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Clinical Translational IIT Study of Novel Radiopharmaceutical Targeting FAP—Evaluating the Clinical Imaging of 68Ga-FAPI-GP PET in Patients with Malignant Solid Tumors

Clinical Translational IIT Study of Novel Radiopharmaceutical Targeting FAP—Evaluating the Clinical Imaging of 68Ga-FAPI-GP PET in Patients with Malignant Solid Tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093842
Enrollment
Unknown
Registered
2024-12-12
Start date
2024-12-23
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

Subjects confirmed to have malignant solid tumors by histopathological examination

Interventions

GP-01:68Ga-FAPI-GP01
GP-02:68Ga-FAPI-GP02

Sponsors

Affiliated Hospital of Guilin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.The subject or their legal representative is able to voluntarily sign the informed consent form. 2.Adult subjects (aged 18-80 years), regardless of gender. 3.Commitment to comply with the study procedures and cooperate throughout the entire study. 4.Subjects confirmed to have malignant solid tumors by histopathological examination. 5.Subjects agree to use contraception for at least 28 days following the administration of 68Ga-FAPI.

Exclusion criteria

Exclusion criteria: 1.The subject or their legal representative is unable or unwilling to sign the informed consent form. 2.Unable to comply with the full study procedures. 3.Pregnant or breastfeeding women. 4.Individuals deemed unsuitable for inclusion by the investigator.

Design outcomes

Primary

MeasureTime frame
SUVmax;

Countries

China

Contacts

Public ContactFu Wei

Affiliated Hospital of Guilin Medical University

13977385850@126.com+86 13977385850

Outcome results

None listed

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