CClinicalTrials.gg
RecruitingNCT07489495Updated Sep 25, 2026

A Clinical Study of Belzutifan (MK-6482) and Zanzalintinib in People With Renal Cell Carcinoma (RCC) (LITESPARK-034/LS-034/MK-6482-034)

A Phase 3 interventional study of Belzutifan and Zanzalintinib in Carcinoma, Renal Cell, sponsored by Merck Sharp & Dohme LLC. Recruiting at 92 sites in 19 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-25.

Sponsored by Merck Sharp & Dohme LLC · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
758
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Researchers are looking for new ways to treat advanced renal cell carcinoma (RCC).

A standard (usual) treatment for certain people with RCC is belzutifan (a study medicine), which is a targeted therapy. Targeted therapy is a treatment that works to control how specific types of cancer cells grow and spread. Researchers want to learn if adding another targeted therapy called zanzalintinib (another study medicine) can treat more people with advanced RCC than belzutifan alone.

The goal of this study is to learn if people who receive belzutifan and zanzalintinib live longer overall and without the cancer getting worse compared to people who receive belzutifan and placebo.

02

Conditions studied

  • Carcinoma, Renal Cell
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

The main inclusion criteria include but are not limited to the following:

  • Has a histologically confirmed diagnosis of unresectable, advanced renal cell carcinoma (RCC) with clear cell component (with or without sarcomatoid features) ie, Stage IV RCC per American Joint Committee on Cancer (8th Edition)
  • Has measurable disease per Response Evaluation Criteria In Solid Tumors Version 1.1 (RECIST 1.1)
  • Has received no more than 3 prior systemic regimens for RCC, including only 1 prior anti-Programmed Cell Death-1/Programmed Cell Death 1 Ligand 1 therapy

Exclusion criteria

Exclusion Criteria:

For exclusion criteria: The main exclusion criteria include but are not limited to the following:

  • Has any of the following: a pulse oximeter reading \<92% at rest, requires intermittent supplemental oxygen, or required chronic supplemental oxygen
  • Has clinically significant cardiovascular disease within 12 months from first dose of study intervention
  • Has deep vein thrombosis within 3 months before randomization unless stable, asymptomatic, and treated with therapeutic anticoagulation for at least 4 weeks before randomization
  • Has a left ventricular ejection fraction ≤50% or below the institutional (or local laboratory) normal range as determined by multigated acquisition or echocardiogram
  • Has had major surgery within 8 weeks before randomization
  • Has current pneumonitis/interstitial lung disease
  • Has a history of human immunodeficiency virus infection
  • Has Hepatitis B or Hepatitis C virus infection
  • Has a known additional malignancy that is progressing or has required active treatment within the past 3 years
  • Has a history of solid organ transplant
  • Has not adequately recovered from major surgery or has ongoing surgical complications
04

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
758 participants (estimated)

Study arms

  • Experimental
    Belzutifan + Zanzalintinib

    Participants will receive 120 mg belzutifan orally and 60 mg zanzalintinib once daily for approximately 24 months.

    Drug: Belzutifan · Drug: Zanzalintinib

  • Active comparator
    Belzutifan + Placebo

    Participants will receive 120 mg belzutifan orally and zanzalintinib-matching placebo once daily for approximately 24 months.

    Drug: Belzutifan · Drug: Placebo

Interventions

  • DrugBelzutifan

    Tablet for oral administration.

    Also known as: MK-6482, PT2977, WELIREG

  • DrugZanzalintinib

    Tablet for oral administration.

    Also known as: XL092

  • DrugPlacebo

    Zanzalintinib-matching placebo tablet for oral administration.

05

What researchers measure

Primary outcomes

  1. Progression-free Survival (PFS)

    PFS is defined as the time from randomization to the first documented disease progression per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) based on blinded independent central review (BICR) or death due to any cause, whichever occurs first.

    Time frame: Up to approximately 30 months

  2. Overall Survival (OS)

    OS is defined as the time from randomization to death due to any cause.

    Time frame: Up to approximately 50 months

Secondary outcomes

  1. Objective Response Rate (ORR)

    ORR is defined as the percentage of participants who have achieved confirmed Complete Response (CR: disappearance of all target lesions) or a Partial Response (PR: at least a 30% decrease in the sum of diameters of target lesions) per RECIST 1.1 as assessed by BICR.

