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Psoriatic ArthritisPhase 4CONTROLNCT02814175

A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

A Phase 4 study testing methotrexate (MTX) and adalimumab (ADA) in people with Psoriatic Arthritis, run by AbbVie at 60 sites in 14 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

An interventional Phase 4 open-label, randomized, controlled, parallel-group, multi-country study in participants with psoriatic arthritis (PsA) consisting of 2 parts: Part 1 (Day 1 up to Week 16) is designed to compare the achievement of minimal disease activity (MDA) between participants randomized to either… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Psoriatic Arthritis
What is being tested?
methotrexate (MTX) and adalimumab (ADA)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
246 participants
Where
60 sitesin 14 countries
Study dates
5 Aug 2016to 19 Mar 2020
Phase
Phase 4
Are there results?
Yes, posted in the registrySummary in the doctors' view

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

Who may be able to join

  • PsA diagnosis established at least 4 weeks prior to the date of the Screening visit and confirmed by ClASsification of Psoriatic Arthritis (CASPAR) criteria
  • Not in MDA at the time of screening
  • Has 3 or more tender and 3 or more swollen joints
  • Treated with methotrexate 15 mg (weekly) for at least 4 weeks

Who cannot join

  • Contraindications to adalimumab therapy and/or known hypersensitivity to adalimumab or its excipients
  • History of methotrexate intolerance/toxicity
  • Medical conditions(s) precluding methotrexate dose increase above 15 mg
  • Had prior exposure to any tumor necrosis factor (TNF) inhibitor, other mechanism of action biologic DMARD (bDMARD) or any systemic biologic agent in general

Trial locations and contacts

60 sites in 14 countries.

