Mirikizumab

drug
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Also known as LY-3074828LY3074828Mirikizumab-mrkzOmvoh

Summary

Mirikizumab (CHEMBL3990014) is an approved antibody (ATC L04AC24); indicated across 5 conditions including crohn disease and ulcerative colitis.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Antibody
  • ATC class: L04AC24
  • Indications: 5 conditions
  • Clinical trials: 39

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL3990014
NameMirikizumab
TypeAntibody
Max phase4
ATCL04AC24

Also known as: LY-3074828, LY3074828, Mirikizumab, Mirikizumab-mrkz, Omvoh, MIRIKIZUMAB

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

5 indications (3 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
Crohn disease4MONDO:0005011EFO:0000384
ulcerative colitis4MONDO:0005101EFO:0000729
immune system disorder4MONDO:0005046EFO:0000540
psoriasis3MONDO:0005083EFO:0000676
inflammatory bowel disease3MONDO:0005265EFO:0003767

Clinical trials

Total trials: 39.

Phase distribution

PhaseTrials
PHASE115
PHASE312
PHASE26
PHASE45
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06997965PHASE4NOT_YET_RECRUITINGOpen-label Single-arm Study to Assess the Efficacy of Mirikizumab in Patients With Inflammatory Strictures Due to CD
NCT07059130PHASE4NOT_YET_RECRUITINGEvaluating the Efficacy and Safety of Mirikizumab in Adults Over 60 With Moderate to Severe Crohn’s Disease and Ulcerative Colitis
NCT07235904PHASE4RECRUITINGEfficacy of Top-down Therapy With Mirikizumab Versus Standard of Care With Azathioprine in Patients With Newly Diagnosed Moderate-to-severe Ulcerative Colitis
NCT07612267PHASE4NOT_YET_RECRUITINGA Study to Measure Mirikizumab Levels in Breast Milk of Lactating Participants Receiving Mirikizumab Therapeutically for an Approved Indication
NCT06626165PHASE4COMPLETEDAssociation Between Effectiveness of Mirikizumab and UC Patients With High Neutrophilic Infiltration in Epithelium of the Colonic Mucosa
NCT03519945PHASE3ACTIVE_NOT_RECRUITINGA Study to Evaluate the Long-Term Efficacy and Safety of Mirikizumab in Participants With Moderately to Severely Active Ulcerative Colitis (LUCENT 3)
NCT04232553PHASE3ACTIVE_NOT_RECRUITINGA Long-term Extension Study of Mirikizumab (LY3074828) in Participants With Crohn’s Disease
NCT04844606PHASE3RECRUITINGA Master Protocol (AMAZ): A Study of Mirikizumab (LY3074828) in Pediatric Participants With Ulcerative Colitis or Crohn’s Disease (SHINE-ON)
NCT05509777PHASE3RECRUITINGA Study of Mirikizumab (LY3074828) in Pediatric Participants With Crohn’s Disease
NCT05767021PHASE3ACTIVE_NOT_RECRUITINGA Study of Mirikizumab (LY3074828) in Participants With Moderately to Severely Active Ulcerative Colitis
NCT06937086PHASE3RECRUITINGMirikizumab Administered at the Same Time as Tirzepatide in Adult Participants With Moderately to Severely Active Ulcerative Colitis and Obesity or Overweight: Phase 3b Study
NCT06937099PHASE3RECRUITINGMirikizumab and Tirzepatide Administered in Adult Participants With Moderately to Severely Active Crohn’s Disease and Obesity or Overweight
NCT03482011PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Mirikizumab (LY3074828) in Participants With Moderate-to-Severe Plaque Psoriasis
NCT03518086PHASE3COMPLETEDAn Induction Study of Mirikizumab in Participants With Moderately to Severely Active Ulcerative Colitis (LUCENT 1)
NCT03535194PHASE3COMPLETEDA Study to Assess if Mirikizumab is Effective and Safe Compared to Secukinumab and Placebo in Moderate to Severe Plaque Psoriasis (OASIS-2)
NCT03556202PHASE3TERMINATEDA Long-term Study to Evaluate Safety and Maintenance of Treatment Effect of LY3074828 in Participants With Moderate-to-Severe Plaque Psoriasis (OASIS-3)
NCT03926130PHASE3COMPLETEDA Study of Mirikizumab (LY3074828) in Participants With Crohn’s Disease
NCT06598943PHASE2RECRUITINGA Study of Eltrekibart and Mirikizumab in Adult Patients With Moderately to Severely Active Ulcerative Colitis
NCT07186101PHASE2RECRUITINGLY4268989 (MORF-057) Co-Administered With Mirikizumab in Adults With Moderately to Severely Active Ulcerative Colitis:
NCT02589665PHASE2COMPLETEDA Study of Mirikizumab (LY3074828) in Participants With Moderate to Severe Ulcerative Colitis
NCT02891226PHASE2COMPLETEDA Study of Mirikizumab (LY3074828) in Participants With Active Crohn’s Disease
NCT02899988PHASE2COMPLETEDA Study of Mirikizumab (LY3074828) in Participants With Moderate to Severe Plaque Psoriasis
NCT04004611PHASE2COMPLETEDA Study of Mirikizumab (LY3074828) in Children and Teenagers With Ulcerative Colitis (UC)
NCT07446101PHASE1RECRUITINGA Study of Mirikizumab Solution (LY3074828) in Healthy Participants
NCT03053622PHASE1COMPLETEDA Study of Mirikizumab (LY3074828) Injection in Healthy Participants
NCT03188510PHASE1COMPLETEDA Study of Two Different Formulations of LY3074828 in Healthy Participants
NCT03220126PHASE1COMPLETEDA Study to Assess the Amount of LY3074828 That Gets Into the Body When Given With LY9999QS, in Healthy Participants
NCT03456713PHASE1COMPLETEDA Study of LY3074828 in Healthy Participants
NCT03662100PHASE1COMPLETEDA Study of Two Formulations of LY3074828 in Healthy Participants
NCT03718884PHASE1COMPLETEDA Study of Mirikizumab in Participants With Plaque Psoriasis
NCT03748940PHASE1COMPLETEDStudy of LY3074828 in Healthy Participants
NCT03886948PHASE1COMPLETEDA Study of Injections of LY3074828 in Healthy Participants
NCT04548219PHASE1COMPLETEDA Study to Compare Two Different Formulations of Mirikizumab in Healthy Participants
NCT04607733PHASE1COMPLETEDA Study of Mirikizumab in Healthy Participants
NCT05069896PHASE1COMPLETEDA Study to Compare Two Formulations of Mirikizumab (LY3074828) in Healthy Participants
NCT05515601PHASE1COMPLETEDA Bioequivalence Study of Mirikizumab (LY3074828) in Healthy Participants
NCT05644353PHASE1COMPLETEDA Bioequivalence Study of Mirikizumab (LY3074828) Solution in Healthy Participants
NCT06475729PHASE1COMPLETEDA Bioequivalence Study of Citrate Free Mirikizumab (LY3074828) in Healthy Participants
NCT06249555Not specifiedRECRUITINGVOICE-Early Response to Vedolizumab and IL-23 Antagonists in Participants With Crohn’s Disease: A Prospective Observational Study

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).