Study to Assess the Efficacy and Safety of Lanreotide Autogel in Chinese Participants With GEP-NETs
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ABSTRACT: This study will be conducted to support the registration of the lanreotide Autogel 120 mg formulation in China for the treatment of GEP-NETs and treatment of clinical symptoms of NETs.
The study will include a screening period of up to 4 weeks followed by a 48-week intervention period. After completion of the main study period, approximately five participants will continue in a self/partner injection cohort with lanreotide Autogel 120 mg every 28 days for 24 weeks.
DISEASE(S): Neuroendocrine Tumors,Pancreatic Neoplasms,Stomach Neoplasms,Gastroenteropancreatic Neuroendocrine Tumor,Intestinal Neoplasms
PROVIDER: 2374905 | ecrin-mdr-crc |
REPOSITORIES: ECRIN MDR
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