🔎 Trials Near Me

Home › Biliary Tract Cancer › NCT07221253

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

RecruitingPhase 3

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)

Who can join

Ages 18 and older · All sexes

Full eligibility 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.

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.

About the study

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.

What is being tested

Sponsor: AstraZeneca · Participants: 1,100 · Started: Dec 4, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07221253

Locations in the U.S.

AlabamaResearch Site, Birmingham
ArizonaResearch Site, Phoenix
Research Site, Tucson
CaliforniaResearch Site, Duarte
Research Site, Los Angeles
Research Site, Orange
Research Site, Palo Alto
ColoradoResearch Site, Aurora
ConnecticutResearch Site, Hartford
Research Site, New Haven
District of ColumbiaResearch Site, Washington D.C.
Research Site, Washington D.C. (Not yet recruiting)
FloridaResearch Site, Gainesville
Research Site, Jacksonville
Research Site, Miami (Not yet recruiting)
GeorgiaResearch Site, Marietta
IllinoisResearch Site, Chicago (Not yet recruiting)
Research Site, Chicago
IndianaResearch Site, Indianapolis (Not yet recruiting)
KentuckyResearch Site, Louisville
MarylandResearch Site, Baltimore
MichiganResearch Site, Ann Arbor (Not yet recruiting)
Research Site, Detroit (Not yet recruiting)
MinnesotaResearch Site, Rochester
NebraskaResearch Site, Omaha (Not yet recruiting)
New MexicoResearch Site, Santa Fe
New YorkResearch Site, Mineola
Research Site, New York
Research Site, New York
OklahomaResearch Site, Oklahoma City (Not yet recruiting)
OregonResearch Site, Portland (Not yet recruiting)
PennsylvaniaResearch Site, Lancaster
Research Site, Philadelphia
Research Site, Pittsburgh
Rhode IslandResearch Site, Providence
South DakotaResearch Site, Pierre
Research Site, Sioux Falls
TennesseeResearch Site, Nashville (Not yet recruiting)
TexasResearch Site, Houston (Not yet recruiting)
WashingtonResearch Site, Seattle (Not yet recruiting)

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.