    Time frame: Up to approximately 30 months

  2. Duration of Response (DOR)

    DOR is defined as the interval from the first documented evidence of a CR (disappearance of all target lesions) or a PR (at least a 30% decrease in the sum of diameters of target lesions) per RECIST 1.1 until Progressive Disease (PD) or death due to any cause, whichever occurs first, in participants demonstrating a best confirmed response of CR or PR. Per RECIST 1.1, PD is defined as at least a 20% increase in the sum of diameters of target lesions. In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5 mm. The appearance of one or more new lesions is also considered PD.

    Time frame: Up to approximately 30 months

  3. Number of Participants Who Experience One or More Adverse Events (AEs)

    An AE is any unfavorable and unintended sign, symptom, or disease temporally associated with the use of a medicinal product or protocol-specified procedure, whether or not considered related to the medicinal product or protocol-specified procedure. Any worsening of a preexisting condition that is temporally associated with the use of the Sponsor's product, is also an AE. The number of participants who experience an AE will be reported.

    Time frame: Up to approximately 25 months

  4. Number of Participants who Discontinue Study Treatment Due to an AE

    An AE is any unfavorable and unintended sign, symptom, or disease temporally associated with the use of a medicinal product or protocol-specified procedure, whether or not considered related to the medicinal product or protocol-specified procedure. Any worsening of a preexisting condition that is temporally associated with the use of the Sponsor's product, is also an AE. The number of participants who discontinue study treatment due to an AE will be reported.

    Time frame: Up to approximately 24 months

  5. Change from Baseline in European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30) Global Health Status (Item 29) and Quality of Life (Item 30) Combined Score

    EORTC QLQ-C30 is a questionnaire to assess the overall quality of life (QoL) of cancer patients. Participant responses to questions regarding Global Health Status (GHS; "How would you rate your overall health during the past week?") and QoL ("How would you rate your overall quality of life during the past week?") are scored on a 7-point scale (1= Very poor to 7=Excellent). The combined score of GHS (Item 29) and QoL (Item 30) is computed by averaging the raw scores of the 2 items and then applying a linear transformation to standardize the average score, so that the combined scores range from 0-100. A higher score indicates a better outcome. The change from baseline in GHS and QoL combined score will be presented.

    Time frame: Baseline and up to approximately 25 months

  6. Change from Baseline in the EORTC QLQ-C30 Physical Functioning (Items 1-5) Combined Score

    EORTC QLQ-C30 is a questionnaire to assess the overall QoL of cancer patients. Participant responses to 5 questions about their physical functioning (Items 1 to 5) are scored on a 4-point scale (1=Not at All to 4=Very Much). The combined score of items 1 to 5 was computed by averaging the raw scores of the 5 items and then applying a linear transformation to standardize the average score, so that the combined scores range from 0-100. A higher score indicates a better outcome. The change from baseline in EORTC QLQ-C30 physical functioning (Items 1-5) combined score will be presented.

    Time frame: Baseline and up to approximately 25 months

  7. Change from Baseline in the EORTC QLQ-C30 Role Functioning (Items 6 and 7) Combined Score

    The EORTC QLQ-C30 is a cancer specific health-related quality of life questionnaire. The role functioning score is based on participant responses to questions scored on a 4-point scale (1=Not at All to 4=Very Much). The combined score was computed by averaging the raw scores of Items 6 and 7 and then applying a linear transformation to standardize the average score, so that the combined scores range from 0-100. Higher scores indicate better role functioning. The change from baseline in EORTC QLQ-C30 Role Functioning (Items 6 and 7) combined score will be reported.

    Time frame: Baseline and up to approximately 25 months

  8. Change From Baseline in Disease Symptoms Using the Functional Assessment of Cancer Therapy-Kidney Symptom Index-Disease-related Symptoms (FKSI-DRS) (Items 1-9) Score

    The FKSI-DRS index consists of a 9-item questionnaire that assesses the extent of participant symptoms from kidney cancer. Each item is scored on a 5-point scale (0=not at all to 4=very much). FKSI-DRS total score ranged from 0 (most severe symptoms) to 36 (no symptoms) with a higher score indicating a better outcome.