60 sites in 14 countries

United States12 sites
  • Ochsner Clinic Foundation /ID# 155178

    Baton Rouge, Louisiana, 70836-6455

  • Metroplex Clinical Research /ID# 162486

    Dallas, Texas, 75231

  • Altoona Ctr Clinical Res /ID# 152087

    Duncansville, Pennsylvania, 16635

  • LeJenue Research Associates /ID# 200093

    Miami, Florida, 33126

  • Coastal Carolina Health Care /ID# 152088

    New Bern, North Carolina, 28562

  • Shores Rheumatology, PC /ID# 162697

    Saint Clair Shores, Michigan, 48081

  • Swedish Medical Center /ID# 162051

    Seattle, Washington, 98104

  • West Virginia Research Inst /ID# 157815

    South Charleston, West Virginia, 25309

  • AZ Arthritis & Rheum Research /ID# 161796

    Sun City, Arizona, 85351

  • Deerbrook Medical Associates /ID# 158655

    Vernon Hills, Illinois, 60061

  • PMG Research of Wilmington LLC /ID# 152089

    Wilmington, North Carolina, 28401

  • Clinical Pharmacology Study Gr /ID# 161057

    Worcester, Massachusetts, 01605

Other trials in United States

Canada8 sites
  • The Waterside Clinic /ID# 151938

    Barrie, Ontario, L4M 6L2

  • Rheumatology Research Assoc /ID# 161600

    Edmonton, Alberta, T5M 0H4

  • Adachi Medicine Prof. Corp /ID# 152575

    Hamilton, Ontario, L8N 1Y2

  • Ctr. de Rheum de l'est du QC /ID# 151937

    Rimouski, Quebec, G5L 8W1

  • Groupe de Recherche en Maladies Osseuses /ID# 205693

    Sainte-Foy, Quebec, G1V 3M7

  • St. Clare's Mercy Hospital /ID# 159680

    St. John's, Newfoundland and Labrador, A1C 5B8

  • Percuro Clinical Research, Ltd /ID# 161601

    Victoria, British Columbia, V8V 3M9

  • Manitoba Clinic /ID# 151939

    Winnipeg, Manitoba, R3A 1M3

Other trials in Canada

Spain6 sites
  • Hospital Univ Germans Trias I Pujol /ID# 151760

    Badalona, 08916

  • Hospital Universitario Reina S /ID# 151761

    Córdoba, 14004

  • Hospital Manises /ID# 162778

    Manises, 46940

  • Corporac Sanitaria Parc Tauli /ID# 151759

    Sabadell, Barcelona, 08208

  • Hospital Univ Canarias /ID# 206489

    Santa Cruz de Tenerife, 38320

  • Hospital de Viladecans /ID# 163875

    Viladecans, 8840

Other trials in Spain

Australia5 sites
  • Royal Prince Alfred Hospital /ID# 153144

    Camperdown, New South Wales, 2050

  • Optimus Clinical Research Pty. /ID# 153145

    Kogarah, New South Wales, 2217

  • Liverpool Hospital /ID# 153147

    Liverpool, New South Wales, 2170

  • Box Hill Hospital /ID# 153146

    Melbourne, Victoria, 3128

  • BJC Health /ID# 153875

    Parramatta, New South Wales, 2150

Other trials in Australia

Germany5 sites
  • Fachpraxis fuer Rheumatologie und Osteologie /ID# 203982

    Bruchhausen-Vilsen, Lower Saxony, 27305

  • CIRI GmbH /ID# 152228

    Frankfurt, 60590

  • Hamburger Rheuma I /ID# 164055

    Hamburg, 22391

  • Universitaetsklinik Heidelberg /ID# 152229

    Heidelberg, Baden-Wurttemberg, 69120

  • Univ Hosp Schleswig-Holstein, Campus Kiel, Klinik furer Innere Medizin /ID# 152231

    Kiel, Schleswig-Holstein, 24105

Other trials in Germany

United Kingdom5 sites
  • Royal National Hosp for Rheuma /ID# 152767

    Bath, BA1 1RL

  • Western General Hospital /ID# 155195

    Edinburgh, EH4 2XU

  • Altnagelvin Area Hospital /ID# 152766

    Londonderry, BT47 6SB

  • Central Manchester University /ID# 152765

    Manchester, M13 9WL

  • Lancashire Care NHS Foundation /ID# 152769

    Preston, BT47 3EN

Other trials in United Kingdom

Poland4 sites
  • ClinicMed Badurski i wspolnicy SJ /ID# 151987

    Bialystok, 15-879

  • McBk Sc /Id# 163089

    Grodzisk Mazowiecki, Masovian Voivodeship, 05-825

  • SANUS Szpital Specjalistyczny /ID# 151988

    Stalowa Wola, Podkarpackie Voivodeship, 37-450

  • Centrum Medyczne AMED /ID# 164047

    Warsaw, Masovian Voivodeship, 01-518

Other trials in Poland

Colombia3 sites
  • Centro de Investigacion en Reumatologia y Especialidades Medicas- CIREEM SAS /ID# 151954

    Bogota, Cundinamarca, 110221

  • Riesgo de Fractura S.A - CAYRE /ID# 153817

    Bogotá, 111121

  • San Vicente Fundacion /Id# 171324

    Medellín, 050034

Other trials in Colombia

Italy3 sites
  • Universita di Catanzaro Magna Graecia /ID# 152013

    Catanzaro, Calabria, 88100

  • Azienda Ospedaliera Policlinic /ID# 152011

    Rome, 00161

  • A.O. Universitaria Senese /ID# 152012

    Siena, 53100

Other trials in Italy

Brazil2 sites
  • Hospital de Clinicas de Porto Alegre /ID# 152345

    Porto Alegre, Rio Grande do Sul, 90035-903

  • Faculdade de Medicina do ABC /ID# 152344

    Santo André, São Paulo, 09060-870

Other trials in Brazil

Bulgaria2 sites
  • MHAT Trimontsium /ID# 152658

    Plovdiv, 4000

  • Diag Consult Ctr 17 Sofia EOOD /ID# 152657

    Sofia, 1505

Other trials in Bulgaria

Czechia2 sites
  • Revmatolog s.r.o. /ID# 151753

    Jihlava, Jihlava, 586 01

  • Nuselská poliklinika, Revmatologie /ID# 151754

    Prague, Praha 4, 140 00

Other trials in Czechia

Puerto Rico2 sites
  • Dr. Ramon L. Ortega-Colon, MD /ID# 152957

    Carolina, 00983

  • GCM Medical Group, PSC /ID# 152091

    San Juan, 00917

Other trials in Puerto Rico

Qatar1 site
  • Hamad Hospital /ID# 152334

    Doha, Baladiyat ad Dawhah

Other trials in Qatar

About this study

Official title: A Phase 4 Open-label Randomized Controlled Study COmparing the Effectiveness of Adalimumab iNTROduction and Methotrexate Dose escaLation in Subjects With Psoriatic Arthritis (CONTROL)

An interventional Phase 4 open-label, randomized, controlled, parallel-group, multi-country study in participants with psoriatic arthritis (PsA) consisting of 2 parts: Part 1 (Day 1 up to Week 16) is designed to compare the achievement of minimal disease activity (MDA) between participants randomized to either adalimumab in combination with methotrexate (MTX) or MTX alone escalated to the highest recommended or tolerable dose; Part 2 (Week 16 through Week 32) is designed to evaluate the maintenance or achievement of MDA on 4 different treatment regimens using adalimumab and/or MTX, with participant allocation based on the initial randomized treatment and achievement of MDA in Part 1, and with rescue treatment option.

