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Plaque PsoriasisPhase 3NCT06088043

A Study About How Well TAK-279 Works and Its Safety in Participants With Moderate-to-severe Plaque Psoriasis During 52 Weeks of Treatment

A Phase 3 study testing TAK-279 and Apremilast in people with Plaque Psoriasis, run by Takeda at 132 sites in 10 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
693 participants
Where
132 sitesin 10 countries
Study dates
6 Nov 2023to 22 Oct 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

132 sites in 10 countries.

132 sites in 10 countries

United States27 sites
  • Bellaire Dermatology Associates

    Bellaire, Texas, 77401-3505

  • Bexley Dermatology Research - Probity - PPDS

    Bexley, Ohio, 43209

  • Accellacare of Cary

    Cary, North Carolina, 27518-7414

  • Clinical Research Center of the Carolinas, LLC

    Charleston, South Carolina, 29407-5347

  • Kindred Hair & Skin Center - CAR

    Columbia, Maryland, 21046-1246

  • Driven Research LLC

    Coral Gables, Florida, 33134-3901

  • FXM Clinical Research Ft. Lauderdale, LLC

    Fort Lauderdale, Florida, 33308-5211

  • First OC Dermatology - Fountain Valley

    Fountain Valley, California, 92708-3701

  • Center for Dermatology Clinical Research

    Fremont, California, 94538-1614

  • Henderson Clinical Trials

    Henderson, Nevada, 89052-5016

  • Direct Helpers Research Center

    Hialeah, Florida, 33012-3618

  • Leavitt Clinical Research - 1542 Elk Creek Dr

    Idaho Falls, Idaho, 83404-8322

  • Dawes Fretzin Clinical Research Group-7910 N Shadeland Ave

    Indianapolis, Indiana, 46256-4697

  • Dartmouth Hitchcock Medical Center

    Lebanon, New Hampshire, 03766-1937

  • UCLA University of California Los Angeles

    Los Angeles, California, 90024

  • Marietta Dermatology & The Skin Cancer Center - Marietta

    Marietta, Georgia, 30060-7902

  • FXM Clinical Research Miami, LLC

    Miami, Florida, 33175-3582

  • International Clinical Research-Tennessee LLC

    Murfreesboro, Tennessee, 37130-2450

  • Northwell Health Physician Partners Dermatology at Lake Success - BRANY - PPDS

    New York, New York, 10003-3314

  • Renstar Medical Research -21 NE 1st Ave

    Ocala, Florida, 34470-6657

  • Saguaro Dermatology Associates, LLC - Probity - PPDS

    Phoenix, Arizona, 85008-3884

  • ALLCUTIS Research, LLC.

