Efficacy and Safety Study of SHP647 as Induction Therapy in Participants With Moderate to Severe Ulcerative Colitis (FIGARO UC 301)

A Phase 3 Randomized, Double-blind, Placebo-controlled, Parallel-group Efficacy and Safety Study of SHP647 as Induction Therapy in Subjects With Moderate to Severe Ulcerative Colitis (FIGARO UC 301)

The purpose of this study is to evaluate the efficacy of SHP647 in inducing remission, based on composite score of participant-reported symptoms and centrally read endoscopy, in participants with moderate to severe ulcerative colitis (UC).

Study Overview

• Status: Terminated
• Conditions: Ulcerative Colitis
• Intervention / Treatment: Drug: Ontamalimab; Other: Placebo

• Study Type: Interventional
• Enrollment (Actual): 380
• Phase: Phase 3

Contacts and Locations

Study Locations

• Australia
  • New South Wales
    • Concord, New South Wales, Australia, 2139
      • Concord Repatriation General Hospital
    • Liverpool, New South Wales, Australia, 2170
      • Liverpool Hospital
  • Queensland
    • Herston, Queensland, Australia, 4029
      • Royal Brisbane & Women's Hospital
    • South Brisbane, Queensland, Australia, 4101
      • Mater Hospital Brisbane
  • South Australia
    • Adelaide, South Australia, Australia, 5000
      • Royal Adelaide Hospital
  • Victoria
    • Fitzroy, Victoria, Australia, 3065
      • St Vincents Hospital Melbourne - PPDS
    • Melbourne, Victoria, Australia, 3004
      • The Alfred Hospital
• Austria
  • Klagenfurt am Wörthersee, Austria, 9020
    • Klinikum Klagenfurt am Woerthersee
  • Salzburg, Austria, 5020
    • Salzburger Landeskliniken
  • St. Pölten, Austria, 3100
    • Universitätsklinikum St. Pölten
  • Wels, Austria, 4600
    • Klinikum Wels-Grieskirchen GmbH
  • Wien, Austria, 1090
    • Medizinische Universitat Wien (Medical University of Vienna)
  • Kärnten
    • St. Veit an der Glan, Kärnten, Austria, 9300
      • A.ö. Krankenhaus der Barmherzigen Brüder
  • Steiermark
    • Graz, Steiermark, Austria, 8036
      • LKH-Universitätsklinikum Klinikum Graz
• Brazil
  • Goiás
    • Goiânia, Goiás, Brazil, 74535-170
      • Instituto Goiano de Gastroenterologia e Endoscopia Digestiva Ltda
  • Rio Grande Do Sul
    • Passo Fundo, Rio Grande Do Sul, Brazil, 99010-260
      • Hospital da Cidade de Passo Fundo
  • São Paulo
    • Santo André, São Paulo, Brazil, 09190-510
      • CEMEC - Centro Multidisciplinar de Estudos Clínicos
• Croatia
  • Bjelovar, Croatia, 43000
    • Opca bolnica Bjelovar
  • Osijek, Croatia, 31000
    • Clinical Hospital Centre Osijek
  • Split, Croatia, 21000
    • University Hospital Centre Split
  • Virovitica, Croatia, 33000
    • General Hospital Virovitica
  • Vukovar, Croatia, 32000
    • General County Hospital Vukovar and Croatian Veterans Hospital
  • Zadar, Croatia, 23 000
    • General Hospital Zadar
  • Grad Zagreb
    • Zagreb, Grad Zagreb, Croatia, 10000
      • University hospital center Zagreb
  • Karlovacka Županija
    • Karlovac, Karlovacka Županija, Croatia, 47000
      • Opca bolnica Karlovac
• Czechia
  • Praha 4, Czechia, 140 21
    • Institut Klinicke a Experimentalni Mediciny
  • Praha 7, Czechia, 170 04
    • ISCARE I.V.F. a.s.
  • Usti nad Labem, Czechia, 401 13
    • Krajská zdravotní, a.s. - Masarykova nemocnice v Ústí nad Labem, o.z.
  • Usti nad Orlici, Czechia, 562 18
    • Nemocnice Pardubickeho kraje, a.s. Orlickoustecka nemocnice
  • Královéhradecký Kraj
    • Hradec Kralove, Královéhradecký Kraj, Czechia, 500 12
      • Hepato-Gastroenterologie HK, s. r. o.
  • Olomoucký Kraj
    • Olomouc, Olomoucký Kraj, Czechia, 779 00
      • PreventaMed s.r.o.
• Germany
  • Berlin, Germany, 13353
    • Charité - Universitätsmedizin Berlin
  • Berlin-Zehlendorf, Germany, 14163
    • Gastroenterologische Facharztpraxis am Mexikoplatz
  • Biberach an der Riss, Germany, 88400
    • Sana Klinikum Biberach
  • Frankfurt, Germany, 60590
    • Universitätsklinikum Frankfurt
  • Hamburg, Germany, 22559
    • Asklepios Westklinikum Hamburg Ggmbh
  • Köln, Germany, 50937
    • Uniklinik Köln
  • Munich, Germany, 81675
    • Klinikum rechts der Isa der Technischen Universitaet Muenchen
  • Baden-Württemberg
    • Ulm, Baden-Württemberg, Germany, 89081
      • Universitatsklinikum Ulm
  • Nordrhein-Westfalen
    • Aachen, Nordrhein-Westfalen, Germany, 52074
      • Universitatsklinikum der RWTH Aachen
    • Münster, Nordrhein-Westfalen, Germany, 48159
      • Gastro Campus Research GbR
  • Schleswig-Holstein
    • Kiel, Schleswig-Holstein, Germany, 24105
      • Universitätsklinikum Schleswig-Holstein
  • Thüringen
    • Jena, Thüringen, Germany, 07747
      • Universitätsklinikum Jena
• Israel
  • Jerusalem, Israel, 91031
    • Shaare Zedek Medical Center
  • Jerusalem, Israel, 91120
    • Hadassah Medical Center - PPDS
  • Nahariya, Israel, 22100
    • Galilee Medical Center
  • Nazareth, Israel, 16100
    • Nazareth EMMS Hospital
  • Tel Aviv, Israel, 6423906
    • Tel Aviv Sourasky Medical Center PPDS
  • Tiberias, Israel, 15208
    • Baruch Padeh Poriya Medical Center
• Italy
  • Bologna, Italy, 40138
    • Azienda Ospedaliero Universitaria Di Bologna - Policlinico S Orsola Malpighi
  • Novara, Italy, 28100
    • A.O.U. Maggiore della Carità
  • Pavia, Italy, 27100
    • Fondazione IRCCS Policlinico San Matteo di Pavia
  • Roma, Italy, 00168
    • Fondazione Policlinico Universitario A Gemelli
  • Roma, Italy, 00161
    • La Sapienza-Università di Roma-Policlinico Umberto I
  • Rozzano (MI), Italy, 20089
    • Istituto Clinico Humanitas
  • Torino, Italy, 10126
    • Azienda Ospedaliera Citta Della Salute E Della Scienza Di Torino
  • Torino, Italy, 10128
    • Azienda Ospedaliera Ordine Mauriziano di Torino
  • Calabria
    • Catanzaro, Calabria, Italy, 88100
      • Azienda Ospedaliera Mater Domini di Catanzaro
  • Emilia-Romagna
    • Modena, Emilia-Romagna, Italy, 41124
      • Azienda Ospedaliero Universitaria Di Modena Policlinico
  • Lazio
    • Roma, Lazio, Italy, 00152
      • Azienda Ospedaliera San Camillo Forlanini
  • Puglia
    • San Giovanni Rotondo (FG), Puglia, Italy, 71013
      • Ospedale Casa Sollievo Della Sofferenza IRCCS
  • Toscana
    • Firenze, Toscana, Italy, 50134
      • Azienda Ospedaliera Universitaria Careggi
  • Veneto
    • Negrar, Veneto, Italy, 37024
      • Ospedale Sacro Cuore Don Calabria
    • Padova, Veneto, Italy, 35128
      • Azienda Ospedale Università Padova - Dipartimento Salute della Donna e del Bambino - INCIPIT - PIN
• Japan
  • Abiko-shi, Chiba, Japan, 270-1168
    • Tokatsu Tsujinaka Hospital
  • Hakodate, Japan, 040-0001
    • Hakodate Koseiin Hakodate Goryoukaku Hospital
  • Koga, Japan, 306-0232
    • Yuai Memorial Hospital
