CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 60 enrolled
Drug / intervention
AG013736drug
Likely dose
AG-013736 5 mg orally twice dailyAI-extracted
Key inclusion· 2
  • Histologically documented thyroid cancer with metastases
  • Failed radioactive iodine (131I) treatment or 131I is not appropriate therapy (e.g., due to lack of iodine uptake)
Key exclusion· 2
  • Central lung lesions involving major blood vessels (arteries or veins)
  • History of hemoptysis

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

Search/NCT00094055
NCT00094055Phase 2Completed

Phase 2 Study of the Anti-Angiogenesis Agent AG-013736 in Patients With Metastatic Thyroid Cancer Who Are Refractory to or Not Suitable Candidates for 131 I Treatment

Pfizer·interventional·Posted Oct 11, 2004·Updated Jun 26, 2012

In Brief

A Phase 2 clinical trial evaluating AG013736 for Thyroid Neoplasms. Completed, enrolled 60 participants across 9 sites.

Detailed Summary

This is a Phase 2 study being conducted at multiple centers in the United States. Patients having thyroid cancer that has spread to other parts of the body (i.e., metastatic) are eligible to participate. Patients must have disease that was not controlled by previous treatment with radioactive iodine (131I) or not be good candidates for such treatment. The purpose of the study is to test whether the angiogenesis inhibitor AG-013736 is an effective treatment for metastatic thyroid cancer as shown by the number of patients in the study who experience significant and durable tumor shrinkage.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedOct 11, 2004
Enrollment StartSep 1, 2004
Primary CompletionJan 1, 2009
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 21.7 years ago

Interventions

AG013736drug

AG013736, tablets 5 mg BID daily until tumor progression or toxicity