    Portsmouth, New Hampshire, 03801-6822

  • Arlington Dermatology

    Rolling Meadows, Illinois, 60008-3811

  • UC Davis Dermatology Clinic

    Sacramento, California, 95816-3370

  • Progressive Clinical Research PA - San Antonio

    San Antonio, Texas, 78213-2250

  • Revival Research Corporation - Michigan - ClinEdge - PPDS

    Troy, Michigan, 48084-3536

  • Grekin Skin Institute

    Warren, Michigan, 48088-3671

Other trials in United States

China20 sites
  • Peking University People's Hospital

    Beijing, Beijing Municipality, 100044

  • Beijing Friendship Hospital, Capital Medical University - PPDS

    Beijing, Beijing Municipality, 100050

  • Peking University Third Hospital

    Beijing, Beijing Municipality, 100191

  • Beijing Tongren Hospital, Capital Medical University

    Beijing, Beijing Municipality, 100730

  • The First Affiliated Hospital of Chongqing Medical University

    Chongqing, Chongqing Municipality, 400016

  • The First Affiliated Hospital of Fujian Medical University

    Fuzhou, Fujian, 350005

  • Dermatology Hospital of Southern Medical University

    Guangzhou, Guangdong, 510091

  • Sun Yat-sen Memorial Hospital, Sun Yat-sen University

    Guangzhou, Guangdong, 510120

  • Zhujiang Hospital of Southern Medical University

    Guangzhou, Guangdong, 510280

  • Zhejiang Provincial People's Hospital

    Hangzhou, Zhejiang, 310000

  • Shandong Provincial Hospital

    Jinan, Shandong, 250021

  • Shanghai Skin Disease Hospital

    Shanghai, Shanghai Municipality, 200020

  • The First Hospital of China Medical University

    Shenyang, Liaoning, 110001

  • The University of Hong Kong - Shenzhen Hospital

    Shenzhen, Guangdong, 518053

  • The First Hospital of Hebei Medical University

    Shijiazhuang, Hebei, 050031

  • The 1st Affiliated Hospital of Wenzhou Medical University - Nanbaixiang Campus

    Wenzhou, Zhejiang, 325000

  • Renmin Hospital of Wuhan University

    Wuhan, Hubei, 430060

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

    Wuhan, Hubei

  • The Second Affiliated Hospital of Xi'an Jiaotong University

    Xi'an, Shaanxi, 710004

  • General Hospital of Ningxia Medical University

    Yinchuan, Ningxia, 750004

Other trials in China

Poland19 sites
  • ClinicMed Daniluk, Nowak Spólka Komandytowa

    Bialystok, Podlaskie Voivodeship, 15-879

  • Centrum Medyczne Bydgoszcz- PRATIA - PPDS

    Bydgoszcz, 85-796

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

    Gdansk, Pomeranian Voivodeship, 80-382

  • Copernicus Podmiot Leczniczy Sp. z o.o. - al. Jana Pawla II 50

    Gdansk, Pomeranian Voivodeship, 80-462

  • Derm-art

    Gdynia, Pomeranian Voivodeship, 81-415

  • Centrum Medyczne Katowice - PRATIA - PPDS

    Katowice, Silesian Voivodeship, 40-081

  • Centrum Medyczne PROMED

    Krakow, 31-411

  • Uniwersytecki Szpital Kliniczny im. WAM - Centralny Szpital Weteranow-Lodz-ul. Plac J. Hallera 1

    Lodz, 90-647

  • Dermoklinika-Centrum Medyczne s.c

    Lódz, Lódzkie, 90-436

  • Clinical Best Solutions - Lublin

    Lublin, Lublin Voivodeship, 20-078

  • Rheumatology Clinic NZOZ Lecznica MAK-MED

    Nadarzyn, Masovian Voivodeship, 05-830

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

    Poznan, Greater Poland Voivodeship, 60-702

  • Twoja Przychodnia SCM - Slowackiego

    Szczecin, West Pomeranian Voivodeship, 71-500

  • Clinical Best Solutions - Warszawa

    Warsaw, Masovian Voivodeship, 00-710

  • MICS Centrum Medyczne Warszawa - MICS - PPDS

    Warsaw, Masovian Voivodeship, 00-874

  • High-Med Przychodnia Specjalistyczna

    Warsaw, Masovian Voivodeship, 01-817

  • Klinika Reuma Park sp . zoo Sp.k.

    Warsaw, Masovian Voivodeship, 02-665

  • Klinika Ambroziak - Kosiarzy 9A

    Warsaw, Masovian Voivodeship, 02-953

  • Cityclinic Przychodnia Lekarsko Psychologiczna Matusiak Spółka Partnerska

    Wroclaw, Lower Silesian Voivodeship, 50-566

Other trials in Poland

South Korea15 sites
  • The Catholic University of Korea, Bucheon St. Mary's Hospital

