AzTrials
AzTrials

Plaque PsoriasisPhase 3NCT06108544

A Study About How Well TAK-279 Works and Its Safety in Participants With Moderate-to-severe Plaque Psoriasis During 60 Weeks of Treatment With a Withdrawal and Retreatment Period

A Phase 3 study testing TAK-279 and Apremilast in people with Plaque Psoriasis, run by Takeda at 217 sites in 16 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The main aim of this study is to show how well TAK-279 reduces the skin plaques compared to placebo, in participants with moderate-to-severe plaque psoriasis. Participants will be assigned to one of the 3 study treatments (TAK-279, apremilast (an approved treatment), or a placebo). Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Plaque Psoriasis
What is being tested?
TAK-279 and Apremilast
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
1,108 participants
Where
217 sitesin 16 countries
Study dates
6 Nov 2023to 7 Nov 2025
Phase
Phase 3
Are there results?
None posted in the registry

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

  • Plaque psoriasis for at least 6 months.
  • Moderate to severe disease.
  • Candidate for phototherapy or systemic therapy.

Who cannot join

  • Other forms of psoriasis.
  • History of recent infection.
  • Prior exposure to TAK-279 or active comparator.
  • Other protocol defined inclusion/exclusion criteria apply.

Trial locations and contacts

217 sites in 16 countries.

217 sites in 16 countries

United States66 sites
  • David Fivenson MD Dermatology PLLC

    Ann Arbor, Michigan, 48103-9746

  • University of Michigan Hospital - 1500 E Medical Center Dr

    Ann Arbor, Michigan, 48109-5360

  • Arlington Research Center

    Arlington, Texas, 76011-3800

  • Divine Dermatology and Aesthetics, LLC

    Atlanta, Georgia, 30315-2042

  • Advanced Medical Research, PC

    Atlanta, Georgia, 30342-1418

  • Oakland Hills Dermatology - 3400 Auburn Rd

    Auburn Hills, Michigan, 48326-3396

  • UT Physicians Dermatology - Bellaire Station

    Bellaire, Texas, 77401-3535

  • Allcutis Research LLC

    Beverly, Massachusetts, 01915

  • Zenith Research, Inc.

    Beverly Hills, California, 90211-1705

  • Total Dermatology

    Birmingham, Alabama, 35205

  • Beacon Clinical Research LLC

    Brockton, Massachusetts, 02301

  • DS Research - 1005 E. Lewis & Clark Pkwy Indiana Location

    Clarksville, Indiana, 47129-2201

  • ClinOhio Research Services

    Columbus, Ohio, 43213-4445

  • Modern Research Associates

    Dallas, Texas, 75231-6077

  • Revival Research Corporation - Florida - ClinEdge - PPDS

    Doral, Florida, 33122-1902

  • Duke Dermatology Clinic

    Durham, North Carolina, 27710-4000

  • Psoriasis Treatment Center of Central New Jersey

    East Windsor, New Jersey, 08520

  • UNISON Clinical Trials (Shahram Jacobs md inc.)

    Encino, California, 91436-2428

  • Wright State Physicians

    Fairborn, Ohio, 45324

  • Johnson Dermatology Clinic

    Fort Smith, Arkansas, 72916-6103

  • First OC Dermatology Research Inc.

    Fountain Valley, California, 92708-3701

  • Minnesota Clinical Study Center

    Fridley, Minnesota, 55432-3134

  • North Texas Center for Clinical Research

    Frisco, Texas, 75034

  • Cumberland Skin Center for Clinical Research - Objective Health - PPDS

    Hermitage, Tennessee, 37076-3497

  • Cahaba Dermatology Skin Health Center

    Hoover, Alabama, 35244-2111

  • Burke Pharmaceutical Research

    Hot Springs, Arkansas, 71913-6475

  • Dermatology & Advanced Aesthetics

    Lake Charles, Louisiana, 70605-1213

  • Vivida Dermatology - Flamingo Rd - Probity - PPDS

    Las Vegas, Nevada, 89119-5190

  • Long Beach Research Institute, LLC

    Long Beach, California, 90805-4587

  • Metropolis Dermatology Downtown LA - Probity - PPDS

    Los Angeles, California, 90017-5310

  • Skin Sciences, PLLC

    Louisville, Kentucky, 40217-1444

  • DS Research of Kentucky

    Louisville, Kentucky, 40241-6162

  • Skin Care Physicians of Georgia

    Macon, Georgia, 31217-3861

  • Apex Clinical Research Center

    Mayfield Heights, Ohio, 44124-4005

  • Florida Academic Centers Research

    Miami, Florida, 33136-1003

  • San Marcus Research Clinic Inc

    Miami Lakes, Florida, 33014-5602

  • FXM Research Miramar

    Miramar, Florida, 33027-4714

  • Tennessee Clinical Research Center

    Nashville, Tennessee, 37215-2888

  • Mount Sinai Doctors -234 E 85th St

    New York, New York, 10029-6504

  • Sadick Research Group

    New York, New York, 10075-0385

  • Virginia Clinical Research - 6160 Kempsville Cir

    Norfolk, Virginia, 23507

  • Northridge Clinical Trials

    Northridge, California, 91325-4122

  • Skin Specialists PC

    Omaha, Nebraska, 68144

  • Austin Institute for Clinical Research, Inc. - Pflugerville - ClinEdge - PPDS

    Pflugerville, Texas, 78660-6148

  • Medical Dermatology Specialists

    Phoenix, Arizona, 85006-2722

  • University of Pittsburgh Medical Center-3601 5th Ave

    Pittsburgh, Pennsylvania, 15213-3403

  • Oregon Medical Research Center PC

    Portland, Oregon, 97239-4501

  • ALLCUTIS Research, LLC.

