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Clinical Trial Details


Research Study Summary

Patients are needed to participate in a clinical research study for the treatment of Acromegaly

Research Study Title

Somatuline® Depot (Lanreotide) Injection for Acromegaly (SODA): A Post-marketing Observational Study


To assess the safety and effectiveness of Somatuline® Depot (lanreotide) Injection when administered by a health care professional (HCP), the patient, the patient's partner or parent/guardian as part of their routine acromegaly care.

To Learn more

Both Male and Female



Overall Status


Lead Sponsor



79 Months

Facility Type



Both Male and Female ages up to N/A

Inclusion Criteria:

  • The patient must have a clinical diagnosis of acromegaly

  • The patient must be treated with Somatuline® Depot (including patients newly prescribed Somatuline® Depot)

  • The patient or legally authorized representative must be able to understand the protocol and give signed informed consent. Assent from the patient should also be obtained, where appropriate. Signed informed consent and assent must be obtained before any study-related activities are conducted.

Exclusion Criteria:

  • Symptomatic, untreated biliary lithiasis

  • Known hypersensitivity to somatostatin analogs or related compounds (e.g., octreotide)

Site Locations (1)

Country State City Zip Facility and Contact
United States New Jersey Basking Ridge 07920 Ipsen


Ipsen Central Contact


NCT ID: NCT00686348

Date Last Changed: November 25, 2014

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