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Study of Patritumab Deruxtecan in Participants With Gastrointestinal Cancers (MK-1022-011) (HERTHENA-PanTumor02)

Gastrointestinal Cancer

Researchers 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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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation Criteria

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

Study Location

Sunnybrook Research Institute - Odette Cancer Centre ( Site 0206)
Sunnybrook Research Institute - Odette Cancer Centre ( Site 0206)
Toronto, Ontario
Canada

Contact Study Team

Primary Contact

Study Coordinator

416-480-5000 x64270
McGill University Health Centre ( Site 0202)
McGill University Health Centre ( Site 0202)
Montreal, Quebec
Canada

Contact Study Team

Primary Contact

Study Coordinator

5145772241
QEII Health Sciences Centre - Victoria General Site ( Site 0200)
QEII Health Sciences Centre - Victoria General Site ( Site 0200)
Halifax, Nova Scotia
Canada

Contact Study Team

Primary Contact

Study Coordinator

9024736106
Study Sponsored By
Merck Sharp & Dohme LLC
Participants Required
More Information
Study ID: NCT06596694