- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne 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
Przegląd badań
Status
Szczegółowy opis
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.
Typ studiów
Zapisy (Szacowany)
Faza
- Faza 4
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Dr Sadia Maqsood Awan Assistant Professor Pharmacology FPGMI Lahore, MBBS, M.phil,MHPE
- Numer telefonu: 03335032495
- E-mail: sadia_maqsood_awan@yahoo.com
Kopia zapasowa kontaktu do badania
- Nazwa: Dr Mudassra yaseen HOD pharmacology FPGMI, Lahore, MBBS, M.phil, CMT, PhD
- Numer telefonu: 03334162630
- E-mail: Drmudassarayaseen@gmail.com
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
Akceptuje zdrowych ochotników
Opis
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
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: 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.
|
|
Eksperymentalny: 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.
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Change in the Disease activity score(DAS 28)
Ramy czasowe: 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
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Frequency & severity of opportunistic infections
Ramy czasowe: 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
|
Inne miary wyników
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Lipid profile
Ramy czasowe: 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
|
Współpracownicy i badacze
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
- Choroby układu mięśniowo-szkieletowego
- Artretyzm
- Choroby stawów
- Choroby reumatyczne
- Choroby tkanki łącznej
- Choroby Autoimmunologiczne
- Choroby układu odpornościowego
- Choroby skóry i tkanki łącznej
- Zapalenie stawów, reumatoidalne
- Związki heterocykliczne
- Związki heterocykliczne, 2-ring
- Związki heterocykliczne, sterowanie stopieniem
- Pterins
- Perydyny
- Aminopterina
- Metotreksat
- upadacitinib
Inne numery identyfikacyjne badania
- TERC/SC/INT/2026/47
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
produkt wyprodukowany i wyeksportowany z USA
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