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Search / Trial NCT05667064

Imfinzi/Imjudo uHCC Japan PMS _ Japan Post-Marketing Surveillance (PMS) Study

Launched by ASTRAZENECA · Dec 19, 2022

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is looking at the safety of a combination treatment called IMJUDO and IMFINZI, as well as IMFINZI on its own, for patients with a type of liver cancer known as unresectable hepatocellular carcinoma (HCC). The goal is to gather information on how well these treatments work in real-world settings after they have been approved for use.

If you or a loved one has been diagnosed with unresectable HCC and are receiving either the combination therapy or just IMFINZI, you may be eligible to participate in this study. There are no specific age or gender requirements, so all patients receiving these treatments can join. Participants will have the opportunity to contribute to important research while receiving standard care. It’s a great way to help advance our understanding of these therapies and improve treatment options for others in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • All patients who receive IMJUDO and IMFINZI combination therapy or IMFINZI monotherapy for their unresectable HCC.
  • -
  • Exclusion Criteria:
  • -

About Astrazeneca

AstraZeneca is a global biopharmaceutical company dedicated to the discovery, development, and commercialization of innovative medicines across various therapeutic areas, including oncology, cardiovascular, respiratory, and autoimmune diseases. With a strong commitment to scientific research and patient-centric solutions, AstraZeneca leverages cutting-edge technology and a robust pipeline to address unmet medical needs. The company collaborates with healthcare professionals, academic institutions, and other organizations to advance clinical trials and deliver transformative therapies, aiming to improve health outcomes and enhance the quality of life for patients worldwide.

Locations

Chiba, , Japan

Fukuoka, , Japan

Kumamoto, , Japan

Niigata, , Japan

Oita, , Japan

Osaka, , Japan

Saitama, , Japan

Tokyo, , Japan

Gifu, , Japan

Nagasaki, , Japan

Okayama, , Japan

Yamagata, , Japan

Hiroshima, , Japan

Kyoto, , Japan

Toyama, , Japan

Kagoshima, , Japan

Tochigi, , Japan

Kochi, , Japan

Fukushima, , Japan

Miyazaki, , Japan

Shizuoka, , Japan

Yamaguchi, , Japan

Gunma, , Japan

Hyogo, , Japan

Ibaraki, , Japan

Kanagawa, , Japan

Nagano, , Japan

Wakayama, , Japan

Akita, , Japan

Tottori, , Japan

Ehime, , Japan

Hokkaido, , Japan

Aichi, , Japan

Nara, , Japan

Tokushima, , Japan

Aomori, , Japan

Kagawa, , Japan

Okinawa, , Japan

Saga, , Japan

Fukui, , Japan

Iwate, , Japan

Mie, , Japan

Miyagi, , Japan

Shiga, , Japan

Shimane, , Japan

Ishikawa, , Japan

Yamanashi, , Japan

Patients applied

0 patients applied

Trial Officials

Toshimitsu Tokimoto

Study Director

AstraZeneca KK

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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