    Time frame: Baseline and up to approximately 25 months

  9. Time to Deterioration (TTD) in EORTC QLQ-C30 Global Health Status (Item 29) and Quality of Life (Item 30) Combined Score

    EORTC QLQ-C30 is a questionnaire to assess QoL of cancer patients. Participant responses to questions on GHS ("How would you rate your overall health during the past week?") and QoL ("How would you rate your overall QoL during the past week?") were scored on a 7-point scale (1= Very poor to 7=Excellent). The combined score of GHS (Item 29) and QoL (Item 30) was computed by averaging raw scores of the 2 items and applying a linear transformation to standardize the average score, so that the combined scores range from 0-100. A higher score indicates a better outcome. TTD was defined as the time from baseline to first onset of ≥10-point negative change (decrease) from baseline in GHS-QoL combined score. A longer TTD indicates a better outcome.

    Time frame: Up to approximately 25 months

  10. TTD in EORTC QLQ-C30 Physical Functioning (Items 1-5) Score

    EORTC QLQ-C30 is a questionnaire to assess the overall QoL of cancer patients. Participant responses to 5 questions about their physical functioning (Items 1 to 5) are scored on a 4-point scale (1=Not at All to 4=Very Much). The combined score of items 1 to 5 was computed by averaging the raw scores of the 5 items and then applying a linear transformation to standardize the average score, so that the combined scores range from 0-100. A higher score indicates a better outcome. TTD was defined as the time from baseline to first onset of ≥10-point negative change (decrease) from baseline in physical functioning (Items 1 to 5). A longer TTD indicates a better outcome.

    Time frame: Up to approximately 25 months

  11. TTD in EORTC QLQ-C30 Role Functioning (Items 6 and 7) Score

    EORTC QLQ-C30 is a questionnaire to assess the overall QoL of cancer patients. Participant responses to questions about their role functioning (Items 6 and 7) are scored on a 4-point scale (1=Not at All to 4=Very Much). The combined score of Items 6 and 7 was computed by averaging the raw scores of the items and then applying a linear transformation to standardize the average score, so that the combined scores range from 0-100. A higher score indicates a better outcome. TTD was defined as the time from baseline to first onset of ≥10-point negative change (decrease) from baseline in role functioning (Items 6 and 7). A longer TTD indicates a better outcome.

    Time frame: Up to approximately 25 months

  12. TTD in Disease Symptoms Using the FKSI-DRS (Items 1-9) Score

    TTD is defined as time from the first dose of study treatment to the date of deterioration of FKSI-DRS score. The FKSI-DRS index consists of a 9-item questionnaire that assesses the extent of participant symptoms from kidney cancer. Each item is scored on a 5-point scale (0=not at all to 4=very much). FKSI-DRS total score ranged from 0 (most severe symptoms) to 36 (no symptoms) with a higher score indicating a better outcome. Deterioration is defined as a 3-point decrease (i.e. lower score) in symptom score and the time to true deterioration is the time to first onset of 3 or more decreases from baseline with confirmation under right-censoring rule (the last observation). A longer TTD indicates a better outcome.

