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Comparison of Effectiveness and Safety of Tofacitinib Versus Upadacitinib as Add-on to Methotrexate in Rheumatoid Arthritis

4 juin 2026 mis à jour par: Tahira Shaukat, Sheikh Zayed Federal Postgraduate Medical Institute

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

Aperçu de l'étude

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Estimé)

100

Phase

  • Phase 4

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

  • Nom: Dr Sadia Maqsood Awan Assistant Professor Pharmacology FPGMI Lahore, MBBS, M.phil,MHPE
  • Numéro de téléphone: 03335032495
  • E-mail: sadia_maqsood_awan@yahoo.com

Sauvegarde des contacts de l'étude

  • Nom: Dr Mudassra yaseen HOD pharmacology FPGMI, Lahore, MBBS, M.phil, CMT, PhD
  • Numéro de téléphone: 03334162630
  • E-mail: Drmudassarayaseen@gmail.com

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Non

La description

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 d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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.
Expérimental: 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.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in the Disease activity score(DAS 28)
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Frequency & severity of opportunistic infections
Délai: 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.

  • Grade 1 (Mild): Asymptomatic or mild infection; no or minimal intervention required
  • Grade 2 (Moderate): Symptomatic infection requiring medical treatment (e.g., oral antibiotics/antivirals); no hospitalization
  • Grade 3 (Severe): Severe infection requiring hospitalization or intravenous therapy
  • Grade 4 (Life-threatening): Life-threatening infection requiring urgent intervention/ICU care
  • Grade 5: Death related to infection
From enrollment in the study to 6 months of treatment

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Lipid profile
Délai: 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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

5 juillet 2026

Achèvement primaire (Estimé)

5 mars 2027

Achèvement de l'étude (Estimé)

10 mai 2027

Dates d'inscription aux études

Première soumission

29 avril 2026

Première soumission répondant aux critères de contrôle qualité

4 juin 2026

Première publication (Réel)

9 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

9 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

4 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

produit fabriqué et exporté des États-Unis.

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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