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New study tests if early drug use can stop psoriasis from becoming chronic

NCT ID NCT06742333

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether early use of the drug bimekizumab can delay or prevent chronic inflammation in people with mild plaque psoriasis. 40 adults with recent-onset or long-standing mild psoriasis will receive either bimekizumab injections or a topical steroid cream. The goal is to see if bimekizumab can keep the disease from becoming a long-term problem.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

About 40 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jul 2025

Expected to finish

Jan 2029

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 45 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Men and women 2. ≥ 18 and \<45 years 3. Plaque psoriasis without psoriatic arthritis 4. Patients with mild psoriasis PASI \>2 and \<6 5. Patient with at least one lesion on the elbows, or the knees, or the lower back to be recorded as target lesion (additional lesions in other areas on top are allowed) 6. Disease duration less than 6 months (short duration psoriasis) or \>2 years (long duration psoriasis) 7. The psoriasis lesions should not having being treated by any topical treatment for at least 2 weeks 8. For women of childbearing potential, an effective contraception (estroprogestative pill, contraceptive implant, IUD, condoms or tubal ligation) should be used for more than one month before the inclusion in the study. A urine pregnancy test (βHCG in urines) will be performed. Thus, a woman who is permanently sterile and therefore unable to procreate should not be subjected to pregnancy tests. Women who are sexually abstinent are not requested to use a contraception. However, they must agree to take one if they want to become sexually active. 9. Affiliation to a social security system 10. Signed informed consent 11. Patient willing and able to attend all study visits Exclusion Criteria: 1. Pregnant or breast-feeding women. Or women who plan to get pregnant during the study duration. 2. Concomitant use of topical or systemic immunosuppressive medication or steroids in the past 12 weeks 3. Personal history of skin cancer 4. Personal history of cancer of less than 5 years 5. Patients with active infection 6. Abnormal blood counts (neutrophils \<1500/mm3 and platelets \<150 000/mm3) and/or positive HIV, HVB and HVC testing at screening. 7. Patients with personal history of keloid scars 8. Patients with personal history of hypersentitivity to xylocaine and/or adrenalin 9. Vulnerable people: minors, adult under guardianship or deprived of freedom 10. Participants in other clinical therapeutic studies involving a drug that could interfere with the present evaluation

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    7 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • CHITS

    RECRUITING

    Toulon, 83000, France

  • CHU Saint-Etienne

    RECRUITING

    Saint-Etienne, 42055, France

  • CHU de Nice - Hôpital de l'Archet

    RECRUITING

    Nice, Alpes-Maritimes, 06200, France

  • Cabinet Dermatologie Dr RUER

    RECRUITING

    Martigues, 13500, France

  • Hôpital Edouard Herriot

    RECRUITING

    Lyon, 69003, France

  • Hôpital Saint-Joseph

    RECRUITING

    Marseille, 13005, France

  • Médipole Villeurbanne

    ENROLLING_BY_INVITATION

    Villeurbanne, 69100, France

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Other studies related to the condition(s) this trial covers.