Last reviewed · How we verify

Mirikizumab - IV

Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives · FDA-approved active Small molecule

Mirikizumab is a monoclonal antibody that selectively inhibits IL-23 signaling by binding to the p19 subunit of IL-23, reducing inflammatory responses in the gut.

Mirikizumab is a monoclonal antibody that selectively inhibits IL-23 signaling by binding to the p19 subunit of IL-23, reducing inflammatory responses in the gut. Used for Ulcerative colitis, Crohn's disease.

At a glance

Generic nameMirikizumab - IV
Also known asLY3074828
SponsorGroupe d'Etude Therapeutique des Affections Inflammatoires Digestives
Drug classIL-23 inhibitor monoclonal antibody
TargetIL-23 p19 subunit
ModalitySmall molecule
Therapeutic areaImmunology / Gastroenterology
PhaseFDA-approved

Mechanism of action

IL-23 is a key cytokine driving Th17 cell differentiation and intestinal inflammation. By blocking the p19 subunit of IL-23, mirikizumab prevents IL-23-mediated immune activation while preserving IL-12 signaling, which is important for antimicrobial immunity. This selective IL-23 inhibition reduces pathogenic T cell responses in inflammatory bowel disease.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: