CClinicalTrials.gg
RecruitingNCT06997497Updated Sep 21, 2026

A Clinical Study of Calderasib (MK-1084) With Targeted Therapy and Chemotherapy in People With Colorectal Cancer (MK-1084-012/KANDLELIT-012)

A Phase 3 interventional study of Calderasib and Oxaliplatin in Colon Adenocarcinoma and Rectal Adenocarcinoma, sponsored by Merck Sharp & Dohme LLC. Recruiting at 238 sites in 29 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-21.

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

Phase
Phase 3
Study type
Interventional
Enrollment
477
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Researchers are looking for other ways to treat locally advanced or metastatic colorectal cancer (mCRC) that is unresectable and has a gene mutation called KRAS G12C.

Standard (or usual) treatments for this type of colorectal cancer may include mFOLFOX6 with or without bevacizumab. Researchers want to learn if adding calderasib (the study medicine) and cetuximab to mFOLFOX6 can treat locally advanced or mCRC with the KRAS G12C mutation. Calderasib and cetuximab are targeted therapies.

The goals of this study are to learn:

  • About the safety of calderasib with cetuximab and mFOLFOX6 and if people tolerate the treatments
  • If people who receive calderasib with cetuximab and mFOLFOX6 live longer without mCRC growing or spreading compared to people who receive mFOLFOX6 with or without bevacizumab.
Read the detailed description

This study will have 2 parts.

02

Conditions studied

  • Colon Adenocarcinoma
  • Rectal Adenocarcinoma
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 locally advanced unresectable or metastatic (unresectable Stage III or Stage IV as defined by American Joint Committee on Cancer [AJCC] eighth edition) colorectal adenocarcinoma
  • Part 2 only: Has not received systemic anticancer therapy for locally advanced unresectable or metastatic colorectal cancer; an exception is permitted for 1-2 cycles of FOLFOX or 1 cycle of CAPOX as optional chemotherapy before or during the screening period
  • Demonstrates presence of a Kirsten rat sarcoma viral oncogene homolog G12C (KRAS G12C) mutation
  • Human immunodeficiency virus (HIV)-infected participants must have well controlled HIV on antiretroviral therapy (ART)
  • Participants who are Hepatitis B surface antigen (HBsAg) positive are eligible if they have received hepatitis B virus (HBV) antiviral therapy and have undetectable HBV viral load
  • Participants with history of hepatitis C virus (HCV) infection are eligible if HCV viral load is undetectable

Exclusion criteria

Exclusion Criteria:

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

  • Has active inflammatory bowel disease requiring immunosuppressive medication or previous clear history of inflammatory bowel disease (eg, Crohn's disease, ulcerative colitis, chronic diarrhea)
  • Has uncontrolled, significant cardiovascular disease or cerebrovascular disease
  • Has known partial or complete dihydropyrimidine dehydrogenase (DPD) deficiency
  • HIV-infected participants with a history of Kaposi's sarcoma and/or Multicentric Castleman's Disease
  • Has received prior systemic anticancer therapy including investigational agents within 4 weeks before randomization, with the exception of the optional chemotherapy
  • Has 1 or more conditions that, in the opinion of the investigator, make the participant ineligible for treatment with bevacizumab
  • Has known additional malignancy that is progressing or has required active treatment within the past 3 years
  • Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis or leptomeningeal disease
  • Has active infection requiring systemic therapy
  • Has not adequately recovered from major surgery or have ongoing surgical complications
  • Has a history of (noninfectious) pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease
04

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
477 participants (estimated)

Study arms

  • Experimental
    Calderasib + Cetuximab + mFOLFOX6

    Participants will receive calderasib orally, cetuximab per label every 2 weeks (Q2W), and mFOLFOX6 chemotherapy: oxaliplatin per label every 2 weeks (Q2W), leucovorin or levofolinate calcium per label Q2W, and 5-fluorouracil (5-FU) per label Q2W. Treatment will continue until criteria for discontinuation is met.