    Portsmouth, New Hampshire, 03801-03804

  • Lawrence J Green, MD LLC

    Rockville, Maryland, 20850-6363

  • Texas Dermatology and Laser Specialists

    San Antonio, Texas, 78218-3128

  • Dermatology Clinical Research Center of San Antonio

    San Antonio, Texas, 78229-3409

  • TCR Medical Corporation

    San Diego, California, 92123-1523

  • University Clinical Trials

    San Diego, California, 92123

  • Dermatology Institute and Skin Care Center

    Santa Monica, California, 90404-2216

  • NorthShore Medical Group Dermatology - Skokie

    Skokie, Illinois, 60077-1049

  • Derm Research Center of NY

    Stony Brook, New York, 11790

  • Houston Center for Clinical Research, LLC

    Sugar Land, Texas, 77479-1001

  • Lenus Research & Medical Group

    Sweetwater, Florida, 33172-2741

  • Advanced Clinical Research Institute (ACRI) - Florida

    Tampa, Florida, 33607-6429

  • Olympian Clinical Research - 6331 Memorial Hwy

    Tampa, Florida, 33615

  • Montefiore Dermatology - BRANY - PPDS

    The Bronx, New York, 10467-1402

  • Noble Clinical Research

    Tucson, Arizona, 85704-7892

  • Center For Clinical Studies, LTD. LLP - 451 N Texas Ave

    Webster, Texas, 77598-4927

  • Center For Clinical Studies,LTD. LLP - 451 N Texas Ave

    Webster, Texas, 77598-4927

  • The Skin Surgery Center for Clinical Research - Objective Health - PPDS

    Winston-Salem, North Carolina, 27103-7109

  • Wake Forest Baptist Health Department of Dermatology - 4618 Country Club Rd

    Winston-Salem, North Carolina, 27157-0001

Other trials in United States

Poland35 sites
  • NZOZ Osteo Medic SC Artur Racewicz Jerzy Supronik

    Bialystok, Podlaskie Voivodeship, 15-351

  • Centrum Uslug Medycznych MaxMed

    Bochnia, 32-700

  • Centrum Medyczne Chojnice - PRATIA - PPDS

    Chojnice, Pomeranian Voivodeship, 89-600

  • Ambulatorium Barbara Bazela

    Elblag, 82-300

  • Centrum Badan Klinicznych PI-House sp. z o.o.

    Gdansk, Pomeranian Voivodeship, 80-546

  • AES - DRS - Synexus Polska Sp. z o.o. Oddzial w Gdyni

    Gdynia, Pomeranian Voivodeship, 81-537

  • AES - DRS - Synexus Polska Sp. z o.o. Oddzial w Katowicach

    Katowice, Silesian Voivodeship, 40-040

  • Centrum Medyczne Angelius Provita

    Katowice, Silesian Voivodeship, 40-611

  • Pro Familia Altera Sp. z o.o.

    Katowice, Silesian Voivodeship, 40-648

  • Globe Badania Kliniczne Spólka z o.o. - Klodzko

    Klodzko Dolnoslaskie, 57-300

  • Centrum Medyczne ALL-MED

    Krakow, Lesser Poland Voivodeship, 30-033

  • Krakowskie Centrum Medyczne - FutureMeds - PPDS

    Krakow, Lesser Poland Voivodeship, 31-501

  • MCM Krakow - PRATIA - PPDS

    Krakow, 30-727

  • Diamond Clinic

    Krakow, 31-559

  • Centrum Terapii Wspolczesnej

    Lódz, Lódzkie, 90-338

  • Luxderm Specjalistyczny Gabinet Dermatologiczny Dorota Krasowska

    Lublin, Lublin Voivodeship, 20-573

  • ETG Lublin - PPDS

    Lublin, 20-314

  • Twoja Przychodnia Nowosolskie Centrum Medyczne sp. z o.o

    Nowa Sól, Lubusz Voivodeship, 67-100

  • ETYKA Osrodek Badan Klinicznych

    Olsztyn, 10-117

  • DermoDent Centrum Medyczne Aldona Czajkowska Rafał Czajkowski, s.c.

    Osielsko, 86-031

  • Dermedic Jacek Zdybski

    Ostrowiec Świętokrzyski, Świętokrzyskie Voivodeship, 27-400

  • Ostrowieckie Centrum Medyczne

    Ostrowiec Świętokrzyski, Świętokrzyskie Voivodeship, 27-400

  • Solumed Centrum Medyczne

    Poznan, Greater Poland Voivodeship, 60-101

  • Twoja Przychodnia PCM

    Poznan, Greater Poland Voivodeship, 61-293

  • ETG Siedlce - PPDS

    Siedlce, Masovian Voivodeship, 08-110

  • ClinMedica Research

    Skierniewice, Lódzkie, 96-100

  • RCMed Oddzial Sochaczew

    Sochaczew, Masovian Voivodeship, 96-500

  • MICS Centrum Medyczne Torun - MICS - PPDS

    Torun, Ohio, 87-100

  • Clinical Research Group Sp. z o.o

    Warsaw, Masovian Voivodeship, 01-142

  • AES - DRS - Synexus Polska Sp. z o.o. Oddzial w Warszawie

    Warsaw, Masovian Voivodeship, 02-672

  • ETG Warszawa - PPDS

    Warsaw, Masovian Voivodeship, 02-677

  • FutureMeds - Targowek - PPDS

    Warsaw, Masovian Voivodeship, 03-291

  • Royalderm

    Warsaw

  • WroMedica

    Wroclaw, Lower Silesian Voivodeship, 51-685

  • dermMEDICA Sp. z o.o

    Wroclaw, 51-503

Other trials in Poland

Canada22 sites
  • Dermatology Research Institute, Inc. - Probity - PPDS

    Calgary, Alberta, T3A 2N1

  • Alberta DermaSurgery Centre - Probity - PPDS

    Edmonton, Alberta, T6G 1C2 Canada

  • VIDA Dermatology - Probity - PPDS

    Edmonton, Alberta, T6H 4J8

  • Brunswick Dermatology Centre - Probity - PPDS

    Fredericton, New Brunswick, E3B 1G9

  • Lima's Excellence In Allergy And Dermatology Research (Leader) Inc. - Probity - PPDS