  • Koganei, Japan, 184-0003
    • Kawabe Clinic
  • Koshigaya, Japan, 343-8555
    • Dokkyo Medical University Saitama Medical Center
  • Kurume-shi, Japan, 839-0809
    • Hidaka Coloproctology Clinic
  • Nagakute, Japan, 480-1195
    • Aichi Medical University Hospital
  • Nishinomiya, Japan, 663-8014
    • Nishinomiya Municipal Central Hospital
  • Onomichi, Japan
    • Onomichi General Hospital
  • Otsu-Shi, Japan, 520-2192
    • Shiga University of Medical Science Hospital
  • Sapporo, Japan, 065-0033
    • Sapporo Higashi Tokushukai Hospital
  • Hokkaidô
    • Sapporo-shi, Hokkaidô, Japan, 004-0041
      • Sapporo Tokushukai Hospital
  • Kanagawa
    • Sagamihara, Kanagawa, Japan, 252-5188
      • Sagamihara Kyodo Hospital
  • Tokyo
    • Minato-ku, Tokyo, Japan, 105-8471
      • Jikei University Hospital
    • Minato-ku, Tokyo, Japan, 108-8642
      • Kitasato University Kitasato Institute Hospital
    • Ome, Tokyo, Japan, 198-0042
      • Ome Municipal General Hospital
  • Ôita
    • Beppu, Ôita, Japan, 874-0833
      • Shinbeppu Hospital
• Lithuania
  • Kaunas, Lithuania, LT-50009
    • Hospital of Lithuanian University of Health Sciences Kaunas Clinics
  • Vilnius, Lithuania, LT- 08661
    • Vilnius University Hospital Santaros Klinikos
  • Vilnius, Lithuania, LT-10207
    • Vilnius City Clinical Hospital
• Netherlands
  • Amsterdam, Netherlands, 1081 HV
    • VU Medisch Centrum
  • Amsterdam, Netherlands, 1105 AZ
    • Academisch Medisch Centrum Amsterdam
  • Noord-Brabant
    • Tilburg, Noord-Brabant, Netherlands, 5022 GC
      • ETZ-Elisabeth
  • Noord-Holland
    • Alkmaar, Noord-Holland, Netherlands, 1815 JD
      • NWZ, location Alkmaar
  • Zuid-Holland
    • Leiden, Zuid-Holland, Netherlands, 2333 ZA
      • Leids Universitair Medisch Centrum
• Poland
  • Bydgoszcz, Poland, 85-168
    • Szpital Uniwersytecki nr 2 im. dr Jana Biziela w Bydgoszczy
  • Bydgoszcz, Poland, 85-796
    • Centrum Medyczne Pratia Bydgoszcz
  • Czestochowa, Poland, 42-200
    • Centrum Medyczne Czestochowa - PRATIA - PPDS
  • Gdynia, Poland, 81-338
    • Centrum Medyczne Gdynia - PRATIA - PPDS
  • Józefów, Poland, 05-410
    • BioVirtus Centrum Medyczne
  • Katowice, Poland, 40-659
    • Nzoz All Medicus
  • Katowice, Poland, 40-211
    • Szpital Zakonu Bonifratrow pw. Aniolow Strozow w Katowicach
  • Krakow, Poland, 31-315
    • Centrum Medyczne A-Z Clinic Mateusz Sidor, Piotr Puc-Lekarze Spolka Partnerska
  • Ksawerow, Poland, 95-054
    • Centrum Opieki Zdrowotnej Orkan-Med Stec-Michalska sp. j.
  • Lodz, Poland, 91-034
    • Med Gastr Sp.z.o.o Sp.k
  • Nowa Sól, Poland, 67-100
    • Twoja Przychodnia - Centrum Medyczne Nowa Sol
  • Piaseczno, Poland, 05-500
    • Centrum Innowacyjnych Terapii
  • Poznan, Poland
    • Clinical Research Center Spółka z Ograniczoną Odpowiedzialnością, Medic-R Spółka Komandytowa
  • Rzeszow, Poland, 35-302
    • Korczowski Bartosz, Gabinet Lekarski
  • Szczecin, Poland, 71-685
    • Sonomed Sp. z o.o.
  • Warsaw, Poland, 00-635
    • Centrum Zdrowia MDM
  • Warszawa, Poland, 02-507
    • Centralny Szpital Kliniczny MSW
  • Zamosc, Poland, 22-400
    • Samodzielny Publiczny Szpital Wojewodzki im. Papieza Jana Pawla II
  • Dolnoslaskie
    • Wroclaw, Dolnoslaskie, Poland, 50-449
      • Melita Medical
    • Wroclaw, Dolnoslaskie, Poland, 53-114
      • Lexmedica
  • Kujawsko-pomorskie
    • Bydgoszcz, Kujawsko-pomorskie, Poland, 85-079
      • Vitamed Galaj i Cichomski sp.j.
    • Torun, Kujawsko-pomorskie, Poland, 87-100
      • Gastromed Kopon Zmudzinski i Wspolnicy Sp.j.Specjalistyczne Centrum Gastrologii i Endoskopii Specj
    • Wloclawek, Kujawsko-pomorskie, Poland, 87-800
      • Centrum Diagnostyczno - Lecznicze Barska sp. z o.o.
  • Lódzkie
    • Lódz, Lódzkie, Poland, 90-302
      • Niepubliczny Zaklad Opieki Zdrowotnej CENTRUM MEDYCZNE Szpital Swietej Rodziny
    • Lódz, Lódzkie, Poland, 93-338
      • Instytut Centrum Zdrowia Matki Polki
    • Lódz, Lódzkie, Poland, 90-647
      • SPZOZ Uniwersytecki Szpital Kliniczny im. Wojskowej Akademii Medycznej UM w Lodzi
  • Malopolskie
    • Krakow, Malopolskie, Poland, 31-501
      • Krakowskie Centrum Medyczne
  • Mazowieckie
    • Warszawa, Mazowieckie, Poland, 03-580
      • Niepubliczny Zakład Opieki Zdrowotnej VIVAMED
    • Warszawa, Mazowieckie, Poland, 04-749
      • Miedzyleski Szpital Specjalistyczny w Warszawie
    • Warszawa, Mazowieckie, Poland, 01-868
      • Centrum Medyczne Warszawa - PRATIA - PPDS
  • Podlaskie
    • Bialystok, Podlaskie, Poland, 15-276
      • Uniwersytecki Szpital Kliniczny w Bialymstoku
  • Pomorskie
    • Sopot, Pomorskie, Poland, 81-756
      • ENDOSKOPIA Sp. z o.o.
  • Slaskie
    • Tychy, Slaskie, Poland, 43-100
      • H-T. Centrum Medyczne Endoterapia
  • Swietokrzyskie
    • Konskie, Swietokrzyskie, Poland, 26-200
      • Szpital Specjalistyczny sw Lukasza - Oddzial Gastroenterologii
  • Zachodniopomorskie
    • Szczecin, Zachodniopomorskie, Poland, 71-434
      • Twoja Przychodnia - Szczecinskie Centrum Medyczne
• Romania
  • Bucharest, Romania, 022328
    • Fundeni Clinical Institute
  • Bucharest, Romania, 010825
    • Dr.Carol Davila Emergency University Central Military Hospital
  • Bucharest, Romania, 020125
    • Colentina Clinical Hospital
  • Bucharest, Romania, 021105
    • Prof. Dr. Matei Bals Institute of Infectious Diseases
  • Bucharest, Romania, 011025
    • Sana Monitoring SRL
  • Bucuresti, Romania, 031864
    • Centrul Medical Hifu Terramed Conformal S.R.L.
  • Constanta, Romania, RO-900591
    • Affidea Romania SRL
  • Iasi, Romania, 700506
    • Gastromedica Srl
  • Oradea, Romania, 410066
    • Dr. Tirnaveanu Amelita Private Practice
  • Timisoara, Romania, 300002
    • Dr. Goldis Gastroenterology Center SRL
  • Cluj
    • Cluj-Napoca, Cluj, Romania, 400006
      • Cluj-Napoca Emergency Clinical County Hospital
• Russian Federation
  • Kazan, Russian Federation, 420064
    • Kazan State Medical University
  • Moscow, Russian Federation, 111123
    • Moscow Clinical Scientific Center
  • Moscow, Russian Federation, 129110
    • Moscow Regional Research Clinical Institute Na Mfvladimirskiy
  • Nizhny Novgorod, Russian Federation, 603126
    • Nizhegorodskaya Regional Clinical Hospital n.a. Semashko
  • Novosibirsk, Russian Federation, 630117
    • Research Institute of Physiology and Basic Medicine
  • Rostov-on-Don, Russian Federation, 344022
    • Rostov State Medical University
  • Rostov-on-Don, Russian Federation, 344091
    • Rostov State Medical University
  • Saint Petersburg, Russian Federation
    • Russian Medical Military Academy n.a. S.M. Kirov
  • Saint-Petersburg, Russian Federation, 191119
    • Union Clinic, LLC
  • Samara, Russian Federation, 443011
