TTrialPathMatch Me to Trials
← Back to trials
RecruitingHepatobiliary Cancers

Observational Study Protocol: LIVER-R

Eligible age

18–130 yrs

Accepts

All genders

Locations

14 states

Healthy volunteers

No

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

Check my eligibility →

About this study

Given the number of anticipated durvalumab-based treatment launches in the hepatobiliary cancer space over the next 3 years, there is a need to capture contemporary real-world data across these indications. LIVER-R is a multicountry, multicenter, observational study of patients with a confirmed diagnosis of hepatobiliary cancer treated with a durvalumab-based regimen as part of routine clinical practice or early access program (EAP). The study design will include primary and secondary data collection. The primary objective of this study is to evaluate the effectiveness of durvalumab-based regimens in real-world settings as measured by real-world overall survival. Other endpoints include demographics, clinical characteristics, clinically significant events of interest, treatment patterns, concomitant medications, and other real-world clinical endpoints (such as duration of treatment, progression-free survival, time to treatment progression, time to next treatment, recurrence-free survival, and time to treatment recurrence).

Sponsor: AstraZeneca

You may qualify if…

  • 1. Age ≥18 years and a lawful adult in the country at the index date
  • 2. Confirmed presence of malignancy of primary hepatobiliary cancer (i.e., uHCC or aBTC) by the treating physician
  • 3. Type of hepatobiliary cancer indication is approved to be treated (i.e., positive phase 3 clinical trial read out for HIMALAYA or TOPAZ 1) with a durvalumab based regimen in the respective country or was administered as part of an EAP
  • 4. Informed consent was obtained as per country level regulations on or after the index date

You may not qualify if…

  • 1. Currently/was participating or plans to participate in any clinical trial for investigational treatment for hepatobiliary cancers on or after the diagnosis date until the index date
  • 2. Received other systemic therapies for hepatobiliary cancer indication on or after diagnosis date through the index date (e.g., uHCC or aBTC patient who received a systemic treatment for unresectable HCC or advanced BTC, respectively, prior to initiating durvalumab based regimen)
  • 3. Received a liver transplant during the baseline period

Where it's recruiting

Alabama

Birmingham · Mobile

Arizona

Phoenix

California

Coronado · Los Angeles · Walnut Creek

Florida

Clermont · Gainesville · Tampa

Georgia

Augusta

Illinois

Evergreen Park · Hinsdale

Louisiana

Baton Rouge

Missouri

Osage Beach

New York

White Plains

Ohio

Canton

Pennsylvania

Bethlehem · Lancaster · Philadelphia · Pittsburgh

Source: ClinicalTrials.gov · NCT06252753 · last updated 2026-07-17