    Hamilton, Ontario, L8L 3C3

  • Dermatrials Research

    Hamilton, Ontario, L8N 1Y2

  • DermEffects - Probity - PPDS

    London, Ontario, N6H 5L5

  • Lynderm Research Inc - Probity - PPDS

    Markham, Ontario, L3P 1X3

  • DermEdge Research - Probity - PPDS

    Mississauga, Ontario, L4Y 4C5

  • The Centre for Clinical Trials Inc. - Probity - PPDS

    Oakville, Ontario, L6J 7W5

  • Oshawa Clinic-117 King St

    Oshawa, Ontario, L1R 1R7

  • SKiN Centre for Dermatology - Peterborough - Probity - PPDS

    Peterborough, Ontario, K9J 1Z2

  • CaRe Clinic-Red Deer

    Red Deer, Alberta, T4N 7C3

  • Centre For Dermatology and Cosmetic Surgery - Probity - PPDS

    Richmond Hill, Ontario, L4B 1M5

  • Dr. S. K. Siddha Medicine Professional Corporation - Probity - PPDS

    Richmond Hill, Ontario, L4C 9M7

  • Skinsense Medical Research - 411 2nd Ave N - Probity - PPDS

    Saskatoon, Saskatchewan, S7K 0H6

  • Canadian Dermatology Centre - Probity - PPDS

    Toronto, Ontario, M3B 0A7

  • Toronto Research Centre - Probity - PPDS

    Toronto, Ontario, M3H 5Y8

  • Alliance Clinical Trials - Probity - PPDS

    Waterloo, Ontario, N2J 1C4

  • Siena Medical Research

    Westmount, Quebec, H3Z 2S6

  • XLR8 Medical Research - Probity - PPDS

    Windsor, Ontario, N8X 3V6

  • Wiseman Dermatology Research Inc. - Probity - PPDS

    Winnipeg, Manitoba, R3E 0V9

Other trials in Canada

Bulgaria16 sites
  • Multiprofile Hospital for Active Treatment - Dobrich AD

    Dobrich, 9300

  • Medical Center Asklepii OOD

    Dupnitsa, Kyustendil, 2600

  • MBAL Skin Systems, Doganovo

    Elin Pelin, Sofia, 2115

  • Multiprofile Hospital For Active Treatment Dr Tota Venkova

    Gabrovo, 5300

  • Diagnostic Consultative Center Sveti Georgi EOOD

    Haskovo, 6300

  • Medical Center Medconsult Pleven OOD

    Pleven, 5800

  • Medical Center Exacta Medica - Vasil Levski 60

    Pleven, 5801

  • University Multiprofile Hospital for Active Treatment -Dr. Georgi Stranski -Gen. V. Vazov Str 91

    Pleven

  • Medical Center Unimed EOOD

    Sevlievo, Gabrovo, 5400

  • Diagnostic and Consulting Center Aleksandrovska EOOD

    Sofia, Sofia-Grad, 1431

  • Diagnostic Consultative Centre - Focus-5 - LZIP EOOD

    Sofia, Sofia-Grad, 1463

  • Medical Center Hera EOOD

    Sofia, Sofia-Grad, 1510

  • Diagnostic Consultative Center XXVIII - Sofia - EOOD

    Sofia, Sofia-Grad, 1592

  • Ambulatory for Specialized Medical Care- Group Practice in Dermatology - Clinic EuroDerma OOD

    Sofia, Sofia-Grad, 1606

  • Military Medical Academy Multiprofile Hospital for Active Treatment - Sofia

    Sofia, Sofia-Grad, 1606

  • MC Comac Medical - IRN - PPDS

    Sofia, Sofia-Grad, 1612

Other trials in Bulgaria

China13 sites
  • China-Japan Friendship Hospital

    Beijing, Beijing Municipality, 100029

  • The Third Xiangya Hospital of Central South University

    Changsha, Hunan, 410013

  • West China Hospital Sichuan University

    Chengdu, Sichuan, 610041

  • Guangdong Provincial People's Hospital

    Guangzhou, Guangdong, 510080

  • Sir Run Run Shaw Hospital Zhejiang University School of Medicine - Qingchun Campus

    Hangzhou, Zhejiang, 310016

  • The Second Affiliated Hospital of Kunming Medical University

    Kunming, Yunnan, 650000

  • The Second Affiliated Hospital of Nanchang University

    Nanchang, Jiangxi, 330008

  • The First Affiliated Hospital With Nanjing Medical University(Jiangsu Province Hospital)

    Nanjing, Jiangsu, 210029

  • Huashan Hospital Fudan University - PPDS

    Shanghai, 200040

  • First Hospital of Shanxi Medical University

    Taiyuan, Shanxi, 030001

  • Tongji Hospital Tongji Medical College Huazhong University of Science and Technology

    Wuhan, Hubei, 430030

  • Henan Provincial People's Hospital

    Zhengzhou, Henan, 450003

  • Affiliated Hospital of Jiangsu University

    Zhenjiang, Jiangsu, 212001

Other trials in China

Czechia10 sites
  • Pratia Brno s.r.o. - PRATIA - PPDS

    Brno, South Moravian, 602 00

  • Dermamedica, s.r.o. - Kozni Ambulance Nachod

    Náchod, Hradec Králové Region, 547 01

  • Nemocnice AGEL Novy Jicin a.s

    Nový Jičín, Moravian-Silesian Region, 741 01

  • Dermskin s.r.o.

    Olomouc, Olomouc Region, 779 00

  • CCR Ostrava s.r.o.

    Ostrava, Moravian-Silesian Region, 702 00

  • Pratia Pardubice a.s. - PRATIA - PPDS

    Pardubice, 530 02

  • Praglandia s.r.o.

    Prague, Ohio, 150 00

  • CLINTRIAL s.r.o.

    Prague, Praha, Hlavní Mesto, 100 00

  • Fakultni nemocnice Kralovske Vinohrady

    Prague, 100 34

  • Prof. MUDr. Petr Arenberger, DrSc. - CRC - PPDS

    Prague, 110 00

Other trials in Czechia

United Kingdom9 sites
  • St Luke's Hospital

    Bradford, West Yorkshire, BD5 0NA

  • Accellacare of Yorkshire

    Chorley, Lancashire, PR7 7NA

  • Accellacare of Northamptonshire

    Harrow, Middlesex, HA1 3UJ

  • Velocity Clinical Research, High Wycombe - PPDS

    High Wycombe, Buckinghamshire, HP11 2QW

  • 4 Medical Clinical Solutions (4MCS) Swinton - PPDS

    Ilford, Essex, IG1 4HP

  • Whipps Cross Hospital

    London, London, City of, E11 1NR

  • Velocity Clinical Research, North London - PPDS

    London, Middlesex, N12 8BU

  • Accellacare - North London Clinical Studies Centre

    Northwood, Middlesex, HA6 2RN

  • Salford Royal Hospital - PPDS

    Salford, Lancashire, M6 8HD

Other trials in United Kingdom

Latvia8 sites
  • Semigallia

    Kuldīga, LV-3301

  • Adoria

    Riga, Ohio, LV-1011

  • Riga 1st Hospital

    Riga, LV-1001

  • Health Center 4, Center of Diagnostics

    Riga, LV-1003

  • J. Kisis

    Riga, LV-1003

  • Veseliba un estetika

    Riga, LV-1009

  • Health Center 4, Clinic of Dermatology

    Riga, LV-1013

  • Smite Aija doctor practice in dermatology, venerology

    Talsi, Talsu Aprinkis, LV-3201

Other trials in Latvia

Germany7 sites
  • Fachklinik Bad Bentheim

    Bad Bentheim, Lower Saxony, 48455

  • FutureMeds - Berlin - PPDS

    Berlin, 10629

  • Klinische Forschung Dresden GmbH (KFGN) - PRATIA - PPDS

    Dresden, Saxony, 01069

  • Praxis fur Dermatologie and Venerologie

    Dresden, Saxony, 01097

  • SRH Wald-Klinikum Gera GmbH

    Gera, Thuringia, 07548

  • Dermatologikum Hamburg

    Hamburg, 20354

  • Medizinisches Versorgungszentrum DermaKiel GmbH

    Kiel, 24148

Other trials in Germany

Hungary6 sites
  • Debreceni Egyetem Klinikai Kozpont Nagyerdei Campus

    Debrecen, Hajdú-Bihar, 4032

  • Somogy Varmegyei Kaposi Mor Oktato Korhaz

    Kaposvár, Somogy County, 7400

  • Pécsi Tudomanyegyetem - Vasvari Pal u.

