Study completion date changed from estimate of Aug 2026 to Sep 21, 2026
Eligibility criteria expanded, about 13 words
Secondary endpoints: details revised at 1 of 1 entry
Site details revised at 9 of 102 sites
NotableResults first posted: Dec 15, 2025
Primary endpoint revised
Enrollment target: 282 to 280
Secondary endpoint revised
v33
MinorStudy sites revised (102)v32
NotableLead sponsor: Morphic Therapeutic, Inc to Morphic Therapeutic, Inc. (A Wholly Owned Subsidiary of Eli Lilly and Company)
Study sites: 125 to 102
Start date: Oct 31, 2022 to Nov 21, 2022
v31
MinorEnrollment target: estimated 280 to confirmed 282
Primary completion date changed from estimate of Dec 2024 to Nov 28, 2024
v30
Show 28 earlier versionsHide 28 earlier versions
MinorTrial status: Recruiting to Active, Not Recruiting
Study sites: 137 to 125
Primary completion date: May 2025 to Dec 2024
Study completion date: Jul 2025 to Aug 2026
v29
MinorSite details revised at 2 of 137 sitesv28
MinorSite details revised at 1 of 137 sitesv27
MinorStudy sites: 24 to 137v26
MinorSite details revised at 1 of 24 sitesv25
MinorStudy sites: 23 to 24v24
MinorSite details revised at 3 of 23 sitesv23
MinorStudy sites: 22 to 23v22
MinorStudy sites: 21 to 22v21
MinorStudy sites: 20 to 21v20
MinorStudy sites: 19 to 20v19
MinorStudy sites: 18 to 19v18
MinorStudy sites: 17 to 18v17
MinorStudy sites: 18 to 17v16
MinorStudy sites: 17 to 18v15
MinorRe-verified, no change to tracked fieldsv14
MinorStudy sites: 16 to 17v13
MinorStudy sites: 15 to 16v12
MinorStudy sites: 14 to 15v11
MinorStudy sites: 13 to 14v10
MinorStudy sites: 12 to 13v9
MinorStudy sites: 11 to 12v8
MinorStudy sites: 10 to 11v7
MinorStudy sites: 9 to 10v6
MinorStudy sites: 8 to 9v5
MinorStudy sites: 7 to 8v4
MinorStudy sites: 2 to 7v3
MinorStudy title shortened, about 2 wordsv2
MinorStudy First Submitted
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This is a Phase 2b randomized, double-blind, placebo-controlled study to evaluate the safety and efficacy of three active dose regimens of MORF-057 in adult patients with moderately to severely active Ulcerative Colitis (UC).