Phase 1 Thyroid Cancer Trial, Recruiting NCT07438847 Sponsor: SHAOYAN LIU Condition: Thyroid Cancer
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Phase 1 Thyroid Cancer Trial, Recruiting

NCT07438847
Recruiting Phase 1

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 1
Sponsor
SHAOYAN LIU
Registry
ClinicalTrials.gov
Start date
1 January 2026
Est. completion
31 December 2026

Where this trial is recruiting

🇨🇳 China

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov