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Plaque PsoriasisMARCOPOLONCT01677598

A Study to Evaluate Ustekinumab in Patients With Plaque Psoriasis in Asia-Pacific Countries

An observational study of Plaque Psoriasis, run by Janssen Research & Development, LLC at 9 sites in 5 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to determine how patients use ustekinumab (label-recommended or other/missed dose interval) in Asia-Pacific countries. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Plaque Psoriasis
How many people
169 participants
Where
9 sitesin 5 countries
Study dates
2 Dec 2011to 30 Nov 2013
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients at least 18 years of age with a diagnosis of plaque psoriasis, according to the dermatologists' clinical judgment

Who may be able to join

  • Have a diagnosis of plaque psoriasis, according to the dermatologists' clinical judgment
  • Agree to initiate treatment with ustekinumab on the same day as enrollment into the study
  • Have not received anti-IL12/23 therapies within 6 months prior to enrollment into the study

Who cannot join

  • Has difficulty understanding questions posed by any of the questionnaires
  • Are currently participating in an investigational drug clinical study

Trial locations and contacts

9 sites in 5 countries.

9 sites in 5 countries

South Korea4 sites
  • Study site

    Incheon

  • Study site

    Seongnam-Si, Gyeonggi-Do

  • Study site

    Seoul

  • Study site

    Suwon

Other trials in South Korea

Malaysia2 sites
  • Study site

    Johor Bahru

  • Study site

    Pulau Pinang

Other trials in Malaysia

Indonesia1 site
  • Study site

    Jakarta Pusat

Other trials in Indonesia

Singapore1 site
  • Study site

    Singapore

Other trials in Singapore

Taiwan1 site
  • Study site

    Taipei

Other trials in Taiwan

About this study

Official title: A Study to Evaluate Ustekinumab in Clinical Practice in Patients With Plaque Psoriasis in Asia-Pacific Countries

The purpose of this study is to determine how patients use ustekinumab (label-recommended or other/missed dose interval) in Asia-Pacific countries.

Read the detailed description

This is an open-label (all people know the identity of the medication), multicenter, Phase 4, observational study (no study medication was administered during the study) designed to assess how patients will use ustekinumab (label-recommended or other/missed dose interval) in Asia-Pacific countries. The study will consist of 4 study visits which will take place over the duration of 1 year. At the first visit (ie, Week 0), eligibility for the study will be determined (it will be screening and baseline visit). At each subsequent visit (Weeks 16, 28, and 52), exposure to ustekinumab will be recorded, questionnaires for efficacy will be completed, and information about adverse events and concomitant medications will be collected. As many patient reported outcome questionnaires as possible will be administered, depending on the availability of validated translations. Safety will be assessed by monitoring of adverse events, vital signs and physical examination.

Being tested
No intervention
Keywords
Plaque Psoriasis, Ustekinumab, CNTO 1275, Asia-Pacific

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • No interventionDrug

    Also called CNTO 1275

    No intervention will be administered during study. This will be an observational study in patients using ustekinumab as label-recommended or other/missed dose interval in Asia-Pacific countries

Study groups in NCT01677598
Study groupRoleWhat they receive
Patients with plaque psoriasisPatients with plaque psoriasis using ustekinumab in Asia-Pacific countries.
Receives: Drug: No intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of psoriasis patients who use ustekinumab with label-recommended interval or other/missed dose interval

    Number of psoriasis patients who use ustekinumab with label-recommended interval or other/missed dose interval will be assessed at Weeks 0, 16, 28, 52.

    Measured: up to 52 weeks

Secondary outcomes (13)
  1. Epidemiologic characteristics of the psoriasis population

    Epidemiologic characteristics of the psoriasis patients (sex, age, race, weight height, and peak disease level) will be determined.

    Measured: Week 0

  2. Change from baseline (Week 0) in Psoriasis Area and Severity Index (PASI) score at Weeks 16, 28 and 52

    The PASI is a physician-administered assessment tool used for assessing and grading the severity of psoriatic lesions and their response to therapy. The PASI produces a numeric score that can range from 0 (no disease) to 72 (maximal disease).

    Measured: Baseline (Week 0), Weeks 16, 28 and 52

  3. Change from baseline (Week 0) in Nail Psoriasis Severity Index (NAPSI) score at Weeks 16, 28, and 52

    NAPSI is used for assessing and grading the severity of nail psoriasis. Each nail is divided with imaginary horizontal and longitudinal lines into quadrants. Each nail is given a score for nail matrix psoriasis (0 to 4) and nail bed psoriasis (0 to 4) depending on the presence of any of the features of nail psoriasis in the 4 quadrants as: 0 (none), 1 (present in 1/4 nail), 2 (2/4), 3 (3/4), and 4 (4/4). Each nail gets a matrix score and a nail bed score, the total of which is the score for that nail (0 to 8). Each nail is evaluated, and the sum of all the nails is the total NAPSI score. The sum of the scores from all nails is 0 to 160 (Both finger and toe nails are included). Higher scores indicate worsening.

