An Observational Study of Octreotide Subcutaneous Depot in Patients With Acromegaly

NCT07583563 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2026-05-13

No results posted yet for this study

Summary

The purpose of this study is to collect long-term (up to two years) safety and effectiveness of octreotide subcutaneous depot in patients with acromegaly in the real-world setting.

Conditions

Interventions

DRUG

Octreotide subcutaneous depot

Commercially available octreotide subcutaneous depot treatment administered by participants for a maximum duration up to 2 years in the study

Sponsors & Collaborators

  • Camurus AB

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-05-31
Primary Completion
2029-05-31
Completion
2029-05-31

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07583563 on ClinicalTrials.gov