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

  • STATUS
    Recruiting
  • End date
    Dec 31, 2024
  • participants needed
    210
  • sponsor
    Ipsen
Updated on 12 August 2023
fasting
lanreotide
igf1

Summary

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.

Details
Condition Acromegaly
Clinical Study IdentifierNCT05431803
SponsorIpsen
Last Modified on12 August 2023

Eligibility

Yes No Not Sure

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
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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