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.
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
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
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
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
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
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
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
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
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
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
Bulgaria2 sites
MHAT Trimontsium /ID# 152658
Plovdiv, 4000
Diag Consult Ctr 17 Sofia EOOD /ID# 152657
Sofia, 1505
Czechia2 sites
Revmatolog s.r.o. /ID# 151753
Jihlava, Jihlava, 586 01
Nuselská poliklinika, Revmatologie /ID# 151754
Prague, Praha 4, 140 00
Puerto Rico2 sites
Dr. Ramon L. Ortega-Colon, MD /ID# 152957
Carolina, 00983
GCM Medical Group, PSC /ID# 152091
San Juan, 00917
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.
- Conditions
- Psoriatic Arthritis
- 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 group | Role | What they receive |
|---|---|---|
| Part 1: MTX Escalated Dose | Active comparator | Methotrexate (MTX) escalated to 20 - 25 mg or highest tolerable dose every week (ew) Receives: Drug: methotrexate (MTX) |
| Part 1: ADA + MTX | Experimental | Adalimumab (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 Dose | Active comparator | Participants 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 Dose | Active comparator | Participants 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: ADA | Experimental | Participants 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 + MTX | Experimental | Participants 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.
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)
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
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
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
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
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
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
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
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
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
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
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
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.
- First posted27 Jun 2016 (estimated)
- Study start5 Aug 2016
- Primary completion23 Sep 2019
- Study completion19 Mar 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Psoriatic ArthritisStudies of the same condition, open and under way.
- More trials run by AbbVieThe 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
- Interventional
- Phase
- Phase 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 246 participants (actual)
Sponsor and investigators
- Lead sponsor
- AbbVie
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- AbbVie Inc., Study director, AbbVie
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
- Results posted
- Yes, on ClinicalTrials.gov
- 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
Study at a glance
From the registry record, last updated by the sponsor on 23 Nov 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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)
- ClinicalTrials.gov ID
- NCT02814175
- Acronym / sponsor ID
- CONTROL / M14-496
- Conditions
- Psoriatic Arthritis
- Keywords
- Psoriatic Arthritis
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 246 participants (actual)
- Lead sponsor
- AbbVieIndustry (pharma, biotech, devices)
- Study start
- 5 Aug 2016 (actual)
- Primary completion
- 23 Sep 2019 (actual)
- Study completion
- 19 Mar 2020 (actual)
- First posted
- 27 Jun 2016 (estimated)
- Results
- Posted 23 Nov 2020
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 6
| Arm | Type | Receives |
|---|---|---|
| Part 1: MTX Escalated Dose | Active comparator | Drug: methotrexate (MTX)Methotrexate (MTX) escalated to 20 - 25 mg or highest tolerable dose every week (ew) |
| Part 1: ADA + MTX | Experimental | Drug: methotrexate (MTX), Biological: adalimumab (ADA)Adalimumab (ADA) 40 mg every other week (eow) in combination with MTX 15 mg ew |
| Part 2: MTX Escalated Dose | Active comparator | Drug: methotrexate (MTX)Participants 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 |
| Part 2: ADA + MTX Escalated Dose | Active comparator | Drug: methotrexate (MTX), Biological: adalimumab (ADA)Participants 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 |
| Part 2: ADA | Experimental | Biological: adalimumab (ADA)Participants 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 |
| Part 2: ADA ew + MTX | Experimental | Drug: methotrexate (MTX), Biological: adalimumab (ADA)Participants 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 |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- 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
Key exclusion criteria (4 listed)
- 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
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 |
|---|---|---|
| methotrexate (MTX) | Drug | Part 1: ADA + MTX, Part 1: MTX Escalated Dose, Part 2: ADA + MTX Escalated Dose, Part 2: ADA ew + MTX, Part 2: MTX Escalated Dose |
| adalimumab (ADA) | Biological | Part 1: ADA + MTX, Part 2: ADA, Part 2: ADA + MTX Escalated Dose, Part 2: ADA ew + MTX |
Primary outcome
Percentage of Participants Achieving Minimal Disease Activity (MDA) (Non-responder Imputation [NRI]) (Part 1)
Time frame: Week 16
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).
12 secondary outcomes
Change in Dermatology Life Quality Index (DLQI) Score From Baseline (Part 1)
Time frame: From Day 1 to Week 16
Change in Tender Dactylitic Digit Count From Baseline for Participants With Presence of Dactylitis at Baseline (Part 1)
Time frame: From Day 1 to Week 16
Change in Disease Activity Score 28 (DAS28)-C-reactive Protein (CRP) Score From Baseline (Part 1)
Time frame: From Day 1 to Week 16
Change in Psoriatic Arthritis Impact of Disease Score (PsAID) Score From Baseline (Part 1)
Time frame: From Day 1 to Week 16
Percentage of Participants Achieving American College of Rheumatology (ACR) 20/50/70 Response (Part 1)
Time frame: Week 16
Change in Leeds Enthesitis Index (LEI) From Baseline (Part 1) for Participants With Presence of LEI at Baseline
Time frame: From Day 1 to Week 16
Percentage of Participants in MDA in Part 2 of the Study (Week 32)
Time frame: Week 32
Change in Psoriatic Arthritis Disease Activity Score (PASDAS) From Baseline (Part 1)
Time frame: From Day 1 to week 16
Change in Short Form Health Survey 36 (SF-36) Score From Baseline (Part 1)
Time frame: From Day 1 to Week 16
Change in HAQ-DI Score From Baseline (Part 1)
Time frame: From Day 1 to Week 16
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)
Time frame: Week 16
Change in Disease Activity in Psoriatic Arthritis Score (DAPSA) Score From Baseline (Part 1)
Time frame: From Day 1 to Week 16
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Nov 2020.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 38288922Coates 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.
- Individual participant dataSharing planned: 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.
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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.
AbbVie Inc. study director
AbbVie
60 sites in 14 countries: see every site and its status.
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.