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.
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Puerto Rico1 site
GCM Medical Group, PSC -62 Calle Jose Marti
San Juan, 00909-3004
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.
- Conditions
- Plaque Psoriasis
- 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 group | Role | What they receive |
|---|---|---|
| TAK-279 | Experimental | Not described Receives: Drug: TAK-279 |
| Placebo | Placebo comparator | Not described Receives: Drug: Placebo |
| Apremilast | Active comparator | Not described Receives: Drug: Apremilast |
What is being measured
The primary outcome is the main question the study is designed to answer.
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
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)
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Number of Participants With Clinically Significant Abnormalities in Vital Signs
Measured: Up to week 69
Number of Participants With Clinically Significant Laboratory Values
Measured: Up to week 69
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.
- First posted31 Oct 2023
- Study start6 Nov 2023
- Primary completion6 Dec 2024
- Study completion7 Nov 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Plaque PsoriasisStudies of the same condition, open and under way.
- More trials run by TakedaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 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)
Sponsor and investigators
- Lead sponsor
- Takeda
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Study Director, Study director, Takeda
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.
Study at a glance
From the registry record, last updated by the sponsor on 20 Nov 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT06108544
- Acronym / sponsor ID
- TAK-279-3002
- Conditions
- Plaque Psoriasis
- Keywords
- Drug Therapy, Latitude Psoriasis 2, Latitude Research Program
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 1,108 participants (actual)
- Lead sponsor
- TakedaIndustry (pharma, biotech, devices)
- Study start
- 6 Nov 2023 (actual)
- Primary completion
- 6 Dec 2024 (actual)
- Study completion
- 7 Nov 2025 (actual)
- First posted
- 31 Oct 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| TAK-279 | Experimental | Drug: TAK-279 |
| Placebo | Placebo comparator | Drug: Placebo |
| Apremilast | Active comparator | Drug: Apremilast |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Plaque psoriasis for at least 6 months.
- Moderate to severe disease.
- Candidate for phototherapy or systemic therapy.
Key exclusion criteria (4 listed)
- Other forms of psoriasis.
- History of recent infection.
- Prior exposure to TAK-279 or active comparator.
- Other protocol defined inclusion/exclusion criteria apply.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| TAK-279Specified drug on specified days. | Drug | TAK-279 |
| PlaceboSpecified drug on specified days. | Drug | Placebo |
| ApremilastSpecified drug on specified days. | Drug | Apremilast |
Primary outcome
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 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.
Percentage of Participants Achieving ≥75% Improvement from Baseline in Psoriasis Area and Severity Index (PASI) Score at Week 16 Comparing TAK-279 Against Placebo
Time frame: Baseline, Week 16
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.
52 secondary outcomes
Percentage of Participants Achieving 90% Improvement from Baseline in PASI (PASI-90) at Week 16 Comparing TAK-279 Against Placebo
Time frame: Baseline, Week 16
Percentage of Participants Achieving an sPGA of Clear (0) at Week 16 Comparing TAK-279 Against Placebo
Time frame: Week 16
Percentage of Participants Achieving PASI-100 at Week 16 Comparing TAK-279 Against Placebo
Time frame: Week 16
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
Time frame: Baseline, Week 16
Percentage of Participants Achieving PASI-75 at Week 4 Comparing TAK-279 Against Placebo
Time frame: Week 4
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
Time frame: Week 16
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
Time frame: Week 16
Change from Baseline in Nail Psoriasis Severity Index (NAPSI) at Week 16 Among Participants With Nail Involvement at Baseline Comparing TAK-279 Against Placebo