Being tested
methotrexate (MTX), adalimumab (ADA)
Keywords
Psoriatic Arthritis
Medical subject headings
Arthritis, Psoriatic

What participants receive

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

  • methotrexate (MTX)Drug

  • adalimumab (ADA)Biological

Study groups in NCT02814175
Study groupRoleWhat they receive
Part 1: MTX Escalated DoseActive comparatorMethotrexate (MTX) escalated to 20 - 25 mg or highest tolerable dose every week (ew)
Receives: Drug: methotrexate (MTX)
Part 1: ADA + MTXExperimentalAdalimumab (ADA) 40 mg every other week (eow) in combination with MTX 15 mg ew
Receives: Drug: methotrexate (MTX); Biological: adalimumab (ADA)
Part 2: MTX Escalated DoseActive comparatorParticipants achieving minimal disease activity (MDA) at Week 16 on MTX escalated to 20 -25 mg or highest tolerable dose ew, continued with the same MTX dose
Receives: Drug: methotrexate (MTX)
Part 2: ADA + MTX Escalated DoseActive comparatorParticipants not achieving MDA at Week 16 on MTX escalated to 20 - 25 mg or highest tolerable dose ew, received ADA 40 mg eow in combination with MTX 20 - 25 mg or highest tolerable dose ew
Receives: Drug: methotrexate (MTX); Biological: adalimumab (ADA)
Part 2: ADAExperimentalParticipants achieving MDA at Week 16 on ADA 40 mg eow plus MTX 15 mg ew, had MTX completely withdrawn at Week 16 and continued receiving ADA as monotherapy
Receives: Biological: adalimumab (ADA)
Part 2: ADA ew + MTXExperimentalParticipants not achieving MDA at Week 16 on ADA 40 mg eow plus MTX 15 mg ew, had ADA escalated to 40 mg ew in combination with MTX 15 mg ew
Receives: Drug: methotrexate (MTX); Biological: adalimumab (ADA)

What is being measured

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

  1. Percentage of Participants Achieving Minimal Disease Activity (MDA) (Non-responder Imputation [NRI]) (Part 1)

    Minimal disease activity (MDA) for psoriatic arthritis (PsA) was defined as fulfilling at least 5 of the following 7 criteria: tender and swollen joint counts (TJC) ≤ 1 (out of TJC68 assessed in this study), swollen joint count (SJC) ≤ 1 (out of SJC66 assessed in this study), Psoriasis Area and Severity Index (PASI) ≤ 1 or body surface area (BSA) ≤ 3; Patient's assessment of pain visual analogue scale (VAS) ≤ 15, Patient's global assessment of disease activity (PtGA) VAS ≤ 20, Health Assessment Questionnaire Disability Index (HAQ-DI) score ≤ 0.5, and tender entheseal points ≤ 1 (out of 8 assessed in this study).

    Measured: Week 16

Secondary outcomes (12)
  1. Change in Dermatology Life Quality Index (DLQI) Score From Baseline (Part 1)

    The Dermatology Life Quality Index (DLQI) score is a measure of participant's quality of life (QOL) related to skin disease.The DLQI questionnaire consists of 10 questions concerning participants' perception of the impact of skin diseases on different aspects of their health related QOL over the last week. The items of the DLQI encompass aspects such as symptoms and feelings, daily activities, leisure, work or school, personal relationships and the side effects of treatment. The range of possible DLQI scores is 0 to 30, with a score of 0 indicating no effect at all on a participant's life and a score of 30 indicating extremely large effect on participant's life. A decrease in DLQI score indicates improvement.

    Measured: From Day 1 to Week 16

  2. Change in Tender Dactylitic Digit Count From Baseline for Participants With Presence of Dactylitis at Baseline (Part 1)

    Hands and feet bilaterally were assessed for the presence/absence of dactylitis and associated tenderness for participants with presence of dactylitis at baseline. The tender dactylitic digit count is equal to the number of swollen and painful digits (range 0 to 20). A decrease indicates improvement.