    Bucheon-si, Gyeonggido, 14647

  • Seoul National University Bundang Hospital

    Bundang-Gu, Gyeonggido, 13620

  • CHA Bundang Medical Center, CHA University - PPDS

    Bundang-Gu Seongnam-Si, Gyeonggido, 13496

  • Chungnam National University Hospital

    Daejeon, Daejeon Gwang'yeogsi, 35015

  • Konkuk University Medical Center

    Gwangjin-Gu, Seoul Teugbyeolsi, 05030

  • Chosun University Hospital

    Gwangju, Gwangju Gwang'yeogsi, 61453

  • Seoul National University Hospital

    Jongno-Gu, Seoul Teugbyeolsi, 03080

  • Georgia Skin and Cancer Clinic

    Savannah, Georgia, 31419-1768

  • The Catholic University of Korea, Seoul St. Mary's Hospital

    Seocho-Gu, Seoul Teugbyeolsi, 06591

  • Pusan National University Hospital

    Seogu, Busan Gwangyeogsi, 49241

  • Soon Chun Hyang University Hospital Seoul

    Seoul, Seoul Teugbyeolsi, 04401

  • Ewha Womans University Seoul Hospital

    Seoul, Seoul Teugbyeolsi, 07804

  • Kyung Hee University Hospital

    Seoul, 02447

  • Chung-Ang University Hospital

    Seoul, 06973

  • Yonsei University Wonju Severance Christian Hospital

    Wŏnju, 26426

Other trials in South Korea

Japan14 sites
  • Fukuoka University Hospital

    Fukuoka, Hukuoka, 814-0180

  • Tokai University Hospital

    Isehara-Shi, Kanagawa, 259-1143

  • Teikyo University Hospital

    Itabashi-Ku, Tokyo, 173-0003

  • Saruwatari Dermatology Clinic

    Kagoshima, Kagoshima-ken, 892-0826

  • Ohyama Dermatology Clinic

    Kumamoto, 861-4101

  • Nagoya City University Hospital

    Nagoya, Aiti, 467-0802

  • Takagi Dermatological Clinic

    Obihiro-Shi, Hokkaidô, 080-0013

  • Dermatology and Ophthalmology Kume Clinic

    Sakaishi, Ôsaka, 593-8324

  • JR Sapporo Hospital

    Sapporo, Hokkaidô, 060-0033

  • Medical Corporation Kojinkai Sapporo Skin Clinic

    Sapporo, Hokkaidô, 060-0063

  • Jichi Medical University Hospital

    Shimotsuke-Shi, Tochigi, 329-0431

  • Tokyo Medical University Hospital

    Shinjuku-Ku, Tokyo, 160-0023

  • JCHO Tokyo Yamate Medical Center

    Shinjuku-Ku, Tokyo, 169-0073

  • Tokyo Teishin Hospital

    Sumida-Ku, Tokyo

Other trials in Japan

Canada10 sites
  • CCA Medical Research - Probity - PPDS

    Ajax, Ontario, L1S 7K8

  • SimcoDerm Medical and Surgical Dermatology Centre - Probity - PPDS

    Barrie, Ontario, L4M 7G1

  • Beacon Dermatology - Probity - PPDS

    Calgary, Alberta, T3A 2N1

  • Kingsway Clinical Research - Probity - PPDS

    Etobicoke, Ontario, M8X 1Y9

  • Guelph Dermatology Research - Probity - PPDS

    Guelph, Ontario, N1H 1B1

  • Mediprobe Research Inc

    London, Ontario, N5X 2P1

  • North Bay Dermatology Center - Probity - PPDS

    North Bay, Ontario, P1B 3Z7

  • North York Research Inc. - Probity - PPDS

    North York, Ontario, M2M 4J5

  • Enverus Medical Research - Probity - PPDS

    Surrey, British Columbia, V3R 6A7

  • Research Toronto - Probity - PPDS

    Toronto, Ontario, M4W 2N4

Other trials in Canada

Italy8 sites
  • Presidio Ospedaliero Gaspare Rodolico

    Catania, Sicily, 95123

  • Azienda Usl Toscana Centro - Firenze

    Florence, Tuscany, 50125

  • IRCCS Az. Osp. Universitaria San Martino- IST

    Genoa, Liguria, 16132

  • ASL 1 L'Aquila - Presidio Ospedaliero San Salvatore

    L’Aquila, Abruzzo, 67100

  • Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico -Via Pace 9

    Milan, Lombardy, 20122

  • Azienda Ospedaliera Universitaria Luigi Vanvitelli - Via Pansini 5

    Naples, Campania, 80131

  • IRCCS Istituto Clinico Humanitas

    Rozzano, Lombardy, 20089

  • IRCCS Policlinico San Donato

    San Donato Milanese, Lombardy, 20097

Other trials in Italy

Taiwan8 sites
  • National Taiwan University Hospital - Hsin-Chu Branch

    Hsinchu, 300

  • Kaohsiung Veterans General Hospital

    Kaohsiung City, 81362

  • Taipei Medical University Shuang Ho Hospital

    New Taipei City, 23561

  • National Cheng Kung University Hospital

    Tainan, 70403

  • Mackay Memorial Hospital-Taipei branch

    Taipei, 104

  • Taipei Veterans General Hospital

    Taipei, 11217

  • Chang Gung Memorial Hospital, Linkou

    Taoyuan City, 33305

  • National Taiwan University Hospital

    Zhong Zheng Qu, 100

Other trials in Taiwan

Australia7 sites
  • The Skin Center - Probity - PPDS

    Benowa, Queensland, 4217

  • Veracity Clinical Research Pty Ltd

    Brisbane, Queensland, 4102

  • Skin Health Institute Inc - Probity - PPDS

    Carlton, Victoria, 3053

  • Sinclair Dermatology-East Melbourne

    East Melbourne, Victoria, 3002

  • St George Dermatology and Skin Cancer Center - Probity - PPDS

    Kogarah, New South Wales, 2217

  • Alfred Health

    Parkville, Victoria, 3004

  • Royal Melbourne Hospital

    Parkville, Victoria, 3050

Other trials in Australia

Germany4 sites
  • Hautarztpraxis Mahlow

    Blankenfelde-Mahlow, Brandenburg, 15831

  • Universitätsklinikum Schleswig-Holstein - Campus Lübeck

    Lübeck, Schleswig-Holstein, 23562

  • Universitätsklinikum Münster

    Münster, North Rhine-Westphalia, 48149

  • Klinikum Oldenburg AöR

    Oldenburg, Lower Saxony, 26133

Other trials in Germany

About this study

