Comparison of Effectiveness and Safety of Tofacitinib Versus Upadacitinib as Add-on to Methotrexate in Rheumatoid Arthritis
Effectiveness and Safety of Tofacitinib Versus Upadacitinib as Add-on to Methotrexate in Rheumatoid Arthritis; Comparative Clinical Study
The goal of this interventional study is to learn, whether Tofacitinib or upadacitinib is more effective in treating the patients of Rheumatoid Arthritis. It will also learn about the safety of these two agents. The main questions it aims to answer are:
- Which JAK inhibitor (Tofacitinib or Upadacitinib) is more effective to improve the disease activity of Rheumatoid arthritis in Pakistani population?
- What is the Disease Activity scores, ESR, CRP, RA factor level of patients?
- What are the side effects of both drugs, during the study time?
Participants:
- Of Group A will be taking 5mg Tofacitinib oral daily for 6 months along with 25mg of once weekly dose of oral Methotrexate, whereas of Group B will be taking 15mg Upadacitinib oral daily for 6 months along with 25mg of once weekly dose of oral methotrexate.
- Will Visit the clinic once at 3 months and then 6 months for checkups and tests
- Will Keep a diary of any infection, treatment taken, duration of infection
- Will inform the researcher about any unusual side effect during the study
研究概览
地位
条件
详细说明
This study will be conducted in the Department of Pharmacology in collaboration with Rheumatology Department of Shaikh Zayed Medical Complex, Lahore.
The study population will consist of adult patients with diagnosis of RA on the basis of EULAR 2010 Classification Criteria: Moderate to severe disease activity indicated by DAS28 >3.2 and those with Inadequate response to methotrexate (MTX) characterized by Persistent active disease on ≥12 weeks of MTX treatment.
Sample size was estimated considering the following clinically significant variables: infection rate, thrombotic events, and cessation of treatment as a result of remission according to scientific publications. The maximum sample size was estimated among these methods in order to have adequate power.
If infection rate was considered as a key safety parameter, and taking into account the event rates of 0.7 and 1.2 per 100 patient-years for Tofacitinib and Upadacitinib, respectively22, the sample size would be 116 patients (58 per group) at 95% confidence interval and 80% power. In the case of thrombotic events with an assumed event rate of 0.2 and 0.4 per 100 patient-years23, the required sample size would be 100 patients (50 per group) at 95% confidence interval and 90% power.
Adult patients aged ≥18 years, regardless of gender will be included in the study. Whereas the following patients will not be included:
- Other autoimmune rheumatic disorders (SLE, psoriatic arthritis, AS, etc.)
- Administration of any biologic DMARD in the previous three months
- History of a serious infection (e.g., active tuberculosis or sepsis)
- Previous or existing history of recurrent infections or immunosuppressive status
- History of any malignancy in the last five years.
- Current chemotherapy, radiotherapy or intake of any genotoxic drug
- Severe liver impairment (e.g., ALT/AST >3× ULN)
- Severe renal impairment (e.g., estimated GFR <30 mL/min)
- Severe Haematological Abnormalities: Hb <8 g/dL, TLC <3,000 /mm³, Platelets <100,000 /mm³
- Past or present deep vein thrombosis or pulmonary embolism
- Pregnant or lactating women
- Women of reproductive age who are not practicing adequate contraception measures
Data collection procedure:
After the Evaluation by rheumatologist and prescribing the tofacitinib or Upadacitinib, an informed consent will be taken from the patient. Baseline investigations and history will be taken and added to the data collection sheet (Attached at the end). Patients will be followed vigilantly and then the clinical evaluation & biochemical investigations will be recorded at 3 months and 6 months.
Statistical Analysis:
All analyses will be conducted according to the ITT principle. A per protocol analysis will also be performed as sensitivity analysis. Two-sided p ≤ 0.05 will be considered statistically significant.
Continuous variable will be presented as mean±SD/median (IQR) and categorical variables will be presented as frequency (%).
Comparison of proportion between groups will be performed using the Chi-square/Fisher's exact test and effect sizes will be calculated as Risk difference, relative risk (RR) with 95% confidence interval.
Change in DAS28 will be compared by using Independent sample t-test/Mann Whitney-U test. Repeated measures analysis (mixed model/ANOVA) will be used to see the groups and time effect simultaneously. ACR responses will be analyzed by using Chi-square test Comparison of incidence rate between groups will be performed using Chi-square/Fisher's exact test and rates will be presented as proportion and/or incidences per 100 patient years.
研究类型
注册 (估计的)
阶段
- 第四阶段
联系人和位置
学习联系方式
- 姓名:Dr Sadia Maqsood Awan Assistant Professor Pharmacology FPGMI Lahore, MBBS, M.phil,MHPE
- 电话号码:03335032495
- 邮箱:sadia_maqsood_awan@yahoo.com
研究联系人备份
- 姓名:Dr Mudassra yaseen HOD pharmacology FPGMI, Lahore, MBBS, M.phil, CMT, PhD
- 电话号码:03334162630
- 邮箱:Drmudassarayaseen@gmail.com
参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
Inclusion Criteria:
- • Adult patients aged ≥18 years, regardless of gender
Exclusion Criteria:
• Other autoimmune rheumatic disorders (SLE, psoriatic arthritis, AS, etc.)
- Administration of any biologic DMARD in the previous three months
- History of a serious infection (e.g., active tuberculosis or sepsis)
- Previous or existing history of recurrent infections or immunosuppressive status
- History of any malignancy in the last five years.
- Current chemotherapy, radiotherapy or intake of any genotoxic drug
- Severe liver impairment (e.g., ALT/AST >3× ULN)
- Severe renal impairment (e.g., estimated GFR <30 mL/min)
- Severe Haematological Abnormalities: Hb <8 g/dL, TLC <3,000 /mm³, Platelets <100,000 /mm³
- Past or present deep vein thrombosis or pulmonary embolism
- Pregnant or lactating women
- Women of reproductive age who are not practicing adequate contraception measures
学习计划
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:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Tofacitinib
5mg tofacitinib BD(oral) daily + 25mg Methotrexate oral once in a week
|
There is no comparative study of tofacitinib with upadacitinib in Pakistan, as upadacitinib is recently been available here.
There is no study yet in pakistan to compare the effectiveness and safety of these two JAK inhibitors in Pakistani population.
|
|
实验性的:Upadacitinib
15mg Upadacitinib OD(oral) daily + 25mg Methotrexate oral once in a week
|
There is no comparative study of tofacitinib with upadacitinib in Pakistan, as upadacitinib is recently been available here.
There is no study yet in pakistan to compare the effectiveness and safety of these two JAK inhibitors in Pakistani population.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Change in the Disease activity score(DAS 28)
大体时间:From enrollment in the study to 6 months of treatment
|
Change in Disease Activity Score-28 ranges from 0 to 10, with ≤2.6 indicates remission, 2.6-3.2
low disease activity, ≥ 3.2-5.1 moderate activity, ≥ 5.1 high disease activity.
|
From enrollment in the study to 6 months of treatment
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Frequency & severity of opportunistic infections
大体时间:From enrollment in the study to 6 months of treatment
|
Severity of opportunistic infections according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0, which classifies adverse events from Grade 1 (mild) to Grade 5 (death)21.
|
From enrollment in the study to 6 months of treatment
|
其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Lipid profile
大体时间:From enrollment in the study to 6 months of treatment
|
Change in Lipid Profile; Total cholesterol >200 mg/dL , LDL >130 mg/dL ,HDL <40 mg/dL, Triglycerides >150 mg/dL
|
From enrollment in the study to 6 months of treatment
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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