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Clinical Trials List

Protocol NumberD702NC00001
NCT Number(ClinicalTrials.gov Identfier)NCT07221253
Not yet recruiting

2025-11-07 - 2029-09-25

Phase III

Recruiting8

ICD-10C26.9

Malignant neoplasm of ill-defined sites within the digestive system

ICD-10Z51.12

Encounter for antineoplastic immunotherapy

ICD-9159.9

Malignant neoplasm of ill-defined sites within the digestive organs and peritoneum

Phase III, Randomized, Open-label, Global, Multicenter Study of Rilvegostomig or Durvalumab in Combination With Chemotherapy as a First-line Treatment for Patients With Advanced Biliary Tract Cancer (ARTEMIDE-Biliary02)

  • Trial Applicant

  • Sponsor

  • Trial scale

    Multi-Regional Multi-Center

  • Update

    2026/04/08

Investigators and Locations

Principal Investigator Ming-Huang Chen Division of Hematology & Oncology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator Tai-Jan Chiu Division of Hematology & Oncology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator Li-Yuan Bai Division of Hematology & Oncology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator Jen-Shi Chen Division of Hematology & Oncology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator Huey-En Tzeng Division of Hematology & Oncology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator Chih-Hung Hsu Division of Hematology & Oncology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator 饒坤銘 Division of Hematology & Oncology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator Yan-Shen Shan

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Condition/Disease

Biliary Tract Cancer

Objectives

The purpose of ARTEMIDE-Biliary02 was to evaluate the efficacy and safety of rilvegostomig plus chemotherapy compared to durvalumab plus chemotherapy as first-line treatment for patients with advanced (unresectable or metastatic) biliary tract cancer.

Test Drug

Injectables

Active Ingredient

Rilvegostomig (AZD2936)
Durvalumab

Dosage Form

270
270

Dosage

750mg/vial
500mg/vial

Endpoints

By evaluating overall survival (OS) in the PD-L1 ≥ 1% population, we demonstrated the efficacy of rilvegostomig plus chemotherapy compared to durvalumab plus chemotherapy.

Inclution Criteria

Key inclusion Criteria:

Histologically confirmed adenocarcinoma of the biliary tract, including intra-hepatic or extra-hepatic cholangiocarcinoma (CCA) and gallbladder carcinoma (GBC).
Unresectable locally advanced or metastatic BTC, previously untreated in the advanced disease setting
Known PD-L1 status assessed at a central laboratory using an acceptable tumor sample.
Measurable disease by RECIST 1.1 criteria using CT or MRI and is suitable for accurate repeated measurements.
ECOG Performance Status of 0 or 1 with no deterioration (ie, ECOG PS > 1) over the previous 2 weeks prior to baseline at screening and prior to randomization.
Adequate bone marrow and organ function.

Exclusion Criteria

Key exclusion Criteria:

Ampullary carcinoma
Any prior systemic therapy received for unresectable, locally advanced or metastatic BTC.
Any prior exposure to any other therapy targeting immune-regulatory receptors or mechanisms.
Any concurrent chemotherapy, radiotherapy, immunotherapy, investigational, biologic, or hormonal therapy for cancer treatment other than those under investigation in this study.
Active or prior documented autoimmune or inflammatory disorders requiring chronic treatment with steroids or other immunosuppressive treatment.
Active or ongoing interstitial lung disease/pneumonitis (of any grade), serious chronic gastrointestinal conditions associated with diarrhea, or active non-infectious skin disease (including any grade rash, urticaria, dermatitis, ulceration, or psoriasis) requiring systemic treatment.

The Estimated Number of Participants

  • Taiwan

    97 participants

  • Global

    1100 participants