    Drug: Calderasib · Drug: Oxaliplatin · Drug: Leucovorin/levofolinate calcium · Drug: 5-Fluorouracil · Biological: Cetuximab

  • Active comparator
    mFOLFOX6

    Participants will receive mFOLFOX6 chemotherapy: oxaliplatin per label Q2W, leucovorin or levofolinate calcium per label Q2W, and 5-fluorouracil (5-FU) per label Q2W. Participants may also receive bevacizumab or bevacizumab biosimilar Q2W at the investigator's discretion. Treatment will continue until criteria for discontinuation is met.

    Drug: Oxaliplatin · Drug: Leucovorin/levofolinate calcium · Drug: 5-Fluorouracil · Drug: Bevacizumab · Drug: Bevacizumab biosimilar

Interventions

  • DrugCalderasib

    Oral tablet

    Also known as: MK-1084

  • DrugOxaliplatin

    Per label

  • DrugLeucovorin/levofolinate calcium

    Per label

  • Drug5-Fluorouracil

    Per label

  • BiologicalCetuximab

    Per label

    Also known as: Erbitux

  • DrugBevacizumab

    Per label

    Also known as: Avastin

  • DrugBevacizumab biosimilar

    Per label

    Also known as: MVASI

05

What researchers measure

Primary outcomes

  1. Number of Participants Experiencing Dose-Limiting Toxicity (DLT)

    A DLT is defined as the occurrence of protocol-specified toxicities if assessed by the investigator to be possibly, probably, or definitely related to study intervention administration.

    Time frame: Up to approximately 28 days

  2. Part 1: Number of Participants Who Experience an Adverse Event (AE)

    An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of a study intervention.

    Time frame: Up to approximately 44 months

  3. Part 1: Number of Participants Who Discontinue Study Treatment Due to an AE

    An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of a study intervention.

    Time frame: Up to approximately 44 months

  4. Progression Free Survival (PFS)

    PFS is defined as the time from randomization to the first documented disease progression or death due to any cause, whichever occurs first.

    Time frame: Up to approximately 44 months

Secondary outcomes

  1. Objective Response Rate (ORR)

    ORR is defined as a confirmed complete response (CR: the disappearance of all target lesions) or partial response (PR: at least a 30% decrease in the sum of diameters of target lesions) per Response Evaluation Criteria In Solid Tumors (RECIST) 1.1 as assessed by blinded independent central review (BICR). The percentage of participants who experience CR or PR as assessed by BICR will be presented.

    Time frame: Up to approximately 3 years

  2. Overall Survival (OS)

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

    Time frame: Up to approximately 5 years

  3. Duration of Response (DOR)

    For participants who demonstrate a confirmed Complete Response (CR: disappearance of all target lesions) or Partial Response (PR: at least a 30% decrease in the sum of diameters of target lesions) per RECIST 1.1, DOR is defined as the time from first documented evidence of CR or PR until progressive disease (PD) or death. 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. DOR as assessed by BICR will be presented.

    Time frame: Up to approximately 4 years

  4. Part 2: Number of Participants with an Adverse Event (AE)

    An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of a study intervention.

    Time frame: Up to approximately 5 years

  5. Part 2: Number of Participants who Discontinue Study Treatment Due to an AE

    An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of a study intervention.

    Time frame: Up to approximately 5 years

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

    The EORTC QLQ-C30 is a cancer specific health-related quality-of life (QoL) questionnaire. Participant responses to the questions regarding Global Health Status (GHS; "How would you rate your overall health during the past week?") and Quality of Life (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). Using linear transformation, raw scores are standardized, so that scores range from 0 to 100. The change from baseline in GHS (EORTC QLQ-C30 Item 29) and QoL (EORTC QLQ-C30 Item 30) combined score will be presented. A higher score indicates a better outcome.

