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

4 giugno 2026 aggiornato da: 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

Panoramica dello studio

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Stimato)

100

Fase

  • Fase 4

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Dr Sadia Maqsood Awan Assistant Professor Pharmacology FPGMI Lahore, MBBS, M.phil,MHPE
  • Numero di telefono: 03335032495
  • Email: sadia_maqsood_awan@yahoo.com

Backup dei contatti dello studio

  • Nome: Dr Mudassra yaseen HOD pharmacology FPGMI, Lahore, MBBS, M.phil, CMT, PhD
  • Numero di telefono: 03334162630
  • Email: Drmudassarayaseen@gmail.com

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

No

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.
Sperimentale: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in the Disease activity score(DAS 28)
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Frequency & severity of opportunistic infections
Lasso di tempo: 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

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Lipid profile
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

5 luglio 2026

Completamento primario (Stimato)

5 marzo 2027

Completamento dello studio (Stimato)

10 maggio 2027

Date di iscrizione allo studio

Primo inviato

29 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

4 giugno 2026

Primo Inserito (Effettivo)

9 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

9 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

4 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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