An International, Non-Interventional, Post-Authorization Long-Term Safety Study of Lutathera®, in Patients with Unresectable or Metastatic, Well-Differentiated, Somatostatin Receptor Positive, Gastroenteropancreatic Neuroendocrine Tumours (SALUS Study)

03/10/2018
14/03/2024
EU PAS number:
EUPAS25735
Study
Ongoing
Documents
Study protocol
Initial protocol
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Updated protocol
English (863.44 KB - PDF) View document
Study results
Study report
Other information
Study, other information
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