Phase 1 Thyroid Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have been diagnosed with thyroid cancer that has been confirmed by a laboratory test, and if it is a certain type (differentiated thyroid cancer), a specialist has determined it no longer responds to radioactive iodine treatment.
- Your cancer has been shown to be growing or spreading based on recent scans, using a standard measurement system called RECIST 1.1.
- You have already had surgery to remove tumors in the neck area that could be removed, but the cancer has now spread to areas that cannot be surgically removed.
- You previously received a targeted drug treatment that was stopped because of side effects, because it wasn't working, or because you chose to stop it.
- You have at least one tumor that can be measured on a CT or MRI scan (meeting specific size requirements).
- A special type of scan (68Ga-CTR-FAPI PET/CT) shows that more than half of your tumors have a high uptake of a specific tracer (confirm with trial site for technical details).
- Your doctor estimates you are expected to live longer than 6 months.
- You are able to carry out basic daily activities, with your overall health and functioning rated at a certain level or better (confirm with trial site).
- Any side effects from previous cancer treatments have mostly cleared up, except for things like hair loss or certain long-term effects considered permanent.
- If you are able to have children, you agree to use effective birth control during treatment and for several months after the last dose (4 months for males, 7 months for females).
- You are willing to take part and have signed a consent form.
Who may not be able to join:
- Some of your tumors show up on a CT or MRI scan but do not show up on the special tracer scan (68Ga-CTR-FAPI PET/CT).
- You have previously received a type of radiation treatment delivered through the bloodstream, except for radioactive iodine (131I).
- You have received any systemic cancer treatment (such as chemotherapy, targeted therapy, immunotherapy, or certain traditional medicines) within the 4 weeks before starting the trial.
- You have taken part in another clinical trial for a drug or medical device within the 4 weeks before starting the trial.
- Your major organs (such as liver, kidneys, or heart) are not functioning well enough (confirm with trial site for specific thresholds).
- You have serious or poorly controlled other health conditions.
- You have fluid buildup around your lungs or in your abdomen that needs treatment or is considered uncontrolled.
- You have had an active infection within the 4 weeks before starting the trial.
- You are pregnant, breastfeeding, or planning to become pregnant.
- You have a known allergy to contrast dyes used in scans.
- You have had brain or spinal cord metastases that have caused symptoms.
- You currently have or are being treated for another type of cancer.
- You have had surgery requiring general anesthesia within the 8 weeks before starting the trial.
- You have had a heart attack or stroke within the 8 weeks before starting the trial.
- You have severe claustrophobia (fear of enclosed spaces, which could affect your ability to have scans).
- The trial doctor feels there is any other reason you should not take part, such as difficulty following the treatment plan or attending follow-up visits.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Yansong Lin, M.D., Peking Union Medical College Hospital
Phone: 0086-18500487274
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Incidence and severity of adverse events, frequency of dose-limiting toxicities and maximum tolerated dose of 177Lu-CTR-FAPI in patients with thyroid cancer.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.