    Pécs, 7632

  • Szegedi Tudomanyegyetem

    Szeged, Csongrád megye, 6720

  • Allergo-Derm Bakos Kft- Szolnok-Baross utca 20

    Szolnok, Jász-Nagykun-Szolnok, 5000

  • Vas Varmegyei Markusovszky Egyetemi Oktatokorhaz

    Szombathely, Vas County, 9700

Other trials in Hungary

Spain6 sites
  • Hospital Universitario Germans Trias i Pujol

    Badalona, Barcelona, 08915

  • Hospital de La Santa Creu i Sant Pau

    Barcelona, 08041

  • Hospital Universitario de Gran Canaria Doctor Negrin

    Las Palmas de Gran Canaria, 35010

  • Hospital Clinico San Carlos

    Madrid, 28040

  • Hospital Universitario La Paz - PPDS

    Madrid, 28046

  • Hospital de Manises

    Manises, Valencia, 46940

Other trials in Spain

Argentina5 sites
  • Conexa Investigación Clínica S.A.

    Buenos Aires, C1012

  • STAT Research S.A.

    Buenos Aires, C1023AAB

  • Instituto de Neumonologia y Dermatologia

    Buenos Aires, C1425BEA

  • Centro de Investigacion Clínica - CEDIC

    Ciudad Autónomade Buenos Aires, C1060ABN

  • Centro de Investigaciones Médicas Tucumán - PPDS

    San Miguel de Tucumán, T4000

Other trials in Argentina

Greece5 sites
  • Hospital A.Syggros

    Athens, Attica, 161 21

  • University General Hospital ''ATTIKON''

    Chaïdári, Attica, 124 62

  • University Hospital of Ioannina

    Loannina, Loannina, 455 00

  • Hospital Of Skin And Venereal Diseases of Thessaloniki

    Thessaloniki, 546 43

  • Papageorgiou General Hospital of Thessaloniki

    Thessaloniki, 564 29

Other trials in Greece

Israel5 sites
  • HaEmek Medical Center

    Afula, 18101

  • Hadassah Medical Center- Ein Kerem - PPDS

    Jerusalem, Jerusalem, 9112002

  • Rabin Medical Center - PPDS

    Petah Tikva, 49100

  • The Chaim Sheba Medical Center - PPDS

    Ramat Gan, Tel Aviv, 52621

  • Tel Aviv Sourasky Medical Center Ichilov - PPDS 27004

    Tel Aviv, Tel Aviv, 64239

Other trials in Israel

France3 sites
  • Centre Hospitalier Le Mans

    Le Mans, Ohio, 72037

  • AP-HM- Hôpital de La Timone

    Marseille, 13885

  • Hôpital Charles Nicolle-1 Rue de Germont

    Rouen, 76031

Other trials in France

Puerto Rico1 site
  • GCM Medical Group, PSC -62 Calle Jose Marti

    San Juan, 00909-3004

Other trials in Puerto Rico

About this study

Official title: A Phase 3, Randomized, Multicenter, Double-Blind, Placebo- and Active Comparator-Controlled Study With a Randomized Withdrawal and Retreatment Period to Evaluate the Efficacy, Safety, and Tolerability of TAK-279 in Subjects With Moderate-to-Severe Plaque Psoriasis

The main aim of this study is to show how well TAK-279 reduces the skin plaques compared to placebo, in participants with moderate-to-severe plaque psoriasis. Participants will be assigned to one of the 3 study treatments (TAK-279, apremilast (an approved treatment), or a placebo). Participants will be in the study for up to 69 weeks.

Read the detailed description

The drug being tested in this study is called TAK-279. TAK-279 is being tested to treat people with moderate to severe plaque psoriasis.

The study will enroll approximately 1000 patients. Participants will be randomly assigned (by chance, like flipping a coin) to one of the three treatment groups for TAK-279, placebo, or apremilast in a ratio of 2:1:1 which will remain undisclosed to the patient and investigator during the study (unless there is an urgent medical need):

  • TAK-279
  • Apremilast
  • Placebo

This multi-center trial will be conducted worldwide. The overall time to participate in this study is 69 weeks. Participants will go through a screening process to make sure they meet the rules for taking part in the study. This will take up to 35 days. If participants meet the study rules, they will be treated for up to 60 weeks. There will be a safety follow-up visit 4 weeks after their last day of treatment.

Being tested
TAK-279, Placebo, Apremilast
Keywords
Drug Therapy, Latitude Psoriasis 2, Latitude Research Program

What participants receive

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

  • TAK-279Drug

    Specified drug on specified days.

  • PlaceboDrug

    Specified drug on specified days.

  • ApremilastDrug

    Specified drug on specified days.

Study groups in NCT06108544
Study groupRoleWhat they receive
TAK-279ExperimentalNot described
Receives: Drug: TAK-279
PlaceboPlacebo comparatorNot described
Receives: Drug: Placebo
ApremilastActive comparatorNot described
Receives: Drug: Apremilast

What is being measured

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

  1. Percentage of Participants Achieving a Static Physician's Global Assessment (sPGA) of Clear (0) or Almost Clear (1) With a ≥2-Point Decrease from Baseline at Week 16 Comparing TAK-279 Against Placebo

    The sPGA is a 5-point scale of an average assessment of all psoriatic lesions based on erythema, scaling, and induration. The average of the 3 scales, rounded to the nearest whole number, is the final sPGA score. The sPGA score ranges from 0 to 4 (0 = Clear; 1 = Almost clear; 2 = Mild; 3 = Moderate; 4 = Severe). Higher scores indicate more severe disease activity. 'Clear' and 'Almost clear' will include all participants who score a 0 or 1.

    Measured: Baseline, Week 16

  2. Percentage of Participants Achieving ≥75% Improvement from Baseline in Psoriasis Area and Severity Index (PASI) Score at Week 16 Comparing TAK-279 Against Placebo

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing at least 75% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Baseline, Week 16

Secondary outcomes (52)
  1. Percentage of Participants Achieving 90% Improvement from Baseline in PASI (PASI-90) at Week 16 Comparing TAK-279 Against Placebo

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing at least 90% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Baseline, Week 16

  2. Percentage of Participants Achieving an sPGA of Clear (0) at Week 16 Comparing TAK-279 Against Placebo

    The sPGA is a 5-point scale of an average assessment of all psoriatic lesions based on erythema, scaling, and induration. The average of the 3 scales, rounded to the nearest whole number, is the final sPGA score. The sPGA score ranges from 0 to 4 (0 = Clear; 1 = Almost clear; 2 = Mild; 3 = Moderate; 4 = Severe). Higher scores indicate more severe disease activity. Higher scores indicate worsening. 'Clear' will include all participants who score a 0.