    • Medical University Reaviz
  • Samara, Russian Federation, 443029
    • Private Healthcare Institution Clinical Hospital RZD-Medicina of Samara city
  • Samara, Russian Federation, 443093
    • Medical Company Hepatolog, LLC
  • Saratov, Russian Federation, 410053
    • SHI Regional Clinical Hospital
  • Smoensk, Russian Federation, 214018
    • Smolensk Regional Clinical Hospital
  • St. Petersburg, Russian Federation, 195257
    • St. Elizabeth Municipal Clinical Hospital
  • St. Petersburg, Russian Federation, 197022
    • First St. Petersburg State Medical University n.a. I.P Pavlov
  • Stavropol, Russian Federation, 355017
    • Stavropol State Medical University
  • Tyumen, Russian Federation, 625026
    • Regional Consulting and Diagnostics Centre
• Serbia
  • Belgrade, Serbia, 11080
    • Clinical Hospital Center ''Bezanijska Kosa''
  • Nis, Serbia, 18000
    • University Clinical Center Nis
  • Vrsac, Serbia, 26300
    • General Hospital Vrsac
  • Šumadijski Okrug
    • Kragujevac, Šumadijski Okrug, Serbia, 34000
      • University Clinical Center Kragujevac
• South Africa
  • Gauteng
    • Johannesburg, Gauteng, South Africa, 1619
      • CLINRESCO, ARWYP Medical Suites
    • Pretoria, Gauteng, South Africa, 0002
      • Dr. J Breedt
  • Western Cape
    • Claremont, Western Cape, South Africa, 7708
      • Dr JP Wright
• United Kingdom
  • Aberdeen, United Kingdom, AB25 2ZN
    • Aberdeen Royal Infirmary - PPDS
  • Edinburh, United Kingdom, EH4 2XU
    • Western General Hospital Edinburgh - PPDS
  • Newport, United Kingdom, NP20 2UB
    • Royal Gwent Hospital - PPDS
  • Wolverhampton, United Kingdom, WV10 0QP
    • New Cross Hospital
  • Bury
    • Lancashire, Bury, United Kingdom, BL9 7TD
      • Fairfield General Hospital - PPDS
    • Lancashire, Bury, United Kingdom, BL9 7TD
      • Pennine Acute Hospitals Trust
  • London, City Of
    • London, London, City Of, United Kingdom, E11 1NR
      • Whipps Cross University Hospital
  • Northumberland
    • North Shields, Northumberland, United Kingdom, NE29 8NH
      • North Tyneside General Hospital
  • Shropshire
    • Shrewsbury, Shropshire, United Kingdom, SY3 8XQ
      • Royal Shrewsbury Hospital
• United States
  • Arkansas
    • Little Rock, Arkansas, United States, 72209
      • Atria Clinical Research - Clinedge - PPDS
  • California
    • Lancaster, California, United States, 93534
      • OM Research LLC - Lancaster - ClinEdge - PPDS
    • Rialto, California, United States, 92377
      • Inland Empire Liver Foundation
  • Colorado
    • Colorado Springs, Colorado, United States, 80907
      • Asthma and Allergy Associates PC - CRN - PPDS
    • Colorado Springs, Colorado, United States, 80906
      • Peak Gastroenterology Associates
  • Florida
    • Coral Gables, Florida, United States, 33134
      • Advanced Clinical Research Network
    • Miami, Florida, United States, 33144
      • Nuren Medical and Research Center
    • Naples, Florida, United States, 34102
      • Gastroenterology Group Of Naples
    • Orlando, Florida, United States, 32810
      • Omega Research Consultants LLC - Clinedge - PPDS
    • Saint Augustine, Florida, United States, 32086
      • East Coast Institute for Research, LLC
  • Georgia
    • Columbus, Georgia, United States, 31904
      • Gastrointestinal Diseases, Inc. Research
  • Illinois
    • Chicago, Illinois, United States, 60611
      • Northwestern University
    • Chicago, Illinois, United States, 60637
      • University of Chicago Medical Center
  • Indiana
    • Evansville, Indiana, United States, 47714
      • Medisphere Medical Research Center LLC
    • Michigan City, Indiana, United States, 46360
      • LaPorte County Institute for Clinical Research
  • Louisiana
    • Lake Charles, Louisiana, United States, 70601
      • Clinical Trials of Swla Llc
    • Shreveport, Louisiana, United States, 71105
      • Louisiana Research Center LLC
  • Massachusetts
    • Boston, Massachusetts, United States, 02114
      • Massachusetts General Hospital
  • Mississippi
    • Ocean Springs, Mississippi, United States, 39564
      • Digestive Health Center PA
  • New York
    • Brooklyn, New York, United States, 11215
      • New York Total Medical Care PC
  • North Carolina
    • Statesville, North Carolina, United States, 28677
      • Piedmont Healthcare
  • Ohio
    • Cincinnati, Ohio, United States, 45219
      • Consultants For Clinical Research Inc
    • Cincinnati, Ohio, United States, 45249
      • Consultants For Clinical Research Inc
    • Fairfield, Ohio, United States, 45014
      • Consultants For Clinical Research Inc
  • Pennsylvania
    • Pittsburgh, Pennsylvania, United States, 15212
      • Allegheny Center for Digestive Health
    • Wyomissing, Pennsylvania, United States, 19610
      • Digestive Disease Associates
  • Tennessee
    • Germantown, Tennessee, United States, 38138
      • Gastro One
    • Nashville, Tennessee, United States, 37232
      • Vanderbilt University Medical Center
    • Union City, Tennessee, United States, 38261
      • Advanced Gastroenterology-Union City
  • Texas
    • Baytown, Texas, United States, 77521
      • Inquest Clinical Research/Coastal Gastroenterology Associates, PA
    • Cypress, Texas, United States, 77429
      • Northside Gastroenterology
    • Tomball, Texas, United States, 77375
      • DM Clinical Research - ERN - PPDS
  • Utah
    • Bountiful, Utah, United States, 84010
      • HP Clinical Research
  • Washington
    • Seattle, Washington, United States, 98195
      • University of Washington
    • Seattle, Washington, United States, 98195
      • Digestive Health Center at UWMC
    • Tacoma, Washington, United States, 98405
      • CHI Franciscan Digestive Care Associates
  • West Virginia
    • Elkins, West Virginia, United States, 26241
      • Exemplar Research, Inc. - Elkins
    • Morgantown, West Virginia, United States, 26506
      • West Virginia University Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 14 years to 78 years (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Participants and/or their parent or legally authorized representative must have an understanding, ability, and willingness to fully comply with study procedures and restrictions.
• Participants must be able to voluntarily provide written, signed, and dated informed consent and/or assent, as applicable, to participate in the study.
• Participants must be between greater than or equal to (>=)16 and <=80 years of age at the time of the signing of the informed consent/assent form.
• Participants less than (<) 18 years of age must weigh >=40 kg and must have body mass index (BMI) >=16.5 kilogram per square meter (kg/m^2).

