Study of Patritumab Deruxtecan in Participants With Gastrointestinal Cancers (MK-1022-011) (HERTHENA-PanTumor02)
Gastrointestinal CancerResearchers want to learn if patritumab deruxtecan (MK-1022) can treat certain gastrointestinal (GI) cancers. The GI cancers being studied are advanced (the cancer has spread to other parts of the body). The goals of this study are to learn:
* About the safety and how well people tolerate of patritumab deruxtecan
* How many people have the cancer respond (get smaller or go away) to treatment
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Conditions de participation
-
Sexe:
ALL -
Âges admissibles:
18 and up
Critères de participation
Inclusion Criteria:
The main inclusion criteria include but are not limited to the following:
* Has one of the following cancers:
* Unresectable or metastatic colorectal cancer.
* Advanced and/or unresectable biliary tract cancer (BTC)
* Hepatocellular carcinoma (HCC) not amenable to locoregional therapy
* Locally advanced unresectable or metastatic gastroesophageal cancer
* Has received prior therapy for the cancer.
* Has recovered from any side effects due to previous cancer treatment
Exclusion Criteria:
The main exclusion criteria include but are not limited to the following:
* Has a history of (noninfectious) interstitial lung disease (ILD) or pneumonitis that required steroids, or has current ILD or pneumonitis, and/or suspected ILD or pneumonitis that cannot be ruled out by standard diagnostic assessments at Screening
* Has clinically severe respiratory compromise (based on the investigator's assessment) resulting from intercurrent pulmonary illnesses
* Has evidence of any leptomeningeal disease
* Has clinically significant corneal disease
* Has uncontrolled, significant cardiovascular disease or cerebrovascular disease
* Has evidence of ongoing uncontrolled systemic bacterial, fungal, or viral infection
Lieu de l'étude
Sunnybrook Research Institute - Odette Cancer Centre ( Site 0206)
Sunnybrook Research Institute - Odette Cancer Centre ( Site 0206)Toronto, Ontario
Canada
Contactez l'équipe d'étude
Study Coordinator
416-480-5000 x64270McGill University Health Centre ( Site 0202)
McGill University Health Centre ( Site 0202)Montreal, Quebec
Canada
Contactez l'équipe d'étude
Study Coordinator
5145772241QEII Health Sciences Centre - Victoria General Site ( Site 0200)
QEII Health Sciences Centre - Victoria General Site ( Site 0200)Halifax, Nova Scotia
Canada
Contactez l'équipe d'étude
Study Coordinator
9024736106- Étude parrainée par
- Merck Sharp & Dohme LLC
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT06596694