Title : 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.

Pub. Date : 2018 Nov

PMID : 29855175






4 Functional Relationships(s)
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1 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 interleukin 17A Homo sapiens
2 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 interleukin 17A Homo sapiens
3 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 interleukin 17A Homo sapiens
4 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 interleukin 17A Homo sapiens