabolic ratio of midazolam is used to assess the activity of CYP3A4.
次要结局
- Long-term change in CYP3A4 activity assessed by midazolam metabolic ratio.(12 weeks)
- Short-term change in CYP1A2 activity assessed by caffeine metabolic ratio.(3 weeks)
- Long-term change in CYP1A2 activity assessed by caffeine metabolic ratio.(12 weeks)
- Short-term change in CYP2B6 activity assessed by efavirenz metabolic ratio.(3 weeks)
- Long-term change in CYP2B6 activity assessed by efavirenz metabolic ratio.(12 weeks)
- Short-term change in CYP2C9 activity assessed by losartan metabolic ratio.(3 weeks)
- Long-term change in CYP2C9 activity assessed by losartan metabolic ratio.(12 weeks)
- Short-term change in CYP2C19 activity assessed by omeprazole metabolic ratio.(3 weeks)
- Long-term change in CYP2C19 activity assessed by omeprazole metabolic ratio.(12 weeks)
- Short-term change in CYP2D6 activity assessed by metoprolol metabolic ratio.(3 weeks)
- Long-term change in CYP2D6 activity assessed by metoprolol metabolic ratio.(12 weeks)
研究者
Ann-Cathrine Dunvald
Principal investigator
University of Southern Denmark