A Study to Test the Efficacy and Safety of Bimekizumab in the Treatment of Subjects With Active Psoriatic Arthritis

NCT ID: NCT03895203

Last Updated: 2026-01-27

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

852 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-04-03

Study Completion Date

2022-07-11

Brief Summary

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This is a study to demonstrate the clinical efficacy, safety and tolerability of bimekizumab administered subcutaneously (sc) compared with placebo in the treatment of subjects with active Psoriatic Arthritis (PsA).

Detailed Description

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Conditions

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Psoriatic Arthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Bimekzumab dosage regimen

Subjects randomized to this arm will receive assigned bimekizumab dosage regimen and placebo to maintain the blinding with adalimumab and placebo arms during the Treatment Period.

Group Type EXPERIMENTAL

Bimekizumab

Intervention Type DRUG

Subjects will receive bimekizumab at pre-specified time-points.

Placebo

Intervention Type OTHER

Subjects will receive placebo at pre-specified time-points.

Adalimumab dosage regimen

Subjects randomized to this arm will receive the assigned adalimumab dosage regimen during the Treatment Period.

Group Type ACTIVE_COMPARATOR

Adalimumab

Intervention Type DRUG

Adalimumab will be administered according to the labeling recommendations.

Placebo

Subjects randomized to this arm will receive placebo during the Double-Blind Treatment Period and will be reallocated to receive bimekizumab dosage regimen during the Maintenance Period.

Group Type PLACEBO_COMPARATOR

Bimekizumab

Intervention Type DRUG

Subjects will receive bimekizumab at pre-specified time-points.

Placebo

Intervention Type OTHER

Subjects will receive placebo at pre-specified time-points.

Interventions

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Bimekizumab

Subjects will receive bimekizumab at pre-specified time-points.

Intervention Type DRUG

Adalimumab

Adalimumab will be administered according to the labeling recommendations.

Intervention Type DRUG

Placebo

Subjects will receive placebo at pre-specified time-points.

Intervention Type OTHER

Other Intervention Names

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BKZ UCB4940 HUMIRA® PBO

Eligibility Criteria

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Inclusion Criteria

* An Institutional Review Board (IRB)/Independent Ethics Committee (IEC) approved written Informed Consent form is signed and dated by the subject
* Subject is male or female at least 18 years of age
* Female subject must be postmenopausal, permanently sterilized or willing to use a highly effective method of contraception
* Documented diagnosis of adult-onset Psoriatic Arthritis (PsA) meeting the Classification Criteria for Psoriatic Arthritis (CASPAR) for at least 6 months prior to Screening with active PsA and must have at Baseline tender joint count (TJC) \>=3 out of 68 and swollen joint count (SJC) \>=3 out of 66
* Subject must be negative for rheumatoid factor and anti-cyclic citrullinated peptide (CCP) antibodies
* Subject must have at least 1 active psoriatic lesion(s) and/or a documented history of psoriasis (PSO)
* Subject must be a suitable candidate for treatment with adalimumab and has no contraindications to receive adalimumab as per the local label as assessed by the Investigator
* Subjects currently taking NSAIDs, cyclooxygenase 2 (COX-2) inhibitors, analgesics (including mild opioids), corticosteroids, methotrexate (MTX), leflunomide (LEF), sulfasalazine (SSZ), hydroxychloroquine (HCQ) AND/OR apremilast can be allowed if they fulfill specific requirements prior to study entry

Exclusion Criteria

* Female subjects who are breastfeeding, pregnant, or plan to become pregnant during the study
* Subjects with current or prior exposure to any biologics for the treatment of Psoriatic Arthritis (PsA) or Psoriasis (PSO)
* Subject has an active infection or a history of recent serious infections
* Subject has known tuberculosis (TB) infection, is at high risk of acquiring TB infection, or has current or history of nontuberculous mycobacterium (NTMB) infection
* Subject has a diagnosis of inflammatory conditions other than PSO or PsA. Subjects with a diagnosis of Crohn's disease, ulcerative colitis, or other inflammatory bowel disease (IBD) are allowed as long as they have no active symptomatic disease at Screening or Baseline
* Subject had acute anterior uveitis within 6 weeks of Baseline
* Subject has any active malignancy or history of malignancy within 5 years prior to the Screening Visit EXCEPT treated and considered cured cutaneous squamous or basal cell carcinoma, or in situ cervical cancer
* Subject has a form of PSO other than chronic plaque-type (eg, pustular, erythrodermic and guttate PSO, or drug-induced PSO)
* Presence of active suicidal ideation, or moderately severe major depression or severe major depression
* Subject has a history of chronic alcohol or drug abuse within 6 months prior to Screening
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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UCB Biopharma SRL