    Measured: Week 16

  3. Percentage of Participants Achieving PASI-100 at Week 16 Comparing TAK-279 Against Placebo

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing 100% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Week 16

  4. Percentage of Participants Achieving a Scalp-specific Physician's Global Assessment (ssPGA) of Clear (0) or Almost Clear (1) With a ≥2-Point Decrease from Baseline at Week 16 Comparing TAK-279 Against Placebo

    ssPGA assesses the overall severity of active psoriasis on the participant's scalp. Scalp lesions will be evaluated in terms of clinical signs of erythema, induration, and scaling and scored on 5-point ssPGA scale where 0=absence of disease and 4=severe disease. Higher scores indicate worsening.

    Measured: Baseline, Week 16

  5. Percentage of Participants Achieving PASI-75 at Week 4 Comparing TAK-279 Against Placebo

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing 75% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Week 4

  6. Percentage of Participants with a Baseline Dermatology Life Quality Index (DLQI) Score ≥2 who Achieve DLQI Score of 0 or 1 at Week 16 Comparing TAK-279 Against Placebo

    The DLQI is a 10-item validated questionnaire completed by the participant or caregiver used to assess the impact of skin disease on the participant's quality of life (QoL) during the previous week. The 10 questions cover the following topics: symptoms, embarrassment, shopping and home care, clothes, social and leisure, sport, work or study, close relationships, sex, and treatment. Each question is scored from 0=not at all, 1=a little, 2=a lot, and 3=very much, giving a total score ranging from 0 to 30. A high score is indicative of a poor QoL. DLQI scores indicate: 0-1 (no effect on participant's life), 2-5 (small effect on participant's life), 6-10 (moderate effect on participant's life), 11-20 (very large effect on participant's life), 21-30 (extremely large effect on participant's life).

    Measured: Week 16

  7. Percentage of Participants With a Baseline Psoriasis Symptoms and Signs Diary (PSSD) ≥1 who Achieve Weekly Mean PSSD Symptom Score of 0 at Week 16 Comparing TAK-279 Against Placebo

    The PSSD is an 11-item validated questionnaire that assesses symptoms (itch, pain, stinging, burning, and skin tightness) and participant-observable signs (skin dryness, cracking, scaling, shedding/flaking, redness, and bleeding) of moderate-to-severe plaque psoriasis. These symptoms and signs will be evaluated by asking participants to assign a numerical score representing of worst intensity over the last 24-hour on a scale from 0 to 10, with 0 indicating absence of symptoms or signs and 10 indicating worst imaginable symptoms or signs. The PSSD is a composite score calculated based on the scores for each question that can range between 0 and 100. A higher score indicates more severe disease.

    Measured: Week 16

  8. Change from Baseline in Nail Psoriasis Severity Index (NAPSI) at Week 16 Among Participants With Nail Involvement at Baseline Comparing TAK-279 Against Placebo

    The NAPSI quantifies severity of nail psoriasis by evaluating the presence or absence of psoriatic manifestations on the nail matrix (pitting, leukonychia, red spots on lunula, crumbling) and nail bed (onycholysis, splinter hemorrhages, subungual hyperkeratosis, oil drop [salmon patch dyschromia]). Each nail will be scored for both nail matrix and nail bed psoriasis for each quadrant (ranging from 0 [absence of psoriasis] to 4 [presence of psoriasis in all 4 quadrants]). The total NAPSI score equals the sum of scores for all of the finger nails evaluated and ranges from 0 to 80. Higher scores indicate more severe psoriasis.

    Measured: Baseline, Week 16

  9. Change from Baseline in Body Surface Area (BSA) Affected by Psoriasis at Week 16 Comparing TAK-279 Against Placebo

    Psoriasis BSA will be assessed by means of the handprint method, where the surface of the palm and 5 digits of the participant's hand represents 1% BSA. The sum of handprints equates to the total surface area of involvement.

    Measured: Week 16

  10. Percentage Change from Baseline in BSA Affected by Psoriasis at Week 16 Comparing TAK-279 Against Placebo

    Psoriasis BSA will be assessed by means of the handprint method, where the surface of the palm and 5 digits of the participant's hand represents 1% BSA. The sum of handprints equates to the total surface area of involvement.

    Measured: Week 16

  11. Percentage of Participants Achieving a Physician's Global Assessment (PGA) of the Hands and/or Feet of Clear (0) or Almost Clear (1) With a ≥2-Point Decrease From Baseline at Week 16 Comparing TAK-279 Against Placebo

    PGA is a 5-point scale and a score of 0 to 4 should be assigned, based on the category that best describes the severity of active psoriasis of the participant's hands and/or feet (palmoplantar), where 0=clear and 4=severe. Higher scores indicate worsening of severity. It will be evaluated for participants with the presence of active hand or foot psoriasis on Day 1.

    Measured: Baseline, Week 16

  12. Change from Baseline in DLQI at Week 16 Comparing TAK-279 Against Placebo

    The DLQI is a 10-item validated questionnaire completed by the participant or caregiver used to assess the impact of skin disease on the participant's QoL during the previous week. The 10 questions cover the following topics: symptoms, embarrassment, shopping and home care, clothes, social and leisure, sport, work or study, close relationships, sex, and treatment. Each question is scored from 0=not at all, 1=a little, 2=a lot, and 3=very much, giving a total score ranging from 0 to 30. A high score is indicative of a poor QoL. DLQI scores indicate: 0-1 (no effect on participant's life), 2-5 (small effect on participant's life), 6-10 (moderate effect on participant's life), 11-20 (very large effect on participant's life), 21-30 (extremely large effect on participant's life). It will be evaluated for participants with a baseline DLQI score ≥2.

    Measured: Baseline, Week 16

  13. Change from Baseline in the Short Form-36 Health Survey (SF-36) Version 2 Scores at Week 16 Comparing TAK-279 Against Placebo

    The SF-36 is a self-administered, validated questionnaire designed to measure generic health-related QoL. This 36-item questionnaire measures 8 domains, including physical and social functioning, physical and emotional role limitations, bodily pain, general health, vitality, mental health, physical and social functioning, physical and emotional role limitations, bodily pain, general health, vitality, mental health. Two summary scores, including the physical component summary (PCS) and mental component summary (MCS), will be calculated ranging from 0 (worst) to 100 (best). Higher scores indicate better QoL.

