NotablePrimary completion pushed from Apr 2027 to Sep 2028
MinorEligibility criteria expanded, about 14 words
Site details revised at 4 of 46 sites
MinorSite details revised at 1 of 46 sitesv20
MinorSite details revised at 2 of 46 sitesv19
MinorSite details revised at 2 of 46 sitesv18
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MinorSite details revised at 1 of 46 sitesv17
MinorSite details revised at 2 of 46 sitesv16
MinorPrimary completion pushed from Feb 2027 to Apr 2027
Study completion pushed from Dec 2029 to Feb 2030
Study sites: 45 to 46
v15
NotableRecruitment openedv14Show 4 more changesShow less
Enrollment increased: 360 → 460 participants
Start date changed from estimate of Apr 2026 to Apr 17, 2026
Eligibility criteria expanded, about 49 words
Site details revised at 45 of 45 sites
MinorStudy sites: 44 to 45v13
NotableStart date: Feb 2026 to Apr 2026v12
MinorStudy sites: 40 to 44v11
MinorStudy sites: 33 to 40v10
MinorStudy sites: 32 to 33v9
MinorStudy sites: 28 to 32v8
MinorStudy sites: 22 to 28v7
MinorStudy sites: 19 to 22v6
MinorStudy sites: 15 to 19v5
MinorStudy sites: 13 to 15v4
MinorStudy sites: 9 to 13v3
MinorRe-verified, no change to tracked fieldsv2
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.
The main purpose of this study is to evaluate safety and efficacy, and measure how much LY4584180 gets into the bloodstream and how long it takes the body to eliminate it in patients with previously treated blood cancers. For each participant, the study could last about 9 months or possibly longer including screening.