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

AstraZeneca
NCT IDNCT05775159ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

294

Study length

about 4.5 years

Ages

18+

Locations

10 sites in AL, CA, FL +5

What this study is about

Researchers are testing a treatment (Volrustomig or Rilvegostomig) alone or with other cancer drugs to see if it helps people with advanced liver or bile duct cancer. The trial will last for about 1648 days and involve around 294 participants.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Bevacizumab
  • 2.Take Cisplatin
  • 3.Take Gemcitabine
  • +3 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVInjection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

bevacizumab, cisplatin (Platinum chemotherapy; crosslinks DNA to stop replication), gemcitabine, lenvatinib

Drug routes

infusion, injection, intravenous, injection (Injection), oral (Oral Capsule)

Endpoints

Primary: Objective response rate (ORR), Progression free survival (PFS), The number of participants with adverse events/serious adverse events

Secondary: Disease Control Rate (DCR), Duration Of Response (DOR), Objective response rate (ORR), Overall Survival (OS), Pharmacokinetics of novel immunomodulators: Maximum plasma concentration of the study drug (Cmax), Pharmacokinetics of novel immunomodulators: Time to maximum plasma concentration of the study drug (T-max), Progression free survival (PFS)