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ACTIVE NOT RECRUITING Phase 3

Evaluate Durvalumab and Tremelimumab +/- Lenvatinib in Combination With TACE in Patients With Locoregional HCC

NCT05301842 · View on ClinicalTrials.gov ↗

Study Summary

A global study to evaluate transarterial chemoembolization (TACE) in combination with durvalumab, tremelimumab and lenvatinib therapy in patients with locoregional hepatocellular carcinoma

Conditions Studied

Interventions

  • DRUG Lenvatinib
  • DRUG Durvalumab
  • DRUG Tremelimumab
  • PROCEDURE Transarterial Chemoembolization (TACE)

Study Locations (20)

Other

  • Research Site — Brussels
  • Research Site — Ghent
  • Research Site — Barretos
  • Research Site — Brasília
  • Research Site — Niterói
  • Research Site — Porto Alegre
  • Research Site — Rio de Janeiro
  • Research Site — Santa Maria

Alabama

  • Research Site — Birmingham
  • Research Site — Mobile

New York

  • Research Site — Commack
  • Research Site — New York

Texas

  • Research Site — Dallas
  • Research Site — Houston

Arizona

  • Research Site — Yuma

California

  • Research Site — Glendale

Georgia

  • Research Site — Atlanta

Maryland

  • Research Site — Baltimore

Trial Details

FieldValue
Enrollment Target 760 participants
Start Date 2022-03-28
Est. Completion 2027-02-26
Phase Phase 3

Sponsor

AstraZeneca

1,053 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05301842

The ClinicalTrials.gov registry entry for NCT05301842 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 760 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AstraZeneca, which has 1,053 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Hepatocellular Carcinoma appearing as the primary indexed condition, and to 4 interventions — of which Lenvatinib is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05301842 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Other, Alabama, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05301842 about?

NCT05301842 is a clinical study titled "Evaluate Durvalumab and Tremelimumab +/- Lenvatinib in Combination With TACE in Patients With Locoregional HCC". A global study to evaluate transarterial chemoembolization (TACE) in combination with durvalumab, tremelimumab and lenvatinib therapy in patients with locoregional hepatocellular carcinoma

What is the current status of trial NCT05301842?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 760 participants. The study started on 2022-03-28. Estimated completion is 2027-02-26.

What conditions does trial NCT05301842 study?

This clinical trial studies the following conditions: Hepatocellular Carcinoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05301842?

The interventions under investigation include: Lenvatinib (DRUG), Durvalumab (DRUG), Tremelimumab (DRUG), Transarterial Chemoembolization (TACE) (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05301842?

This trial is sponsored by AstraZeneca, which has 1,053 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05301842 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Georgia, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial