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Clinical Trial Summary

This study consists of two phases. The phase I study is designed to investigate the safety and tolerability of Satoreotide tetraxetan following fractionated i.v. administrations in pre-treated subjects with locally advanced or metastatic cancers expressing sstr2 as identified by Satoreotide trizoxetan Positron Emission Tomography (PET/CT) scans. This phase will encompass both radioactivity escalation and peptide mass dose evaluation. Phase II will assess the efficacy of Satoreotide tetraxetan in subjects in selected indications, in a basket design.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03773133
Study type Interventional
Source Ipsen
Contact
Status Terminated
Phase Phase 1/Phase 2
Start date May 14, 2019
Completion date October 10, 2019