• Participants must have a documented diagnosis of UC for >=3 months before screening. The following must be available in each participant's source documentation:

  1. A biopsy report to confirm the histological diagnosis.
  2. A report documenting disease duration based upon prior colonoscopy. Note: If this documentation is not available at the time of screening, a colonoscopy with biopsy to confirm the diagnosis is required during the screening period.
• Participants must be willing to undergo a flexible sigmoidoscopy or colonoscopy, including biopsy sample collection, during screening after all other inclusion criteria have been met.
• Participants must have moderate to severe active UC, defined as a total Mayo score of >=6, including a centrally read endoscopic subscore >=2, rectal bleeding subscore >=1, and stool frequency subscore >=1 at baseline.
• Participants must have evidence of UC extending proximal to the rectum (ie, not limited to proctitis).
• Participants must have had an inadequate response to, or lost response to, or had an intolerance to at least 1 conventional treatment such as mesalamine (5-aminosalicylate [ASA]), glucocorticoids, immunosuppressants (azathioprine [AZA], 6-mercaptopurine [6-MP], or methotrexate [MTX]), or anti-tumor necrosis factor (TNF).
• Participants receiving any treatment(s) for UC are eligible provided they have been, and are anticipated to be, on a stable dose for the designated period of time.
• Participants are males or nonpregnant, nonlactating females who, if sexually active, agree to comply with the contraceptive requirements of the protocol, or females of nonchildbearing potential.

Exclusion Criteria:

- Participants with indeterminate colitis, microscopic colitis, non-steroidal anti-inflammatory drug-induced colitis, ischemic colitis, infectious colitis, or clinical/histologic findings suggestive of Crohn's disease.

• Participants with colonic dysplasia or neoplasia. (Participants with prior history of adenomatous polyps will be eligible if the polyps have been completely removed.)
• Participants with past medical history or presence of toxic megacolon.
• Participants with colonic stricture, past medical history of colonic resection, a history of bowel surgery within 6 months before screening, or who are likely to require surgery for UC during the treatment period.
• Participants at risk for colorectal cancer must have a colonoscopy performed during the screening period with results available within 10 days before the baseline visit, unless the participant has had a surveillance colonoscopy performed within 1 year prior to screening, and any adenomatous polyps found at that examination have been excised. Colonoscopy report and pathology report (if biopsies are obtained) from the colonoscopy performed during screening or in the prior year confirming no evidence of dysplasia and colon cancer must be available in the source documents.

Participants at risk for colorectal cancer include, but are not limited to:

1. Participants with extensive colitis for >=8 years or disease limited to left side of colon (ie, distal to splenic flexure) for >=10 years before screening, regardless of age.