    Time frame: Up to approximately 25 months

06

Study locations

89 of 92 sites recruiting
  • Northwest Georgia Oncology Centers, a Service of Wellstar Cobb Hospital ( Site 0102)
    Marietta, Georgia 30060, United States
    • Study Coordinator · Contact · 770-281-5124
    Recruiting
  • Washington University School of Medicine ( Site 0114)
    St Louis, Missouri 63110, United States
    • Study Coordinator · Contact · 314-362-7355
    Recruiting
  • Memorial Sloan Kettering Cancer Center ( Site 0126)
    New York, New York 10065, United States
    • Study Coordinator · Contact · 347-798-9213
    Recruiting
  • The West Clinic, P.C. ( Site 0115)
    Germantown, Tennessee 38138, United States
    • Study Coordinator · Contact · 901-683-0055
    Recruiting
  • Centro Oncologico Korben ( Site 0254)
    CABA, Buenos Aires C1426AHB, Argentina
    • Study Coordinator · Contact · +541159507952
    Recruiting
  • Hospital Italiano de Buenos Aires ( Site 0253)
    Ciudad de Buenos Aires, Buenos Aires 1181, Argentina
    • Study Coordinator · Contact · +541149590200
    Recruiting
  • Instituto de Investigaciones Clinicas Mar del Plata ( Site 0250)
    Mar del Plata, Buenos Aires B7600FZO, Argentina
    • Study Coordinator · Contact · +542234963224
    Recruiting
  • Centro Privado de RMI Río Cuarto S.A. II ( Site 0255)
    Río Cuarto, Córdoba Province X5800ALB, Argentina
    • Study Coordinator · Contact · +543584620273
    Recruiting
  • Sanatorio Parque ( Site 0251)
    Rosario, Santa Fe Province S2000DSV, Argentina
    • Study Coordinator · Contact · +5493416955611
    Recruiting
  • Instituto de Oncología de Rosario ( Site 0257)
    Rosario, Santa Fe Province S2000KZE, Argentina
    • Study Coordinator · Contact · +543414484830
    Recruiting
  • Instituto Alexander Fleming ( Site 0252)
    CABA, C1426ANZ, Argentina
    • Study Coordinator · Contact · +541132218900
    Recruiting
  • Centro Oncológico Riojano Integral ( Site 0256)
    La Rioja, X5004BAL, Argentina
    • Study Coordinator · Contact · +543804436443X108
    Recruiting
  • COE (Centro Oncológico de Excelencia) ( Site 0259)
    San Juan, J5402BGA, Argentina
    • Study Coordinator · Contact · +54 2644229585
    Recruiting
  • Macquarie University ( Site 2700)
    Macquarie University, New South Wales 2109, Australia
    Suspended
  • Princess Alexandra Hospital ( Site 2703)
    Woolloongabba, Queensland 4102, Australia
    Suspended
  • Peter MacCallum Cancer Centre ( Site 2702)
    Melbourne, Victoria 3000, Australia
    Suspended
  • CEDOES ( Site 0303)
    Vitória, Espírito Santo 29055-450, Brazil
    • Study Coordinator · Contact · +552721250202
    Recruiting
  • Instituto do Câncer e Transplante de Curitiba ( Site 0300)
    Curitiba, Paraná 80510-130, Brazil
    • Study Coordinator · Contact · +55 41 99205-7755
    Recruiting
  • Liga Norte Riograndense Contra o Câncer ( Site 0307)
    Natal, Rio Grande do Norte 59062-000, Brazil
    • Study Coordinator · Contact · +55 84 4009-5595
    Recruiting
  • Hope - Humanizacao Em Oncologia, Pesquisa E Ensino ( Site 0306)
    Ribeirão Preto, São Paulo 14026-610, Brazil
    • Study Coordinator · Contact · +55 16 3913-8181
    Recruiting
  • Fundação Faculdade Regional de Medicina de São José do Rio Preto ( Site 0302)
    São José do Rio Preto, São Paulo 15090-000, Brazil
    • Study Coordinator · Contact · +55 17 3201-5054
    Recruiting
  • The Ottawa Hospital Cancer Centre ( Site 0003)
    Ottawa, Ontario K1H 8L6, Canada
    • Study Coordinator · Contact · 613-737-7700
    Recruiting
  • IC La Serena Research ( Site 0405)
    La Serena, Coquimbo Region 1720430, Chile
    • Study Coordinator · Contact · 56958646664
    Recruiting
  • Clínica Puerto Montt ( Site 0404)
    Port Montt, Los Lagos Region 5500243, Chile