    Measured: From Day 1 to Week 16

  3. Change in Disease Activity Score 28 (DAS28)-C-reactive Protein (CRP) Score From Baseline (Part 1)

    The Disease Activity Score 28 (DAS28) is a validated index of rheumatoid arthritis disease activity but is also used in PsA clinical trials. DAS28 is a composite score calculated using a mathematical formula based on the scores for these scales. DAS28 includes tender and swollen joint counts, PtGA, and acute phase reactant (CRP in this study). DAS28 scores range from 0 to 10, with higher scores indicating more disease activity. A larger negative change in the DAS28 score indicates greater improvement.

    Measured: From Day 1 to Week 16

  4. Change in Psoriatic Arthritis Impact of Disease Score (PsAID) Score From Baseline (Part 1)

    Psoriatic Arthritis Impact of Disease Score (PsAID) was developed by an European League Against Rheumatism (EULAR) initiative and is a validated patient self-reported tool to assess the impact of PsA on the participant's life. The PsAID is a composite score calculated using a mathematical formula based on the scores for each component. PsAID-9 was developed for clinical trials and was used in this study. The PsAID-9 is calculated based on 9 Numerical rating scales (NRS) questions that include pain, fatigue, skin, work and/or leisure activities, function, discomfort, sleep, coping, and anxiety). Each NRS is assessed as a number between 0 and 10. PsAID scores range from 0 to 10, with higher scores indicating worse status. A larger negative change in the PsAID-9 score indicates greater improvement.

    Measured: From Day 1 to Week 16

  5. Percentage of Participants Achieving American College of Rheumatology (ACR) 20/50/70 Response (Part 1)

    The ACR is a standard criteria originally developed to measure the effectiveness of various arthritis medications or treatments in clinical trials for RA, but is also widely used in PsA. The ACR measures improvement in tender joint count (TJC) or swollen joint count (SJC), and improvement in at least 3 of the following 5 parameters: Patient Global Assessment (PtGA), Physician's Global Assessment of Disease Activity (PhGA), physical function (using HAQ-DI) and acute phase reactant (using CRP). ACR 20/50/70 response is achieved if ≥ 20%/≥ 50%/≥ 70% improvement in tender joint count (TJC) or swollen joint count (SJC) as well as a ≥ 20%/≥ 50%/≥ 70% improvement in ≥ 3 of the other 5 parameters.

    Measured: Week 16

  6. Change in Leeds Enthesitis Index (LEI) From Baseline (Part 1) for Participants With Presence of LEI at Baseline

    The Leeds Enthesitis Index (LEI) is an enthesitis measure developed specifically for PsA and assesses the presence or absence of tenderness at the following 3 bilateral enthesial sites: medial femoral condyles, lateral epicondyles of the humerus, and Achilles tendon insertions for participants with presence of LEI at baseline.Tenderness on examination is recorded as either present (1) or absent (0) for each of the 6 sites, for an overall score range of 0 to 6. A decrease in LEI indicates improvement.

    Measured: From Day 1 to Week 16

  7. Percentage of Participants in MDA in Part 2 of the Study (Week 32)

    MDA for PsA was defined as fulfilling at least 5 of the following 7 criteria: TJC ≤ 1 (out of TJC68 assessed in this study), SJC ≤ 1 (out of SJC66 assessed in this study), PASI ≤ 1 or BSA ≤ 3; Patient's assessment of pain VAS ≤ 15, PtGA VAS ≤ 20, HAQ-DI score ≤ 0.5, and tender entheseal points ≤ 1 (out of 8 assessed in this study).

    Measured: Week 32

  8. Change in Psoriatic Arthritis Disease Activity Score (PASDAS) From Baseline (Part 1)

    Psoriatic Arthritis Disease Activity Score (PASDAS) is a weighted disease activity measure developed specifically for PsA. It includes PhGA, PtGA, SF-36 PCS, SJC, TJC, Leeds enthesitis count, tender dactylitic count and hsCRP lab test. The PASDAS is a composite score calculated using a mathematical formula based on the scores for each component. The PASDAS is unitless, with a typical score range between 0 and 10. Smaller values on PASDAS indicate a better condition; a negative change from baseline indicates improvement.

    .

    Measured: From Day 1 to week 16

  9. Change in Short Form Health Survey 36 (SF-36) Score From Baseline (Part 1)

    The Short Form Health Survey 36 (SF-36) is a generic measure to assess participant's general health/well-being (health related quality of life); short version 2 (SF-36v2) was used. SF-36 determined participants' overall quality of life by assessing 1) limitations in physical functioning due to health problems; 2) limitations in usual role because of physical health problems; 3) bodily pain; 4) general health perceptions; 5) vitality; 6) limitations in social functioning because of physical or emotional problems; 7) limitations in usual role due to emotional problems; and 8) general mental health. Items 1-4 comprise physical component of the SF-36. Scores on each item were summed and averaged (PCS; range = 0-100). Items 5-8 comprise mental component of the SF-36. Scores on each item were summed and averaged (mental component score [MCS]; range = 0-100). Larger values on SF-36 indicate a better condition. A positive change from Baseline in either PCS or MCS indicates improvement.