    Time frame: Baseline and up to approximately 5 years

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

    The EORTC QLQ-C30 is a cancer specific health-related quality-of-life questionnaire. Participant responses to 5 questions about their physical functioning (Items 1-5) are scored on a 4-point scale (1=Not at All to 4=Very Much). Higher scores indicate better physical functioning. 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 5 years

  8. 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). Higher scores indicate better role functioning. The change from baseline in EORTC QLQ-C30 Role Functioning (Items 6 and 7) combined score will be presented.

    Time frame: Baseline and up to approximately 5 years

  9. Change from Baseline in the EORTC-QLQ-C30 Appetite Loss (Item 13) Score

    The EORTC QLQ-C30 is a cancer specific health-related quality-of life questionnaire, including a single-item scale score for appetite loss (QLQ-C30 Item 13). For this item, individual responses to the question "Have you lacked appetite?" are given on a 4-point scale (1=Not at all; 4=Very much). Scores are transformed to a range from 0-100, with a lower score indicating a better outcome. The change from baseline in the EORTC QLQ-C30 appetite loss (Item 13) scale score will be presented.

    Time frame: Baseline and up to approximately 5 years

  10. Change from Baseline in the EORTC-Quality of Life Questionnaire-Colorectal Cancer-Specific 29 Items (QLQ-CR29) Bloating (Item 37) Score

    The EORTC QLQ-CR29 is a health-related quality-of life questionnaire specific for colorectal cancer, including a single-item scale score for bloating (QLQ-CR29 Item 37). For this item, individual responses to the question "Did you have a bloated feeling in your abdomen?" are given on a 4-point scale (1=Not at all; 4=Very much). Scores are transformed to a range from 0-100, with a lower score indicating a better outcome. The change from baseline in the EORTC QLQ-CR29 bloating (Item 37) scale score will be presented.

    Time frame: Baseline and up to approximately 5 years

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

    The EORTC QLQ-C30 is a cancer specific health-related quality-of-life questionnaire. TTD is defined as the time from baseline to the first onset of a ≥10-point deterioration (decrease) from baseline in global health status (GHS) (EORTC QLQ-C30 Item 29) \& quality of life (QoL) combined score (EORTC QLQ-C30 Item 30). Using linear transformation, raw scores are standardized, so that scores range from 0 to 100. The TTD, as assessed based on a ≥10-point negative change (decrease) from baseline in GHS and QoL combined score, will be presented. A longer TTD indicates a better outcome.

    Time frame: Baseline and up to approximately 5 years

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

    The EORTC QLQ-C30 is a cancer specific health-related quality-of-life questionnaire. TTD is defined as the time from baseline to the first onset of a ≥10-point deterioration (decrease) from baseline in physical functioning score (EORTC QLQ-C30 Items 1-5). Using linear transformation, raw scores are standardized, so that scores range from 0 to 100. The TTD, as assessed based on a ≥10-point negative change (decrease) from baseline in GHS and QoL combined score, will be presented. A longer TTD indicates a better outcome.

    Time frame: Baseline and up to approximately 5 years

  13. TTD in EORTC QLQ-C30 Role Functioning (Items 6 and 7) 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'). Higher scores indicate better role functioning. The TTD, as assessed based on a ≥10-point negative change (decrease) from baseline in role functioning score, will be presented. A longer TTD indicates a better outcome.

    Time frame: Baseline and up to approximately 5 years

  14. TTD in EORTC QLQ-C30 Appetite Loss (Item 13) Score

    The EORTC QLQ-C30 is a cancer specific health-related quality-of-life questionnaire. TTD is defined as the time from baseline to the first onset of a ≥10-point deterioration (decrease) from baseline in appetite loss score (EORTC QLQ-C30 Item 13). Using linear transformation, raw scores are standardized, so that scores range from 0 to 100. The TTD, as assessed based on a ≥10-point negative change (decrease) from baseline in physical functioning score, will be presented. A longer TTD indicates a better outcome.

