A Study of Cabozantinib Compared With Placebo in Subjects With Radioiodine-refractory Differentiated Thyroid Cancer Who Have Progressed After Prior Vascular Endothelial Growth Factor Receptor (VEGFR) -Targeted Therapy
Condition(s) studied
Investigational drug(s) / intervention(s)
Cabozantinib: Tablets containing 60-mg or 20-mg cabozantinib once daily orally.
Placebo: Tablets containing placebo equivalent of 60-mg or 20-mg cabozantinib once daily orally.
Study summary
The objective of this study is to evaluate the effect of cabozantinib compared with placebo on progression free survival (PFS) and objective response rate (ORR) in subjects with Radioiodine-Refractory Differentiated Thyroid Cancer (DTC) who have progressed after prior vascular endothelial growth factor receptor (VEGFR)-Targeted therapy.
Eligibility
Primary outcome measure(s)
- Progression Free Survival (PFS) — Up to approximately twenty months after the first subject is randomized. Time from randomization to the earlier of the following events: radiographic PD as determined by the blinded independent central review (BIRC) or death due to any cause.
Time to the earlier of either radiographic progressive disease (PD) or death from any cause. - Objective Response Rate (ORR) — Six months after 100 subjects are randomized. Time from randomization to best overall response of confirmed complete response (CR) or confirmed partial response (PR) per BIRC per RECIST 1.1.
Proportion of subjects with the best overall response of complete response (CR) or partial response (PR).
Trial sites (164)
| Facility | City | Region | Status |
|---|---|---|---|
| Exelixis Clinical Site #2 | Newport Beach | California | |
| Exelixis Clinical Site #98 | Sacramento | California | |
| Exelixis Clinical Site #69 | San Francisco | California | |
| Exelixis Clinical Site #10 | Stanford | California | |
| Exelixis Clinical Site #3 | Torrance | California | |
| Exelixis Clinical Site #9 | Aurora | Colorado | |
| Exelixis Clinical Site #21 | New Haven | Connecticut | |
| Exelixis Clinical Site #4 | Washington D.C. | District of Columbia | |
| Exelixis Clinical Site #94 | Miami | Florida | |
| Exelixis Clinical Site #93 | Orlando | Florida | |
| Exelixis Clinical Site #6 | Tampa | Florida | |
| Exelixis Clinical Site #164 | Chicago | Illinois | |
| Exelixis Clinical Site #54 | Lexington | Kentucky | |
| Exelixis Clinical Site #153 | Boston | Massachusetts | |
| Exelixis Clinical Site #80 | Ann Arbor | Michigan | |
| Exelixis Clinical Site #78 | Detroit | Michigan | |
| Exelixis Clinical Site #22 | Detroit | Michigan | |
| Exelixis Clinical Site #63 | Columbia | Missouri | |
| Exelixis Clinical Site #42 | St Louis | Missouri | |
| Exelixis Clinical Site #11 | Omaha | Nebraska | |
| Exelixis Clinical Site #118 | Morristown | New Jersey | |
| Exelixis Clinical Site #76 | Charlotte | North Carolina | |
| Exelixis Clinical Site #19 | Durham | North Carolina | |
| Exelixis Clinical Site #7 | Cincinnati | Ohio | |
| Exelixis Clinical Site #5 | Bethlehem | Pennsylvania | |
| Exelixis Clinical Site #1 | Philadelphia | Pennsylvania | |
| Exelixis Clinical Site #75 | Pittsburgh | Pennsylvania | |
| Exelixis Clinical Site #134 | Charleston | South Carolina | |
| Exelixis Clinical Site #68 | Nashville | Tennessee | |
| Exelixis Clinical Site #8 | Houston | Texas | |
| Exelixis Clinical Site #113 | Seattle | Washington | |
| Exelixis Clinical Site #96 | Pergamino | Buenos Aires | |
| Exelixis Clinical Site #97 | Caba | Argentina | |
| Exelixis Clinical Site #129 | Córdoba | Argentina | |
| Exelixis Clinical Site #17 | St Leonards | New South Wales | |
| Exelixis Clinical Site #25 | Waratah | New South Wales | |
| Exelixis Clinical Site #86 | Bedford Park | South Australia | |
| Exelixis Clinical Site #24 | Melbourne | Victoria | |
| Exelixis Clinical Site #12 | Herston | Australia | |
| Exelixis Clinical Site #62 | Salzburg | Austria |
+ 124 more sites — see the full list on the official registry below.
On this site
📄 Cabometyx (cabozantinib) drug profile →More Exelixis trials in South Korea
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT03690388 on ClinicalTrials.gov ↗ ← All trials in South Korea