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Efficacy of Tofacitinib for the Treatment of Psoriatic Arthritis: Pooled Analysis of Two Phase 3 Studies
by
Coates, Laura C
, Papp, Kim A
, Ports, William C
, Menon, Sujatha
, Hendrikx, Thijs
, Wang, Cunshan
, Juan Jesus Gomez-Reino
, Nash, Peter
, Wu, Joseph
, Fleischmann, Roy
, Kanik, Keith S
in
Clinical trials
/ Drug therapy
/ Inhibitor drugs
/ Psoriasis
/ Psoriatic arthritis
2018
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Efficacy of Tofacitinib for the Treatment of Psoriatic Arthritis: Pooled Analysis of Two Phase 3 Studies
by
Coates, Laura C
, Papp, Kim A
, Ports, William C
, Menon, Sujatha
, Hendrikx, Thijs
, Wang, Cunshan
, Juan Jesus Gomez-Reino
, Nash, Peter
, Wu, Joseph
, Fleischmann, Roy
, Kanik, Keith S
in
Clinical trials
/ Drug therapy
/ Inhibitor drugs
/ Psoriasis
/ Psoriatic arthritis
2018
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Efficacy of Tofacitinib for the Treatment of Psoriatic Arthritis: Pooled Analysis of Two Phase 3 Studies
by
Coates, Laura C
, Papp, Kim A
, Ports, William C
, Menon, Sujatha
, Hendrikx, Thijs
, Wang, Cunshan
, Juan Jesus Gomez-Reino
, Nash, Peter
, Wu, Joseph
, Fleischmann, Roy
, Kanik, Keith S
in
Clinical trials
/ Drug therapy
/ Inhibitor drugs
/ Psoriasis
/ Psoriatic arthritis
2018
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Efficacy of Tofacitinib for the Treatment of Psoriatic Arthritis: Pooled Analysis of Two Phase 3 Studies
Journal Article
Efficacy of Tofacitinib for the Treatment of Psoriatic Arthritis: Pooled Analysis of Two Phase 3 Studies
2018
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Overview
IntroductionTofacitinib is an oral Janus kinase inhibitor for the treatment of psoriatic arthritis (PsA). This post hoc analysis assessed the efficacy of tofacitinib using pooled data from two phase 3 studies of patients with active PsA.MethodsData were pooled from OPAL Broaden (NCT01877668) and OPAL Beyond (NCT01882439). Patients had active PsA and either an inadequate response (IR) to ≥ 1 conventional synthetic disease-modifying antirheumatic drug (csDMARD) and were tumor necrosis factor inhibitor (TNFi)-naïve (OPAL Broaden), or had IR to ≥ 1 TNFi (OPAL Beyond). Pooled data included tofacitinib 5 or 10 mg twice daily (BID; to month 6) and placebo (to month 3; patients then switched to tofacitinib 5 or 10 mg BID). Patients also received one background csDMARD. Endpoints included American College of Rheumatology (ACR)20 response and change from baseline in Health Assessment Questionnaire-Disability Index (HAQ-DI) at month 3 (primary endpoints), ACR50/70 response, HAQ-DI response (decrease from baseline ≥ 0.35) and improvements in painful and swollen joint counts, psoriasis, enthesitis and dactylitis to month 6.ResultsA total of 710 patients were included (tofacitinib 5 mg BID: 238; tofacitinib 10 mg BID: 236; placebo: 236). Primary endpoints showed significant improvements at month 3 in patients receiving tofacitinib 5 or 10 mg BID vs. placebo. Significant improvements in HAQ-DI response, painful and swollen joints, psoriasis, enthesitis and dactylitis vs. placebo were observed for both tofacitinib doses at month 3. Efficacy was maintained to month 6 (final pooled time point).ConclusionsIn a pooled analysis of csDMARD-IR/TNFi-naïve and TNFi-IR patients, tofacitinib was superior to placebo at month 3 across four PsA domains: peripheral arthritis, psoriasis, enthesitis and dactylitis.Trial RegistrationOPAL Broaden (NCT01877668); OPAL Beyond (NCT01882439).FundingPfizer Inc.
Publisher
Springer Nature B.V
Subject
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