drugset / Trial / NCT03086343

A Phase 3 Study to Compare Upadacitinib to Abatacept in Subjects With Rheumatoid Arthritis on Stable Dose of Conventional Synthetic Disease- Modifying Antirheumatic Drugs (csDMARDs) Who Have an Inadequate Response or Intolerance to Biologic DMARDs

NCT03086343 ↗

Phase 3 Completed 657 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study objective of Period 1 was to compare the safety and efficacy of upadacitinib 15 mg once daily (QD) to abatacept on a background of conventional synthetic disease-modifying antirheumatic drugs (csDMARDs) for the treatment of signs and symptoms of rheumatoid arthritis (RA) in biologic disease-modifying antirheumatic drug (bDMARD)-inadequate response or bDMARD-intolerant participants with moderately to severely active RA. The study objective of Period 2 is to evaluate the long-term safety, tolerability, and efficacy of upadacitinib 15 mg QD in participants with RA who had completed Period 1.

Timeline

Start
2017-05-09
Primary completion
2019-06-13
Completion
2023-06-06

Outcome

Met primary endpoint

registry analysis (non-inferiority test); Upadacitinib 15 mg vs Abatacept; p < 0.001; LS Mean Difference -0.52 (95% CI -0.69 to -0.35); ANCOVA; NCT03086343 ↗

release “SELECT-CHOICE clinical trial, showing that RINVOQ™ (upadacitinib, 15 mg, once daily) met the primary endpoint of non-inferiority” abbvie.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Abatacept Other / unclassified 500 mg Intravenous
Comparator Abatacept Other / unclassified 750 mg Intravenous
Comparator Abatacept Other / unclassified 1000 mg Intravenous
Subject Upadacitinib Small molecule 15 mg Oral
Subject Upadacitinib Small molecule 30 mg Oral

Indications