    Time frame: Baseline and up to approximately 5 years

  15. TTD in EORTC QLQ-CR29 Bloating (Item 37) Score

    The EORTC QLQ-CR29 is a health-related quality-of life questionnaire specific for colorectal cancer, including a single-item scale score for bloating (QLQ-CR29 Item 37). TTD is defined as the time from baseline to the first onset of a ≥10-point deterioration (decrease) from baseline in bloating score (QLQ-CR29 Item 37). Using linear transformation, raw scores are standardized, so that scores range from 0 to 100. The TTD, as assessed based on a ≥10-point negative change (decrease) from baseline in appetite loss score, will be presented. A longer TTD indicates a better outcome.

    Time frame: Baseline and up to approximately 5 years

06

Study locations

238 of 238 sites recruiting
  • Mayo Clinic - Arizona ( Site 0090)
    Phoenix, Arizona 85054, United States
    • Study Coordinator · Contact · 480-301-8000
    Recruiting
  • Los Angeles Hematology Oncology Medical Group ( Site 0084)
    Los Angeles, California 90017, United States
    • Study Coordinator · Contact · 213-533-9655
    Recruiting
  • UCLA Hematology/Oncology - Santa Monica ( Site 0088)
    Santa Monica, California 90404, United States
    • Study Coordinator · Contact · 310-794-6500
    Recruiting
  • University of Colorado Health - Harmony-Cancer Care and Hematology - Ft. Collins ( Site 0087)
    Fort Collins, Colorado 80528, United States
    • Study Coordinator · Contact · 970-493-6337
    Recruiting
  • Rocky Mountain Cancer Centers (RMCC) ( Site 8000)
    Lone Tree, Colorado 80124, United States
    • Study Coordinator · Contact · 303-925-0700
    Recruiting
  • Florida Cancer Specialists - South ( Site 7002)
    Fort Myers, Florida 33901, United States
    • Study Coordinator · Contact · 239-274-9930
    Recruiting
  • Mayo Clinic in Florida ( Site 0092)
    Jacksonville, Florida 32224, United States
    • Study Coordinator · Contact · 904-953-5380
    Recruiting
  • Orlando Health Cancer Institute ( Site 0065)
    Orlando, Florida 32806, United States
    • Study Coordinator · Contact · 321-841-6780
    Recruiting
  • Florida Cancer Specialists - North ( Site 7001)
    St. Petersburg, Florida 33705, United States
    • Study Coordinator · Contact · 727-216-1143
    Recruiting
  • Florida Cancer Specialists - East ( Site 7000)
    West Palm Beach, Florida 33401, United States
    • Study Coordinator · Contact · 561-366-4100
    Recruiting
  • Piedmont Atlanta Hospital ( Site 2002)
    Atlanta, Georgia 30318, United States
    • Study Coordinator · Contact · 404-605-3068
    Recruiting
  • Saint Alphonsus Regional Medical Center ( Site 0085)
    Boise, Idaho 83706, United States
    • Study Coordinator · Contact · 208-367-2121
    Recruiting
  • Endeavor Health ( Site 2027)
    Evanston, Illinois 60201, United States
    • Study Coordinator · Contact · 847-570-2112
    Recruiting
  • Accellacare of Duly ( Site 2015)
    Lisle, Illinois 60532, United States
    • Study Coordinator · Contact · 630-545-7760
    Recruiting
  • University of Iowa ( Site 0074)
    Iowa City, Iowa 52242, United States
    • Study Coordinator · Contact · 319-356-4200
    Recruiting
  • University of Kentucky ( Site 0055)
    Lexington, Kentucky 40536, United States
    • Study Coordinator · Contact · 859-218-1758
    Recruiting
  • Norton Cancer Institute, Audubon Hospital Campus ( Site 0054)
    Louisville, Kentucky 40217, United States
