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NCT06973291 · ClinicalTrials.gov registry record · Phase 3

A Study Comparing Zasocitinib (TAK-279) With Deucravacitinib in Adults With Plaque Psoriasis

A Phase 3 study of Plaque Psoriasis, sponsored by Takeda.

Active
Registry status
Phase 3
Development phase
606
Enrollment target
20
Study locations

NCT06973291: Active Phase 3 study of Plaque Psoriasis, sponsored by Takeda.

NCT06973291 is a Phase 3 study of Plaque Psoriasis that is active but no longer recruiting, run by Takeda. The registered enrollment target is 606 participants, above the 402-participant average among 45 other Plaque Psoriasis trials with a reported enrollment target (51% higher). The trial reports 20 study locations across 13 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06973291, a Phase 3 study of Plaque Psoriasis, is active but no longer recruiting, sponsored by Takeda.

ACTIVE NOT RECRUITING
Registry status
Phase 3
Development phase
606 participants
Enrollment target
20
Study locations

Study Summary

The main aim of this study is to assess whether zasocitinib works better than deucravacitinib in treating participants with moderate-to-severe plaque psoriasis. Participants will take one tablet daily of either zasocitinib or a matching placebo, along with one capsule daily of either over-encapsulated deucravacitinib or a matching placebo, for a duration of 16 weeks. Participants will be in the study for up to 25 weeks, which includes screening period of up to 35 days, a 16-week treatment period, and a 4-week safety follow-up period.

Primary Outcome

PASI is a measure of the average erythema, induration/infiltration, and desquamation/scaling of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72 (less than or equal to \[\<=\] 3 representing mild disease, greater than or equal to \[\>=3\] to 15 representing moderate disease, and \>=15 indicating severe disea

Conditions Studied

Interventions

  • DRUG Deucravacitinib
  • DRUG Zasocitinib
  • DRUG Placebo to match zasocitinib
  • DRUG Placebo to match deucravacitinib

Study Locations (20)

California

  • Zenith Research, Inc. - Beverly Hills
  • First OC Dermatology Research Inc. - Fountain Valley
  • UNISON Clinical Trials (Shahram Jacobs md inc.) - Sherman Oaks

Florida

  • Direct Helpers Research Center - Hialeah
  • San Marcus Research Clinic Inc - Miami Lakes
  • Advanced Clinical Research Institute - Tampa

Arkansas

  • Johnson Dermatology - Fort Smith
  • Burke Pharmaceutical Research - Hot Springs

Connecticut

  • Central Connecticut Dermatology, PLLC - Cromwell
  • Yale University School of Medicine - New Haven

Illinois

  • Arlington Dermatology - Rolling Meadows
  • Endeavor Health Clinical Trials - Skokie

Indiana

  • Dawes Fretzin Clinical Research Group, LLC - Indianapolis

Maryland

  • Lawrence J Green, MD LLC - Rockville

Michigan

  • Henry Ford Health System - Detroit

Trial Details

FieldValue
Enrollment Target 606 participants
Start Date 2025-07-09
Est. Completion 2026-07-03
Phase Phase 3
Takeda

408 total trials

What the registry record for NCT06973291 still lists

NCT06973291 is an interventional study that assigns participants to a tested intervention. The registered 606 participants enrollment target is mid-sized for trials with a published cap, above the 402-participant average among 45 other Plaque Psoriasis trials with a reported enrollment target (51% higher).

The record links to 1 condition, with Plaque Psoriasis appearing as the primary indexed condition, and to 4 interventions - of which Deucravacitinib is the first listed.

NCT06973291 names 20 study sites across 13 states, led by California, Florida, Arkansas.

Frequently Asked Questions

What is clinical trial NCT06973291 about?

NCT06973291 is a clinical study titled "A Study Comparing Zasocitinib (TAK-279) With Deucravacitinib in Adults With Plaque Psoriasis". The main aim of this study is to assess whether zasocitinib works better than deucravacitinib in treating participants with moderate-to-severe plaque psoriasis. Participants will take one tablet daily of either zasocitinib or a matching placebo, along with one capsule daily of either over-encapsula...

What is the current status of trial NCT06973291?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 606 participants. The study started on 2025-07-09. Estimated completion is 2026-07-03.

What conditions does trial NCT06973291 study?

This clinical trial studies the following conditions: Plaque Psoriasis.

What interventions are being tested in trial NCT06973291?

The interventions under investigation include: Deucravacitinib (DRUG), Zasocitinib (DRUG), Placebo to match zasocitinib (DRUG), Placebo to match deucravacitinib (DRUG).

Who is sponsoring clinical trial NCT06973291?

This trial is sponsored by Takeda, which has 408 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06973291 being conducted?

This trial has 20 study locations across Arkansas, California, Connecticut, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Plaque Psoriasis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06973291's enrollment target sits among peer trials

606 12th of 45 higher than 34 of 45 other Plaque Psoriasis trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Plaque Psoriasis trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06973291, the US trial registry maintained by the National Library of Medicine. NCT06973291 (mid enrollment · wide site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.