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PET imaging of [18F]AlF-ETN for assessment of EphA2 Presence in Solid Tumors

PET imaging of [18F]AlF-ETN for assessment of EphA2 Presence in Solid Tumors

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090839
Enrollment
Unknown
Registered
2024-10-14
Start date
2024-10-19
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

Tumor

Interventions

A:Dynamic PET/CT scan to assess the biodistribution, pharmacokinetics and dosimetry of [18F]AlF-ETN in human
B:Using PET/CT to evaluate tumor uptake of [18F]AlF-ETN in patients with malignant solid tumors

Sponsors

Cancer Hospital Chinese Academy of Medical Sciences Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Healthy Volunteers: Aged between 18 and 80 years old, capable of cooperating independently to complete the examinations; having full comprehension and voluntarily participating in this experiment, and signing the informed consent form. ? Malignant Tumor Patients: Patients with confirmed malignant tumors such as pancreatic cancer, gastric cancer, colorectal cancer, squamous cell carcinoma of the head and neck, cervical cancer, ovarian cancer, endometrial cancer, breast cancer, esophageal cancer, lung cancer, etc., who have not received tumor-related treatments yet; aged between 18 and 80 years old, capable of cooperating independently to complete the examinations; having full comprehension and voluntarily participating in this experiment, and signing the informed consent form.

Exclusion criteria

Exclusion criteria: Severe abnormal of liver function, kidney function or blood routine test; Pre-pregnancy, pregnant or lactating women; Unable to lie flat for half an hour; Suffering from claustrophobia or other mental illness; Unable to understand the examination process or unable to cooperate; Other circumstances that the investigator considers inappropriate for trial participation.

Design outcomes

Primary

MeasureTime frame
safety;Standard intake value;

Countries

China

Contacts

Public ContactXuejuan Wang

Cancer Hospital Chinese Academy of Medical Sciences

xuejuan_wang@hotmail.com+86 138 1085 1485

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026