Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05044234 · ClinicalTrials.gov registry record · Phase 2

A Study to Assess Adverse Events and Disease Activity With Cedirogant (ABBV-157) in Adult Participants With Moderate to Severe Psoriasis

A Phase 2 study, sponsored by AbbVie.

Terminated
Registry status
Phase 2
Development phase
156
Enrollment target

NCT05044234 is a Phase 2 study that was terminated before completion, run by AbbVie. The registered enrollment target is 156 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05044234, a Phase 2 study, was terminated before completion, sponsored by AbbVie.

TERMINATED
Registry status
Phase 2
Development phase
156 participants
Enrollment target

Study Summary

Psoriasis is a chronic disease characterized by marked inflammation and thickening of the skin that results in thick, scaly skin plaques. This study assessed how safe and effective cedirogant (ABBV-157) was compared to placebo in adult participants with moderate to severe psoriasis. Efficacy and safety-related measurements assessed disease activity in participants with plaque psoriasis. Cedirogant (ABBV-157) is an investigational drug being developed for the treatment of chronic plaque psoriasis. Participants were put into 1 of 4 groups, called treatment arms and each group received a different treatment. There was a 1 in 4 chance that participants were assigned to placebo. Participants received oral daily doses of cedirogant or placebo capsules for 16 weeks. There may have been a higher burden for participants in this study compared to usual standard of care. Participants attended regular visits per routine clinical practice. The effect of the treatment was checked by medical assessments, checking for side effects, and questionnaires.

Interventions

  • DRUG Placebo
  • DRUG Cedirogant

Trial Details

FieldValue
Enrollment Target 156 participants
Start Date 2021-11-16
Est. Completion 2022-11-30
Phase Phase 2

Sponsor

AbbVie

526 total trials

What the Registry Record Tells You About NCT05044234

The ClinicalTrials.gov registry entry for NCT05044234 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 156 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AbbVie, which has 526 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT05044234 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05044234 about?

NCT05044234 is a clinical study titled "A Study to Assess Adverse Events and Disease Activity With Cedirogant (ABBV-157) in Adult Participants With Moderate to Severe Psoriasis". Psoriasis is a chronic disease characterized by marked inflammation and thickening of the skin that results in thick, scaly skin plaques. This study assessed how safe and effective cedirogant (ABBV-157) was compared to placebo in adult participants with moderate to severe psoriasis. Efficacy and saf...

What is the current status of trial NCT05044234?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 156 participants. The study started on 2021-11-16. Estimated completion is 2022-11-30.

What interventions are being tested in trial NCT05044234?

The interventions under investigation include: Placebo (DRUG), Cedirogant (DRUG).

Who is sponsoring clinical trial NCT05044234?

This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.