drugset / Trial / NCT00454220

Study to Determine the Dose, the Safety and Effectiveness of a New Drug, Modified Release rhTSH, in Patients With Multinodular Goiter

NCT00454220 ↗

Phase 2 Completed 96 enrolled Genzyme, a Sanofi Company
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study is to determine the safety and effectiveness of 2 different doses of modified-release recombinant human thyroid stimulating hormone (MRrhTSH) when administered with radioiodine in patients with multinodular goiter, a condition that involves the enlargement of the thyroid gland. We will also evaluate the safety and effectiveness of radioiodine therapy alone in these patients. The goal of the treatment is to determine if there was a reduction in the size of the goiter and to study if goiter symptoms have improved after 6 months and after 36 months.

Timeline

Start
2007-07
Primary completion
2011-07
Completion
2011-07

Drugs

EvaluationDrugModalityDoseRoute
Subject MRrhTSH Protein / enzyme biologic 0.01 mg Intramuscular
Subject MRrhTSH Protein / enzyme biologic 0.03 mg Intramuscular

Indications