ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional

Rilvegostomig + Chemotherapy as Adjuvant Therapy for Biliary Tract Cancer After Resection (ARTEMIDE-Biliary01)

ClinicalTrials.gov ID: NCT06109779

Public ClinicalTrials.gov record NCT06109779. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 8, 2026, 10:48 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Global Study of Rilvegostomig in Combination With Chemotherapy as Adjuvant Treatment After Resection of Biliary Tract Cancer With Curative Intent (ARTEMIDE-Biliary01)

Study identification

NCT ID
NCT06109779
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
757 participants

Conditions and interventions

Interventions

  • Capecitabine Drug
  • Gemcitabine/Cisplatin Drug
  • Placebo Drug
  • Rilvegostomig Drug
  • S-1 [Tegafur/Oteracil/gimeracil] Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 3, 2023
Primary completion
Jan 1, 2029
Completion
May 2, 2030
Last update posted
Mar 3, 2026

2023 – 2030

United States locations

U.S. sites
22
U.S. states
18
U.S. cities
22
Facility City State ZIP Site status
Research Site Birmingham Alabama 35233
Research Site Phoenix Arizona 85054
Research Site Los Angeles California 90089
Research Site Orange California 92868
Research Site Stanford California 94305
Research Site Aurora Colorado 80045
Research Site Littleton Colorado 80129
Research Site Washington D.C. District of Columbia 20007
Research Site Jacksonville Florida 32224
Research Site Atlanta Georgia 30322
Research Site Chicago Illinois 60637
Research Site Iowa City Iowa 52242
Research Site Kansas City Kansas 66160
Research Site Lexington Kentucky 40506
Research Site New Orleans Louisiana 70121
Research Site Grand Rapids Michigan 49503
Research Site Rochester Minnesota 55905
Research Site St Louis Missouri 63110
Research Site Commack New York 11725
Research Site Mineola New York 11501
Research Site Philadelphia Pennsylvania 19144
Research Site Dallas Texas 75246

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 155 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06109779, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 3, 2026 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06109779 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →