PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 28681115-5 2017 Results have already been obtained from phase 3 studies for tofacitinib, a Janus kinase inhibitor as well as for the antibodies brodalumab, bimekizumab and ABT-122 that inhibit the IL17-signaling pathway. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 156-159 interleukin 17A Homo sapiens 181-185 29364523-1 2018 ABT-122 is an IgG1 dual-variable domain immunoglobulin that specifically blocks TNF-alpha and IL-17A. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 0-3 interleukin 17A Homo sapiens 94-100 29855172-9 2018 CONCLUSION: Over the 12-week study period, dual inhibition of TNF and IL-17A with ABT-122 produced a safety profile consistent with that of adalimumb used for inhibition of TNF alone. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 82-85 interleukin 17A Homo sapiens 70-76 29855175-0 2018 Phase II Study of ABT-122, a Tumor Necrosis Factor- and Interleukin-17A-Targeted Dual Variable Domain Immunoglobulin, in Patients With Psoriatic Arthritis With an Inadequate Response to Methotrexate. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 18-21 interleukin 17A Homo sapiens 56-71 29855175-1 2018 OBJECTIVE: To investigate the safety and efficacy of ABT-122, a tumor necrosis factor (TNF)- and interleukin-17A (IL-17A)-targeted dual variable domain immunoglobulin, in patients with active psoriatic arthritis (PsA) who have experienced an inadequate response to methotrexate. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 53-56 interleukin 17A Homo sapiens 97-112 29855175-1 2018 OBJECTIVE: To investigate the safety and efficacy of ABT-122, a tumor necrosis factor (TNF)- and interleukin-17A (IL-17A)-targeted dual variable domain immunoglobulin, in patients with active psoriatic arthritis (PsA) who have experienced an inadequate response to methotrexate. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 53-56 interleukin 17A Homo sapiens 114-120 30032191-0 2018 Dual inhibition of tumour necrosis factor and interleukin-17A with ABT-122: open-label long-term extension studies in rheumatoid arthritis or psoriatic arthritis. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 67-70 interleukin 17A Homo sapiens 46-61 29855175-10 2018 CONCLUSION: Dual neutralization of TNF and IL-17A with ABT-122 had efficacy and safety that was similar to, and not broadly differentiated from, that of adalimumab over a 12-week treatment course in patients with PsA. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 55-58 interleukin 17A Homo sapiens 43-49 28941216-0 2017 Safety, Tolerability, and Pharmacodynamics of ABT-122, a Tumor Necrosis Factor- and Interleukin-17-Targeted Dual Variable Domain Immunoglobulin, in Patients With Rheumatoid Arthritis. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 46-49 interleukin 17A Homo sapiens 84-98 28941216-2 2017 ABT-122 is a novel dual variable domain immunoglobulin that selectively and simultaneously targets human TNF and IL-17A. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 0-3 interleukin 17A Homo sapiens 113-119 28941216-13 2017 CONCLUSION: The results of these phase I studies suggest that dual neutralization of TNF and IL-17 with ABT-122 has characteristics acceptable for further exploration of therapeutic potential in TNF- and IL-17A-driven immune-mediated inflammatory diseases. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 104-107 interleukin 17A Homo sapiens 93-98 28941216-13 2017 CONCLUSION: The results of these phase I studies suggest that dual neutralization of TNF and IL-17 with ABT-122 has characteristics acceptable for further exploration of therapeutic potential in TNF- and IL-17A-driven immune-mediated inflammatory diseases. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 104-107 interleukin 17A Homo sapiens 204-210