Phase 2 Thyroid Cancer Trial, Recruiting NCT03099356 Sponsor: University of Michigan Rogel Cancer Center Condition: Thyroid Cancer
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Phase 2 Thyroid Cancer Trial, Recruiting

NCT03099356
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 type of thyroid cancer called differentiated thyroid cancer (confirmed by a lab test), with or without spread to other parts of the body, and it cannot be fully cured — or you have chosen to decline curative treatment
  • Your cancer can be measured on a scan (tumors larger than 10mm) and has been getting worse over time based on standard measurement guidelines
  • You have already tried radioactive iodine (I-131) treatment and it did not work, or your doctor has determined you are not a suitable candidate for it
  • You are 18 years of age or older
  • You are well enough to carry out daily activities with little to no limitation (confirm with trial site for exact fitness level required)
  • You are expected to live for at least 12 weeks or more
  • You have not had radioactive iodine (I-131) treatment in the past 24 weeks (or 4 weeks if a follow-up scan showed no sign of disease)
  • Your blood, kidney, and liver are functioning well enough to handle treatment (confirm with trial site for specific levels required)
  • If you are a woman who could become pregnant, you have had a negative pregnancy test within 3 days before starting treatment
  • You are willing and able to sign a consent form after being fully informed about the trial
  • You are able and willing to attend appointments, take the study medication, and follow all trial procedures

Who may not be able to join:

  • Genetic testing of your tumor tissue (called Foundation One or Next Generation Sequencing) cannot be done, or has not previously been done
  • You have had chemotherapy, targeted therapy, or radiation treatment within the past 4 weeks
  • You have taken part in another experimental treatment within the past 4 weeks
  • You have had radioactive iodine (I-131) treatment within the past 24 weeks (or 4 weeks if a follow-up scan was clear)
  • You have previously been treated with a type of drug called an mTOR inhibitor
  • You are currently taking certain medicines that strongly affect how the body processes drugs (called CYP3A4 or P-glycoprotein inhibitors or inducers) and cannot stop taking them at least one week before starting this trial
  • You have a stomach or bowel condition that could affect how your body absorbs the trial medications, including if you rely on a feeding tube for medicines
  • You have a serious uncontrolled medical condition or active infection that could prevent you from safely receiving the treatment
  • You have a known allergy or sensitivity to either of the trial drugs: cyclophosphamide or sirolimus
  • You have a known blockage in your urinary tract
  • You have dementia or a significant mental health condition that would prevent you from understanding and agreeing to take part in the trial
  • You are able to have children but are unwilling or unable to use reliable contraception or practice abstinence during the trial
  • You are currently pregnant or breastfeeding
  • You are currently living in prison

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: Paul Swiecicki, M.D., University of Michigan Rogel Cancer Center

Phone: 1-800-865-1125

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
Sponsor
University of Michigan Rogel Cancer Center
Registry
ClinicalTrials.gov
Start date
27 April 2017
Est. completion
1 December 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Percentage of patients that respond to treatment

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