← Eichor
Study identifier: NCT06849180 Synced from ClinicalTrials.gov · July 27, 2026
● Recruiting

Novel Subtypes and Treatment Strategies of Patients with Unresectable Combined Hepatocellular Cholangiocarcinoma Based on Multimodal Data

Condition: Combined Hepatocellular-cholangiocarcinoma · Combined Hepatocellular Carcinoma and Cholangiocarcinoma · Combined Hepatocellular and Cholangiocarcinoma  ·  Sponsor: Zhongda Hospital

PhaseN/A
Planned participants198
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study focused on exploring new comprehensive treatment strategies for patients with unresectable combined hepatocellular-cholangiocarcinoma, classifying patients with CHC subtypes based on the combination of artificial intelligence and multi-omics, and exploring the optimal treatment strategies for patients with different subtypes, helping clinicians to screen the most beneficial groups of various treatment schemes, and providing new ideas for safe treatment of high-risk patients.

This description comes directly from the study's public registry record.

Talk to the study team

Gao-Jun Teng, M.D  ·  +86-02583272121  ·  gjteng@vip.sina.com

Always discuss trial participation with your own doctor first.

Locations (1)

Zhongda HospitalNanjing, Jiangsu, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06849180