    Measured: Baseline, Week 16

  14. Change from Baseline in the EuroQoL 5-Dimension 5-Level Questionnaire (EQ-5D-5L) Scores at Week 16 Comparing TAK-279 Against Placebo

    EQ-5D-5L includes 5 dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) and 5 response levels for each domain (1=no problems, 2=slight problems, 3=moderate problems, 4=severe problems, and 5=extreme problems). The scores in the 5 dimensions will be summarized into a health state index score. The health state index value is a single value on a scale from less than 0 to 1 (negative values are valued as worse than dead) with higher scores indicating better health; 0=a health state equivalent to death, and 1=perfect health.

    Measured: Baseline, Week 16

  15. Change in Work Productivity and Activity Impairment-Psoriasis (WPAI-PSO) Questionnaire Scores at Week 16 Comparing TAK-279 Against Placebo

    The WPAI-PSO consists of 6 questions to determine employment status, hours missed from work because of psoriasis, hours missed from work for other reasons, hours actually worked, the degree to which psoriasis affected work productivity while at work, and the degree to which psoriasis affected activities outside of work. Four scores are derived: absenteeism, presenteeism (reduced productivity while at work), an overall work impairment score that combines absenteeism and presenteeism and impairment in activities performed outside of work. Each WPAI score will be expressed as impairment percentages (0-100) with higher numbers indicating greater impairment and less productivity, that is, worse outcomes.

    Measured: Week 16

  16. Percentage of Participants Achieving an sPGA of Clear (0) or Almost Clear (1) With a ≥2-Point Decrease from Baseline at Week 16 Comparing TAK-279 Against Apremilast

    The sPGA is a 5-point scale of an average assessment of all psoriatic lesions based on erythema, scaling, and induration. The average of the 3 scales, rounded to the nearest whole number, is the final sPGA score. The sPGA score ranges from 0 to 4 (0 = Clear; 1 = Almost clear; 2 = Mild; 3 = Moderate; 4 = Severe). Higher scores indicate more severe disease activity. Higher scores indicate worsening. 'Clear' and 'Almost clear' will include all participants who score a 0 or 1.

    Measured: Baseline to Week 16

  17. Percentage of Participants Achieving PASI-75 at Week 16 Comparing TAK-279 Against Apremilast

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing at least 75% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Week 16

  18. Percentage of Participants Achieving PASI-90 at Week 16 Comparing TAK-279 Against Apremilast

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing at least 90% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Week 16

  19. Percentage of Participants Achieving an sPGA of Clear (0) or Almost Clear (1) With a ≥2-Point Decrease from Baseline at Week 24 Comparing TAK-279 Against Apremilast

    The sPGA is a 5-point scale of an average assessment of all psoriatic lesions based on erythema, scaling, and induration. The average of the 3 scales, rounded to the nearest whole number, is the final sPGA score. The sPGA score ranges from 0 to 4 (0 = Clear; 1 = Almost clear; 2 = Mild; 3 = Moderate; 4 = Severe). Higher scores indicate more severe disease activity. 'Clear' and 'Almost clear' will include all participants who score a 0 or 1.

    Measured: Baseline to Week 24

  20. Percentage of Participants Achieving PASI-75 at Week 24 Comparing TAK-279 Against Apremilast

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing at least 75% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Week 24

  21. Percentage of Participants Achieving PASI-90 at Week 24 Comparing TAK-279 Against Apremilast

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing at least 90% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Week 24

  22. Change from Baseline in Weekly Mean PSSD Symptom Score at Week 16 Comparing TAK-279 Against Apremilast

    The PSSD is an 11-item validated questionnaire that assesses symptoms (itch, pain, stinging, burning, and skin tightness) and participant-observable signs (skin dryness, cracking, scaling, shedding/flaking, redness, and bleeding) of moderate-to-severe plaque psoriasis. These symptoms and signs will be evaluated by asking participants to assign a numerical score representing of worst intensity over the last 24-hour on a scale from 0 to 10, with 0 indicating absence of symptoms or signs and 10 indicating worst imaginable symptoms or signs. The PSSD is a composite score calculated based on the scores for each question that can range between 0 and 100. A higher score indicates more severe disease.

    Measured: Baseline to Week 16

  23. Percentage of Participants Achieving an ssPGA of Clear (0) or Almost Clear (1) With a ≥2-Point Decrease from Baseline at Week 16 Comparing TAK-279 Against Apremilast

    ssPGA assesses the overall severity of active psoriasis on the participant's scalp. Scalp lesions will be evaluated in terms of clinical signs of erythema, induration, and scaling and scored on 5-point ssPGA scale where 0=absence of disease and 4=severe disease. Higher scores indicate worsening.

    Measured: Baseline to Week 16

  24. Percentage of Participants Achieving PASI-100 at Week 16 Comparing TAK-279 Against Apremilast

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing 100% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Week 16

  25. Percentage of Participants Achieving PASI-100 at Week 24 Comparing TAK-279 Against Apremilast

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing 100% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Week 24

  26. Percentage of Participants Achieving an sPGA of Clear (0) at Week 16 Comparing TAK-279 Against Apremilast

    The sPGA is a 5-point scale of an average assessment of all psoriatic lesions based on erythema, scaling, and induration. The average of the 3 scales, rounded to the nearest whole number, is the final sPGA score. The sPGA score ranges from 0 to 4 (0 = Clear; 1 = Almost clear; 2 = Mild; 3 = Moderate; 4 = Severe). Higher scores indicate more severe disease activity. 'Clear' will include all participants who score a 0.

    Measured: Week 16

  27. Percentage of Participants with a Baseline DLQI Score ≥2 who Achieve DLQI Score of 0/1 at Week 16 Comparing TAK-279 Against Apremilast

    The DLQI is a 10-item validated questionnaire completed by the participant or caregiver used to assess the impact of skin disease on the participant's QoL during the previous week. The 10 questions cover the following topics: symptoms, embarrassment, shopping and home care, clothes, social and leisure, sport, work or study, close relationships, sex, and treatment. Each question is scored from 0=not at all, 1=a little, 2=a lot, and 3=very much, giving a total score ranging from 0 to 30. A high score is indicative of a poor QoL. DLQI scores indicate: 0-1 (no effect on participant's life), 2-5 (small effect on participant's life), 6-10 (moderate effect on participant's life), 11-20 (very large effect on participant's life), 21-30 (extremely large effect on participant's life).

