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Tofacitinib or adalimumab versus placebo in rheumatoid arthritis
Ronald F van Vollenhoven1, Roy Fleischmann, Stanley Cohen
1Karolinska Institute, Stockholm.
Background:
Tofacitinib (CP-690,550) is a novel oral Janus kinase inhibitor that is being investigated for the treatment of rheumatoid arthritis.
Methods:
In this 12-month, phase 3 trial, 717 patients who were receiving stable doses of methotrexate were randomly assigned to 5 mg of tofacitinib twice daily, 10 mg of tofacitinib twice daily, 40 mg of adalimumab once every 2 weeks, or placebo. At month 3, patients in the placebo group who did not have a 20% reduction from baseline in the number of swollen and tender joints were switched in a blinded fashion to either 5 mg or 10 mg of tofacitinib twice daily; at month 6, all patients still receiving placebo were switched to tofacitinib in a blinded fashion. The three primary outcome measures were a 20% improvement at month 6 in the American College of Rheumatology scale (ACR 20); the change from baseline to month 3 in the score on the Health Assessment Questionnaire-Disability Index (HAQ-DI) (which ranges from 0 to 3, with higher scores indicating greater disability); and the percentage of patients at month 6 who had a Disease Activity Score for 28-joint counts based on the erythrocyte sedimentation rate (DAS28-4[ESR]) of less than 2.6 (with scores ranging from 0 to 9.4 and higher scores indicating greater disease activity).
Results:
At month 6, ACR 20 response rates were higher among patients receiving 5 mg or 10 mg of tofacitinib (51.5% and 52.6%, respectively) and among those receiving adalimumab (47.2%) than among those receiving placebo (28.3%) (P<0.001 for all comparisons). There were also greater reductions in the HAQ-DI score at month 3 and higher percentages of patients with a DAS28-4(ESR) below 2.6 at month 6 in the active-treatment groups than in the placebo group. Adverse events occurred more frequently with tofacitinib than with placebo, and pulmonary tuberculosis developed in two patients in the 10-mg tofacitinib group. Tofacitinib was associated with an increase in both low-density and high-density lipoprotein cholesterol levels and with reductions in neutrophil counts.
Conclusions:
In patients with rheumatoid arthritis receiving background methotrexate, tofacitinib was significantly superior to placebo and was numerically similar to adalimumab in efficacy. (Funded by Pfizer; ORAL Standard ClinicalTrials.gov number, NCT00853385.).
Insights
Tofacitinib demonstrated superior efficacy compared to placebo in treating rheumatoid arthritis patients on methotrexate. This oral Janus kinase inhibitor showed results comparable to adalimumab, with some increased adverse events observed.
Area of Science:
- Rheumatology
- Immunology
- Pharmacology
Background:
- 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 under investigation for RA treatment.
Purpose of the Study:
- To evaluate the efficacy and safety of tofacitinib in patients with rheumatoid arthritis.
- To compare tofacitinib with adalimumab and placebo in a 12-month, Phase 3 trial.
Main Methods:
- 717 RA patients on stable methotrexate were randomized to tofacitinib (5mg or 10mg BID), adalimumab (40mg Q2W), or placebo.
- Primary outcomes included ACR 20 response at 6 months, HAQ-DI change at 3 months, and DAS28-4(ESR) < 2.6 at 6 months.
- Blinded switching from placebo to tofacitinib occurred at months 3 and 6 for non-responders.
Main Results:
- Tofacitinib (5mg and 10mg) and adalimumab showed significantly higher ACR 20 response rates (51.5%, 52.6%, 47.2%) versus placebo (28.3%) at 6 months.
- Active treatment groups demonstrated greater HAQ-DI score reductions and higher rates of DAS28-4(ESR) < 2.6 compared to placebo.
- Adverse events were more frequent with tofacitinib; pulmonary tuberculosis occurred in two patients on 10mg tofacitinib. Lipid levels increased, and neutrophil counts decreased.
Conclusions:
- Tofacitinib is significantly more effective than placebo for RA patients on background methotrexate.
- Efficacy of tofacitinib was numerically similar to adalimumab.
- Tofacitinib treatment was associated with increased adverse events, including infections and laboratory abnormalities.
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