Drug class
Interleukin 23 Antagonists
Interleukin-23 antagonists are a therapeutic class of targeted biologic agents designed to disrupt the proinflammatory signaling pathways driven by interleukin-23. Read more about Interleukin 23 Antagonists
13 drugs in this class 4 manufacturers
Drugs in Interleukin 23 Antagonists
SKYRIZI PEN (risankizumab-rzaa)
TREMFYA PEN (guselkumab)
OMVOH MIRIKIZUMAB (docusate sodium)
TREMFYA (guselkumab)
TREMFYA (guselkumab)
ILUMYA (tildrakizumab-asmn)
SKYRIZI (risankizumab-rzaa)
OMVOH (mirikizumab-mrkz)
Interleukin-23 antagonists are a therapeutic class of targeted biologic agents designed to disrupt the proinflammatory signaling pathways driven by interleukin-23.
These agents, primarily monoclonal antibodies such as guselkumab, risankizumab, tildrakizumab, and mirikizumab, selectively bind to the unique p19 subunit of interleukin-23, thereby preventing its interaction with cell-surface receptors and inhibiting downstream inflammatory cascades, particularly the activation and differentiation of T-helper 17 cells.
Clinically, this class is primarily utilized to treat chronic immune-mediated inflammatory disorders, including moderate-to-severe plaque psoriasis, active psoriatic arthritis, and inflammatory bowel diseases such as Crohn's disease and ulcerative colitis.
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nih.gov
Interleukin-23 antagonists are a therapeutic class of targeted biologic agents designed to disrupt the proinflammatory signaling pathways driven by interleukin-23 These agents, primarily monoclonal antibodies such as guselkumab, risankizumab, tildrakizumab, and mirikizumab, selectively bind to the unique p19 subunit of interleukin-23, thereby preventing its interaction with cell-surface receptors and inhibiting downstream inflammatory cascades, particularly the activation and differentiation of ...
-
nih.gov
Interleukin-23 antagonists are a therapeutic class of targeted biologic agents designed to disrupt the proinflammatory signaling pathways driven by interleukin-23 These agents, primarily monoclonal antibodies such as guselkumab, risankizumab, tildrakizumab, and mirikizumab, selectively bind to the unique p19 subunit of interleukin-23, thereby preventing its interaction with cell-surface receptors and inhibiting downstream inflammatory cascades, particularly the activation and differentiation of ...
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fda.gov
These agents, primarily monoclonal antibodies such as guselkumab, risankizumab, tildrakizumab, and mirikizumab, selectively bind to the unique p19 subunit of interleukin-23, thereby preventing its interaction with cell-surface receptors and inhibiting downstream inflammatory cascades, particularly the activation and differentiation of T-helper 17 cells Clinically, this class is primarily utilized to treat chronic immune-mediated inflammatory disorders, including moderate-to-severe plaque psorias...
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fda.gov
These agents, primarily monoclonal antibodies such as guselkumab, risankizumab, tildrakizumab, and mirikizumab, selectively bind to the unique p19 subunit of interleukin-23, thereby preventing its interaction with cell-surface receptors and inhibiting downstream inflammatory cascades, particularly the activation and differentiation of T-helper 17 cells Clinically, this class is primarily utilized to treat chronic immune-mediated inflammatory disorders, including moderate-to-severe plaque psorias...
-
fda.gov
These agents, primarily monoclonal antibodies such as guselkumab, risankizumab, tildrakizumab, and mirikizumab, selectively bind to the unique p19 subunit of interleukin-23, thereby preventing its interaction with cell-surface receptors and inhibiting downstream inflammatory cascades, particularly the activation and differentiation of T-helper 17 cells Clinically, this class is primarily utilized to treat chronic immune-mediated inflammatory disorders, including moderate-to-severe plaque psorias...
-
fda.gov
These agents, primarily monoclonal antibodies such as guselkumab, risankizumab, tildrakizumab, and mirikizumab, selectively bind to the unique p19 subunit of interleukin-23, thereby preventing its interaction with cell-surface receptors and inhibiting downstream inflammatory cascades, particularly the activation and differentiation of T-helper 17 cells Clinically, this class is primarily utilized to treat chronic immune-mediated inflammatory disorders, including moderate-to-severe plaque psorias...
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