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Thiazolidinedione
Rosiglitazone for Thyroid Cancer
Phase 2
Waitlist Available
Led By Electron Kebebew, MD
Research Sponsored by University of California, San Francisco
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Diagnosis of differentiated thyroid cancer
More than 3 months since prior chemotherapy
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Study Summary
This trial is studying the effects of rosiglitazone on patients with locoregionally extensive or metastatic thyroid cancer.
Who is the study for?
This trial is for adults with advanced thyroid cancer who've had a scan in the last 18 months, have certain levels of thyroglobulin, and show little to no uptake on radioactive iodine scans. They should not be pregnant or nursing, must use contraception if fertile, and can't have severe heart disease or allergies to thiazolidinediones.Check my eligibility
What is being tested?
The study tests how well rosiglitazone works in making thyroid tumor cells more sensitive to radioactive iodine. It's for those whose cancer has spread locally or further and who didn't respond well to surgery and radioactive iodine treatment.See study design
What are the potential side effects?
Rosiglitazone may cause fluid retention leading to swelling, weight gain, fatigue, headache, muscle pain; it might also affect liver function and increase risk of bone fractures.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have been diagnosed with differentiated thyroid cancer.
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It has been over 3 months since my last chemotherapy session.
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My cancer has spread to nearby areas or other parts of my body.
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I have had thyroid surgery and radioactive iodine treatment, but my condition did not improve.
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My heart condition does not severely limit my daily activities.
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I have no cancer other than possibly basal cell skin cancer.
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I have never received more than 800 mCi of radioiodine treatment.
Select...
My condition cannot be treated with surgery.
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I am 18 years old or older.
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I am not taking levothyroxine.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Radioiodine uptake and thyroglobulin level at 6 months and 1 year
Secondary outcome measures
Side effects of drug at 2 months
Find a Location
Who is running the clinical trial?
National Cancer Institute (NCI)NIH
13,667 Previous Clinical Trials
40,926,141 Total Patients Enrolled
University of California, San FranciscoLead Sponsor
2,506 Previous Clinical Trials
15,238,530 Total Patients Enrolled
Electron Kebebew, MDPrincipal InvestigatorUniversity of California, San Francisco
4 Previous Clinical Trials
505 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My cancer has spread to nearby areas or other parts of my body.I have had thyroid surgery and radioactive iodine treatment, but my condition did not improve.I am positive for Tg-antibodies regardless of Tg levels.I have been diagnosed with differentiated thyroid cancer.I have never received more than 800 mCi of radioiodine treatment.It has been over 3 months since my last chemotherapy session.I have had radiation therapy before.My heart condition does not severely limit my daily activities.I have no cancer other than possibly basal cell skin cancer.My condition cannot be treated with surgery.I am 18 years old or older.Not applicable.I am not taking levothyroxine.
Research Study Groups:
This trial has the following groups:Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
How secure are patients who utilize this particular remedy?
"There is limited data confirming the safety of this intervention, so it earned a score of 2."
Answered by AI
Are there any vacancies open in this clinical assessment for participants?
"The information on clinicaltrials.gov reveals that this trial is not currently seeking patients, as the last update was posted in January of 2014. Despite this inactive status, there are 476 other studies actively recruiting participants right now."
Answered by AI
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