Psoriasis Clinical Trial

A Study to Evaluate the Efficacy and Safety of Bimekizumab Compared to Placebo and an Active Comparator in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis

Summary

This is a study to compare the efficacy of bimekizumab versus placebo and an active comparator in the treatment of subjects with moderate to severe chronic plaque psoriasis (PSO).

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Must be at least 18 years of age
Chronic plaque psoriasis (PSO) for at least 6 months prior to the Screening Visit
Psoriasis Area Severity Index (PASI) >=12 and body surface area (BSA) affected by PSO >=10% and Investigator's Global Assessment (IGA) score >=3 on a 5-point scale
Subject is a candidate for systemic PSO therapy and/or phototherapy
Female subject of child bearing potential must be willing to use highly effective method of contraception

Exclusion Criteria:

Subject has an active infection (except common cold), a recent serious infection, or a history of opportunistic or recurrent chronic infections
Subject has concurrent acute or chronic viral hepatitis B or C or human immunodeficiency virus (HIV) infection
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 any other condition, including medical or psychiatric, which, in the Investigator's judgment, would make the subject unsuitable for inclusion in the study
Presence of active suicidal ideation or positive suicide behavior
Presence of moderately severe major depression or severe major depression
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

Study is for people with:

Psoriasis

Phase:

Phase 3

Estimated Enrollment:

567

Study ID:

NCT03370133

Recruitment Status:

Completed

Sponsor:

UCB Biopharma SRL

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There are 25 Locations for this study

See Locations Near You

Ps0009 946
Phoenix Arizona, 85032, United States
Ps0009 910
Bakersfield California, 93309, United States
Ps0009 919
San Diego California, 92103, United States
Ps0009 906
Boca Raton Florida, 33486, United States
Ps0009 909
Boynton Beach Florida, 33437, United States
Ps0009 912
Coral Gables Florida, 33134, United States
Ps0009 907
Miami Florida, 33144, United States
Ps0009 903
Ocala Florida, 34471, United States
Ps0009 921
Ormond Beach Florida, 32174, United States
Ps0009 918
Tampa Florida, 33612, United States
Ps0009 941
Alpharetta Georgia, 30022, United States
Ps0009 911
Plainfield Indiana, 46168, United States
Ps0009 900
West Des Moines Iowa, 50265, United States
Ps0009 905
Overland Park Kansas, 66215, United States
Ps0009 922
Baton Rouge Louisiana, 70809, United States
Ps0009 917
Troy Michigan, 48084, United States
Ps0009 915
Saint Louis Missouri, 63117, United States
Ps0009 958
Omaha Nebraska, 68144, United States
Ps0009 901
Portsmouth New Hampshire, 03801, United States
Ps0009 908
East Windsor New Jersey, 08520, United States
Ps0009 923
Albuquerque New Mexico, 87106, United States
Ps0009 913
New York New York, 10029, United States
Ps0009 920
Portland Oregon, 97210, United States
Ps0009 924
Houston Texas, 77004, United States
Ps0009 914
San Antonio Texas, 78213, United States
Ps0009 004
Fremantle , , Australia
Ps0009 005
Phillip , , Australia
Ps0009 002
Westmead , , Australia
Ps0009 009
Woolloongabba , , Australia
Ps0009 050
Bruxelles , , Belgium
Ps0009 052
Liège , , Belgium
Ps0009 051
Loverval , , Belgium
Ps0009 673
Halifax , , Canada
Ps0009 652
Oakville , , Canada
Ps0009 651
Richmond Hill , , Canada
Ps0009 650
Surrey , , Canada
Ps0009 653
Toronto , , Canada
Ps0009 657
Waterloo , , Canada
Ps0009 218
Bonn , , Germany
Ps0009 209
Darmstadt , , Germany
Ps0009 214
Erlangen , , Germany
Ps0009 208
Frankfurt/Main , , Germany
Ps0009 210
Friedrichshafen , , Germany
Ps0009 211
Hamburg , , Germany
Ps0009 212
Heidelberg , , Germany
Ps0009 213
Mahlow , , Germany
Ps0009 205
Osnabrück , , Germany
Ps0009 217
Schweinfurt , , Germany
Ps0009 254
Budapest , , Hungary
Ps0009 255
Budapest , , Hungary
Ps0009 253
Orosháza , , Hungary
Ps0009 259
Szekszárd , , Hungary
Ps0009 300
Roma , , Italy
Ps0009 303
Roma , , Italy
Ps0009 629
Asahikawa , , Japan
Ps0009 605
Bunkyō-Ku , , Japan
Ps0009 607
Chiyoda , , Japan
Ps0009 610
Chuo Ku , , Japan
Ps0009 601
Fukuoka , , Japan
Ps0009 619
Gifu , , Japan
Ps0009 620
Hamamatsu , , Japan
Ps0009 608
Itabashi-Ku , , Japan
Ps0009 627
Itabashi-Ku , , Japan
Ps0009 609
Kobe , , Japan
Ps0009 600
Kurume , , Japan
Ps0009 622
Matsumoto , , Japan
Ps0009 604
Minato-Ku , , Japan
Ps0009 623
Morioka , , Japan
Ps0009 621
Nagoya , , Japan
Ps0009 625
Nankoku , , Japan
Ps0009 624
Obihiro , , Japan
Ps0009 611
Osaka , , Japan
Ps0009 614
Osaka , , Japan
Ps0009 603
Sapporo , , Japan
Ps0009 617
Sendai , , Japan
Ps0009 613
Shimotsuke , , Japan
Ps0009 602
Shinagawa-Ku , , Japan
Ps0009 612
Shinjuku-Ku , , Japan
Ps0009 618
Shinjuku-Ku , , Japan
Ps0009 626
Shinjuku-Ku , , Japan
Ps0009 628
Shinjuku-Ku , , Japan
Ps0009 615
Sumida , , Japan
Ps0009 606
Takaoka , , Japan
Ps0009 616
Tsu , , Japan
Ps0009 362
Białystok , , Poland
Ps0009 369
Białystok , , Poland
Ps0009 371
Bydgoszcz , , Poland
Ps0009 358
Katowice , , Poland
Ps0009 357
Kielce , , Poland
Ps0009 374
Poznań , , Poland
Ps0009 350
Warsaw , , Poland
Ps0009 351
Warsaw , , Poland
Ps0009 367
Wrocław , , Poland
Ps0009 370
Wrocław , , Poland
Ps0009 372
Łódź , , Poland
Ps0009 400
Moscow , , Russian Federation
Ps0009 402
Moscow , , Russian Federation
Ps0009 403
Moscow , , Russian Federation
Ps0009 404
Saint Petersburg , , Russian Federation
Ps0009 556
Cardiff , , United Kingdom
Ps0009 551
Dundee , , United Kingdom
Ps0009 553
Edgbaston , , United Kingdom
Ps0009 552
Liverpool , , United Kingdom
Ps0009 550
Manchester , , United Kingdom
Ps0009 555
Salford , , United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Psoriasis

Phase:

Phase 3

Estimated Enrollment:

567

Study ID:

NCT03370133

Recruitment Status:

Completed

Sponsor:


UCB Biopharma SRL

How clear is this clinincal trial information?

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