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J6Z-MC-IIBD - A Master Protocol for Phase 2, Randomized, Controlled Studies of Multiple Interventions for the Treatment of Adults With Moderately to Severely Active Ulcerative Colitis or Crohn’s Disease J6Z-MC-CD01 - A Phase 2, Multicenter, Randomized, Open-Label, Active-Controlled Study to Investigate LY4395089/Mirikizumab Co-administration Compared with Mirikizumab in Adults with Moderately to Severely Active Crohn’s Disease

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-524112-11-00
Enrollment
7
Registered
2026-06-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

J6Z-MC-IIBD - Colitis, Ulcerative Crohn Disease J6Z-MC-CD01 - Crohn Disease

Brief summary

J6Z-MC-CD01 - Percentage of Participants with Crohn’s Disease who Achieve Endoscopic Response, J6Z-MC-IIBD - The proportion of participants who achieve the following at Week 12 of Study Period 1: UC: endoscopic improvement CD: endoscopic response

Interventions

DRUGMirikizumab

Sponsors

Eli Lilly & Co.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
J6Z-MC-CD01 - Percentage of Participants with Crohn’s Disease who Achieve Endoscopic Response, J6Z-MC-IIBD - The proportion of participants who achieve the following at Week 12 of Study Period 1: UC: endoscopic improvement CD: endoscopic response

Outcome results

None listed

Source: EU CTIS · Data processed: Jun 12, 2026