Phase 2 Thyroid Cancer Trial, Recruiting NCT05607407 Sponsor: Case Comprehensive Cancer Center Condition: Thyroid Cancer
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Phase 2 Thyroid Cancer Trial, Recruiting

NCT05607407
Recruiting Phase 2

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 a high-grade brain tumor (WHO grade 4 glioma) that has been confirmed by lab testing, and surgery to remove part or all of the tumor is already planned.
  • You have never been treated with a drug called methimazole for this brain tumor.
  • You are 18 years of age or older.
  • You are well enough to carry out most daily activities (a doctor will assess this using a standard scale).
  • Your blood counts, liver function, kidney function, and blood clotting are within acceptable ranges based on tests done within the last 21 days (confirm specific values with trial site).
  • If you take blood thinners (such as warfarin), your levels must be stable and within a safe range, with no active or high-risk bleeding.
  • Your thyroid function levels are within an acceptable range based on tests done within the last 21 days.
  • If you could become pregnant, you must have a negative pregnancy test within the last 21 days, and both you and your partner must agree to use reliable birth control during the trial and for 30 days after the last dose of the study drug.
  • You are able to swallow whole tablets.
  • Enough time has passed since your last treatment — for example, at least 4 weeks after surgery, 6 weeks after certain chemotherapy drugs, or 2 weeks after other investigational treatments (exact waiting times depend on what treatment you received — confirm with trial site).
  • If you are HIV-positive, your virus levels must be undetectable, you must be on a stable HIV treatment regimen, and you must not need preventive antibiotics or antifungal medications.
  • If you have or have had hepatitis B, the virus must be undetectable while on appropriate treatment.
  • If you have or have had hepatitis C, you must have been successfully treated and cured, or currently be on treatment with an undetectable viral load.
  • Your doctor believes you are a suitable candidate for chemotherapy after your surgery.
  • You are able to understand the study and are willing to sign a consent form.

Who may not be able to join:

  • You still have significant side effects from a previous treatment that have not mostly resolved (exceptions may apply for hair loss or nerve-related symptoms — confirm with trial site).
  • You are currently taking part in another clinical trial involving an experimental treatment.
  • You have had an allergic reaction to a drug that is chemically similar to methimazole.
  • You have an uncontrolled ongoing illness, such as an active infection, serious heart problems, or a mental health or personal situation that would make it difficult to follow the study requirements.
  • You have another cancer whose history or treatment could interfere with how this trial measures safety or effectiveness (other prior or current cancers may still be acceptable — confirm with trial site).
  • You have a significant ongoing digestive condition that causes frequent or severe diarrhea (such as Crohn's disease or a malabsorption disorder).
  • You are pregnant or currently breastfeeding.
  • You have a known history of an overactive thyroid (hyperthyroidism) or underactive thyroid (hypothyroidism).
  • You are unable or unwilling to swallow tablets.
  • You have a serious medical, laboratory, or mental health concern that, in your doctor's judgment, makes this trial unsuitable for you.

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 2: approximately ~30% 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: David Peereboom, MD, Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center

Phone: 216-445-6068

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 2
Registry
ClinicalTrials.gov
Start date
30 January 2023
Est. completion
1 September 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Progression Free Survival (PFS) Rate

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