Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at Los Angeles, California and other locations
Dates
study started
study ends around

Description

Summary

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.

Official Title

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)

Keywords

Biliary Tract Cancer, Rilvegostomig, Durvalumab, Bispecific Antibody, PD-L1, TIGIT, Initially Unresectable, Recurrent, Intra-hepatic cholangiocarcinoma, Extra-hepatic cholangiocarcinoma, Gallbladder cancer, Biliary Tract Neoplasms, Recurrence, Gallbladder Neoplasms, Gemcitabine, Cisplatin, Gemcitabine/Cisplatin

Eligibility

You can join if…

Open to people ages 18 years and up

  • 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.

You CAN'T join if...

  • 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

  • Research Site accepting new patients
    Los Angeles California 90095 United States
  • Research Site accepting new patients
    Duarte California 91010 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
AstraZeneca
Links
Sign up for this study
ID
NCT07221253
Phase
Phase 3 Biliary Tract Cancer Research Study
Study Type
Interventional
Participants
Expecting 1100 study participants
Last Updated