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18F-FAPI & FDG PET/MRI assisting the precise treatment of thyroid-related eye diseases with teprotumumab and evaluating its efficacy, a prospective study

18F-FAPI & FDG PET/MRI assisting the precise treatment of thyroid-related eye diseases with teprotumumab and evaluating its efficacy, a prospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113667
Enrollment
Unknown
Registered
2025-12-01
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Thyroid-related eye disease

Interventions

Experimental Group:teprotumumab treatment

Sponsors

Shanghai Tenth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meet the TED diagnostic criteria; 2.EUGOGO classification: Moderate to severe; 3. Age: 18-80 years old 4. The subjects are willing and able to abide by the prescribed treatment plan and assessment time.

Exclusion criteria

Exclusion criteria: 1. Known to be allergic to any component of testuzumab or have had a previous allergic reaction to monoclonal antibody drugs; 2. Pregnant women, those with prohibited implants in their bodies, or those with claustrophobia who are not suitable for PET/MRI; 3. There are any other pre-existing diseases, metabolic disorders, abnormal physical examination or clinical laboratory test results, and there is reason to suspect that there may be diseases or conditions that lead to contraindications for the use of the investigational drug, or affect the interpretation of the research results, or put the subjects at high risk of treatment complications; 4. During the study period, other treatments for TED were received, including drug therapy (local or systemic glucocorticoids, traditional immunosuppressants and other biological agents), orbital radiotherapy, or surgical treatment, etc. 5. Those who the researchers believe are not suitable to participate in this clinical trial for other reasons.

Design outcomes

Primary

MeasureTime frame
Molecular imaging parameters of 18F-FAPI & FDG PET/MRI;

Countries

China

Contacts

Public ContactChunjun Sheng, Chao Ma

Shanghai Tenth People's Hospital

ponymachao@163.com+86 189 1768 5931

Outcome results

None listed

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