Time frame: Baseline, Week 16
Change from Baseline in Body Surface Area (BSA) Affected by Psoriasis at Week 16 Comparing TAK-279 Against Placebo
Time frame: Week 16
Percentage Change from Baseline in BSA Affected by Psoriasis at Week 16 Comparing TAK-279 Against Placebo
Time frame: Week 16
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
Time frame: Baseline, Week 16
Change from Baseline in DLQI at Week 16 Comparing TAK-279 Against Placebo
Time frame: Baseline, Week 16
Change from Baseline in the Short Form-36 Health Survey (SF-36) Version 2 Scores at Week 16 Comparing TAK-279 Against Placebo
Time frame: Baseline, Week 16
Change from Baseline in the EuroQoL 5-Dimension 5-Level Questionnaire (EQ-5D-5L) Scores at Week 16 Comparing TAK-279 Against Placebo
Time frame: Baseline, Week 16
Change in Work Productivity and Activity Impairment-Psoriasis (WPAI-PSO) Questionnaire Scores at Week 16 Comparing TAK-279 Against Placebo
Time frame: Week 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
Time frame: Baseline to Week 16
Percentage of Participants Achieving PASI-75 at Week 16 Comparing TAK-279 Against Apremilast
Time frame: Week 16
Percentage of Participants Achieving PASI-90 at Week 16 Comparing TAK-279 Against Apremilast
Time frame: Week 16
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
Time frame: Baseline to Week 24
Percentage of Participants Achieving PASI-75 at Week 24 Comparing TAK-279 Against Apremilast
Time frame: Week 24
Percentage of Participants Achieving PASI-90 at Week 24 Comparing TAK-279 Against Apremilast
Time frame: Week 24
Change from Baseline in Weekly Mean PSSD Symptom Score at Week 16 Comparing TAK-279 Against Apremilast
Time frame: Baseline to Week 16
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
Time frame: Baseline to Week 16
Percentage of Participants Achieving PASI-100 at Week 16 Comparing TAK-279 Against Apremilast
Time frame: Week 16
Percentage of Participants Achieving PASI-100 at Week 24 Comparing TAK-279 Against Apremilast
Time frame: Week 24
Percentage of Participants Achieving an sPGA of Clear (0) at Week 16 Comparing TAK-279 Against Apremilast
Time frame: Week 16
Percentage of Participants with a Baseline DLQI Score ≥2 who Achieve DLQI Score of 0/1 at Week 16 Comparing TAK-279 Against Apremilast
Time frame: Week 16
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
Time frame: Week 16
Change from Baseline in NAPSI Among Participants With Nail Involvement at Weeks 16 and 24 Comparing TAK-279 Against Apremilast
Time frame: Baseline, Weeks 16 and 24
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
Time frame: Baseline to Week 24
Change from Baseline in DLQI at Weeks 16 and 24 Comparing TAK-279 Against Apremilast
Time frame: Baseline, Weeks 16 and 24
Change from Baseline in BSA Affected by Psoriasis at Weeks 16 and 24 Comparing TAK-279 Against Apremilast
Time frame: Baseline, Weeks 16 and 24
Percent Change from Baseline in BSA Affected by Psoriasis at Weeks 16 and 24 Comparing TAK-279 Against Apremilast
Time frame: Baseline, Weeks 16 and 24
Percentage of Participants Achieving an sPGA of Clear (0) at Week 24 Comparing TAK-279 Against Apremilast
Time frame: Week 24
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
Time frame: Week 24
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
Time frame: Week 24
Change from Baseline in ssPGA at Weeks 16 and 24 Comparing TAK-279 Against Apremilast
Time frame: Baseline, Weeks 16 and 24
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
Time frame: Baseline, Weeks 16 and 24
Change from Baseline in SF-36 Version 2 Scores at Weeks 16 and 24 Comparing TAK-279 Against Apremilast
Time frame: Baseline, Weeks 16 and 24
Change from Baseline in the EQ-5D-5L Scores at Weeks 16 and 24 Comparing TAK-279 Against Apremilast
Time frame: Baseline, Weeks 16 and 24
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Nov 2025.
- To obtain more information on the study, click here/on this linkLink provided by the sponsor.
- Individual participant dataSharing planned: 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Study Director study director
Takeda
217 sites in 16 countries: see every site and its status.
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.