Profile of Tofacitinib in the Treatment of Ulcerative Colitis: An Evidence-Based Review of Recent Data.
Fumi VaryaniKonstantinos ArgyriouFrank PhillipsEirini TsakiridouGordon William MoranPublished in: Drug design, development and therapy (2019)
Recent advances in the understanding of the pathophysiology of ulcerative colitis (UC) have led to the expansion of our therapeutic arsenal. Conventional treatment options, including aminosalicylates, corticosteroids, thiopurines, and calcineurin inhibitors, fail to control the disease in a significant proportion of patients. Approximately 25-50% of the patients treated with tumor necrosis factor antibodies (anti-TNFα) are primary and secondary non-responders to therapy. Tofacitinib is a novel orally administered small synthetic molecule that inhibits a homologous family of enzymes, termed Janus kinases that modulate multiple key cytokines involved in the pathogenesis of UC. Phase II and III trials showed promising results in UC, leading the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) to approve its administration for the induction and maintenance of remission in moderate-to-severe UC. Herein, we review tofacitinib for the management of UC, its mechanism of action pharmacokinetic properties, efficacy, and safety.
Keyphrases
- ulcerative colitis
- rheumatoid arthritis
- phase ii
- drug administration
- end stage renal disease
- clinical trial
- ejection fraction
- newly diagnosed
- open label
- chronic kidney disease
- peritoneal dialysis
- dna damage
- early onset
- dna repair
- big data
- patient reported outcomes
- machine learning
- human health
- double blind
- patient reported
- study protocol
- artificial intelligence