    Measured: Week 16

  28. Percentage of Participants With a Baseline PSSD ≥1 who Achieve a Weekly Mean PSSD Symptom Score of 0 at Week 16 Comparing TAK-279 Against Apremilast

    The PSSD is an 11-item validated questionnaire that assesses symptoms (itch, pain, stinging, burning, and skin tightness) and participant-observable signs (skin dryness, cracking, scaling, shedding/flaking, redness, and bleeding) of moderate-to-severe plaque psoriasis. These symptoms and signs will be evaluated by asking participants to assign a numerical score representing of worst intensity over the last 24-hour on a scale from 0 to 10, with 0 indicating absence of symptoms or signs and 10 indicating worst imaginable symptoms or signs. The PSSD is a composite score calculated based on the scores for each question that can range between 0 and 100. A higher score indicates more severe disease.

    Measured: Week 16

  29. Change from Baseline in NAPSI Among Participants With Nail Involvement at Weeks 16 and 24 Comparing TAK-279 Against Apremilast

    The NAPSI quantifies severity of nail psoriasis by evaluating the presence or absence of psoriatic manifestations on the nail matrix (pitting, leukonychia, red spots on lunula, crumbling) and nail bed (onycholysis, splinter hemorrhages, subungual hyperkeratosis, oil drop [salmon patch dyschromia]). Each nail will be scored for both nail matrix and nail bed psoriasis for each quadrant (ranging from 0 [absence of psoriasis] to 4 [presence of psoriasis in all 4 quadrants]). The total NAPSI score equals the sum of scores for all of the finger nails evaluated and ranges from 0 to 80. Higher scores indicate more severe psoriasis.

    Measured: Baseline, Weeks 16 and 24

  30. Percentage of Participants Achieving an ssPGA of Clear (0) or Almost Clear (1) With a ≥2-Point Decrease from Baseline at Week 24 Comparing TAK-279 Against Apremilast

    ssPGA assesses the overall severity of active psoriasis on the participant's scalp. Scalp lesions will be evaluated in terms of clinical signs of erythema, induration, and scaling and scored on 5-point ssPGA scale where 0=absence of disease and 4=severe disease. Higher scores indicate worsening.

    Measured: Baseline to Week 24

  31. Change from Baseline in DLQI at Weeks 16 and 24 Comparing TAK-279 Against Apremilast

    The DLQI is a 10-item validated questionnaire completed by the participant or caregiver used to assess the impact of skin disease on the participant's QoL during the previous week. The 10 questions cover the following topics: symptoms, embarrassment, shopping and home care, clothes, social and leisure, sport, work or study, close relationships, sex, and treatment. Each question is scored from 0=not at all, 1=a little, 2=a lot, and 3=very much, giving a total score ranging from 0 to 30. A high score is indicative of a poor QoL. DLQI scores indicate: 0-1 (no effect on participant's life), 2-5 (small effect on participant's life), 6-10 (moderate effect on participant's life), 11-20 (very large effect on participant's life), 21-30 (extremely large effect on participant's life).

    Measured: Baseline, Weeks 16 and 24

  32. Change from Baseline in BSA Affected by Psoriasis at Weeks 16 and 24 Comparing TAK-279 Against Apremilast

    Psoriasis BSA will be assessed by means of the handprint method, where the surface of the palm and 5 digits of the participant's hand represents 1% BSA. The sum of handprints equates to the total surface area of involvement.

    Measured: Baseline, Weeks 16 and 24

  33. Percent Change from Baseline in BSA Affected by Psoriasis at Weeks 16 and 24 Comparing TAK-279 Against Apremilast

    Psoriasis BSA will be assessed by means of the handprint method, where the surface of the palm and 5 digits of the participant's hand represents 1% BSA. The sum of handprints equates to the total surface area of involvement.

    Measured: Baseline, Weeks 16 and 24

  34. Percentage of Participants Achieving an sPGA of Clear (0) at Week 24 Comparing TAK-279 Against Apremilast

    The sPGA is a 5-point scale of an average assessment of all psoriatic lesions based on erythema, scaling, and induration. The average of the 3 scales, rounded to the nearest whole number, is the final sPGA score. The sPGA score ranges from 0 to 4 (0 = Clear; 1 = Almost clear; 2 = Mild; 3 = Moderate; 4 = Severe). Higher scores indicate more severe disease activity. 'Clear' will include all participants who score a 0.

    Measured: Week 24

  35. Percentage of Participants With a Baseline DLQI Score ≥2 who Achieve a DLQI Score of 0/1 at Week 24 Comparing TAK-279 Against Apremilast

    The DLQI is a 10-item validated questionnaire completed by the participant or caregiver used to assess the impact of skin disease on the participant's QoL during the previous week. The 10 questions cover the following topics: symptoms, embarrassment, shopping and home care, clothes, social and leisure, sport, work or study, close relationships, sex, and treatment. Each question is scored from 0=not at all, 1=a little, 2=a lot, and 3=very much, giving a total score ranging from 0 to 30. A high score is indicative of a poor QoL. DLQI scores indicate: 0-1 (no effect on participant's life), 2-5 (small effect on participant's life), 6-10 (moderate effect on participant's life), 11-20 (very large effect on participant's life), 21-30 (extremely large effect on participant's life).

    Measured: Week 24

  36. Percentage of Participants With a Baseline PSSD ≥1 who Achieve a Weekly Mean PSSD Symptom Score of 0 at Week 24 Comparing TAK-279 Against Apremilast

    The PSSD is an 11-item validated questionnaire that assesses symptoms (itch, pain, stinging, burning, and skin tightness) and participant-observable signs (skin dryness, cracking, scaling, shedding/flaking, redness, and bleeding) of moderate-to-severe plaque psoriasis. These symptoms and signs will be evaluated by asking participants to assign a numerical score representing of worst intensity over the last 24-hour on a scale from 0 to 10, with 0 indicating absence of symptoms or signs and 10 indicating worst imaginable symptoms or signs. The PSSD is a composite score calculated based on the scores for each question that can range between 0 and 100. A higher score indicates more severe disease.

    Measured: Week 24

  37. Change from Baseline in ssPGA at Weeks 16 and 24 Comparing TAK-279 Against Apremilast

    ssPGA assesses the overall severity of active psoriasis on the participant's scalp. Scalp lesions will be evaluated in terms of clinical signs of erythema, induration, and scaling and scored on 5-point ssPGA scale where 0=absence of disease and 4=severe disease. Higher scores indicate worsening.

    Measured: Baseline, Weeks 16 and 24

  38. Percentage of Participants Achieving a PGA of the Hands and/or Feet of Clear (0) or Almost Clear (1) With a ≥2-Point Decrease From Baseline at Weeks 16 and 24 Comparing TAK-279 Against Apremilast

    PGA is a 5-point scale and a score of 0 to 4 should be assigned, based on the category that best describes the severity of active psoriasis of the participant's hands and/or feet (palmoplantar), where 0=clear and 4=severe. Higher scores indicate worsening of severity. It will be evaluated for participants with the presence of active hand or foot psoriasis on Day 1.

