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The trial is taking place at:
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Arlington Dermatology | Rolling Meadows, IL

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A Study About How Well TAK-279 Works and Its Safety in Participants With Moderate-to-severe Plaque Psoriasis During 52 Weeks of Treatment

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Takeda

Status and phase

Enrolling
Phase 3

Conditions

Plaque Psoriasis

Treatments

Drug: TAK-279
Drug: Apremilast
Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT06088043
TAK-279-3001
2023-505841-22 (Other Identifier)

Details and patient eligibility

About

The main aim of this study is to show how well TAK-279 reduces the skin plaques compared to placebo, in participants with moderate-to-severe plaque psoriasis. Participants will be assigned to one of the 3 study treatments (TAK-279, apremilast (an approved treatment), or a placebo). Participants will be in the study for up to 56 weeks.

Full description

The drug being tested in this study is called TAK-279. TAK-279 is being tested to treat people with moderate to severe plaque psoriasis.

The study will enroll approximately 600 patients. Participants will be randomly assigned (by chance, like flipping a coin) to one of the following treatment groups in a ratio of 3:1:1 to receive TAK-279, placebo, or apremilast which will remain undisclosed to the participant and study doctor during the study (unless there is an urgent medical need):

TAK-279 Placebo Apremilast

This multi-center trial will be conducted worldwide. Participants will go through a screening process to make sure they meet the rules for taking part in the study. This will take up to 35 days. If participants meet the study rules, they will be treated for up to 52 weeks (1 year). There will be a safety follow-up visit 4 weeks after their last day of treatment.

Enrollment

600 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Plaque psoriasis for at least 6 months.
  2. Moderate to severe disease.
  3. Candidate for phototherapy or systemic therapy.

Exclusion criteria

  1. Other forms of psoriasis.
  2. History of recent infection.
  3. Prior exposure to TAK-279 or active comparator.

Other protocol defined inclusion/exclusion criteria apply.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

600 participants in 3 patient groups, including a placebo group

TAK-279
Experimental group
Treatment:
Drug: TAK-279
Placebo
Placebo Comparator group
Treatment:
Drug: Placebo
Apremilast
Active Comparator group
Treatment:
Drug: Apremilast

Trial contacts and locations

54

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Central trial contact

Takeda Contact

Data sourced from clinicaltrials.gov

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