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NCT04203693Completed

Observational Study of Tildrakizumab in Patients With Moderate to Severe Plaque Psoriasis in Routine Clinical Practice

Observational Study to Assess the Effectiveness, Safety Profile and Real-life Prescribing and Utilization Patterns of Tildrakizumab (Ilumetri®) in Patients With Moderate to Severe Plaque Psoriasis in Routine Clinical Practice. (SAIL)

Source: ClinicalTrials.gov · Last updated 2 Mar 2026

Brief summary (registry, in English)

The observational, non-interventional study will assess the efficacy, safety, prescription and utilization patterns of Tildrakizumab in participants with moderate to severe plaque psoriasis in routine clinical practice.

Status (registry)
Completed
Study type
Observational
Enrollment
331 (actual)
First submitted
10 Dec 2019
Start date
30 Oct 2019
Primary completion date
2 May 2024
Lead sponsor
Almirall, S.A.
Diseases
Psoriasis
NCT number
NCT04203693

What you commit to

  • Study type: Observational
  • Participants enrolled: 331
  • From 30 Oct 2019 to the primary completion date, 2 May 2024
  • 41 sites in 6 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Unable to comply with the requirements of the study or who in the opinion of the study physician should not participate in the study.
  • Participants meeting any of the exclusion criteria specified in the summary of product characteristics (SmPC) of Ilumetri®.

Who the study is looking for

  • Written informed consent form.
  • Age \>= 18years.
  • Moderate to severe chronic plaque psoriasis diagnosis.
  • Participants who have participated in Tildrakizumab (Ilumetri®) clinical trials (Cohort 1) OR participants who, according to the physician's therapeutic decision, should start the treatment with Tildrakizumab (Ilumetri®) (Cohort 2).

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (41)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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BadenAustriaUnknown status
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ViennaAustriaUnknown status
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BrusselsBelgiumUnknown status
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CharleroiBelgiumUnknown status
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GenkBelgiumUnknown status
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GhentBelgiumUnknown status
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HerstalBelgiumUnknown status
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JetteBelgiumUnknown status
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LedeBelgiumUnknown status
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LeuvenBelgiumUnknown status
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MonsBelgiumUnknown status
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AugsburgGermanyUnknown status
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BerlinGermanyUnknown status
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BochumGermanyUnknown status
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CologneGermanyUnknown status
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ErlangenGermanyUnknown status
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GreifswaldGermanyUnknown status
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HalleGermanyUnknown status
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HamburgGermanyUnknown status
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KielGermanyUnknown status
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KielGermanyUnknown status
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LübeckGermanyUnknown status
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MerzigGermanyUnknown status
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MünchenGermanyUnknown status
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OberurselGermanyUnknown status
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QuedlinburgGermanyUnknown status
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NiceFranceUnknown status
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PoitiersFranceUnknown status
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ArezzoItalyUnknown status
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BresciaItalyUnknown status
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CataniaItalyUnknown status
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FlorenceItalyUnknown status
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GenovaItalyUnknown status
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LecceItalyUnknown status
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ModenaItalyUnknown status
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RomaItalyUnknown status
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RomaItalyUnknown status
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RomaItalyUnknown status
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RomaItalyUnknown status
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RozzanoItalyUnknown status
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BredaNetherlandsUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.