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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UCB Cares

Role: STUDY_DIRECTOR

001 844 599 2273

Locations

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Pa0010 50017

Phoenix, Arizona, United States

Site Status

Pa0010 50035

San Diego, California, United States

Site Status

Pa0010 50004

Tustin, California, United States

Site Status

Pa0010 50033

Palm Harbor, Florida, United States

Site Status

Pa0010 50037

Tampa, Florida, United States

Site Status

Pa0010 50039

Atlanta, Georgia, United States

Site Status

Pa0010 50028

Lexington, Kentucky, United States

Site Status

Pa0010 50015

Hagerstown, Maryland, United States

Site Status

Pa0010 50016

St Louis, Missouri, United States

Site Status

Pa0010 50029

Albuquerque, New Mexico, United States

Site Status

Pa0010 50010

Brooklyn, New York, United States

Site Status

Pa0010 50125

Charlotte, North Carolina, United States

Site Status

Pa0010 50040

Dayton, Ohio, United States

Site Status

Pa0010 50020

Duncansville, Pennsylvania, United States

Site Status

Pa0010 50006

Wyomissing, Pennsylvania, United States

Site Status

Pa0010 50008

Johnston, Rhode Island, United States

Site Status

Pa0010 50007

Orangeburg, South Carolina, United States

Site Status

Pa0010 50001

Jackson, Tennessee, United States

Site Status

Pa0010 50012

Memphis, Tennessee, United States

Site Status

Pa0010 50002

Austin, Texas, United States

Site Status

Pa0010 50049

Corpus Christi, Texas, United States

Site Status

Pa0010 50051

Houston, Texas, United States

Site Status

Pa0010 50036

Mesquite, Texas, United States

Site Status

Pa0010 50009

Waco, Texas, United States

Site Status

Pa0010 50050

Beckley, West Virginia, United States

Site Status

Pa0010 30005

Camberwell, , Australia

Site Status

Pa0010 30002

Clayton, , Australia

Site Status

Pa0010 30008

Hobart, , Australia

Site Status

Pa0010 30003

Maroochydore, , Australia

Site Status

Pa0010 30007

Victoria Park, , Australia

Site Status

Pa0010 30006

Woodville, , Australia

Site Status

Pa0010 40003

Genk, , Belgium

Site Status

Pa0010 40002

Leuven, , Belgium

Site Status

Pa0010 40059

Mons, , Belgium

Site Status

Pa0010 50041

Québec, , Canada

Site Status

Pa0010 50042

Rimouski, , Canada

Site Status

Pa0010 50043

Sidney, , Canada

Site Status

Pa0010 50044

Trois-Rivières, , Canada

Site Status

Pa0010 40061

Brno, , Czechia

Site Status

Pa0010 40065

Brno, , Czechia

Site Status

Pa0010 40062

Ostrava, , Czechia

Site Status

Pa0010 40009

Pardubice, , Czechia

Site Status

Pa0010 40013

Prague, , Czechia

Site Status

Pa0010 40014

Prague, , Czechia

Site Status

Pa0010 40015

Prague, , Czechia

Site Status

Pa0010 40063

Prague, , Czechia

Site Status

Pa0010 40066

Prague, , Czechia

Site Status

Pa0010 40010

Uherské Hradiště, , Czechia

Site Status

Pa0010 40012

Zlín, , Czechia

Site Status

Pa0010 40019

Paris, , France

Site Status

Pa0010 40068

Tours, , France

Site Status

Pa0010 40074

Bad Doberan, , Germany

Site Status

Pa0010 40025

Berlin, , Germany

Site Status

Pa0010 40028

Berlin, , Germany

Site Status

Pa0010 40076

Cottbus, , Germany

Site Status

Pa0010 40023

Erlangen, , Germany

Site Status

Pa0010 40117

Frankfurt, , Germany

Site Status

Pa0010 40029

Hamburg, , Germany

Site Status

Pa0010 40071

Hamburg, , Germany

Site Status

Pa0010 40027

Herne, , Germany

Site Status

Pa0010 40078

Leipzig, , Germany

Site Status

Pa0010 40348

Magdeburg, , Germany

Site Status

Pa0010 40026

Ratingen, , Germany

Site Status

Pa0010 40081