    Measured: Baseline, Weeks 16, 28 and 52

  4. Change from baseline in EuroQol 5 Dimensional Questionnaire (EQ-5D) index score and EQ visual analog scale (VAS) at Weeks 16, 28, and 52

    The EQ-5D (EuroQol Group) is a validated generic measure of quality of life which usually requires less than 1 minute to complete (eg, the questionnaire may have questions about mobility, self care, usual activities, pain/discomfort and anxiety/depression.

    Measured: Baseline, Weeks 16, 28 and 52

  5. Change from baseline (Week 0) in Dermatology Life Quality Index (DLQI) score

    The DLQI is a patient-completed 10-item questionnaire that, in addition to evaluating overall quality of life, can be used to assess 6 different aspects that may affect quality of life: symptoms and feelings, daily activities, leisure, work or school performance, personal relationships, and treatment. The aim of this questionnaire is to measure how much your skin problem has affected your life over the last week. For each of 10 questions patient has to select one of the following options: very much, a lot, a little, not at all.

    Measured: Baseline, Weeks 16, 28 and 52

  6. Change from baseline (Week 0) in Patient Benefit Index (PBI) score at Weeks 16, 28, and 52

    The PBI is a patient-defined benefit assessment tool. Patients select personally relevant treatment goals from a standardized list of benefits called the Patient Needs Questionnaire. An evaluation of those treatment goals assessed by the patient is captured on the Patient Benefit Questionnaire. The PBI is calculated from the sum of the benefit items weighted by their respective relevance divided by the number of relevant items. Values between 0 (no benefit) and 4 (maximal patient-defined benefit) are possible.

    Measured: Baseline, Weeks 16, 28 and 52

  7. Number of patients achieving PASI 50, 75, and 90 response (ie, at least 50%, 75% and 90% improvement in PASI)

    Number of patients achieving PASI 50, 75, and 90 response (ie, at least 50%, 75% and 90% improvement in PASI) will be evaluated at Weeks 16, 28, and 52.

    Measured: up to 52 weeks

  8. Number of patients achieving a DLQI improvement (reduction) of greater than or equal to 5 points

    Number of patients achieving a DLQI improvement (reduction) of greater than or equal to 5 points will be evaluated at Weeks 16, 28, and 52.

    Measured: up to 52 weeks

  9. Number of patients achieving a score of 0 or 1 in DLQI

    Number of patients achieving a score of 0 or 1 in DLQI will be evaluated at Weeks 16, 28, and 52.

    Measured: up to 52 weeks

  10. Number of patients achieving an improvement in PBI

    Number of patients achieving an improvement in PBI will be evaluated at Weeks 16, 28, and 52.

    Measured: up to 52 weeks

  11. Number of patients with comorbidities (obesity, hypertension, diabetes, dyslipidemia, and heart disease)

    Number of patients with comorbidities (obesity, hypertension, diabetes, dyslipidemia, and heart disease) will be evaluated at baseline, Weeks 16, 28, and 52.

    Measured: up to 52 weeks

  12. Health Economics/Medical Resource Utilization Questionnaire (HE/MRU)

    Health economic impact using the HE/MRU questionnaire will be assessed at baseline, Weeks 16, 28 and 52. Patients will be asked to complete a HE/MRU questionnaire to collect information on demographics, medical insurances, and use of biologic agents and phototherapy. Sections 1 and 2 are completed by the patient. Sections 3 and 4 are completed by the physician.

    Measured: up to 52 weeks

  13. Change from baseline in productivity VAS at Weeks 16, 28, and 52

    A 10 cm VAS will be used to assess work, school, or at home productivity. Patients will be asked to put a single vertical line across the horizontal line at the spot that they feel best reflects the answer to the question, "How much has your disease affected your daily productivity at work, school or at home in the past 4 weeks?" The score will be recorded as a measurement of the placement of the patient's mark on a 10 cm scale.

    Measured: Baseline, Weeks 16, 28 and 52

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Sep 2012 (estimated)
  2. Study start2 Dec 2011
  3. Primary completion30 Nov 2013
  4. Study completion30 Nov 2013

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
169 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01677598
Sponsor's protocol ID
CR100140
Other IDs
CNTO1275PSO4016
Acronym
MARCOPOLO
Status last verified
Oct 2024
First submitted
30 Aug 2012
Last updated
28 Oct 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No

Questions about this trial

What is this clinical trial studying?

An observational study of Plaque Psoriasis, run by Janssen Research & Development, LLC at 9 sites in 5 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Oct 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 9 sites in South Korea, Malaysia, Indonesia, Singapore, Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of psoriasis patients who use ustekinumab with label-recommended interval or other/missed dose interval (time frame: up to 52 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Oct 2024.

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