Official title: A Phase 3, Randomized, Multicenter, Double-Blind, Placebo- and Active Comparator-Controlled Study 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 61 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 600 patients. Participants will be randomly assigned (by chance, like flipping a coin) to one of the following treatment groups in a ratio of 3:1:1 to receive TAK-279, placebo, or apremilast which will remain undisclosed to the participant and study doctor during the study (unless there is an urgent medical need):

  1. TAK-279
  2. Placebo
  3. Apremilast

This multi-center trial will be conducted worldwide. 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 52 weeks (1 year). 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 1, 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 NCT06088043
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 (PASI-75 Response) 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 (47)
  1. Percentage of Participants Achieving 90% Improvement from Baseline in PASI (PASI-90 Response) 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 and Week 16

  5. 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

  6. 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

  7. 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 and Week 16

  8. 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: Baseline and Week 16

  9. Percent 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: Baseline and Week 16

  10. 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 and Week 16

  11. 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 and Week 16

  12. 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 and Week 16

  13. 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 and Week 16

  14. 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

  15. 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 and Week 16

  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

  17. 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

  18. 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 and Week 24

  19. 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

  20. 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

  21. 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 and Week 16

  22. 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: Week 16

  23. 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

  24. 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

  25. 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

  26. 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

  27. 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

  28. Change from Baseline in NAPSI, Among Participants with Nail Involvement at Baseline 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

  29. 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 and Week 24

  30. 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

  31. 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

  32. 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

  33. 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

  34. 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

  35. 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

  36. 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

  37. 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

  38. 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

  39. 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

  40. 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

  41. Percentage of Participants Achieving an sPGA of Clear (0) or Almost Clear (1) with a >=2-Point Decrease from Baseline at Weeks 24, 40, and 52 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, 40 and 52

  42. Percentage of Participants Achieving PASI-75 at Weeks 24, 40, and 52 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, 40 and 52

  43. Percentage of Participants Achieving PASI-90 at Weeks 24, 40, and 52 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, 40 and 52

  44. 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 56

  45. Number of Participants with Clinically Significant Vital Signs

    Measured: Up to Week 56

  46. Number of Participants with Clinically Significant Laboratory Values

    Measured: Up to Week 56

  47. Number of Participants with Clinically Significant Electrocardiogram (ECG) Findings

    Measured: Up to Week 56

Timeline

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

  1. First posted18 Oct 2023
  2. Study start6 Nov 2023
  3. Primary completion22 Jan 2025
  4. Study completion22 Oct 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
693 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06088043
Sponsor's protocol ID
TAK-279-3001
Other IDs
jRCT2031230583, 2023-505841-22-00, 2023
Status last verified
Oct 2025
First submitted
12 Oct 2023
Last updated
24 Oct 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 132 sites in 10 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 24 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 132 sites in United States, China, Poland, South Korea, Japan and 5 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 24 Oct 2025.

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