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A Study of LY4100511 (DC-853) in Adult Participants With Moderate-to-Severe Plaque Psoriasis

← catalyst calendar

NCT06602219 · results posted

Sponsored by DICE Therapeutics, Inc., a wholly owned subsidiary of Eli Lilly and Company (industry) · LLY — their whole pipeline →.

Phase
Phase 2
Status
Completed
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
222actual
Sites
58
Countries
Canada, Czechia, Germany +4

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
Start2024-10-25actualWhen the study began enrolling
Primary completion2025-07-24actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-09-04actualThe whole study's end, after follow-up
First posted2024-09-19actualWhen this record first appeared on the registry
Results posted2026-08-18actualWhen the sponsor posted results to the registry
Record updated2026-08-18actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Plaque Psoriasis

Interventions

  • Drug: LY4100511
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Percentage of Participants Achieving ≥75% Reduction From Baseline in Psoriasis Area and Severity Index (PASI-75) at Week 12 (LY4100511 Versus Placebo)
measured Week 12

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2025-03-18 · 1.1 MB · Prot_000.pdf
Statistical Analysis Planposted 2025-06-20 · 968 KB · SAP_001.pdf

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