    Measured: Baseline, Weeks 16 and 24

  39. Change from Baseline in SF-36 Version 2 Scores at Weeks 16 and 24 Comparing TAK-279 Against Apremilast

    The SF-36 is a self-administered, validated questionnaire designed to measure generic health-related QoL. This 36-item questionnaire measures 8 domains, including physical and social functioning, physical and emotional role limitations, bodily pain, general health, vitality, mental health, physical and social functioning, physical and emotional role limitations, bodily pain, general health, vitality, mental health. Two summary scores, including the PCS and MCS, will be calculated ranging from 0 (worst) to 100 (best). Higher scores indicate better QoL.

    Measured: Baseline, Weeks 16 and 24

  40. Change from Baseline in the EQ-5D-5L Scores at Weeks 16 and 24 Comparing TAK-279 Against Apremilast

    EQ-5D-5L includes 5 dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) and 5 response levels for each domain (1=no problems, 2=slight problems, 3=moderate problems, 4=severe problems, and 5=extreme problems). The scores in the 5 dimensions will be summarized into a health state index score. The health state index value is a single value on a scale from less than 0 to 1 (negative values are valued as worse than dead) with higher scores indicating better health; 0=a health state equivalent to death, and 1=perfect health.

    Measured: Baseline, Weeks 16 and 24

  41. Change from Baseline in the WPAI-PSO Scores at Weeks 16 and 24 Comparing TAK-279 Against Apremilast

    The WPAI-PSO consists of 6 questions to determine employment status, hours missed from work because of psoriasis, hours missed from work for other reasons, hours actually worked, the degree to which psoriasis affected work productivity while at work, and the degree to which psoriasis affected activities outside of work. Four scores are derived: absenteeism, presenteeism (reduced productivity while at work), an overall work impairment score that combines absenteeism and presenteeism and impairment in activities performed outside of work. Each WPAI score will be expressed as impairment percentages (0-100) with higher numbers indicating greater impairment and less productivity, that is, worse outcomes.

    Measured: Baseline, Weeks 16 and 24

  42. Percentage of Participants Achieving an sPGA of Clear (0) or Almost Clear (1) With a ≥2-Point Decrease from Baseline at Weeks 24 and 40 Comparing TAK-279 Against Apremilast

    The sPGA is a 5-point scale of an average assessment of all psoriatic lesions based on erythema, scaling, and induration. The average of the 3 scales, rounded to the nearest whole number, is the final sPGA score. The sPGA score ranges from 0 to 4 (0 = Clear; 1 = Almost clear; 2 = Mild; 3 = Moderate; 4 = Severe). Higher scores indicate more severe disease activity. 'Clear' and 'Almost clear' will include all participants who score a 0 or 1.

    Measured: Baseline, Weeks 24 and 40

  43. Percentage of Participants Achieving PASI-75 at Weeks 24 and 40 Comparing TAK-279 Against Apremilast

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing at least 75% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Weeks 24 and 40

  44. Percentage of Participants Achieving PASI-90 at Weeks 24 and 40 Comparing TAK-279 Against Apremilast

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing at least 90% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Weeks 24 and 40

  45. Time to Relapse for PASI-75 Responders at Week 40 Comparing TAK-279 Against Placebo

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing at least 75% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Up to Week 60

  46. Percentage of Participants With Maintenance of PASI-75 Response at Week 60 Comparing TAK-279 Against Placebo

    PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Percentage of participants showing at least 75% improvement in PASI score relative to baseline PASI score will be reported.

    Measured: Week 60

  47. Percentage of Participants with Maintenance of sPGA of Clear (0) or Almost Clear (1) With a ≥2-Point Decrease from Baseline at Week 60 Comparing TAK-279 Against Placebo

    The sPGA is a 5-point scale of an average assessment of all psoriatic lesions based on erythema, scaling, and induration. The average of the 3 scales, rounded to the nearest whole number, is the final sPGA score. The sPGA score ranges from 0 to 4 (0 = Clear; 1 = Almost clear; 2 = Mild; 3 = Moderate; 4 = Severe). Higher scores indicate more severe disease activity. 'Clear' and 'Almost clear' will include all participants who score a 0 or 1.

    Measured: Baseline to Week 60

  48. Percentage of Participants With a Disease Relapse Comparing TAK-279 Against Placebo

    Relapse is defined as a percent change from baseline in PASI score that is at least 50% worse than that observed at Week 40. PASI is a measure of the average redness, thickness, and scaliness of psoriatic skin lesions (each graded on a 0 to 4 scale; 0 = none to 4 = very severe), weighted by the area of involvement (head, upper extremities, trunk, and lower extremities). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. Higher scores indicate worsening.

    Measured: Week 40

  49. Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Adverse Events of Special Interest (AESI)

    TEAE is defined as any event emerging or manifesting at or after the initiation of treatment with a study intervention or medicinal product or any existing event that worsens in either intensity or frequency following exposure to the study intervention or medicinal product. An AESI (serious or nonserious) is an adverse event of scientific and medical concern specific to the compound or program, for which ongoing monitoring and rapid communication by the investigator may be appropriate.

    Measured: Up to week 69

  50. Number of Participants With Clinically Significant Abnormalities in Vital Signs

    Measured: Up to week 69

  51. Number of Participants With Clinically Significant Laboratory Values

    Measured: Up to week 69

  52. Number of Participants With Clinically Significant Electrocardiogram (ECG) Findings

    Measured: Up to week 69

Timeline

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

  1. First posted31 Oct 2023
  2. Study start6 Nov 2023
  3. Primary completion6 Dec 2024
  4. Study completion7 Nov 2025

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
1,108 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06108544
Sponsor's protocol ID
TAK-279-3002
Other IDs
2023-505842-24-00, 2023
Status last verified
Nov 2025
First submitted
25 Oct 2023
Last updated
20 Nov 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: Takeda provides access to the de-identified individual participant data (IPD) for eligible studies to aid qualified researchers in addressing legitimate scientific objectives (Takeda's data sharing commitment is available on https://clinicaltrials.takeda.com/takedas-commitment?commitment=5). These IPDs will be provided in a secure research environment following approval of a data sharing request, and under the terms of a data sharing agreement.

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing TAK-279 and Apremilast in people with Plaque Psoriasis, run by Takeda at 217 sites in 16 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 3 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 20 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 217 sites in United States, Poland, Canada, Bulgaria, China and 11 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. Some participants in this study may receive a placebo. 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 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

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

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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 a Static Physician's Global Assessment (sPGA) of Clear (0) or Almost Clear (1) With a ≥2-Point Decrease from Baseline at Week 16 Comparing TAK-279 Against Placebo (time frame: Baseline, Week 16). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 20 Nov 2025.

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