Efficacy of Tofacitinib on Skin Thickening in Diffuse Cutaneous Systemic Sclerosis: A Comparative Study With Methotrexate

Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh

Status and phase

Completed

Phase 4

Conditions

Scleroderma, Systemic

Treatments

Drug: Methotrexate

Drug: Tofacitinib

Study type

Interventional

Funder types

Other

Identifiers

NCT07472166

5230

Details and patient eligibility

About

This study aims to evaluate the efficacy of Tofacitinib compared to Methotrexate (MTX) in reducing skin thickening in patients with diffuse cutaneous systemic sclerosis (dcSSc). Systemic sclerosis is a chronic autoimmune disease characterized by skin fibrosis and internal organ involvement. Despite existing treatments, many patients continue to experience progressive skin and joint symptoms.

Tofacitinib, a Janus kinase (JAK) inhibitor, has shown potential benefit in reducing inflammation and fibrosis in autoimmune diseases. This randomized controlled study will compare the change in Modified Rodnan Skin Score (mRSS), Clinical Disease Activity Index (CDAI), and 12-Item Short Form Survey (SF-12) between the Tofacitinib and Methotrexate groups over the study period.

The study will also monitor adverse events and laboratory parameters to assess drug safety and tolerability.

Enrollment

34 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

1. Diagnosed with systemic sclerosis (SSc) according to the 2013 ACR/EULAR classification criteria 2. Classified as having diffuse cutaneous systemic sclerosis (dcSSc), as defined by LeRoy and Medsger 3. Disease duration of ≤ 36 months, calculated from the onset of the first non-Raynaud's phenomenon manifestation.

4. Modified Rodnan Skin Score (mRSS) between 10 and 45 at the time of screening.

5. Concurrent use of calcium channel blockers and phosphodiesterase-5 inhibitors for the treatment of Raynaud's phenomenon or digital ulcers was permitted.

6. Subjects were aged 18 years and older

Exclusion criteria

1. Presence of a rheumatic disease other than systemic sclerosis, except for fibromyalgia or scleroderma-associated myopathy.

2. Evidence of any active infection, including active tuberculosis 3. Abnormal laboratory values at screening, including:
- Hemoglobin <9 g/dL
- White blood cell count <3.0 × 10⁹/L
- Absolute neutrophil count <1.2 × 10⁹/L
- Platelet count <100 × 10⁹/L
- Absolute lymphocyte count <0.75 × 10⁹/L
- ALT or AST >3× the upper limit of normal (ULN)
- Estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m²
  
  4. Pulmonary function showing forced vital capacity (FVC) ≤ 50% predicted, or DLCO (uncorrected for hemoglobin) ≤ 40% predicted.
  
  5. History of major surgery (including joint surgery) within 8 weeks prior to the screening visit.
  
  6. Use of oral corticosteroids 7. Diagnosis of latent TB at or within 30 days of screening. 8. Positive hepatitis B surface antigen or anti HCV test at or within 30 days of screening.
  
  9. Pregnant or breastfeeding women, females of childbearing potential who were unwilling or unable to use highly effective contraception during the study 10. History or evidence of malignancy 11. Receipt of a live or attenuated vaccine within 6 weeks prior to baseline