    • Study Coordinator · Contact · +56985383586
    Recruiting
  • Fundacion Arturo Lopez Perez ( Site 0401)
    Santiago, Region M. de Santiago 7500921, Chile
    • Study Coordinator · Contact · 56224205098
    Recruiting
  • Bradfordhill ( Site 0400)
    Santiago, Region M. de Santiago 8420383, Chile
    • Study Coordinator · Contact · 56229490970
    Recruiting
  • ONCOCENTRO APYS ( Site 0403)
    Viña del Mar, Valparaiso 2520598, Chile
    • Study Coordinator · Contact · 56323320850
    Recruiting
  • Masarykuv onkologicky ustav ( Site 0903)
    Brno, Brno-mesto 656 53, Czechia
    • Study Coordinator · Contact · +420543132216
    Recruiting
  • Fakultni nemocnice Ostrava ( Site 0904)
    Ostrava, Ostrava Mesto 708 52, Czechia
    • Study Coordinator · Contact · +420597374322
    Recruiting
  • Fakultni nemocnice Hradec Kralove ( Site 0902)
    Hradec Králové, 500 05, Czechia
    • Study Coordinator · Contact · +420727854666
    Recruiting
  • Fakultni nemocnice Olomouc ( Site 0901)
    Olomouc, 779 00, Czechia
    • Study Coordinator · Contact · +420588445923
    Recruiting
  • Fakulti poliklinika ( Site 0906)
    Prague, 128 08, Czechia
    • Study Coordinator · Contact · +420224966405
    Recruiting
  • Fakultni nemocnice v Motole ( Site 0900)
    Prague, 150 06, Czechia
    • Study Coordinator · Contact · +420734236410
    Recruiting
  • Herlev Hospital ( Site 1002)
    Herlev, Capital Region 2730, Denmark
    • Study Coordinator · Contact · 00 45 38689191
    Recruiting
  • Aarhus Universitetshospital, Skejby ( Site 1001)
    Aarhus, Central Jutland 8200, Denmark
    • Study Coordinator · Contact · +4591167472
    Recruiting
  • Centre Antoine Lacassagne ( Site 1209)
    Nice, Alpes-Maritimes 06189, France
    • Study Coordinator · Contact · +33492031538
    Recruiting
  • Hopital Europeen Marseille ( Site 1216)
    Marseille, Bouches-du-Rhone 13003, France
    • Study Coordinator · Contact · +33413427427
    Recruiting
  • LBM ONCOPOLE CLAUDIUS REGAUD ( Site 1215)
    Toulouse, Haute-Garonne 31059, France
    • Study Coordinator · Contact · +33531155050
    Recruiting
  • CHU Angers ( Site 1204)
    Angers, Maine-et-Loire 49933, France
    • Study Coordinator · Contact · +33241354694
    Recruiting
  • Clinique Victor Hugo Le Mans-Oncology-Radiotherapy ( Site 1203)
    Le Mans, Pays de la Loire Region 72000, France
    • Study Coordinator · Contact · +33 243297908
    Recruiting
  • CHU de Saint-Etienne ( Site 1202)
    Saint Priest En Jarez, Pays de la Loire Region 42271, France
    • Study Coordinator · Contact · +33477917082
    Recruiting
  • Universitaetsklinikum Augsburg ( Site 1316)
    Augsburg, Bavaria 86156, Germany
    • Study Coordinator · Contact · +498214002348
    Recruiting
  • klinikum rechts der isar der technischen universität münchen ( Site 1315)
    Munich, Bavaria 81675, Germany
    • Study Coordinator · Contact · 00498941402522
    Recruiting
  • Universitätsklinikum Jena ( Site 1313)
    Jena, Thuringia 07747, Germany
    • Study Coordinator · Contact · +4936419329970
    Recruiting
  • Charité Universitaetsmedizin Berlin - Campus Mitte ( Site 1312)
    Berlin, 10117, Germany
    • Study Coordinator · Contact · +4930450515288
    Recruiting
  • Alexandra General Hospital of Athens ( Site 1400)
    Athens, Attica 115 28, Greece
    • Study Coordinator · Contact · +302132162543
    Recruiting
  • ATTIKON GENERAL UNIVERSITY HOSPITAL ( Site 1401)
    Athens, Attica 124 62, Greece
    • Study Coordinator · Contact · +302105832549
    Recruiting
  • Metropolitan Hospital ( Site 1402)
    Athens, Attica 185 47, Greece
    • Study Coordinator · Contact · +302104809667
    Recruiting
  • Rambam Health Care Campus ( Site 1600)
    Haifa, 3109601, Israel
    • Study Coordinator · Contact · +97247772688
    Recruiting
  • Meir Medical Center. ( Site 1603)