    Measured: From Day 1 to Week 16

  10. Change in HAQ-DI Score From Baseline (Part 1)

    The HAQ-DI is a standardized measure of physical function in arthritis. The HAQ-DI questionnaire contains 20 items divided into 8 domains that measure: dressing and grooming, arising, eating, walking, hygiene, reach, grip, and common daily activities. Participants assessed their ability to do each task over the past week using the following response categories: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). Scores on each task were summed and averaged to provide an overall score ranging from 0 to 3, where 0 represents no disability and 3 very severe, high-dependency disability. HAQ remission indicating normal physical function is defined by HAQ-DI score of < 0.5. Negative change from Baseline indicates improvement.

    Measured: From Day 1 to Week 16

  11. Percentage of Participants Achieving Psoriasis Area and Severity Index (PASI) 75/90/100 Response Among Participants With BSA Greater Than or Equal to 3% at Baseline (Part 1)

    Psoriasis Area and Severity Index (PASI) provides a quantitative assessment of psoriasis lesional burden based on the amount of body surface area involved and the degree of severity of erythema, induration, and scale, weighted by body part. The score ranges from 0 to 72, with 0 indicating no psoriasis and 72 indicating very severe psoriasis. 75/90/100 denotes greater than or equal to 75%/90%/100% improvement in PASI score. A 100% reduction is considered complete clearance of psoriasis.

    Measured: Week 16

  12. Change in Disease Activity in Psoriatic Arthritis Score (DAPSA) Score From Baseline (Part 1)

    Disease Activity in Psoriatic Arthritis Score (DAPSA) score is a the sum of swollen joint count (66 joints), tender joint count (68 joints), CRP (mg/dL), Patient's Assessment of Pain (on a 10-unit VAS;0=no pain, 10=worst possible pain), and Patient's Global Assessment of Disease Activity (arthritis, on a 10-unit VAS; 0 to 100 centimeter [cm] VAS, 0=excellent and 10=poor). Change from baseline in DAPSA measures the change in disease activity, where a negative change indicates an improvement and a positive change indicates worsening of disease activity.

    Measured: From Day 1 to Week 16

Timeline

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

  1. First posted27 Jun 2016 (estimated)
  2. Study start5 Aug 2016
  3. Primary completion23 Sep 2019
  4. Study completion19 Mar 2020

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
246 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02814175
Sponsor's protocol ID
M14-496
Other IDs
2016-000191-21, 2016
Acronym
CONTROL
Status last verified
Oct 2020
First submitted
21 Jun 2016
Last updated
23 Nov 2020
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: AbbVie is committed to responsible data sharing regarding the clinical trials we sponsor. This includes access to anonymized, individual and trial-level data (analysis data sets), as well as other information (e.g., protocols and clinical study reports), as long as the trials are not part of an ongoing or planned regulatory submission. This includes requests for clinical trial data for unlicensed products and indications.

Publications

  • Coates LC, Tillett W, D'Agostino MA, Rahman P, Behrens F, McDearmon-Blondell EL, Bu X, Chen L, Kapoor M, Conaghan PG, Mease P. Comparison between adalimumab introduction and methotrexate dose escalation in patients with inadequately controlled psoriatic arthritis (CONTROL): a randomised, open-label, two-part, phase 4 study. Lancet Rheumatol. 2022 Apr;4(4):e262-e273. doi: 10.1016/S2665-9913(22)00008-X. Epub 2022 Feb 25.

    PubMed 38288922

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing methotrexate (MTX) and adalimumab (ADA) in people with Psoriatic Arthritis, run by AbbVie at 60 sites in 14 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 4 inclusion and 4 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 23 Nov 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 60 sites in United States, Canada, Spain, Australia, Germany and 9 more countries. 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.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 23 Nov 2020). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

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?

Percentage of Participants Achieving Minimal Disease Activity (MDA) (Non-responder Imputation [NRI]) (Part 1) (time frame: Week 16). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02814175, which also lists 1 linked publication.

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 23 Nov 2020; AzTrials last refreshed its copy on 26 Oct 2026.

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