A Study of Rilvegostomig or Durvalumab Plus Chemotherapy for First-Line Treatment of Biliary Tract Cancer (ARTEMIDE-Biliary02)

Sponsor: AstraZeneca

Sponsor score: 40

ClinicalTrials ID:NCT07221253

This study evaluates the efficacy and safety of rilvegostomig vs. durvalumab, both combined with gemcitabine and cisplatin, for advanced biliary tract cancer. Eligible patients have unresectable, untreated BTC with confirmed adenocarcinoma and measurable disease. Interventions include rilvegostomig or durvalumab, administered intravenously, alongside gemcitabine/cisplatin.

Patient Parameters

Program Overview

The purpose of this study is to measure the efficacy and safety of rilvegostomig with gemcitabine plus cisplatin vs. durvalumab with gemcitabine plus cisplatin as first line treatment for patients with advanced BTC.

Eligibility Criteria

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.

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.

Locations

FACILITYZIPCITYSTATE
Research Site35233BirminghamAlabama
Research Site85719TucsonArizona
Research Site91010DuarteCalifornia
Research Site92868OrangeCalifornia
Research Site90404Santa MonicaCalifornia
Research Site94305-5847StanfordCalifornia
Research Site80045AuroraColorado
Research Site20007Washington D.C.District of Columbia
Research Site30060MariettaGeorgia
Research Site60637ChicagoIllinois

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