Thyroid Cancer Trial, Recruiting NCT07068542 Sponsor: Zhejiang Provincial People's Hospital Condition: Thyroid Cancer
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Thyroid Cancer Trial, Recruiting

NCT07068542
Recruiting Not Applicable

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:

  • People aged 18 or older at the time of signing the consent form.
  • People who have been diagnosed through a tissue biopsy with one of the following advanced thyroid cancers that cannot be surgically removed, has spread locally, or has spread to other parts of the body: anaplastic thyroid carcinoma (ATC), poorly differentiated thyroid carcinoma (PDTC), or a type of thyroid cancer that no longer responds to radioactive iodine treatment (including papillary or follicular thyroid cancer).
  • People with ATC or PDTC who either do not have certain specific gene changes (BRAF V600E, RET fusion, NTRK fusion, or ALK fusion), or who do have those gene changes but have already tried and not responded to the standard targeted treatment for them.
  • People with radioactive iodine-resistant thyroid cancer where the cancer meets at least one of these conditions: the cancer does not absorb radioactive iodine, the cancer grew within 12 months of radioactive iodine treatment, the person received a very high cumulative dose of radioactive iodine, the cancer shows up on a specific type of scan (FDG-PET), or prior targeted drug therapy (multi-target TKI) has already been tried and has not worked.
  • People who have at least one area of cancer that can be measured on a scan, based on standard measurement guidelines (RECIST v1.1).
  • People who are well enough to carry out basic daily activities, as assessed by a standard medical scale (ECOG score of 0, 1, or 2).
  • People with a life expectancy of at least 12 weeks.
  • People whose blood cell counts and bone marrow function are within acceptable ranges, as confirmed by blood tests (confirm with trial site for exact values).
  • People whose liver is functioning adequately, as shown by blood test results within acceptable ranges (confirm with trial site for exact values).
  • People whose kidneys are functioning adequately, with kidney filtration above a certain level as calculated by a standard formula (confirm with trial site for exact values).
  • People who do not have an active autoimmune disease that requires ongoing systemic (whole-body) treatment.
  • People who do not have another active cancer that currently requires treatment.
  • People who are willing and able to sign a written consent form.

Who may not be able to join:

  • People who have previously received a treatment specifically targeting a protein called TROP2.
  • People who have previously been treated with a type of drug called a topoisomerase I inhibitor antibody-drug conjugate.
  • People who have previously received certain immune-activating drugs (such as those targeting ICOS, CD40, CD137, GITR, or OX40) or immune cell therapies.
  • People who have had another cancer diagnosis within the past 3 years, unless it was a localised skin cancer or early-stage cervical cancer that was fully treated (confirm with trial site for specific exceptions).
  • People who have cancer that has spread to the brain or spinal cord that is not well-controlled or is causing symptoms — though people whose brain metastases have been treated and have been stable for at least 4 weeks, and who have been off steroid medications for at least 2 weeks, may still be considered (confirm with trial site).
  • People with serious uncontrolled health conditions, including uncontrolled high blood pressure, severe diabetes, or an active infection.
  • People who have a history of a lung condition called interstitial lung disease or non-infectious pneumonitis that required steroid treatment, or who currently have a suspected lung condition of this type.
  • People who still have side effects from previous cancer treatments that are greater than a mild level (Grade 1), except for hair loss or other effects considered clinically minor.
  • People who have had an active autoimmune disease requiring systemic treatment within the past 2 years (standard hormone replacements such as thyroid medication or low-dose steroids are generally not considered in this category — confirm with trial site).
  • People who have been taking steroid medications at a dose higher than 10 mg per day of prednisone (or equivalent) within the 10 days before starting the trial, with exceptions for inhaled, topical, or low-dose replacement steroids (confirm with trial site).
  • People with a known HIV infection, AIDS, or an active syphilis infection.
  • People who have had an organ transplant or bone marrow/stem cell transplant from a donor.
  • People with a known serious allergic reaction to the study drugs or their ingredients.
  • People who have recently received chemotherapy, radiation, immunotherapy, biological therapy, targeted drug therapy, or other systemic immune treatments and have not completed the required waiting period before joining (confirm with trial site for specific timeframes).
  • People who are pregnant or currently breastfeeding.
  • People with serious eye conditions that may affect healing of the surface of the eye, such as severe dry eye syndrome or severe meibomian gland disease.

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 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Minghua Ge, Zhejiang Provincial People's Hospital

Phone: 86-571-85893567

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
Not Applicable
Sponsor
Zhejiang Provincial People's Hospital
Registry
ClinicalTrials.gov
Start date
1 July 2025
Est. completion
31 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall Survival (OS) - ATC Cohort; Progression-Free Survival (PFS) - PDTC and RAIR-DTC Cohorts

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: 28 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