Related Experiment Video
Updated: May 20, 2026

Scaled-Up Preparation of an Intermediate of Upatinib, ACT051-3
Published on: April 7, 2023
[Janus kinase inhibitors]
E Ostermeier1, P Roll, H-P Tony
1Med. Klinik und Poliklinik II, Sektion Rheumatologie/Immunologie, Universitätsklinikum Würzburg, Oberdürrbacherstr. 6, 97080, Würzburg, Deutschland. Ostermeier_E@klinik.uni-wuerzburg.de
Janus kinase (JAK) inhibitors like tofacitinib show over 50% efficacy for rheumatoid arthritis treatment. Safety profiles are comparable to biologics, with common side effects including upper respiratory and urogenital infections.
Area of Science:
- Rheumatology
- Immunology
- Pharmacology
Context:
- Rheumatoid arthritis (RA) is a chronic autoimmune disease.
- Janus kinase (JAK) inhibitors represent a novel therapeutic class for RA.
- Tofacitinib is an oral JAK inhibitor.
Purpose:
- To evaluate the clinical efficacy and safety of tofacitinib in rheumatoid arthritis patients.
- To assess American College of Rheumatology (ACR) 20 response rates.
- To compare the safety profile of tofacitinib with existing biological therapies.
Summary:
- Tofacitinib demonstrated significant clinical efficacy in Phase II and III studies, achieving ACR20 response rates exceeding 50% in both monotherapy and combination with methotrexate (MTX).
- The safety profile of tofacitinib is comparable to established biological treatments for RA.
- The incidence of serious infections was low (3/100 patient-years), with common adverse events including upper respiratory tract and urogenital infections.
Impact:
- Tofacitinib offers a new oral treatment option for rheumatoid arthritis patients.
- The findings support JAK inhibitors as a viable therapeutic strategy for RA management.
- Understanding the safety profile, including common adverse events, is crucial for clinical practice.
More Related Videos
Related Concept Videos
The JAK-STAT Signaling Pathway
Dipeptidyl Peptidase 4 Inhibitors
Inhibitors of Viral Protein Synthesis
PI3K/mTOR/AKT Signaling Pathway
Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors
Inhibitors of Bacterial Protein Synthesis