    • Study Coordinator · Contact · 502-636-7845
    Recruiting
  • Greater Baltimore Medical Center ( Site 0068)
    Baltimore, Maryland 21204, United States
    • Study Coordinator · Contact · 443-849-3051
    Recruiting
  • Mayo Clinic in Rochester, Minnesota ( Site 0091)
    Rochester, Minnesota 55905, United States
    • Study Coordinator · Contact · 507-284-2511
    Recruiting
  • Hattiesburg Clinic ( Site 0064)
    Hattiesburg, Mississippi 39401, United States
    • Study Coordinator · Contact · 601-288-2495
    Recruiting
  • Saint Luke's Cancer Institute ( Site 0082)
    Kansas City, Missouri 64111, United States
    • Study Coordinator · Contact · 816-932-2677
    Recruiting
  • Intermountain Health St. Vincent Regional Hospital - Cancer Centers of Montana ( Site 2000)
    Billings, Montana 59102, United States
    • Study Coordinator · Contact · 406-238-6685
    Recruiting
  • University Of Nebraska Medical Center ( Site 0078)
    Omaha, Nebraska 68198, United States
    • Study Coordinator · Contact · 402-559-4000
    Recruiting
  • Comprehensive Cancer Centers of Nevada ( Site 2026)
    Las Vegas, Nevada 89169, United States
    • Study Coordinator · Contact · 702-952-3400
    Recruiting
  • Renown Regional Medical Center ( Site 0056)
    Reno, Nevada 89502, United States
    • Study Coordinator · Contact · 775-982-4000
    Recruiting
  • John Theurer Cancer Center at Hackensack University Medical Center ( Site 0060)
    Hackensack, New Jersey 07601, United States
    • Study Coordinator · Contact · 551-996-5855
    Recruiting
  • Atlantic Health System ( Site 0093)
    Summit, New Jersey 07901, United States
    • Study Coordinator · Contact · 908-522-2000
    Recruiting
  • San Juan Oncology Associates, P.C ( Site 2011)
    Farmington, New Mexico 87401, United States
    • Study Coordinator · Contact · 505-564-6850
    Recruiting
  • Memorial Sloan Kettering Cancer Center ( Site 0095)
    New York, New York 10065, United States
    • Study Coordinator · Contact · 347-798-9213
    Recruiting
  • Ellis Hospital ( Site 0098)
    Schenectady, New York 12308, United States
    • Study Coordinator · Contact · 518-243-4762
    Recruiting
  • WakeMed Raleigh Campus ( Site 0094)
    Raleigh, North Carolina 27610, United States
    • Study Coordinator · Contact · 919-350-2873
    Recruiting
  • Miami Valley Hospital South ( Site 0075)
    Centerville, Ohio 45459, United States
    • Study Coordinator · Contact · 937-438-2400
    Recruiting
  • St. Luke's University Health Network ( Site 2014)
    Easton, Pennsylvania 18045, United States
    • Study Coordinator · Contact · 484-658-1793
    Recruiting
  • UPMC Hillman Cancer Center ( Site 2024)
    Pittsburgh, Pennsylvania 15232, United States
    • Study Coordinator · Contact · 412-647-2811
    Recruiting
  • Texas Oncology - DFW ( Site 8002)
    Dallas, Texas 75246, United States
    • Study Coordinator · Contact · 214-370-1000
    Recruiting
  • UT Southwestern Medical Center ( Site 0059)
    Dallas, Texas 75390, United States
    • Study Coordinator · Contact · 214-645-9685
    Recruiting
  • Texas Oncology - Northeast Texas ( Site 8001)
    Denison, Texas 75020, United States
    • Study Coordinator · Contact · 903-868-4700
    Recruiting
  • Texas Oncology - San Antonio ( Site 8004)
    San Antonio, Texas 78240, United States
    • Study Coordinator · Contact · 210-595-5300
    Recruiting
  • Community Cancer Trials of Utah ( Site 0086)