Budapest, , Hungary

Site Status

Pa0010 40083

Budapest, , Hungary

Site Status

Pa0010 40032

Debrecen, , Hungary

Site Status

Pa0010 40030

Eger, , Hungary

Site Status

Pa0010 40082

Kistarcsa, , Hungary

Site Status

Pa0010 40079

Szentes, , Hungary

Site Status

Pa0010 40033

Székesfehérvár, , Hungary

Site Status

Pa0010 40080

Szombathely, , Hungary

Site Status

Pa0010 40084

Catania, , Italy

Site Status

Pa0010 40087

Milan, , Italy

Site Status

Pa0010 40085

Pisa, , Italy

Site Status

Pa0010 40086

Reggio Emilia, , Italy

Site Status

Pa0010 20035

Bunkyō City, , Japan

Site Status

Pa0010 20036

Kawachi-Nagano-shi, , Japan

Site Status

Pa0010 20045

Kita-ku, , Japan

Site Status

Pa0010 20049

Kitakyushu, , Japan

Site Status

Pa0010 20044

Minatoku, , Japan

Site Status

Pa0010 20033

Nagoya, , Japan

Site Status

Pa0010 20041

Osaka, , Japan

Site Status

Pa0010 20046

Osaka, , Japan

Site Status

Pa0010 20048

Saitama, , Japan

Site Status

Pa0010 20031

Sapporo, , Japan

Site Status

Pa0010 20042

Sasebo, , Japan

Site Status

Pa0010 20032

Suita, , Japan

Site Status

Pa0010 20043

tabashi City, , Japan

Site Status

Pa0010 20030

Tokyo, , Japan

Site Status

Pa0010 40093

Bialystok, , Poland

Site Status

Pa0010 40119

Bydgoszcz, , Poland

Site Status

Pa0010 40038

Elblag, , Poland

Site Status

Pa0010 40088

Elblag, , Poland

Site Status

Pa0010 40096

Gdynia, , Poland

Site Status

Pa0010 40042

Krakow, , Poland

Site Status

Pa0010 40092

Krakow, , Poland

Site Status

Pa0010 40037

Lublin, , Poland

Site Status

Pa0010 40091

Nowa Sól, , Poland

Site Status

Pa0010 40044

Poznan, , Poland

Site Status

Pa0010 40090

Poznan, , Poland

Site Status

Pa0010 40118

Torun, , Poland

Site Status

Pa0010 40041

Warsaw, , Poland

Site Status

Pa0010 40094

Warsaw, , Poland

Site Status

Pa0010 40097

Warsaw, , Poland

Site Status

Pa0010 40098

Warsaw, , Poland

Site Status

Pa0010 40039

Wroclaw, , Poland

Site Status

Pa0010 40043

Wroclaw, , Poland

Site Status

Pa0010 40095

Wroclaw, , Poland

Site Status

Pa0010 20002

Moscow, , Russia

Site Status

Pa0010 20005

Moscow, , Russia

Site Status

Pa0010 20010

Moscow, , Russia

Site Status

Pa0010 20017

Moscow, , Russia

Site Status

Pa0010 20013

Petrozavodsk, , Russia

Site Status

Pa0010 20012

Ryazan, , Russia

Site Status

Pa0010 20016

Ryazan, , Russia

Site Status

Pa0010 20001

Saint Petersburg, , Russia

Site Status

Pa0010 20003

Saint Petersburg, , Russia

Site Status

Pa0010 20004

Saint Petersburg, , Russia

Site Status

Pa0010 20009

Saint Petersburg, , Russia

Site Status

Pa0010 20083

Saint Petersburg, , Russia

Site Status

Pa0010 20007

Saratov, , Russia

Site Status

Pa0010 20014

Ulyanovsk, , Russia

Site Status

Pa0010 20006

Vladimir, , Russia

Site Status

Pa0010 20008

Yaroslavl, , Russia

Site Status

Pa0010 20015

Yaroslavl, , Russia

Site Status

Pa0010 40045

A Coruña, , Spain

Site Status

Pa0010 40105

Córdoba, , Spain

Site Status

Pa0010 40102

Málaga, , Spain

Site Status

Pa0010 40101

Sabadell, , Spain

Site Status

Pa0010 40104

Santiago de Compostela, , Spain

Site Status

Pa0010 40049

Seville, , Spain

Site Status

Pa0010 40103

Seville, , Spain

Site Status

Pa0010 40106

Seville, , Spain

Site Status

Pa0010 40099

Vigo, , Spain

Site Status

Pa0010 40111

Leeds, , United Kingdom

Site Status

Pa0010 40107

Wolverhampton, , United Kingdom

Site Status

Countries

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United States Australia Belgium Canada Czechia France Germany Hungary Italy Japan Poland Russia Spain United Kingdom