2. Participants >=50 years of age at the time of signing of the informed consent form.

   - Participants have had prior treatment with SHP647.

   - Participants with known or suspected intolerance or hypersensitivity to the investigational product(s), closely related compounds, or any of the stated ingredients.

   - Participants have received anti-TNF treatment within 60 days before baseline.

   - Participants have received any biologic with immunomodulatory properties (other than anti-TNFs) within 90 days before baseline.

   - Participants have received any nonbiologic treatment with immunomodulatory properties (other than their current background UC treatment) within 30 days before baseline.

   - Participants have ever received anti-integrin/adhesion molecule treatment (example (eg): natalizumab, vedolizumab, efalizumab, etrolizumab, or any other investigational anti-integrin/adhesion molecule).

   - Participants have received parenteral or rectal glucocorticoids, or rectal 5-ASA, within 14 days before screening endoscopic procedure.

   - Participants have received leukocyte apheresis or selective lymphocyte, monocyte, or granulocyte apheresis or plasma exchange within 30 days before baseline.

   - Participants have participated in other investigational studies within either 30 days or 5 half-lives of investigational product used in the study (whichever is longer) before baseline.

   - Participants have received a live (attenuated) vaccine within 30 days before the baseline visit.

   - Participants with active enteric infections (positive stool culture and sensitivity), Clostridium difficile infection or pseudomembranous colitis [Participants with C. difficile infection at screening may be allowed re-test after treatment], evidence of active cytomegalovirus infection or Listeria monocytogenes, known active invasive fungal infections such as histoplasmosis or parasitic infections, clinically significant underlying disease that could predispose the participants to infections, or a history of serious infection (requiring parenteral antibiotic and/or hospitalization) within 4 weeks before the baseline visit.

   - Participants with abnormal chest x-ray findings at screening, such as presence of active tuberculosis, general infections, heart failure, or malignancy.

   - Participants with evidence of active or latent infection with Mycobacterium tuberculosis (TB) or participants with this history who have not completed a generally accepted full course of treatment before randomization are excluded. All other participants must have either the Mantoux (purified protein derivative [PPD]) tuberculin skin test or interferon gamma release assay (IGRA) performed.

Participants who have no history of previously diagnosed active or latent tuberculosis are excluded if they have a positive Mantoux (PPD) tuberculin skin test (ie >=5 millimeter [mm] induration) or a positive IGRA (the latter to be tested at the site's local laboratory) during screening or within 12 weeks before screening. If IGRA test cannot be performed locally, a central laboratory may be used, with prior agreement from the sponsor.

1. An IGRA is strongly recommended for participants with a prior Bacillus Calmette-Guerin (BCG) vaccination, but may be used for any participant. Documentation of IGRA product used and the test result must be in the participant's source documentation if performed locally. Acceptable IGRA products include QuantiFERON TB Gold Plus In-Tube Test.
2. If the results of the IGRA are indeterminate, the test may be repeated, and if a negative result is obtained, enrollment may proceed. In participants with no history of treated active or latent tuberculosis, a positive test on repeat will exclude the participant. Participants with a history of active or latent TB infection must follow instructions for "participants with a prior diagnosis of active or latent TB are excluded unless both of the following criteria are met" in this criterion.
3. Participants with repeat indeterminate IGRA results, with no prior TB history, may be enrolled after consultation with a pulmonary or infectious disease specialist who determines low risk of infection (ie, participant would be acceptable for immunosuppressant [eg, anti-TNF] treatment without additional action). This consultation must be included in source documentation.

Results from a chest x-ray, taken within the 12 weeks before or during screening must show no abnormalities suggestive of active TB infection as determined by a qualified medical specialist.

Participants with a prior diagnosis of active or latent TB are excluded unless both of the following criteria are met:

1. The participant has previously received an adequate course of treatment for either latent (eg, 9 months of isoniazid or an acceptable alternative regimen, in a locale where rates of primary multidrug TB resistance are <5%. Participants from regions with higher rates of primary multidrug TB resistance are excluded) or active (acceptable multidrug regimen) TB infection. Evidence of diagnosis and treatment must be included in source documentation. Consultation with a pulmonary or infectious disease specialist to confirm adequate treatment (ie, participant would be acceptable for immunosuppressant [eg, anti-TNF] treatment without additional action) must be performed during the screening period. The consultation report must be included in source documentation prior to enrollment.

2. A chest x-ray performed within 12 weeks before or during screening indicates no evidence of active or recurrent disease, and documentation of interpretation by a qualified medical specialist must be included in source documentation.

   • Participants with a pre-existing demyelinating disorder such as multiple sclerosis or new onset seizures, unexplained sensory motor, or cognitive behavioral, neurological deficits, or significant abnormalities noted during screening.
   • Participants with any unexplained symptoms suggestive of progressive multifocal leukoencephalopathy (PML) based on the targeted neurological assessment during the screening period.
   • Participants with a transplanted organ. Skin grafts to treat pyoderma gangrenosum are allowed.
   • Participants with a significant concurrent medical condition at the time of screening or baseline, including, but not limited to, the following:

1. Any major illness/condition or evidence of an unstable clinical condition (eg, renal, hepatic, hematologic, gastrointestinal (except disease under study), endocrine, cardiovascular, pulmonary, immunologic [eg, Felty's syndrome], or local active infection/infectious illness) that, in the investigator's judgment will substantially increase the risk to the participant if he or she participates in the study.
2. Cancer or history of cancer or lymphoproliferative disease within the previous 5 years (other than resected cutaneous basal cell carcinoma, squamous cell carcinoma, or carcinoma in situ of the uterine cervix that has been treated with no evidence of recurrence).
3. Presence of acute coronary syndrome (eg, acute myocardial infarction, unstable angina pectoris) within 24 weeks before screening.

4. History of significant cerebrovascular disease within 24 weeks before screening.

   • Participants who have had significant trauma or major surgery within 4 weeks before the screening visit, or with any major elective surgery scheduled to occur during the study.
   • Participants with evidence of cirrhosis with or without decompensation.
   • Participants with primary sclerosing cholangitis.
   • Participants with evidence of positive hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb).

Note: If a participant tests negative for HBsAg, but positive for hepatitis B virus (HBcAb), the participant would be considered eligible if no presence of HBV DNA is confirmed by HBV DNA polymerasechainreaction(PCR) reflex testing performed in the central laboratory.

- Participants with chronic hepatitis C (HCV) (positive HCVAb and HCVRNA). Note: Participants who are HCVAb positive without evidence of HCVRNA may be considered eligible (spontaneous viral clearance or previously treated and cured [defined as no evidence of HCV RNA at least 12 weeks prior to baseline]).

- Participants with any of the following abnormalities in hematology and/or serum chemistry profiles during screening.

