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Recruiting Phase 2 Interventional

Study of Novel Immunomodulators as Monotherapy and in Combination With Anticancer Agents in Participants With Advanced Hepatobiliary Cancer

ClinicalTrials.gov ID: NCT05775159

Public ClinicalTrials.gov record NCT05775159. 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 17, 2026, 3:24 AM 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 II, Open-Label, Multi-Drug, Multi-Center, Master Protocol to Evaluate the Efficacy and Safety of Novel Immunomodulators as Monotherapy and in Combination With Anticancer Agents in Participants With Advanced Hepatobiliary Cancer (GEMINI-Hepatobiliary)

Study identification

NCT ID
NCT05775159
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
294 participants

Conditions and interventions

Interventions

  • Bevacizumab Drug
  • Cisplatin Drug
  • Gemcitabine Drug
  • Lenvatinib Drug
  • Rilvegostomig Drug
  • Volrustomig 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
Apr 23, 2023
Primary completion
Oct 26, 2026
Completion
Oct 27, 2027
Last update posted
Apr 16, 2026

2023 – 2027

United States locations

U.S. sites
10
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
Research Site Birmingham Alabama 35233 Recruiting
Research Site Costa Mesa California 92627 Withdrawn
Research Site Los Angeles California 90089 Recruiting
Research Site Orange California 92868 Recruiting
Research Site Miami Beach Florida 33140 Withdrawn
Research Site Dyer Indiana 46311 Withdrawn
Research Site Kansas City Kansas 66103 Recruiting
Research Site New York New York 10065 Recruiting
Research Site Dallas Texas 75251 Withdrawn
Research Site Fairfax Virginia 22031 Withdrawn

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 50 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05775159, 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 Apr 16, 2026 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05775159 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →