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Brief Title: Evaluate the Safety, Tolerability, Biodistribution and Anti Tumour Activity of 177LU-OPS201 With Companion Imaging 68Ga-OPS202 PET/CT in Previously Treated Subjects With Locally Advanced or Metastatic Cancers Expressing Somatostatin Receptor 2 (SSTR2)
Official Title: A Multicentre, Open-Label Phase I/II Study to Evaluate the Safety, Tolerability, Biodistribution and Anti Tumour Activity of 177LU-OPS201 With Companion Imaging 68Ga OPS202 PET/CT in Previously Treated Subjects With Locally Advanced or Metastatic Cancers Expressing Somatostatin Receptor 2 (SSTR2)
Study ID: NCT03773133
Brief 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.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
MD Anderson Cancer Center, Houston, Texas, United States
Medical University of Innsbruck, Innsbruck, , Austria
University Hospital (UZ) Leuven, Leuven, , Belgium
CHU de Marseille - Hôpital la Timone, Marseille, , France
CHU de Bordeaux - Hôpital Haut Lévêque, Pessac, , France
Universitaetsklinikum Essen, Essen, , Germany
University Hospital Basel, Basel, , Switzerland
Royal Marsden Hospital - Surrey, Sutton, , United Kingdom
Name: Ipsen Medical Director
Affiliation: Ipsen
Role: STUDY_DIRECTOR