drugset / Trial / NCT04614766

A Clinical Trial Evaluating the Safety of Combining Lutathera(R) and Azedra(R) to Treat Mid-gut Neuroendocrine Tumors

NCT04614766

Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study is designed to identify the best tolerated doses of Lutathera® and Azedra® when co-administered to treat midgut neuroendocrine tumors. These drugs are radioactive drugs, known as radionuclide therapy, and are both approved in the treatment of midgut neuroendocrine tumor as single agents (not together). Currently, the safest and best tolerated doses of these drugs (when combined) is unknown. That is the purpose of this clinical trial.

Timeline

Start
2022-09-30
Primary completion
2024-04-23
Completion
2024-04-23

Drugs

EvaluationDrugModalityDoseRoute
Subject 131I-MIBG Protein / enzyme biologic Intravenous
Subject 177Lu-DOTATATE Peptide 200 unknown Intravenous