References

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Ritchlin CT, Coates LC, McInnes IB, Mease PJ, Merola JF, Tanaka Y, Asahina A, Gossec L, Gottlieb AB, Warren RB, Ink B, Bajracharya R, Shende V, Coarse J, Landewe RB. Bimekizumab treatment in biologic DMARD-naive patients with active psoriatic arthritis: 52-week efficacy and safety results from the phase III, randomised, placebo-controlled, active reference BE OPTIMAL study. Ann Rheum Dis. 2023 Nov;82(11):1404-1414. doi: 10.1136/ard-2023-224431. Epub 2023 Sep 11.

Reference Type RESULT
PMID: 37696588 (View on PubMed)

Mease PJ, Warren RB, Nash P, Grouin JM, Lyris N, Willems D, Taieb V, Eells J, McInnes IB. Comparative Effectiveness of Bimekizumab and Secukinumab in Patients with Psoriatic Arthritis at 52 Weeks Using a Matching-Adjusted Indirect Comparison. Rheumatol Ther. 2024 Jun;11(3):817-828. doi: 10.1007/s40744-024-00652-7. Epub 2024 Mar 6.

Reference Type RESULT
PMID: 38446397 (View on PubMed)

Kristensen LE, Tillett W, Nash P, Coates LC, Mease PJ, Ogdie A, Gisondi P, Ink B, Prickett AR, Bajracharya R, Taieb V, Lyris N, Lambert J, Walsh JA. Association of achieving clinical disease control criteria and patient-reported outcomes in bimekizumab-treated patients with active psoriatic arthritis: results from two phase III studies. Ther Adv Musculoskelet Dis. 2024 Nov 11;16:1759720X241288071. doi: 10.1177/1759720X241288071. eCollection 2024.

Reference Type RESULT
PMID: 39534481 (View on PubMed)

Mease PJ, Merola JF, Tanaka Y, Gossec L, McInnes IB, Ritchlin CT, Landewe RBM, Asahina A, Ink B, Heinrichs A, Bajracharya R, Shende V, Coarse J, Coates LC. Summary of Research: Safety and Efficacy of Bimekizumab in Patients with Psoriatic Arthritis: 2-Year Results from Two Phase 3 Studies. Rheumatol Ther. 2025 Aug;12(4):609-612. doi: 10.1007/s40744-025-00764-8. Epub 2025 May 10.

Reference Type RESULT
PMID: 40347389 (View on PubMed)

Thaci D, Asahina A, Boehncke WH, Gottlieb AB, Lebwohl M, Warren RB, Edens H, Ink B, Bajracharya R, Coarse J, Merola JF. Bimekizumab Efficacy and Safety in Patients with Psoriatic Arthritis with Substantial Skin and Nail Psoriasis to 1 Year. Dermatol Ther (Heidelb). 2025 Dec 12. doi: 10.1007/s13555-025-01599-5. Online ahead of print.

Reference Type RESULT
PMID: 41381988 (View on PubMed)

Mease PJ, Gensler LS, Orbai AM, Warren RB, Bajracharya R, Ink B, Marten A, Massow U, Shende V, Manente M, Peterson L, White K, Landewe R, Poddubnyy D. Long-term safety of bimekizumab in adult patients with axial spondyloarthritis or psoriatic arthritis: pooled results from integrated phase IIb/III clinical studies. RMD Open. 2025 Apr 6;11(2):e005026. doi: 10.1136/rmdopen-2024-005026.

Reference Type DERIVED
PMID: 40194794 (View on PubMed)

Gladman DD, Mease PJ, Gossec L, Husni ME, Gottlieb AB, Ink B, Bajracharya R, Coarse J, Lyris N, Lambert J, Tillett W. Effect of Bimekizumab on Patient-Reported Outcomes and Work Productivity in Patients With Psoriatic Arthritis: 1-Year Results From 2 Phase III Studies. J Rheumatol. 2025 May 1;52(5):466-478. doi: 10.3899/jrheum.2024-0923.