Note: Screening laboratory tests, if the results are considered by the investigator to be transient and inconsistent with the participant's clinical condition, may be repeated once during the screening period for confirmation. Results must be reviewed for eligibility prior to the screening endoscopy procedure.

1. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels >=3.0×upper limit of normal (ULN).
2. Total bilirubin level >=1.5×ULN or >2.0×ULN if the participant has a known documented history of Gilbert's syndrome.
3. Hemoglobin level <=80 gram per liter (g/L) (8.0 gram per deciliter [g/dL]).
4. Platelet count <=100×10^9 per liter (/L) (100,000 cells per cubic millimeter [mm^3]) or >=1000×10^9/L (1,000,000 cells/mm^3).

5. White blood cell count <=3.5×10^9/L (3500 cells/mm^3). - Absolute neutrophil count (ANC)<2×10^9/L (2000 cells/mm^3).

   • Serum creatinine level >1.5 × ULN or estimated glomerular filtration rate <30 ml/min/1.73m^2 based on the abbreviated Modification of Diet in Renal Disease Study Equation.

Note: If platelet count is <150,000 cells/mm^3, a further evaluation should be performed to rule out cirrhosis, unless another etiology has already been identified.

- Participants with known human immunodeficiency virus (HIV) infection based on documented history, with positive serological test, or positive HIV serologic test at screening, tested at the site's local laboratory in accordance with country requirements or tested at the central laboratory.

Note: A documented negative HIV test within 6 months of screening is acceptable and does not need to be repeated.

- Participants who have, or who have a history of (within 2 years before screening), serious psychiatric disease, alcohol dependency, or substance/drug abuse or dependency of any kind, including abuse of medical marijuana (cannabis).

- Participants with any other severe acute or chronic medical or psychiatric condition or laboratory or electrocardiogram (ECG) abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the participant inappropriate for entry into this study.

• Female participants who are planning to become pregnant during study period.
• Participants who do not agree to postpone donation of any organ or tissue, including male participants who are planning to bank or donate sperm and female participants who are planning to harvest or donate eggs, for the duration of the study and through 16 weeks after last dose of investigational product.
• Participants who are investigational site staff members or relatives of those site staff members or Participants who are Shire employees directly involved in the conduct of study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Ontamalimab 25 mg; Participants will receive 25 milligrams (mg) of ontamalimab (SHP647) subcutaneous (SC) injection using a prefilled syringe (PFS) on Week 0, Week 4 and Week 8.	Drug: Ontamalimab; Participants will receive 1 mL of SHP647 sterile aqueous buffered solution at an appropriate concentration to provide the intended dose of drug (25 or 75 mg).; Other Names: SHP647; PF-00547659
Experimental: Ontamalimab 75 mg; Participants will receive 75 mg of ontamalimab (SHP647) SC injection using PFS on Week 0, Week 4 and Week 8.	Drug: Ontamalimab; Participants will receive 1 mL of SHP647 sterile aqueous buffered solution at an appropriate concentration to provide the intended dose of drug (25 or 75 mg).; Other Names: SHP647; PF-00547659
Placebo Comparator: Placebo; Participants will receive placebo matched to ontamalimab (SHP647) SC injection using PFS on Week 0, Week 4 and Week 8.	Other: Placebo; Participants will receive 1 mL of sterile aqueous buffered solution.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Participants With Remission at Week 12	Remission was defined as a composite score of patient-reported symptoms using daily e-diary and centrally read endoscopy as stool frequency sub-score of 0 or 1 with at least a 1-point change from baseline, rectal bleeding sub-score of 0 and endoscopic sub-score of 0 or 1 (modified, excluded friability). The composite score was a recommended measure consisted of the Mayo score without the physician global assessment (PGA) sub-score and ranged from 0 to 9 points. The Mayo score was a measure of Ulcerative Colitis (UC) disease activity. It ranged from 0 to 12 points and consisted of 4 sub-scores, each graded from 0 to 3 with higher scores indicating more severe disease. The sub-scores were stool frequency (0-3); rectal bleeding (0-3); findings of endoscopy (0-3); PGA (0-3).	At Week 12