    Ogden, Utah 84405, United States
    • Study Coordinator · Contact · 801-689-3909
    Recruiting
  • University of Virginia ( Site 0080)
    Charlottesville, Virginia 22908, United States
    • Study Coordinator · Contact · 434-243-8237
    Recruiting
  • Virginia Cancer Specialists, PC ( Site 0069)
    Fairfax, Virginia 22031, United States
    • Study Coordinator · Contact · 703-280-5390
    Recruiting
  • Fred Hutchinson Cancer Center ( Site 0076)
    Seattle, Washington 98109, United States
    • Study Coordinator · Contact · 206-616-9025
    Recruiting
  • West Virginia University ( Site 2017)
    Morgantown, West Virginia 26506, United States
    • Study Coordinator · Contact · 304-598-4000
    Recruiting
  • Centro de Oncologia e Investigacion Buenos Aires COIBA ( Site 0110)
    Berazategui, Buenos Aires B1884BBF, Argentina
    • Study Coordinator · Contact · +541142262013
    Recruiting
  • Hospital Italiano de Buenos Aires ( Site 0102)
    Ciudad Autonoma de Buenos Aires, Buenos Aires C1199ABB, Argentina
    • Study Coordinator · Contact · +5491155960279
    Recruiting
  • Instituto Alexander Fleming ( Site 0101)
    Mar del Plata, Buenos Aires C1426ANZ, Argentina
    • Study Coordinator · Contact · +5491166936669
    Recruiting
  • Fundacion Estudios Clinicos ( Site 0105)
    Rosario, Santa Fe Province S2000CEJ, Argentina
    • Study Coordinator · Contact · +5493413168137
    Recruiting
  • Sanatorio Parque ( Site 0103)
    Rosario, Santa Fe Province S2000CUB, Argentina
    • Study Coordinator · Contact · +5493464586234
    Recruiting
  • Hospital Privado Universitario de Córdoba ( Site 0108)
    Córdoba, X5016KEH, Argentina
    • Study Coordinator · Contact · +543514688846
    Recruiting
  • Wollongong Hospital ( Site 0453)
    Wollongong, New South Wales 2500, Australia
    • Study Coordinator · Contact · +61242225000
    Recruiting
  • Sunshine Coast University Hospital ( Site 0451)
    Birtinya, Queensland 4575, Australia
    • Study Coordinator · Contact · +61752020000
    Recruiting
  • Monash Health ( Site 0454)
    Clayton, Victoria 3168, Australia
    • Study Coordinator · Contact · +61 03 8572-2941
    Recruiting
  • Western Health-Sunshine & Footscray Hospitals ( Site 0450)
    St Albans, Victoria 3021, Australia
    • Study Coordinator · Contact · +61383959167
    Recruiting
  • Hospital de Câncer de Recife ( Site 0158)
    Recife, Pernambuco 50040-000, Brazil
    • Study Coordinator · Contact · +558132178084
    Recruiting
  • Hospital de Caridade de Ijuí ( Site 0150)
    Ijuí, Rio Grande do Sul 98700-000, Brazil
    • Study Coordinator · Contact · +55 55 981580022
    Recruiting
  • Associação Hospitalar Beneficente São Vicente de Paulo ( Site 0153)
    Passo Fundo, Rio Grande do Sul 99010-080, Brazil
    • Study Coordinator · Contact · +555433164000
    Recruiting
  • Hospital Nossa Senhora da Conceição ( Site 0156)
    Porto Alegre, Rio Grande do Sul 91350-200, Brazil
    • Study Coordinator · Contact · +5551993590437
    Recruiting
  • CEPEN - Centro de Pesquisa e Ensino em Oncologia de Santa Catarina ( Site 0157)
    Florianópolis, Santa Catarina 88020-210, Brazil
    • Study Coordinator · Contact · +554833804828
    Recruiting
  • Fundação Pio XII - Hospital de Câncer de Barretos ( Site 0155)
    Barretos, São Paulo 14784-400, Brazil
    • Study Coordinator · Contact · +551733216600
    Recruiting
  • Fundação Faculdade Regional de Medicina de São José do Rio Preto ( Site 0159)
