Xeljanz (tofacitinib) vs Truxima (rituximab)

Xeljanz (tofacitinib) vs Truxima (rituximab)

Xeljanz (tofacitinib) is an oral Janus kinase inhibitor that is primarily used to treat moderate to severe rheumatoid arthritis, psoriatic arthritis, and ulcerative colitis by modulating the immune system. Truxima (rituximab), on the other hand, is a monoclonal antibody administered through intravenous infusion, used to treat various conditions including rheumatoid arthritis, non-Hodgkin's lymphoma, and chronic lymphocytic leukemia, by targeting specific cells in the immune system. The choice between Xeljanz and Truxima for a patient would depend on the specific condition being treated, the patient's overall health, the potential side effects, and the mode of administration preferred or recommended by the healthcare provider.

Difference between Xeljanz and Truxima

Metric Xeljanz (tofacitinib) Truxima (rituximab)
Generic name Tofacitinib Rituximab
Indications Rheumatoid arthritis, Psoriatic arthritis, Ulcerative colitis Non-Hodgkin's lymphoma, Chronic lymphocytic leukemia, Rheumatoid arthritis, Granulomatosis with polyangiitis, Microscopic polyangiitis
Mechanism of action Janus kinase (JAK) inhibitor CD20-directed cytolytic antibody
Brand names Xeljanz, Xeljanz XR Truxima, Rituxan
Administrative route Oral Intravenous
Side effects Upper respiratory tract infections, Headache, Diarrhea, Nasopharyngitis Infusion reactions, Infections, Body aches, Fatigue
Contraindications Serious infections, Active tuberculosis, Severe hepatic impairment Hepatitis B infection reactivation, Severe infections, Heart failure, Hypersensitivity to murine proteins
Drug class JAK inhibitor Monoclonal antibody
Manufacturer Pfizer Celltrion Healthcare, Genentech (Rituxan)

Efficacy

Xeljanz (Tofacitinib) Efficacy in Rheumatoid Arthritis

Xeljanz (tofacitinib) is an oral medication that is classified as a Janus kinase (JAK) inhibitor. It is approved for the treatment of adults with moderate to severe rheumatoid arthritis (RA) who have had an inadequate response or intolerance to methotrexate. Tofacitinib works by interfering with the JAK-STAT signaling pathway, which plays a key role in the inflammatory process of RA. Clinical trials have demonstrated that Xeljanz can reduce signs and symptoms of RA, improve physical function, and inhibit the progression of joint damage.

Several studies have shown the efficacy of Xeljanz in reducing the disease activity in RA patients. The ACR20 response rate, which is a 20% improvement in RA symptoms, is often used as a benchmark in clinical trials. Xeljanz has been shown to achieve ACR20 in a significant proportion of patients compared to placebo. Additionally, Xeljanz has also been found to be effective in patients who have had an inadequate response to TNF inhibitors, another class of medication commonly used to treat RA.

Truxima (Rituximab) Efficacy in Rheumatoid Arthritis

Truxima (rituximab) is a biosimilar to Rituxan and is a monoclonal antibody that targets the CD20 protein found on the surface of B cells, which are a type of white blood cell involved in the inflammatory process of RA. Truxima is used in combination with methotrexate in adult patients with moderate to severe active RA who have had an inadequate response or intolerance to one or more TNF inhibitor therapies. Clinical trials have shown that rituximab can reduce symptoms of RA, improve physical function, and slow the progression of joint damage.

The efficacy of rituximab in RA has been established through randomized controlled trials that have demonstrated significant improvements in ACR20, ACR50, and ACR70 response rates, which represent 20%, 50%, and 70% improvements in RA symptoms, respectively. The use of rituximab has also been associated with a reduction in the progression of joint damage as seen on X-rays. Additionally, rituximab has been shown to improve quality of life for many patients with RA who have not responded to other treatments.

Regulatory Agency Approvals

Xeljanz
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
Truxima
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)

Access Xeljanz or Truxima today

If Xeljanz or Truxima are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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