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A Study to Evaluate MORF-057 in Adults With Moderately to Severely Active UC

← catalyst calendar

NCT05611671 · results posted

Sponsored by Morphic Therapeutic, Inc. (A Wholly Owned Subsidiary of Eli Lilly and Company) (industry) · LLY — their whole pipeline →.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
280actual
Sites
102
Countries
Australia, Austria, Bulgaria +18

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-11-21actualWhen the study began enrolling
Primary completion2024-11-28actualThe date the last participant is measured for the primary outcome — the readout window
Study completionAug 2026estimatedThe whole study's end, after follow-up
First posted2022-11-10actualWhen this record first appeared on the registry
Results posted2025-12-15actualWhen the sponsor posted results to the registry
Record updated2025-12-15actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Inflammatory Bowel Diseases
  • Colitis, Ulcerative

Interventions

  • Drug: MORF-057 — also filed as LY4268989
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Percentage of Participants in Clinical Remission as Determined Using the Modified Mayo Clinic Score (mMCS)
measured Week 12

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2025-03-27 · 2.1 MB · Prot_000.pdf
Statistical Analysis Planposted 2024-09-18 · 761 KB · SAP_001.pdf

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