    São José do Rio Preto, São Paulo 15090-000, Brazil
    • Study Coordinator · Contact · +55 17 3201-5054
    Recruiting
  • COE Ensino e Pesquisa ( Site 0151)
    São José dos Campos, São Paulo 12242-660, Brazil
    • Study Coordinator · Contact · +5511960903468
    Recruiting
  • Instituto do Cancer Arnaldo Vieira de Carvalho ( Site 0160)
    São Paulo, 01209-000, Brazil
    • Study Coordinator · Contact · +55 11 3225-0155
    Recruiting
  • IBCC - Núcleo de Pesquisa e Ensino ( Site 0154)
    São Paulo, 04014-002, Brazil
    • Study Coordinator · Contact · +551134744222
    Recruiting
  • Cancercare Manitoba ( Site 0009)
    Winnipeg, Manitoba R3E 0V9, Canada
    • Study Coordinator · Contact · 204-787-4156
    Recruiting
  • Moncton Hospital - Horizon Health Network ( Site 0011)
    Moncton, New Brunswick E1C 6Z8, Canada
    • Study Coordinator · Contact · 5068575756
    Recruiting
  • London Health Sciences Centre ( Site 0012)
    London, Ontario N6A 5W9, Canada
    • Study Coordinator · Contact · 5196858500
    Recruiting
  • Princess Margaret Cancer Centre ( Site 0001)
    Toronto, Ontario M5G 2M9, Canada
    • Study Coordinator · Contact · 416-946-4559
    Recruiting
  • CIUSSS- saguenay-Lac-Saint-Jean ( Site 0007)
    Chicoutimi, Quebec G7H 5H6, Canada
    • Study Coordinator · Contact · 41854112342707
    Recruiting
  • Jewish General Hospital ( Site 0006)
    Montreal, Quebec H3T 1E2, Canada
    • Study Coordinator · Contact · 514-340-8222
    Recruiting
  • CIDO SpA ( Site 0212)
    Temuco, Araucania 4810148, Chile
    • Study Coordinator · Contact · +56452657374
    Recruiting
  • Clínica Puerto Montt ( Site 0206)
    Port Montt, Los Lagos Region 5500243, Chile
    • Study Coordinator · Contact · +56652484800
    Recruiting
  • Oncocentro Valdivia ( Site 0204)
    Valdivia, Los Ríos Region 5112129, Chile
    • Study Coordinator · Contact · 56958537020
    Recruiting
  • Fundacion Arturo Lopez Perez ( Site 0201)
    Santiago, Region M. de Santiago 7500921, Chile
    • Study Coordinator · Contact · 56224205098
    Recruiting
  • Centro de Oncología de Precisión ( Site 0207)
    Santiago, Region M. de Santiago 7560908, Chile
    • Study Coordinator · Contact · +56991612199
    Recruiting
  • Clínica UC San Carlos de Apoquindo ( Site 0211)
    Santiago, Region M. de Santiago 7620002, Chile
    • Study Coordinator · Contact · +56991290140
    Recruiting
  • CECIM ( Site 0210)
    Santiago, Region M. de Santiago 8331143, Chile
    • Study Coordinator · Contact · +56226965804
    Recruiting
  • Bradfordhill ( Site 0200)
    Santiago, Region M. de Santiago 8420383, Chile
    • Study Coordinator · Contact · 56229490970
    Recruiting
  • Clínica RedSalud Vitacura ( Site 0202)
    Vitacura, Region M. de Santiago 7650018, Chile
    • Study Coordinator · Contact · +56223954046
    Recruiting
  • ONCOCENTRO APYS ( Site 0203)
    Viña del Mar, Valparaiso 2520598, Chile
    • Study Coordinator · Contact · +56323320850
    Recruiting
  • Anhui Provincial Cancer Hospital ( Site 0803)
    Hefei, Anhui 230031, China
    • Study Coordinator · Contact · 0551-65327666
    Recruiting
  • The Second Affiliated Hospital of Anhui Medical University ( Site 0813)
    Hefei, Anhui 230601, China
    • Study Coordinator · Contact · 0551-63869536
    Recruiting
  • Peking Union Medical College Hospital ( Site 0824)
    Beijing, Beijing Municipality 100730, China
