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✓ Translated by DotMD AI Clinical Council Source: Annals of the rheumatic diseases • Phase III Randomized Trial
Verify Primary Source: NIH PubMed PMID #33272960 ↗

Phase III Randomized Trial: Upadacitinib for psoriatic arthritis refractory to biologics: SELECT-PsA 2 (N = 642)

Original Paper Title: “Upadacitinib for psoriatic arthritis refractory to biologics: SELECT-PsA 2”

Elena Rostova (AI Quant) Rigor Score
93 / 100
Sample Size (Participants)
N = 642
Evidence Classification
Phase III Randomized Trial
Sarah Jenkins, RN (AI Plain-English Editor) • Key Takeaways
  • In this trial of patients with active PsA who had inadequate response or intolerance to at least one biologic DMARD, upadacitinib 15 mg and 30 mg was more effective than placebo over 24 weeks in improving signs and symptoms of PsA.
  • Study Design & Sample: Phase III Randomized Trial published in Annals of the rheumatic diseases (N = 642 human participants).
  • Biostatistical Rigor Score: 93/100 audited by Elena Rostova (AI Biostatistician & openFDA Quant).

What the Study Found (In Plain English)

Published in Annals of the rheumatic diseases (2021), this phase iii randomized trial evaluating 642 human participants investigated: Upadacitinib is a Janus kinase inhibitor under evaluation for the treatment of psoriatic arthritis (PsA). Key clinical takeaway: In this trial of patients with active PsA who had inadequate response or intolerance to at least one biologic DMARD, upadacitinib 15 mg and 30 mg was more effective than placebo over 24 weeks in improving signs and symptoms of PsA.

Dr. Lin (AI Evidence Lead): Statistical Endpoints & Numbers

Primary Endpoint & Quantitative Summary (Annals of the rheumatic diseases, 2021-03-15; N = 642; Rigor 93/100): In this trial of patients with active PsA who had inadequate response or intolerance to at least one biologic DMARD, upadacitinib 15 mg and 30 mg was more effective than placebo over 24 weeks in improving signs and symptoms of PsA.

Study Limitations & Caveats Before You Act

Clinical trials evaluate specific inclusion/exclusion cohorts under protocol-controlled conditions (Phase III Randomized Trial). Individual response, hepatic/renal clearance, CYP450 drug interactions, and baseline comorbidities vary; verify applicability with a board-certified physician before modifying any prescription or supplement regimen.

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