CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 37 enrolled
Drug / intervention
Temsirolimus and Sorafenibdrug
Likely dose
Temsirolimus and Sorafenib 200 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01025453
NCT01025453Phase 2Completed

Phase II Study Evaluating the Combination of Temsirolimus and Sorafenib in the Treatment of Radioactive Iodine Refractory Thyroid Cancer

Memorial Sloan Kettering Cancer Center·interventional·Posted Dec 3, 2009·Updated Aug 15, 2018

In Brief

A Phase 2 clinical trial evaluating Temsirolimus and Sorafenib for Thyroid Cancer. Completed, enrolled 37 participants across 5 sites.

Detailed Summary

The purpose of this study is to find out what effects, good and/or bad, the combination of sorafenib and temsirolimus will have on thyroid cancer. Treatment guidelines from the National Comprehensive Cancer Network include sorafenib as a treatment option for thyroid cancer. Temsirolimus is an intravenous medication that is FDA approved for other type of cancers. In laboratory studies, the addition of temsirolimus to sorafenib works better than sorafenib alone.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsThyroid Cancer
CountriesUnited States

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedDec 3, 2009
Enrollment StartDec 1, 2009
Primary CompletionJan 16, 2018
TodayJul 2, 2026
Enrollment to primary: 8.1 yearsPosted 16.6 years ago

Interventions

Temsirolimus and Sorafenibdrug

Treatment will be with sorafenib 200 mg orally twice a day and temsirolimus 25 mg intravenous weekly. A cycle will be equivalent to 4 weeks of treatment.