Guselkumab in patients with active psoriatic arthritis who were biologic-naive or had previously received TNFα inhibitor treatment (DISCOVER-1): a double-blind …

A Deodhar, PS Helliwell, WH Boehncke, AP Kollmeier… - The Lancet, 2020 - thelancet.com
Background Many patients with psoriatic arthritis have an inadequate response to tumor
necrosis factor (TNF) inhibitors. Guselkumab, a specific inhibitor of interleukin-23 (IL-23) via …

Guselkumab in biologic-naive patients with active psoriatic arthritis (DISCOVER-2): a double-blind, randomised, placebo-controlled phase 3 trial

PJ Mease, P Rahman, AB Gottlieb, AP Kollmeier… - The Lancet, 2020 - thelancet.com
Summary Background The interleukin-23 (IL-23)/T-helper 17 cell pathway is implicated in
psoriatic arthritis pathogenesis. Guselkumab, an IL-23 inhibitor that specifically binds the IL …

Phase 1 clinical results with tandutinib (MLN518), a novel FLT3 antagonist, in patients with acute myelogenous leukemia or high-risk myelodysplastic syndrome …

DJ DeAngelo, RM Stone, ML Heaney, SD Nimer… - Blood, 2006 - ashpublications.org
Abstract Tandutinib (MLN518/CT53518) is a novel quinazoline-based inhibitor of the type III
receptor tyrosine kinases: FMS-like tyrosine kinase 3 (FLT3), platelet-derived growth factor …

Phase II study of single‐agent bortezomib for the treatment of patients with fludarabine‐refractory B‐cell chronic lymphocytic leukemia

S Faderl, K Rai, J Gribben, JC Byrd… - … Journal of the …, 2006 - Wiley Online Library
Therapeutic options are limited and the prognosis is poor for patients with fludarabine‐
refractory B‐cell chronic lymphocytic leukemia (CLL). Bortezomib induces apoptosis in vitro …

Guselkumab plus golimumab combination therapy versus guselkumab or golimumab monotherapy in patients with ulcerative colitis (VEGA): a randomised, double …

BG Feagan, BE Sands, WJ Sandborn… - The Lancet …, 2023 - thelancet.com
Background Despite the introduction of new monoclonal antibodies and oral therapies for
the treatment of ulcerative colitis, clinical remission rates remain low, underscoring the need …

Sirukumab, a human anti-interleukin-6 monoclonal antibody: a randomised, 2-part (proof-of-concept and dose-finding), phase II study in patients with active …

JS Smolen, ME Weinblatt, S Sheng… - Annals of the rheumatic …, 2014 - ard.bmj.com
Objectives The safety and efficacy of sirukumab, an anti-interleukin-6 (IL-6) monoclonal
antibody, were evaluated in a 2-part, placebo-controlled phase II study of patients with active …

Randomized phase II study of bortezomib alone and bortezomib in combination with docetaxel in previously treated advanced non–small-cell lung cancer

MP Fanucchi, FV Fossella, R Belt, R Natale… - Journal of Clinical …, 2006 - ascopubs.org
Purpose To evaluate the efficacy and toxicity of bortezomib±docetaxel as second-line
therapy in patients with relapsed or refractory advanced non–small-cell lung cancer …

Long‐term efficacy and safety of guselkumab, a monoclonal antibody specific to the p19 subunit of interleukin‐23, through two years: Results from a phase III …

IB McInnes, P Rahman, AB Gottlieb… - Arthritis & …, 2022 - Wiley Online Library
Objective To assess long‐term efficacy and safety of guselkumab, an interleukin‐23 p19
subunit (IL‐23p19) inhibitor, in patients with active psoriatic arthritis (PsA) from the phase III …

Efficacy of guselkumab on axial involvement in patients with active psoriatic arthritis and sacroiliitis: a post-hoc analysis of the phase 3 DISCOVER-1 and DISCOVER …

PJ Mease, PS Helliwell, DD Gladman… - The Lancet …, 2021 - thelancet.com
Background Guselkumab was efficacious in reducing signs and symptoms of psoriatic
arthritis in the phase 3 DISCOVER-1 and DISCOVER-2 studies. We aimed to evaluate the …

Efficacy and safety of guselkumab, an interleukin‐23p19–specific monoclonal antibody, through one year in biologic‐naive patients with psoriatic arthritis

IB McInnes, P Rahman, AB Gottlieb… - Arthritis & …, 2021 - Wiley Online Library
Objective Guselkumab, a human monoclonal antibody specific to interleukin‐23p19,
demonstrated efficacy and safety versus placebo through week 24 of the phase III …