Rilvegostomig + Chemotherapy as Adjuvant Therapy for Biliary Tract Cancer After Resection (ARTEMIDE-Biliary01)
Biliary Tract CancerA global study to assess the efficacy and tolerability of rilvegostomig compared to placebo in combination with investigator's choice of chemotherapy in participants with BTC after surgical resection with curative intent.
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Participation Requirements
-
Sex:
ALL -
Eligible Ages:
18 and up
Participation Criteria
Inclusion Criteria:
* Histologically confirmed adenocarcinoma of the biliary tract (intrahepatic or extrahepatic cholangiocarcinoma (CCA) or muscle invasive gallbladder cancer (GBC)) after macroscopically complete resection (R0 or R1)
* Provision of a tumor sample collected at surgical resection.
* Randomization within 12 weeks after resection with adequate healing and removal of drains.
* Confirmed to be disease-free by imaging within 28 days prior to randomization.
* Eastern Cooperative Oncology Group performance status of 0 or 1
Exclusion Criteria:
* Participants with locally-advanced, unresectable, or metastatic disease at initial diagnosis.
* Ampullary cancer, neuroendocrine, mixed neuroendocrine and non-neuroendocrine neoplasms and nonepithelial tumors.
* Any anti-cancer therapy for BTC prior to surgery
* Active or prior documented autoimmune or inflammatory disorders or any severe or uncontrolled systemic disease
* Current or prior use of immunosuppressive medication within 14 days before the first dose
* Thromboembolic event within 3 months
* Active HBV or HCV infection unless treated.
Study Location
Research Site
Research SiteBrampton, Ontario
Canada
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Research Site
Research SiteOttawa, Ontario
Canada
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Research Site
Research SiteHalifax, Nova Scotia
Canada
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Research Site
Research SiteMississauga, Ontario
Canada
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Research Site
Research SiteMontreal, Quebec
Canada
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Research Site
Research SiteVancouver, British Columbia
Canada
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Research Site
Research SiteKingston, Ontario
Canada
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Research Site
Research SiteToronto, Ontario
Canada
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Research Site
Research SiteMoncton, New Brunswick
Canada
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Research Site
Research SiteLondon, Ontario
Canada
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Research Site
Research SiteToronto, Ontario
Canada
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- Study Sponsored By
- AstraZeneca
- Participants Required
- More Information
- Study ID:
NCT06109779