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Comparison between methotrexate and apremilast in Psoriatic Arthritis-a single blind randomized controlled trial
Joydeep Samanta1, Gsrsnk Naidu1, Arghya Chattopadhyay2
1Clinical Immunology and Rheumatology Unit, Department of Internal Medicine, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Methotrexate and apremilast showed similar efficacy for psoriatic arthritis (PsA) patients. Both treatments were safe, with no significant differences in major response rates or adverse events at 24 weeks.
Area of Science:
- Rheumatology
- Clinical Immunology
- Pharmacology
Background:
- Psoriatic arthritis (PsA) is a chronic inflammatory condition affecting joints and entheses.
- Methotrexate and apremilast are established treatments for PsA, but direct comparative efficacy data is limited.
Purpose of the Study:
- To compare the efficacy and safety of methotrexate versus apremilast in adult patients with active psoriatic arthritis.
- To evaluate key clinical response measures including the composite disease activity score (cDAPSA) and American College of Rheumatology (ACR) 20 response.
Main Methods:
- A single-center, physician-blinded, parallel-group, randomized controlled trial.
- Recruited adult PsA patients meeting CASPAR criteria, naive to bDMARDs and JAK inhibitors.
- Assessed major cDAPSA response at 24 weeks as the primary outcome, with secondary outcomes including ACR 20, PASI, enthesitis, dactylitis, and HAQ-DI scores.
Main Results:
- 31 patients were randomized (15 apremilast, 16 methotrexate); 26 completed 24 weeks.
- No significant difference in major cDAPSA response at week 24 between apremilast (20%) and methotrexate (37.5%; p=0.433).
- Secondary outcomes and adverse events showed no significant differences between the groups.
Conclusions:
- Methotrexate and apremilast demonstrate comparable efficacy in treating active psoriatic arthritis over 24 weeks.
- Both agents are well-tolerated, with similar safety profiles in this patient cohort.
- Further research may explore long-term outcomes and specific patient subgroups.
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