- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07636057
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
연구 개요
상태
정황
상세 설명
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.
연구 유형
등록 (추정된)
단계
- 4단계
연락처 및 위치
연구 연락처
- 이름: Dr Sadia Maqsood Awan Assistant Professor Pharmacology FPGMI Lahore, MBBS, M.phil,MHPE
- 전화번호: 03335032495
- 이메일: sadia_maqsood_awan@yahoo.com
연구 연락처 백업
- 이름: Dr Mudassra yaseen HOD pharmacology FPGMI, Lahore, MBBS, M.phil, CMT, PhD
- 전화번호: 03334162630
- 이메일: Drmudassarayaseen@gmail.com
참여기준
자격 기준
공부할 수 있는 나이
- 성인
건강한 자원 봉사자를 받아들입니다
설명
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
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: 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.
|
|
실험적: 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.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Change in the Disease activity score(DAS 28)
기간: 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
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Frequency & severity of opportunistic infections
기간: 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
|
기타 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Lipid profile
기간: 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
|
공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- TERC/SC/INT/2026/47
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
미국에서 제조되어 미국에서 수출되는 제품
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