    Kfar Saba, 4428164, Israel
    • Study Coordinator · Contact · +97297472555
    Recruiting
  • Rabin Medical Center ( Site 1602)
    Petah Tikva, 4941492, Israel
    • Study Coordinator · Contact · 97239378074
    Recruiting
  • Sheba Medical Center ( Site 1601)
    Ramat Gan, 5265601, Israel
    • Study Coordinator · Contact · 97235303030
    Recruiting
  • IRCCS - Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori" ( Site 1809)
    Meldola, Emilia-Romagna 47014, Italy
    • Study Coordinator · Contact · +390543739100
    Recruiting
  • Istituto Clinico Humanitas ( Site 1808)
    Rozzano, Milano 20089, Italy
    • Study Coordinator · Contact · 0282244061
    Recruiting
  • Istituto Oncologico Veneto IRCCS ( Site 1806)
    Catselfranco Veneto, Padova 31033, Italy
    • Study Coordinator · Contact · +39 0423732336
    Recruiting
  • Azienda Ospedaliera Universitaria Careggi ( Site 1807)
    Florence, Tuscany 50134, Italy
    • Study Coordinator · Contact · +390557949648
    Recruiting
  • A.O.U.C. Policlinico di Bari ( Site 1802)
    Bari, 70124, Italy
    • Study Coordinator · Contact · 00390805593767
    Recruiting
  • IRCCS Azienda Ospedaliero-Universitaria di Bologna, Policlinico di Sant'Orsola ( Site 1803)
    Bologna, 40138, Italy
    • Study Coordinator · Contact · +390512142204
    Recruiting
  • Fondazione IRCCS Istituto Nazionale dei Tumori ( Site 1800)
    Milan, 20133, Italy
    • Study Coordinator · Contact · 02 2390 3028
    Recruiting
  • AO Santa Maria della Misericordia ( Site 1805)
    Perugia, 06132, Italy
    • Study Coordinator · Contact · +39 0755784188
    Recruiting
  • Istituto Nazionale Tumori Regina Elena ( Site 1804)
    Roma, 00144, Italy
    • Study Coordinator · Contact · +39 0652666919
    Recruiting
  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS - Università Cattolica del Sacro Cuore ( Site 1801)
    Roma, 00168, Italy
    • Study Coordinator · Contact · 00390630155202
    Recruiting
  • Maastricht UMC+ ( Site 1901)
    Maastricht, Limburg 6229 HX, Netherlands
    • Study Coordinator · Contact · +31433877025
    Recruiting
  • Nederlands Kanker Instituut Antoni van Leeuwenhoek (NKI AVL) ( Site 1900)
    Amsterdam, North Holland 1066 CX, Netherlands
    • Study Coordinator · Contact · +3120 512 9111
    Recruiting
  • Haga Ziekenhuis locatie Leyweg ( Site 1906)
    The Hague, South Holland 2545 AA, Netherlands
    • Study Coordinator · Contact · +3170 210 2143
    Recruiting
  • AIDPORT Sp. z o.o. ( Site 2118)
    Skórzewo, Greater Poland Voivodeship 60-185, Poland
    • Study Coordinator · Contact · +48570783100
    Recruiting
  • Pratia MCM Krakow ( Site 2115)
    Krakow, Lesser Poland Voivodeship 30-727, Poland
    • Study Coordinator · Contact · +48122958160
    Recruiting
  • Mazowiecki Szpital Wojewódzki w Siedlcach-Siedleckie Centrum Onkologii ( Site 2102)
    Siedlce, Masovian Voivodeship 08-110, Poland
    • Study Coordinator · Contact · +48256403300
    Recruiting
  • MTZ Clinical Research Powered by Pratia ( Site 2107)
    Warsaw, Masovian Voivodeship 02-172, Poland
    • Study Coordinator · Contact · +48225725959
    Recruiting
  • Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie - P-Klinika Nowotworów Układu Moczowego ( Site 2100)
    Warsaw, Masovian Voivodeship 02-781, Poland
    • Study Coordinator · Contact · +48225462331
    Recruiting
  • Narodowy Instytut Onkologii - Oddzial w Gliwicach ( Site 2106)
    Gliwice, Silesian Voivodeship 44-102, Poland
    • Study Coordinator · Contact · +48322788237
    Recruiting
  • Severance Hospital, Yonsei University Health System ( Site 2903)
    Seoul, 03722, South Korea
    • Study Coordinator · Contact · +82-2-2228-8138
    Recruiting
  • Asan Medical Center ( Site 2901)
    Seoul, 05505, South Korea
