- |||||||||| Tremfya (guselkumab) / J&J
[VIRTUAL] Guselkumab, an IL-23 Inhibitor That Specifically Binds to the IL23p19-Subunit, for Active Psoriatic Arthritis: One Year Results of a Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Patients Who Were Biologic-Naïve or TNFα Inhibitor-Experienced () - Oct 8, 2020 - Abstract #ACRARHP2020ACR_ARHP_2008; In pts continuing in the study, improvements in skin symptoms, dactylitis, enthesitis, physical function, and quality of life were also maintained through 1 year. GUS 100 mg Q4W and Q8W were safe and well-tolerated through study completion and consistent with GUS safety in PsO.1 Reference: 1.
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[VIRTUAL] Guselkumab Efficacy in Adult Patients with Active Psoriatic Arthritis by Baseline Demographic and Disease Characteristics: Pooled Results of Two Phase 3, Randomized, Placebo-Controlled Studies () - Oct 8, 2020 - Abstract #ACRARHP2020ACR_ARHP_1531; GUS effects on joint (ACR50) and skin (Investigator’s Global Assessment [IGA=0/1 + ≥2-grade reduction from W0] in pts with ≥3% body surface area [BSA] psoriasis and IGA ≥2 at W0) responses were evaluated by pt sex, age, body weight, BMI, PsA duration, tender/swollen joint counts (ACR50 only), % BSA (IGA 0/1 only), CRP, and non-biologic (nb) DMARD/methotrexate (MTX) use at W0. The benefits of guselkumab 100 mg Q4W and Q8W in substantially improving signs and symptoms of active PsA appeared to be consistent irrespective of the baseline characteristics assessed
- |||||||||| Humira (adalimumab) / Eisai, AbbVie, Tremfya (guselkumab) / J&J
[VIRTUAL] Four-Year Efficacy and Safety of Guselkumab in Psoriasis Patients with and Without Psoriatic Arthritis: A Pooled Analysis from VOYAGE 1 and VOYAGE 2 () - Oct 8, 2020 - Abstract #ACRARHP2020ACR_ARHP_1514; 1829 patients were randomized to GUS 100 mg at Weeks 0, 4, and 12, then every 8 weeks (q8wk); PBO at Weeks 0, 4, and 12, GUS at Weeks 16 and 20 then q8wk; or adalimumab (ADA) 80 mg at Week 0, 40 mg at Week 1, then 40 mg q2wk until Week 47 (VOYAGE 1) or Week 23 (VOYAGE 2). Among GUS-treated patients with moderate-to-severe PsO with and without self-reported PsA at baseline, stable, durable, and high levels of skin responses, as well as comparable safety outcomes, through 4 years were observed.
- |||||||||| [VIRTUAL] Comparative Efficacy of Synthetic and Biologic Dmards for Adult Patients with ACTIVE Psoriatic Arthritis in the Russian Federation- A Systematic Review and Network Meta-Analysis () - Oct 3, 2020 - Abstract #ISPOREU2020ISPOR-EU_1847;
Phase II and III randomised controlled trials (RCTs) evaluating efficacy of sDMARDS (tofacitinib, apremilast) and bDMARDS (netakimab, guselkumab, ustekinumab, secukinumab, ixekizumab, adalimumab, etanercept, infliximab, certolizumab, golimumab) for active PsA were identified by systematic literature review performed in Pubmed and Embase databases. Netakimab is one of the most effective treatments for active PsA.
- |||||||||| Stelara (ustekinumab) / J&J
[VIRTUAL] Efficiency of Innovative Biologics Indicated for Moderate-Severe Psoriasis () - Oct 3, 2020 - Abstract #ISPOREU2020ISPOR-EU_1632; Cost analysis per responder (CPR) to achieve PASI100 for IL-17 therapies (brodalumab, secukinumab, ixezikumab), IL-12/23 therapies (ustekinumab), and IL-23 therapies (guselkumab, tildrakizumab, risankizumab) vs. placebo. Brodalumab appears to be a cost-effective alternative versus the current biologic treatments for moderate-severe psoriasis in Spain, being the most cost-efficient alternative within the IL-17 therapeutic group.
- |||||||||| [VIRTUAL] Analysis of the Cost per Responder of Biological Treatments for Moderate to Severe Psoriasis in Argentina () - Oct 3, 2020 - Abstract #ISPOREU2020ISPOR-EU_1136;
CPR at 2 years (PASI 90; 100): Risankizumab ($2,064,565; $3,611,709), Guselkumab ($2,066,014; $3,836,054), Ixekizumab ($2,494,476; $4,412,817), Secukinumab ($2641,173; $5,335,524), Adalimumab ($2,832,516; $7,357,634), Apremilast ($2,961,656; $14,164,442), Ustekinumab ($3,552,613; $9,159,750), Etanercept ($4,267,464; $17,486,194) and Infliximab ($4,933,087; $10.520.182). CONCLUSIONS : Among the therapies evaluated for moderate to severe psoriasis, Risankizumab, Guselkumab and Ixekizumab shown the highest PASI-90/100 response rates; while Risankizumab would have the lowest CPR PASI-90/100 for all time horizons considered.
- |||||||||| Stelara (ustekinumab) / J&J
Clinical, Journal: Therapeutic Targeting of Th17/Tc17 Cells Leads to Clinical Improvement of Lichen Planus. (Pubmed Central) - Oct 1, 2020 These findings show for the first time that therapeutic targeting of Th17/Tc17 cells leads to a pronounced clinical amelioration of mucosal and cutaneous LP and strongly suggests that IL-17-producing T cells are central to disease pathogenesis. Thus, therapeutic targeting of Th17/Tc17 cells opens new therapeutic avenues in the treatment of recalcitrant LP.
- |||||||||| Enrollment open, Trial initiation date, Trial primary completion date, Head-to-Head: BeNeBio: Dose Reduction of IL17 and IL23 Inhibitors in Psoriasis (clinicaltrials.gov) - Sep 15, 2020
P4, N=244, Recruiting, Trial completion date: Mar 2025 --> Jul 2025 Not yet recruiting --> Recruiting | Initiation date: May 2020 --> Aug 2020 | Trial primary completion date: Apr 2023 --> Jul 2023
- |||||||||| Tremfya (guselkumab) / J&J
Journal: Successful use of Guselkumab in the treatment of severe hidradenitis suppurativa. (Pubmed Central) - Sep 13, 2020 Adalimumab and Infliximab are recommended for use in HS Hurley stage 2-3 and there are several reported cases and one case series of successful treatment with Ustekinumab which blocks the p40 subunit of IL-12 and IL-23 . We report a case of successful treatment of HS with a monoclonal antibody (Guselkumab) to the p19 subunit of IL-23.
- |||||||||| [VIRTUAL] Phenotypic switch from psoriasis to atopic eczema secondary to biological therapy () - Sep 9, 2020 - Abstract #BAD2020BAD_134;
Implicated biologics included adalimumab (n = 10); etanercept (n = 1); infliximab (n = 1); ixekizumab (n = 2); secukinumab (n = 4); guselkumab (n = 3); and ustekinumab (n = 10)...Treatment strategies for eczema included topical treatment only; oral immunomodulators (ciclosporin, methotrexate or apremilast); or none...Utilizing the British Association of Dermatologists Biologics and Immunomodulators Register is important to document adverse events; the resulting data could allow a more detailed insight into the clinical features and prevalence of atopic eczema secondary to biologics. In‐depth characterization of the genetic basis, cellular and molecular mechanisms of this phenotypic switch is needed to rationalize therapy selection for these patients.
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