Reference Type DERIVED
PMID: 39892885 (View on PubMed)

Husni ME, Mease PJ, Merola JF, Tillett W, Goldammer N, Ink B, Coarse J, Lambert J, Taieb V, Gladman DD. Bimekizumab provided rapid improvements in patient-reported symptoms and health-related quality of life in patients with active psoriatic arthritis: pooled 16-week results from two phase 3 studies. RMD Open. 2024 Sep 23;10(3):e004464. doi: 10.1136/rmdopen-2024-004464.

Reference Type DERIVED
PMID: 39313302 (View on PubMed)

Mease PJ, Merola JF, Tanaka Y, Gossec L, McInnes IB, Ritchlin CT, Landewe RBM, Asahina A, Ink B, Heinrichs A, Bajracharya R, Shende V, Coarse J, Coates LC. Safety and Efficacy of Bimekizumab in Patients with Psoriatic Arthritis: 2-Year Results from Two Phase 3 Studies. Rheumatol Ther. 2024 Oct;11(5):1363-1382. doi: 10.1007/s40744-024-00708-8. Epub 2024 Aug 31.

Reference Type DERIVED
PMID: 39215949 (View on PubMed)

Mease PJ, Warren RB, Nash P, Grouin JM, Lyris N, Willems D, Taieb V, Eells J, McInnes IB. Comparative Effectiveness of Bimekizumab and Risankizumab in Patients with Psoriatic Arthritis at 52 Weeks Assessed Using a Matching-Adjusted Indirect Comparison. Rheumatol Ther. 2024 Oct;11(5):1403-1412. doi: 10.1007/s40744-024-00706-w. Epub 2024 Aug 9.

Reference Type DERIVED
PMID: 39120849 (View on PubMed)

Mease PJ, Warren RB, Nash P, Grouin JM, Lyris N, Taieb V, Eells J, McInnes IB. Comparative Effectiveness of Bimekizumab and Ustekinumab in Patients with Psoriatic Arthritis at 52 Weeks Assessed Using a Matching-Adjusted Indirect Comparison. Rheumatol Ther. 2024 Oct;11(5):1413-1423. doi: 10.1007/s40744-024-00705-x. Epub 2024 Aug 9.

Reference Type DERIVED
PMID: 39120848 (View on PubMed)

Gossec L, Orbai AM, de Wit M, Coates LC, Ogdie A, Ink B, Coarse J, Lambert J, Taieb V, Gladman DD. Effect of bimekizumab on patient-reported disease impact in patients with psoriatic arthritis: 1-year results from two phase 3 studies. Rheumatology (Oxford). 2024 Sep 1;63(9):2399-2410. doi: 10.1093/rheumatology/keae277.

Reference Type DERIVED
PMID: 38754125 (View on PubMed)

Warren RB, McInnes IB, Nash P, Grouin JM, Lyris N, Willems D, Taieb V, Eells J, Mease PJ. Comparative Effectiveness of Bimekizumab and Guselkumab in Patients with Psoriatic Arthritis at 52 Weeks Assessed Using a Matching-Adjusted Indirect Comparison. Rheumatol Ther. 2024 Jun;11(3):829-839. doi: 10.1007/s40744-024-00659-0. Epub 2024 Mar 15.

Reference Type DERIVED
PMID: 38488975 (View on PubMed)

Maloney A, Dua P, Ahmed GF. Comparative Effectiveness of Bimekizumab in Psoriatic Arthritis: A Model-Based Meta-Analysis of American College of Rheumatology Response Criteria. Clin Pharmacol Ther. 2024 May;115(5):1007-1014. doi: 10.1002/cpt.3135. Epub 2024 Jan 12.

Reference Type DERIVED
PMID: 38073049 (View on PubMed)

McInnes IB, Asahina A, Coates LC, Landewe R, Merola JF, Ritchlin CT, Tanaka Y, Gossec L, Gottlieb AB, Warren RB, Ink B, Assudani D, Bajracharya R, Shende V, Coarse J, Mease PJ. Bimekizumab in patients with psoriatic arthritis, naive to biologic treatment: a randomised, double-blind, placebo-controlled, phase 3 trial (BE OPTIMAL). Lancet. 2023 Jan 7;401(10370):25-37. doi: 10.1016/S0140-6736(22)02302-9. Epub 2022 Dec 6.

Reference Type DERIVED
PMID: 36493791 (View on PubMed)

Provided Documents

Download supplemental materials such as informed consent forms, study protocols, or participant manuals.

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

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2017-002322-20

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

PA0010

Identifier Type: -

Identifier Source: org_study_id

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