    • Study Coordinator · Contact · +82-2-3010-5977
    Recruiting
  • Samsung Medical Center ( Site 2902)
    Seoul, 06351, South Korea
    • Study Coordinator · Contact · +82-2-3410-1767
    Recruiting
  • Hospital Universitario Virgen del Rocio ( Site 2306)
    Seville, Andalusia 41013, Spain
    • Study Coordinator · Contact · +34955013068
    Recruiting
  • Institut Català d'Oncologia - L'Hospitalet ( Site 2305)
    L'Hospitalet de Llobregat, Barcelona 08908, Spain
    • Study Coordinator · Contact · +34932607744
    Recruiting
  • HOSPITAL GENERAL UNIVERSITARIO GREGORIO MARAÑON ( Site 2301)
    Madrid, Madrid, Comunidad de 28007, Spain
    • Study Coordinator · Contact · +34914269393
    Recruiting
  • Hospital Universitari Vall d Hebron ( Site 2303)
    Barcelona, 08035, Spain
    • Study Coordinator · Contact · +34934894350
    Recruiting
  • Hospital Insular de Gran Canaria ( Site 2308)
    Las Palmas, 35016, Spain
    • Study Coordinator · Contact · +34928441738
    Recruiting
  • Hospital Universitario 12 de Octubre ( Site 2300)
    Madrid, 28041, Spain
    • Study Coordinator · Contact · +34913908339
    Recruiting
  • Fundación Instituto Valenciano de Oncología ( Site 2307)
    Valencia, 46009, Spain
    • Study Coordinator · Contact · +34961114229
    Recruiting
  • Hacettepe Universite Hastaneleri ( Site 2500)
    Sıhhiye, Ankara 06230, Turkey (Türkiye)
    • Study Coordinator · Contact · +905439340493
    Recruiting
  • Adana Medical Park Seyhan Hastanesi ( Site 2505)
    Adana, 01140, Turkey (Türkiye)
    • Study Coordinator · Contact · +905372688986
    Recruiting
  • Ankara University Health Practice and Research Hospitals ( Site 2506)
    Ankara, 06620, Turkey (Türkiye)
    • Study Coordinator · Contact · +90 312 595 71 12
    Recruiting
  • Trakya University Medical Faculty Hospital ( Site 2502)
    Edirne, 22030, Turkey (Türkiye)
    • Study Coordinator · Contact · +9005378528123
    Recruiting
  • Koc Universitesi Hastanesi ( Site 2501)
    Istanbul, 34010, Turkey (Türkiye)
    • Study Coordinator · Contact · 0090 850 250 8 250
    Recruiting
  • Western General Hospital ( Site 2608)
    Edinburgh, Edinburgh, City of EH4 2XU, United Kingdom
    • Study Coordinator · Contact · +441315371398
    Recruiting
  • The Beatson West of Scotland Cancer Centre ( Site 2602)
    Glasgow, Glasgow City G12 0YN, United Kingdom
    • Study Coordinator · Contact · +441413019916
    Recruiting
  • Leicester Royal Infirmary ( Site 2604)
    Leicester, Leicestershire LE1 5WW, United Kingdom
    • Study Coordinator · Contact · 0300 303 1573
    Recruiting
  • The Christie Hospital NHS Foundation Trust ( Site 2601)
    Withington, Manchester M20 4BX, United Kingdom
    • Study Coordinator · Contact · 0161 918 2546
    Recruiting
  • University Hospitals Birmingham NHS Foundation Trust ( Site 2610)
    Birmingham, B15 2GW, United Kingdom
    • Study Coordinator · Contact · +4407789651543
    Recruiting
  • University Hospital of Southampton ( Site 2606)
    Southampton, SO16 6YD, United Kingdom
    • Study Coordinator · Contact · 023 8077 7222
    Recruiting
07

References and documents

Individual participant data

Plan to share: Yes — https://trialstransparency.msdclinicaltrials.com/pdf/ProcedureAccessClinicalTrialData.pdf

08

Registry details

Key details

Study ID
NCT07489495
Lead sponsor
Merck Sharp & Dohme LLC
Collaborators
Exelixis
Responsible party
Sponsor
First posted
Mar 24, 2026
Start date
Apr 9, 2026
Primary completion
Nov 27, 2030 (estimated)
Completion
Nov 27, 2030 (estimated)
Last update
Sep 25, 2026

Study contacts

Toll Free Number
Contact
Trialsites@msd.com
1-888-577-8839
Medical Director
study director · Merck Sharp & Dohme LLC

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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