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Participants With Endoscopic Remission at Week 12	Endoscopic remission was defined by centrally read endoscopic sub-score 0 or 1 (modified, excluded friability). The centrally read endoscopic sub-score of Mayo score ranged from 0 to 3 with higher scores indicating more severe disease.	At Week 12
Number of Participants With Clinical Response Based on Composite Score at Week 12	Clinical response based on composite score was defined as a decrease from baseline in the composite score of patient-reported symptoms using daily e-diary and centrally read endoscopy of at least 2 points and at least 30 percent (%), with an accompanying decrease in the sub-score for rectal bleeding greater than or equal to (>=) 1 point or a sub-score for rectal bleeding less than or equal to (<=) 1. The composite score was a recommended measure derived from the Mayo score without the PGA sub-score and ranged from 0 to 9 points. The Mayo score was a measure of UC disease activity. It ranged from 0 to 12 points and consisted of 4 sub-scores, each graded from 0 to 3 with higher scores indicating more severe disease The sub-scores were stool frequency (0-3); rectal bleeding (0-3); findings of endoscopy (0-3); PGA (0-3).	At Week 12
Number of Participants With Partial Mayo Score <=2 With no Individual Sub-score Greater Than (>) 1 at Weeks 4, 8, and 12	The partial Mayo score ranged from 0 to 9 points and consisted of the following 3 sub-scores, each graded from 0 to 3 with higher scores indicating more severe disease: Stool frequency (0-3); Rectal bleeding (0-3); PGA (0-3). The partial Mayo score did not include the endoscopy sub-score.	At Weeks 4, 8, and 12
Number of Participants With Endoscopic Remission With Sub-score of 0 at Week 12	Endoscopic remission was defined by centrally read endoscopic sub-score 0 (modified, excluded friability). The centrally read endoscopic sub-score of Mayo score ranged from 0 to 3 with higher scores indicating more severe disease.	At Week 12
Change From Baseline in Total Sign/Symptom Score Based on PRO-UC Daily e-Diary at Week 12	Total sign/symptom score was the average of the average scores of worst abdominal pain over the past 24 hours and the conversion scale values for number of bowel movements blood, number of bowel movements with urgency, number of bowel movements and number of loose bowel movements, with scale ranged of 0-10, with higher scores indicating higher severity.	Baseline, Week 12
Number of Participants With Clinical Remission at Week 12	Clinical remission was defined by stool frequency (SF) sub-score of 0 or 1 with at least a 1-point change from baseline in stool frequency sub-score, and rectal bleeding sub-score of 0. Rectal bleeding is assessed on a scale from 0-3, where 0: no blood seen, 1: streaks of blood with stool less than half time, 2: obvious blood or streaks of blood with stool most of the time, and 3: blood alone passes. Stool frequency is assessed on a scale from 0-3, where 0: normal number of stools for this participant, 1: 1 to 2 stools more than normal, 2: 3 to 4 stools more than normal, and 3: 5 or more stools more than normal. Higher scores indicated more severe disease.	At Week 12
Number of Participants With Mucosal Healing Based on Endoscopic and Histological Assessment Using the Geboes Score Grading System at Week 12	Mucosal healing was defined by centrally read endoscopic sub-score 0 or 1 (modified, excluded friability) and centrally read Geboes score of <=2. The centrally read endoscopic sub-score of Mayo score ranged from 0 to 3 with higher scores indicating more severe disease. Geboes score grading system was a validated score for evaluating histologic disease activity in UC as follows: Grade 0 equal to (=) structural and architectural changes; Grade 1 = chronic inflammatory infiltrate; Grade 2 = lamina propria neutrophils and eosinophils; Grade 3 = neutrophils in the epithelium; Grade 4 = crypt destruction; Grade 5 = erosions or ulceration. A higher Geboes score indicating more severe disease.	At Week 12
Number of Participants With Remission Based on Total Mayo Score at Week 12	Remission was defined as a total Mayo score of <=2 with no individual sub-score (stool frequency, rectal bleeding, endoscopy [modified, excluded friability], and PGA) exceeding 1. The Total Mayo score ranged from 0 to 12 points and consisted of 4 sub-scores, each graded from 0 to 3 with higher scores indicating more severe disease: stool frequency (0-3); rectal bleeding (0-3); findings of endoscopy (0-3); PGA (0-3).	At Week 12
Number of Participants With Clinical Response Based on Total Mayo Score at Week 12	Clinical response (Mayo) was defined as a decrease from baseline in the total Mayo score of at least 3 points and at least 30%, with an accompanying decrease in the sub-score for rectal bleeding >=1 point or an absolute sub-score for rectal bleeding <=1. The Total Mayo score ranged from 0 to 12 points and consisted of the following 4 sub-scores, each graded from 0 to 3 with higher scores indicating more severe disease: stool frequency (0-3); rectal bleeding (0-3); findings of endoscopy (0-3); PGA (0-3).	At Week 12
Number of Participants With Clinical Remission With Stool Frequency Sub-scores of 0 or 1 and Rectal Bleeding Sub-score of 0 at Weeks 4 and 8	Clinical remission was defined as stool frequency sub-score of 0 or 1 with at least a 1-point change from baseline in stool frequency sub-score, and a rectal bleeding sub-score of 0. Rectal bleeding was assessed on a scale from 0-3, where 0: no blood seen, 1: streaks of blood with stool less than half time, 2: obvious blood or streaks of blood with stool most of the time, and 3: blood alone passes. Stool frequency was assessed on a scale from 0-3, where 0: normal number of stools for this participant, 1: 1 to 2 stools more than normal, 2: 3 to 4 stools more than normal, and 3: 5 or more stools more than normal. Higher scores indicated more severe disease	At Weeks 4 and 8
Number of Participants With Clinical Remission With Both Rectal Bleeding and Stool Frequency Sub-scores of 0 at Weeks 4, 8, and 12	Clinical remission was defined as both rectal bleeding and stool frequency sub-scores of 0. Rectal bleeding was assessed on a scale from 0-3, where 0: no blood seen, 1: streaks of blood with stool less than half time, 2: obvious blood or streaks of blood with stool most of the time, and 3: blood alone passes. Stool frequency was assessed on a scale from 0-3, where 0: normal number of stools for this participant, 1: 1 to 2 stools more than normal, 2: 3 to 4 stools more than normal, and 3: 5 or more stools more than normal. Higher scores indicated more severe disease.	At Weeks 4, 8, and 12
Number of Participants With Deep Remission at Week 12	Deep remission was defined as both endoscopic and rectal bleeding sub-scores of 0, and stool frequency sub-score <=1 and a centrally read Geboes score of <=2. The stool frequency sub-score, rectal bleeding sub-score and endoscopic sub-score of Mayo score ranged from 0 to 3 with higher scores indicating more severe disease. The composite score was a recommended measure consisted of the Mayo score without the PGA sub-score and ranged from 0 to 9 points. Geboes score grading system was a validated score for evaluating histologic disease activity in UC as follows: Grade 0 = structural and architectural changes; Grade 1 = chronic inflammatory infiltrate; Grade 2 = lamina propria neutrophils and eosinophils; Grade 3 = neutrophils in the epithelium; Grade 4 = crypt destruction; Grade 5 = erosions or ulceration. A higher Geboes score indicating more severe disease.	At Week 12
Change From Baseline in Average Worst Abdominal Pain Score Based on Patient Reported Outcome-ulcerative Colitis (PRO-UC) Daily e-Diary at Week 12	PRO-UC daily e-diary data was collected using a daily e-diary during the treatment period. Collection of the daily e-diary data was begun at least 10 days before the baseline visit. Participants were asked to record the signs and symptom data of abdominal pain worst severity, as experienced over the previous 24 hours, in the e-diary. Participant's signs and symptom average scores at each scheduled visit were calculated based on data recorded over the most recent 3 days (consecutive or non-consecutive) of the last 10 days prior to scheduled visit start date excluding the following days: day of any bowel preparation, day of endoscopy, any days between day of bowel preparation and day of endoscopy, and the 2 days after the day of endoscopy. Abdominal pain's worst severity assessment was based on an 11-point numerical rating scale with 0 anchor at "No pain" and 10 at "Worst Imaginable Pain" as experienced over the previous 24 hours, in e-diary. Higher scores indicating more severe pain.	Baseline, Week 12
