Phase 2 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 given written consent approved by an ethics committee
- You are 18 years of age or older
- You have been confirmed by tissue testing to have either: advanced or spreading differentiated thyroid cancer that no longer responds to radioactive iodine treatment (Group A), or anaplastic thyroid cancer (Group B)
- Group A: Your cancer got worse after trying at least one approved drug (Sorafenib, Lenvatinib, or Cabozantinib), and you have had no more than 3 prior drug treatments total
- Group B: You are either starting your first treatment, or you have tried no more than one previous drug treatment
- Your cancer can be seen and measured on scans
- A stored tissue sample from your tumour is available, or you are able to provide a new biopsy sample
- You are generally well enough to carry out light activity and care for yourself (confirm with trial site)
- Your blood counts, liver, kidney, and other lab results meet certain minimum health levels (confirm with trial site)
- If you are a woman who could become pregnant: you agree not to try to get pregnant during the study and for at least 6 months after finishing treatment, have a negative pregnancy test within 7 days before starting, and agree to use effective contraception throughout
- If you are a woman who cannot become pregnant: you are postmenopausal (no periods for at least 1 year) or have had a surgical procedure that prevents pregnancy
- You agree not to breastfeed or donate eggs during the study and for at least 6 months after finishing treatment (if applicable)
- If you are a man: you agree not to donate sperm during the study and for at least 6 months after finishing treatment
- If you are a man whose partner could become pregnant, is pregnant, or is breastfeeding: you agree to use a condom and an additional form of effective contraception during the study and for at least 6 months after finishing treatment
- You agree not to join another treatment-based clinical trial while taking part in this study
Who may not be able to join:
- Your cancer has spread to the brain or central nervous system
- You are still experiencing significant side effects (moderate or severe) from a previous cancer treatment, including surgery, radiation, or drug therapy
- You have had another cancer in the past 3 years, or still have signs of a previous cancer (exceptions may apply for certain skin cancers, fully treated prostate cancer, or fully removed non-invasive cancers — confirm with trial site)
- You have active Hepatitis B, active Hepatitis C, or HIV
- You have HIV with a detectable level of virus in your blood, or you take medications that may interfere with how the study drug works
- You have had a stroke or mini-stroke, or have had a serious heart event such as a heart attack or unstable chest pain within the last 6 months
- You have a history of serious heart rhythm problems or significant heart failure (confirm with trial site)
- You have a significant ongoing lung condition such as severe COPD or another moderate-to-severe breathing illness in the past 6 months
- You have active inflammatory bowel disease (such as ulcerative colitis or Crohn's disease), or have had a bowel blockage or tear in the past 6 months
- Your high blood pressure or diabetes is not well controlled
- You have had major surgery or radiation therapy within the past 4 weeks
- You have received a live vaccine in the past 30 days, or antibiotics in the past week
- You have received chemotherapy, immunotherapy, or other cancer drug treatments within the past 2 weeks
- You have previously been treated with a type of drug called a topoisomerase 1 inhibitor (confirm with trial site)
- You have a known allergy to the study drug (sacituzumab govitecan) or any of its ingredients
- You have other health conditions that your doctor feels would make it unsafe for you to receive or tolerate the treatment
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: Alejandro García-Alvarez, M.D.; Ph.D., Hospital Universitario Vall d´Hebron
Phone: +34 93 434 44 12
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
Objective response rate (ORR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.