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| ID | Type | Description | Link |
|---|---|---|---|
| 2024-517416-30-00 | Other Identifier | EU CT | |
| U1111-1312-2472 | Other Identifier | UTN |
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| Name | Class |
|---|---|
| Daiichi Sankyo | INDUSTRY |
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Researchers are looking for new ways to treat certain types of advanced gastrointestinal (GI) cancers. The study medicine raludotatug deruxtecan (also called MK-5909, R-DXd, or DS-6000a) is a type of medicine called an antibody-drug conjugate (ADC). An ADC attaches to a protein on cancer cells and delivers treatment to destroy those cells.
The main goal of this study is to learn if the cancer responds to treatment (gets smaller or goes away).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Raludotatug Deruxtecan (R-DXd) | Experimental | R-DXd will be administered via IV infusion. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Raludotatug Deruxtecan (R-DXd) | Biological | Administered via intravenous (IV) infusion. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Objective Response Rate (ORR) | ORR is defined as the percentage of participants with 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. The percentage of participants who experience CR or PR as assessed by BICR will be presented. | Approximately 15 months |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants who Experience One or More Adverse Events (AEs) | An adverse event (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. The number of participants who experience an AE will be reported. | Up to approximately 14 months |
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Inclusion Criteria:
The main inclusion criteria include but are not limited to the following:
Has one of the following cancers:
Has received prior therapy for the cancer
Has a life expectancy of at least 3 months
If human immunodeficiency virus (HIV) infected, must have well controlled HIV on antiretroviral therapy (ART)
Exclusion Criteria:
The main exclusion criteria include but are not limited to the following:
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| Name | Affiliation | Role |
|---|---|---|
| Medical Director | Merck Sharp & Dohme LLC | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Yale New Haven Hospital ( Site 0375) | New Haven | Connecticut | 06510 | United States | ||
| Sibley Memorial Hospital ( Site 0372) |
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| Label | URL |
|---|---|
| Merck Clinical Trials Information | View source |
| Plain Language Summary | View source |
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| 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. The number of participants who discontinue study treatment due to an AE will be reported. | Up to approximately 12 months |
| 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. | Up to approximately 49 months |
| Progression Free Survival (PFS) | PFS is defined as the time from first day of study intervention to the first documented progressive disease (PD) or death due to any cause, whichever occurs first as assessed by BICR. Per RECIST 1.1, PD is defined as ≥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 ≥5 mm. The appearance of one or more new lesions is also considered PD. The appearance of one or more new lesions is also considered PD. PFS as assessed by BICR will be presented. | Up to approximately 49 months |
| Overall Survival (OS) | OS is defined as the time from the first dose to death due to any cause. | Up to approximately 49 months |
| Washington D.C. |
| District of Columbia |
| 20016 |
| United States |
| Mt Sinai Comprehensive Cancer Center ( Site 0345) | Miami Beach | Florida | 33140 | United States |
| St. Vincent Healthcare Frontier Cancer Center ( Site 0347) | Billings | Montana | 59102 | United States |
| Morristown Medical Center ( Site 0349) | Morristown | New Jersey | 07960 | United States |
| University Hospitals Cleveland Medical Center ( Site 0369) | Cleveland | Ohio | 44106 | United States |
| University of Virginia Cancer Center ( Site 0365) | Charlottesville | Virginia | 22903 | United States |
| University of Wisconsin Carbone Cancer Center ( Site 0348) | Madison | Wisconsin | 53792 | United States |
| Instituto de Investigaciones Clinicas Mar del Plata ( Site 0001) | Mar del Plata | Buenos Aires | B7600FZO | Argentina |
| Nefra Medical Care - CEMIC Saavedra ( Site 0008) | Buenos Aires | Buenos Aires F.D. | C1431FWO | Argentina |
| Instituto Medico de la Fundacion Estudios Clinicos ( Site 0007) | Rosario | Santa Fe Province | S2000CEJ | Argentina |
| Fundación CORI para la Investigación y Prevención del Cáncer ( Site 0006) | La Rioja | F5300COE | Argentina |
| Sunnybrook Research Institute ( Site 0044) | Toronto | Ontario | M4N 3M5 | Canada |
| Princess Margaret Cancer Centre ( Site 0041) | Toronto | Ontario | M5G 1X6 | Canada |
| Centre Hospitalier de l'Université de Montréal ( Site 0042) | Montreal | Quebec | H2X 3E4 | Canada |
| FALP ( Site 0062) | Santiago | Region M. de Santiago | 7500921 | Chile |
| Centro de Estudios Clínicos SAGA ( Site 0064) | Santiago | Region M. de Santiago | 7501010 | Chile |
| Clínica UC San Carlos de Apoquindo ( Site 0066) | Santiago | Region M. de Santiago | 7620002 | Chile |
| Bradfordhill ( Site 0069) | Santiago | Region M. de Santiago | 8420383 | Chile |
| Centre François Baclesse ( Site 0085) | Caen | Calvados | 14076 | France |
| Institut Regional du Cancer Montpellier ( Site 0084) | Montpellier | Herault | 34298 | France |
| Gustave Roussy ( Site 0081) | Villejuif | Val-de-Marne | 94800 | France |
| Pitie Salpetriere University Hospital ( Site 0082) | Paris | 75013 | France |
| Prince of Wales Hospital ( Site 0122) | Hksar | Hong Kong |
| Queen Mary Hospital ( Site 0121) | Hksar | Hong Kong |
| Institut Català d'Oncologia (ICO) - Badalona ( Site 0222) | Badalona | Barcelona | 08916 | Spain |
| Hospital Universitario Marqués de Valdecilla ( Site 0221) | Santander | Cantabria | 39008 | Spain |
| Hospital Clinic de Barcelona ( Site 0223) | Barcelona | 08036 | Spain |
| Hospital General Universitario Gregorio Marañón ( Site 0225) | Madrid | 28007 | Spain |
| Hospital Universitario Fundacion Jimenez Diaz ( Site 0224) | Madrid | 28040 | Spain |
| Universitaetsspital Basel ( Site 0241) | Basel | Canton of Basel-City | 4031 | Switzerland |
| Hôpitaux Universitaires de Genève (HUG) ( Site 0245) | Geneva | Canton of Geneva | 1211 | Switzerland |
| Universitaetsspital Zuerich ( Site 0242) | Zurich | 8091 | Switzerland |
| China Medical University Hospital ( Site 0267) | Taichung | 40447 | Taiwan |
| Taichung Veterans General Hospital ( Site 0265) | Taichung | 407 | Taiwan |
| National Cheng Kung University Hospital ( Site 0263) | Tainan | 70403 | Taiwan |
| National Taiwan University Hospital ( Site 0261) | Taipei | 10002 | Taiwan |
| Mackay Memorial Hospital ( Site 0266) | Taipei | 104 | Taiwan |
| Taipei Veterans General Hospital ( Site 0262) | Taipei | 112 | Taiwan |
| Ramathibodi Hospital. ( Site 0282) | Bangkok | Bangkok | 10400 | Thailand |
| Faculty of Medicine Siriraj Hospital ( Site 0281) | Bangkok | Bangkok | 10700 | Thailand |
| ID | Term |
|---|---|
| D005770 | Gastrointestinal Neoplasms |
| ID | Term |
|---|---|
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D004066 | Digestive System Diseases |
| D005767 | Gastrointestinal Diseases |
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