Change From Baseline in Diarrhea (Average Loose Bowel Movements) Score Based on PRO-UC Daily e-Diary at Week 12	PRO-UC daily e-diary data was collected using a daily e-diary during the treatment period. Collection of the daily e-diary data was begun at least 10 days before the baseline visit. Participants were asked to record the signs and symptom data for number of loose bowel movement, as experienced over the previous 24 hours, in the e-diary. Participant's signs and symptom average scores at each scheduled visit were calculated based on data recorded over the most recent 3 days (consecutive or nonconsecutive) of the last 10 days prior to the scheduled visit start date excluding the following days: day of any bowel preparation, day of endoscopy, any days between day of bowel preparation and day of endoscopy, and the 2 days after the day of endoscopy. Average number of loose bowel movement ranged from 0-27. Higher scores indicating more frequent bowel movements.	Baseline, Week 12
Change From Baseline in Average Bowel Movements With Urgency Score Based on PRO-UC Daily e-Diary at Week 12	PRO-UC daily e-diary data was collected using a daily e-diary during the treatment period. Collection of the daily e-diary data was begun at least 10 days before the baseline visit. Participants were asked to record the signs and symptom data for number of bowel movement with urgency, as experienced over the previous 24 hours. Participant's signs and symptom average scores at each scheduled visit were calculated based on data recorded over the most recent 3 days (consecutive or nonconsecutive) of the last 10 days prior to the scheduled visit start date excluding the following days: day of any bowel preparation, day of endoscopy, any days between day of bowel preparation and day of endoscopy, and the 2 days after the day of endoscopy. Average number bowel movements urgency ranged from 0 to 27. Higher scores indicating more frequent bowel movements.	Baseline, Week 12
Change From Baseline in Absolute Stool Frequency (Average Number of Bowel Movements) Score Based on PRO-UC Daily e-Diary at Week 12	PRO-UC daily e-diary data was collected using a daily e-diary during the treatment period. Collection of the daily e-diary data was begun at least 10 days before the baseline visit. Participants were asked to record the signs and symptom data for average number of bowel movements, as experienced over the previous 24 hours. Participant's signs and symptom average scores at each scheduled visit were calculated based on data recorded over the most recent 3 days (consecutive or nonconsecutive) of the last 10 days prior to the scheduled visit start date excluding the following days: day of any bowel preparation, day of endoscopy, any days between day of bowel preparation and day of endoscopy, and the 2 days after the day of endoscopy. Average number bowel movements ranged from 0 to 27. Higher scores indicating more frequent bowel movements.	Baseline, Week 12
Change From Baseline in Absolute Rectal Bleeding (Average Number Bowel Movements With Blood) Score Based on PRO-UC Daily e-Diary at Week 12	PRO-UC daily e-diary data was collected using a daily e-diary during the treatment period. Collection of the daily e-diary data was begun at least 10 days before the baseline visit. Participants were asked to record the signs and symptom data for average number of bowel movements with blood, as experienced over the previous 24 hours. Participant's signs and symptom average scores at each scheduled visit were calculated based on data recorded over the most recent 3 days (consecutive or nonconsecutive) of the last 10 days prior to the scheduled visit start date excluding the following days: day of any bowel preparation, day of endoscopy, any days between day of bowel preparation and day of endoscopy, and the 2 days after the day of endoscopy. Average number bowel movements with blood ranged from 0 to 27. Higher scores indicating more frequent bowel movements.	Baseline, Week 12
Change From Baseline in Inflammatory Bowel Disease Questionnaire (IBDQ) Domains Scores at Weeks 8 and 12	IBDQ was a psychometrically validated participant-reported outcome (PRO) instrument for measuring the disease-specific health-related quality of life (HRQL) in participants with inflammatory bowel disease, including UC. The IBDQ consisted of 32 items, which were grouped into 4 domains: bowel function, emotional status, systemic symptoms, and social function The 4 domains were scored as follows: Bowel symptoms: 10 to 70; Systemic symptoms: 5 to 35; Emotional function: 12 to 84; Social function: 5 to 35. Higher scores indicating a better quality of life.	Baseline, Weeks 8 and 12
Change From Baseline in IBDQ Total Scores at Weeks 8 and 12	IBDQ was a psychometrically validated PRO instrument for measuring the disease-specific HRQL in participants with inflammatory bowel disease, included UC. The IBDQ consisted of 32 items, which were grouped into 4 domains: bowel function, emotional status, systemic symptoms, and social function. The 4 domains were scored as follows: Bowel symptoms: 10 to 70; Systemic symptoms: 5 to 35; Emotional function: 12 to 84; Social function: 5 to 35. The total IBDQ score ranged from 32 to 224. For the total score and each domain, a higher score indicating better HRQL. A score of at least 170 corresponds to clinical remission and an increase of at least 16 points was considered to indicate a clinically meaningful improvement.	Baseline, Weeks 8 and 12
Change From Baseline in Short Form-36 Health Survey (SF-36), Version 2, Acute (Physical and Mental Component Summary Scores) at Week 12	SF-36 was a generic quality-of-life instrument that had been widely used to assess health-related quality of life (HRQL) of participants). SF-36 consisted of 36 items that were aggregated into 8 multi-item scales (physical functioning [1=yes, limited a lot to 3=no, not limited at all], role-physical [1=all of the time to 5=none of the time], bodily pain [1=very severe to 6=none], general health [1=poor to 5=excellent], vitality [1=none of the time to 5=all of the time], social functioning [1=all of the time: to 5=none of the time], role emotional [1=all of the time to 5=none of the time] and mental health [1=all of the time to 5=none of the time]). Four domains comprised physical component summary (PCS) score (physical functioning, role-physical, bodily pain, general health) and remaining 4 domains comprised mental component summary (MCS) score (vitality, social functioning, role-emotional, mental health). The scores ranged from 0 to 100. Higher scores indicating better HRQL.	Baseline, Week 12
Change From Baseline in Short Form-36 Health Survey (SF-36), Version 2, Acute (Individual Domain Scores) at Week 12	SF-36 was a generic quality-of-life instrument that had been widely used to assess HRQL of participants. The SF-36 consisted of 36 items that were aggregated into 8 multi-item scales (physical functioning [1=yes, limited a lot to 3=no, not limited at all], role-physical [1=all of the time to 5=none of the time], bodily pain [1=very severe to 6=none], general health [1=poor to 5=excellent], vitality [1=none of the time to 5=all of the time], social functioning [1=all of the time: to 5=none of the time], role emotional [1=all of the time to 5=none of the time] and mental health [1=all of the time to 5=none of the time]), with scores ranged from 0 to 100. Higher scores indicating better HRQL.	Baseline, Week 12
Number of Participants Based on In-patient Hospitalization	Number of participants based on inpatient hospitalization due to all-cause hospitalization, gastrointestinal related, other illness/problem, and who had undergone gastrointestinal related procedures during the entire study period was reported.	Baseline up to Week 12
Median Duration of Total In-patient Days	In-patient days were calculated as Date of discharge - Date of admission + 1. Median duration of total inpatient days during the entire study period was reported.	Baseline up to Week 12

Collaborators and Investigators

• Sponsor: Shire

Publications and helpful links

Helpful Links

• To obtain more information on the study, click here/on this link

Study record dates

Study Major Dates

• Study Start (Actual): February 9, 2018
• Primary Completion (Actual): July 22, 2020
• Study Completion (Actual): October 23, 2020

Study Registration Dates

• First Submitted: August 21, 2017
• First Submitted That Met QC Criteria: August 22, 2017
• First Posted (Actual): August 23, 2017

Study Record Updates

• Last Update Posted (Actual): June 14, 2021
• Last Update Submitted That Met QC Criteria: June 7, 2021
• Last Verified: June 1, 2021

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Digestive System Diseases; Pathologic Processes; Gastrointestinal Diseases; Gastroenteritis; Colonic Diseases; Intestinal Diseases; Inflammatory Bowel Diseases; Ulcer; Colitis; Colitis, Ulcerative
• Other Study ID Numbers: SHP647-301; 2017-000599-27 (EudraCT Number)

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No