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.
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
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.
- Conditions
- Plaque Psoriasis
- 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 group | Role | What they receive |
|---|---|---|
| Patients with plaque psoriasis | Patients 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.
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)
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
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
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
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
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
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
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
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
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
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
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
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
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.
- First posted3 Sep 2012 (estimated)
- Study start2 Dec 2011
- Primary completion30 Nov 2013
- Study completion30 Nov 2013
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Plaque PsoriasisStudies of the same condition, open and under way.
- More trials run by Janssen Research & Development, LLCThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Janssen Research & Development, LLC
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Janssen Research & Development, LLC Clinical Trial, Study director, Janssen Research & Development, LLC
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
Study at a glance
From the registry record, last updated by the sponsor on 28 Oct 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Study to Evaluate Ustekinumab in Clinical Practice in Patients With Plaque Psoriasis in Asia-Pacific Countries
- ClinicalTrials.gov ID
- NCT01677598
- Acronym / sponsor ID
- MARCOPOLO / CR100140
- Conditions
- Plaque Psoriasis
- Keywords
- Plaque Psoriasis, Ustekinumab, CNTO 1275, Asia-Pacific
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 169 participants (actual)
- Lead sponsor
- Janssen Research & Development, LLCIndustry (pharma, biotech, devices)
- Study start
- 2 Dec 2011 (actual)
- Primary completion
- 30 Nov 2013 (actual)
- Study completion
- 30 Nov 2013 (actual)
- First posted
- 3 Sep 2012 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to determine how patients use ustekinumab (label-recommended or other/missed dose interval) in Asia-Pacific countries.
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.
Study design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patients with plaque psoriasis | – | Drug: No interventionPatients with plaque psoriasis using ustekinumab in Asia-Pacific countries. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients at least 18 years of age with a diagnosis of plaque psoriasis, according to the dermatologists' clinical judgment
Key inclusion criteria (3 listed)
- 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
Key exclusion criteria (2 listed)
- Has difficulty understanding questions posed by any of the questionnaires
- Are currently participating in an investigational drug clinical study
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| No interventionAlso: CNTO 1275No 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 | Drug | Patients with plaque psoriasis |
Primary outcome
Number of psoriasis patients who use ustekinumab with label-recommended interval or other/missed dose interval
Time frame: up to 52 weeks
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.
13 secondary outcomes
Epidemiologic characteristics of the psoriasis population
Time frame: Week 0
Change from baseline (Week 0) in Psoriasis Area and Severity Index (PASI) score at Weeks 16, 28 and 52
Time frame: Baseline (Week 0), Weeks 16, 28 and 52
Change from baseline (Week 0) in Nail Psoriasis Severity Index (NAPSI) score at Weeks 16, 28, and 52
Time frame: Baseline, Weeks 16, 28 and 52
Change from baseline in EuroQol 5 Dimensional Questionnaire (EQ-5D) index score and EQ visual analog scale (VAS) at Weeks 16, 28, and 52
Time frame: Baseline, Weeks 16, 28 and 52
Change from baseline (Week 0) in Dermatology Life Quality Index (DLQI) score
Time frame: Baseline, Weeks 16, 28 and 52
Change from baseline (Week 0) in Patient Benefit Index (PBI) score at Weeks 16, 28, and 52
Time frame: Baseline, Weeks 16, 28 and 52
Number of patients achieving PASI 50, 75, and 90 response (ie, at least 50%, 75% and 90% improvement in PASI)
Time frame: up to 52 weeks
Number of patients achieving a DLQI improvement (reduction) of greater than or equal to 5 points
Time frame: up to 52 weeks
Number of patients achieving a score of 0 or 1 in DLQI
Time frame: up to 52 weeks
Number of patients achieving an improvement in PBI
Time frame: up to 52 weeks
Number of patients with comorbidities (obesity, hypertension, diabetes, dyslipidemia, and heart disease)
Time frame: up to 52 weeks
Health Economics/Medical Resource Utilization Questionnaire (HE/MRU)
Time frame: up to 52 weeks
Change from baseline in productivity VAS at Weeks 16, 28, and 52
Time frame: Baseline, Weeks 16, 28 and 52
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Oct 2024.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Janssen Research & Development, LLC Clinical Trial study director
Janssen Research & Development, LLC
9 sites in 5 countries: see every site and its status.
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.