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Real-World Study (RWS) of Lanreotide Autogel (LAN) for the Treatment of Patients With Acromegaly in China

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Ipsen

Status

Completed

Conditions

Acromegaly

Study type

Observational

Funder types

Industry

Identifiers

NCT05431803
CLIN-52030-455

Details and patient eligibility

About

This study aims to assess the one-year effectiveness and safety of LAN among patients with acromegaly in China in routine clinical practice. In addition, the study is designed to understand the real-world treatment patterns and outcomes of LAN among Chinese patients with acromegaly.

Enrollment

129 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants who are able to comply with the protocol
  • Participants with serum IGF-1 level above the ULN for age and sex, and serum fasting GH level above 2.5 μg/L
  • Participants with acromegaly who are naïve to LAN treatment and about to initiate LAN

Exclusion criteria

  • Participants who are currently participating in any investigational study or clinical trial of acromegaly
  • Pregnant participants
  • Participants with hypersensitivity to somatostatin or related peptides or to any of the excipients

Trial contacts and locations

12

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Central trial contact

Ipsen Clinical Study Enquiries

Data sourced from clinicaltrials.gov

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