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A Study to Learn About the Safety, Effects and Pharmacokinetics of Study Medication (PF-07054894) for the Treatment of Ulcerative Colitis

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NCT05549323

Sponsored by Pfizer (industry) · PFE — their whole pipeline →.

Phase
Phase 1
Status
Terminated
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
44actual
Sites
17
Countries
Germany, Poland, United States

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

Why the sponsor stopped it

The study was terminated due to business decision. The decision to terminate the trial was not based on any safety concerns associated with PF-07054894.

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-11-07actualWhen the study began enrolling
Primary completion2025-11-11actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-11-11actualThe whole study's end, after follow-up
First posted2022-09-22actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-02-25actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Ulcerative Colitis

Interventions

  • Drug: PF-07054894
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Part A: Proportion of participants achieving clinical remission at Week 12 in participants with moderate to severe UC.
measured Week 12
Part B: Percent change from baseline in the mMS in participants with mild to moderate UC.
measured Week 12

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