RINVOQ®(upadacitinib) Revmatoid artritt (RA)
RINVOQ er indisert til behandling av moderat til alvorlig aktiv revmatoid artritt hos voksne pasienter som har respondert utilstrekkelig på eller er intolerante overfor ett eller flere sykdomsmodifiserende antirevmatiske legemidler (DMARDs). RINVOQ kan brukes som monoterapi eller i kombinasjon med metotreksat1.
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Dette gjøres via meldeskjema som finnes på nettsiden til Statens Legemiddelverk: www.legemiddelverket.no/meldeskjema.
Referanse: 1. RINVOQ SPC avsnitt 4.1, sist oppdatert 16.09.2021.
The study evaluated 2 doses of upadacitinib, 15 mg and 30 mg QD. The results presented here are for RINVOQ (upadacitinib) 15 mg once daily, which is the approved dose for Rheumatoid Arthritis.
SELECT-EARLY: Study design
A Phase 3 study investigating the efficacy and safety of RINVOQ monotherapy compared with MTX in MTX-naive patients with moderately to severely active RA1
Primary
RINVOQ 15 mg vs MTX for DAS28 (CRP) <2.6 at Week 24 or ACR50 at Week 12
Safety
Adverse events, serious adverse events, adverse event of special interest (e.g., serious infections, opportunistic infections, MACEs, VTEs, malignancies)
ACR: American College of Rheumatology; ACR50: improvement of at least 50% in the American College of Rheumatology core criteria; CDAI: Clinical Disease Activity Index; DAS28 (CRP): disease activity score with 28 joint count (C-reactive protein); JAK: Janus kinase; MACE: major adverse cardiovascular events; MTX: methotrexate; QD: once daily; VTE: venous thromboembolic event.
RINVOQ monotherapy data
SELECT-EARLY: Remission (primary endpoint) and low disease activity at Week 24 in MTX-naive patients1*
*RINVOQ is not indicated for MTX-naive patients.
† P<0.001 vs MTX
DAS28 (CRP): disease activity score with 28 joint counts (C-reactive protein); MTX: methotrexate.
Joint protection with RINVOQ monotherapy
SELECT-EARLY: Inhibition of structural joint damage progression as monotherapy in MTX-naive patients* at Week 241
Change in mTSS for RINVOQ vs MTX at Week 24 was a ranked secondary endpoint controlled for multiplicity. All other data shown for RINVOQ vs MTX were prespecified nonranked endpoints not controlled for multiplicity; nominal P-values are provided.
*RINVOQ is not indicated for MTX-naive patients.
† P≤0.01 vs MTX
||Indicates multiplicity-controlled comparison of RINVOQ vs MTX.
mTSS: modified total Sharp score; MTX:methotrexate.
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Referanser
- RINVOQ SPC avsnitt 5.1, sist oppdatert 21.05.2021.
NO-RNQ-200013v2.0juni/2021