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Study of XmAb942 in Healthy Participants and Participants With Ulcerative Colitis

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NCT06619990 · readout ≤ 620 d

Sponsored by Xencor, Inc. (industry) · XNCR — their whole pipeline →.

Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
270estimated
Sites
90
Countries
Argentina, Australia, Brazil +12

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
Start2024-10-10actualWhen the study began enrolling
Primary completionApr 2028estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJan 2029estimatedThe whole study's end, after follow-up
First posted2024-10-01actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-24actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Ulcerative Colitis (UC)

Interventions

  • Biological: XmAb942
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Incidence, nature, and severity of treatment emergent adverse events (TEAEs) and serious adverse events (SAEs) of XmAb942 in healthy volunteers (Part A)
measured 20 weeks
Incidence, nature, and severity of treatment emergent adverse events (TEAEs) and serious adverse events (SAEs) of XmAb942 in healthy volunteers (Part B)
measured 28 weeks
Clinical remission based on modified mayo score (MMS), defined as MMS ≤ 2 with Mayo endoscopic score (MES) of 1, rectal bleeding subscore (RBS) of 0, and stool frequency subscore (SFS) of 0-1.
measured 12 weeks

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