    • Study Coordinator · Contact · 8613910113193
    Recruiting
  • Peking University First Hospital(Daxing Area) ( Site 0838)
    Beijing, Beijing Municipality 102627, China
    • Study Coordinator · Contact · 010-56957544
    Recruiting
  • Chongqing University Cancer Hospital ( Site 0808)
    Chongqing, Chongqing Municipality 400030, China
    • Study Coordinator · Contact · 13983841209
    Recruiting
  • Chongqing University Three Gorges Hospital ( Site 0837)
    Wanzhou, Chongqing Municipality 404199, China
    • Study Coordinator · Contact · 023-58103019
    Recruiting
  • Fujian Cancer Hospital ( Site 0807)
    Fuzhou, Fujian 350014, China
    • Study Coordinator · Contact · +86 13509339525
    Recruiting
  • The First Affiliated Hospital of Xiamen University ( Site 0806)
    Xiamen, Fujian 361003, China
    • Study Coordinator · Contact · +86 13575559341
    Recruiting
  • Zhongshan Hospital Affiliated to Xiamen University ( Site 1902)
    Xiamen, Fujian 361004, China
    • Study Coordinator · Contact · +8605922292201
    Recruiting
  • Sun Yat-Sen University Cancer Center ( Site 0800)
    Guangzhou, Guangdong 510060, China
    • Study Coordinator · Contact · +86 02087343565
    Recruiting
  • Southern Medical University Nanfang Hospital ( Site 0812)
    Guangzhou, Guangdong 510515, China
    • Study Coordinator · Contact · +86 02062786845
    Recruiting
  • The Sixth Affiliated Hospital of Sun Yat-sen University ( Site 0828)
    Guangzhou, Guangdong 510655, China
    • Study Coordinator · Contact · 020-38254000
    Recruiting
  • The University of Hong Kong - Shenzhen Hospital ( Site 1903)
    Shenzhen, Guangdong 518053, China
    • Study Coordinator · Contact · +86075586913333
    Recruiting
  • Guangxi Medical University Affiliated Tumor Hospital ( Site 0804)
    Nanning, Guangxi 530200, China
    • Study Coordinator · Contact · +86 07715323175
    Recruiting
  • Harbin Medical University Cancer Hospital ( Site 0847)
    Harbin, Heilongjiang 150081, China
    • Study Coordinator · Contact · 0451 86298278
    Recruiting
  • Henan Cancer Hospital ( Site 0822)
    Zhengzhou, Henan 450008, China
    • Study Coordinator · Contact · 037165587161
    Recruiting
  • Tongji Hospital Tongji Medical,Science & Technology ( Site 0839)
    Wuhan, Hubei 430030, China
    • Study Coordinator · Contact · 027-83663940
    Recruiting
  • Hubei Cancer Hospital ( Site 0814)
    Wuhan, Hubei 430079, China
    • Study Coordinator · Contact · 027-87670500
    Recruiting
  • Hunan Cancer Hospital ( Site 0815)
    Changsha, Hunan 410013, China
    • Study Coordinator · Contact · 0731-89762130
    Recruiting
  • The Third Xiangya Hospital of Central South University ( Site 0834)
    Changsha, Hunan 410013, China
    • Study Coordinator · Contact · 0731-88638888
    Recruiting
  • Nanjing Drum Tower Hospital The Affiliated Hospital of Nanjing University Medical School ( Site 0825)
    Nanjing, Jiangsu 210000, China
    • Study Coordinator · Contact · 025-83106666
    Recruiting

Showing the first 100 of 238 sites across 29 countries.

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
NCT06997497
Lead sponsor
Merck Sharp & Dohme LLC
Responsible party
Sponsor
First posted
May 30, 2025
Start date
Jul 16, 2025
Primary completion
Mar 28, 2029 (estimated)
Completion
Oct 27, 2030 (estimated)
Last update
Sep 21, 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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