Phase 3 Thyroid Cancer Trial, Recruiting NCT06860971 Sponsor: Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Condition: Thyroid Cancer
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Phase 3 Thyroid Cancer Trial, Recruiting

NCT06860971
Recruiting Phase 3

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 who are willing to take part voluntarily, sign a consent form, and are able to follow the study requirements.
  • People who have been confirmed through a tissue or cell sample to have locally advanced or metastatic differentiated thyroid cancer.
  • People aged 18 to 74 years old (based on the date the consent form is signed).
  • People whose general physical ability to carry out daily activities is rated at a good level (a standard medical score of 0 or 1 on a scale used by doctors to measure this).
  • People whose life expectancy is estimated to be more than 12 weeks.
  • People who have at least one measurable area of cancer, as confirmed using standard imaging measurement guidelines (RECIST 1.1).
  • People whose cancer has continued to grow after receiving up to 2 rounds (and no more than 3 types) of a specific class of targeted cancer medications that affect blood vessel growth (VEGFR TKI therapies).
  • People whose cancer has been confirmed as no longer responding to radioactive iodine treatment, based on one or more specific medical findings (confirm with trial site for full details).
  • People whose thyroid-stimulating hormone (TSH) level is at or below 0.5 mIU/L while on TSH-suppressing medication.
  • People whose blood test results meet specific thresholds for red blood cells, white blood cells, platelets, liver function, kidney function, clotting ability, and protein levels (confirm with trial site for the exact values required).
  • People of childbearing potential who agree to use effective contraception during the study and for 6 months afterward; women must have a negative pregnancy test within 7 days before joining, and men must also agree to use contraception during and for 6 months after the study.

Who may not be able to join:

  • People who have a type of thyroid cancer called undifferentiated (anaplastic) thyroid carcinoma or medullary thyroid carcinoma.
  • People who have had or currently have another type of cancer, unless it was treated with surgery alone and there has been no return of cancer for 5 or more years, or unless it was a cured cervical carcinoma in situ, a non-melanoma skin cancer, or a superficial bladder tumour of a specific early stage.
  • People who have conditions that make it difficult to take oral (swallowed) medications, such as trouble swallowing, ongoing diarrhoea, or a bowel blockage.
  • People who still have significant side effects from previous cancer treatments that have not improved to a mild level, with some specific exceptions allowed (confirm with trial site for details).
  • People who have a known allergy to any of the inactive ingredients in the study drug.
  • People who have taken part in another clinical trial involving anti-cancer drugs within the 4 weeks before joining this study.
  • People who, in the treating doctor's judgment, have other circumstances that could seriously affect their safety or their ability to complete the study.

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
Phase 3: approximately ~65% 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

Phone: 0731 89762310

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 3
Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Registry
ClinicalTrials.gov
Start date
18 April 2025
Est. completion
1 January 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression - Free Survival (PFS) evaluated by the Independent Review Committee (IRC)

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