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Clinical Application Study of 68Ga-NYM207 PET/CT Imaging in Patients with Hepatocellular Carcinoma

Clinical Application Study of 68Ga-NYM207 PET/CT Imaging in Patients with Hepatocellular Carcinoma

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123817
Enrollment
Unknown
Registered
2026-04-30
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocellular Carcinoma

Interventions

phaseA:68Ga-NYM207
Queue 1:68Ga-NYM207
Queue 2:68Ga-NYM207

Sponsors

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 80 years; no gender restriction. 2. Must meet at least one of the following: (1) Patients with liver lesions planning to undergo surgical resection of the liver lesion within 1 month; (2) Clinically suspected recurrent/metastatic hepatocellular carcinoma; (3) Diagnosed with recurrent/metastatic hepatocellular carcinoma. 3. Before any evaluation, the subject or their legal representative understands and signs a written informed consent form, and the subject is willing and able to comply with all items of this study.

Exclusion criteria

Exclusion criteria: 1.Presence of cancer cachexxia, acute exacerbation of chronic disease, acute infection, immunodeficiency, or any other serious medical condition. 2.Diagnosis of claustrophobia. 3.History of substance abuse or alcoholism. 4.Pregnant or lactating women. 5.Poor venous access, unable to tolerate repeated venipuncture. 6.Receipt of investigational drugs or devices (with unclear efficacy or safety profiles) within the past month. 7.Any condition deemed by the principal investigator as posing actual or potential risk to the participant’s safety during any aspect of the study.

Design outcomes

Primary

MeasureTime frame
Dose;sensitivity ;specificity;Adverse Event (AE);

Secondary

MeasureTime frame
Imaging characteristics;

Countries

China

Contacts

Public ContactLi Huo

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences

huoli@pumch.cn+86 10 6915 5513

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026