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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01840449
Other study ID # A-94-52030-240
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2012
Est. completion date May 2017

Study information

Verified date January 2019
Source Ipsen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to identify predictive factors for the response to Lanreotide treatment in Acromegaly as well as in Neuroendocrine Tumours.


Recruitment information / eligibility

Status Completed
Enrollment 156
Est. completion date May 2017
Est. primary completion date July 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Written informed consent (also mandatory in case of retrospective documentation of subject data)

- Diagnosis of acromegaly or NET with the intention to be treated with ATG or already on treatment with ATG

Exclusion Criteria:

- The subject has already been included in this study

- Participation in an interventional trial

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Somatuline Autogel® 60, 90 or 120 mg


Locations

Country Name City State
Austria University Hospital of Vienna Vienna
Germany ENDOC Hamburg
Switzerland University Hospital Basel Basel

Sponsors (1)

Lead Sponsor Collaborator
Ipsen

Countries where clinical trial is conducted

Austria,  Germany,  Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in biochemical markers (Growth Hormone [GH] & Insulin-like Growth Factor 1 [IGF-1] in acromegaly subjects and Chromogranin A [CgA] in NET subjects) Baseline and 1 year
Secondary Change in biochemical markers (Growth Hormone [GH] & Insulin-like Growth Factor 1 [IGF-1] in acromegaly subjects and Chromogranin A [CgA] in NET subjects) Baseline and 2 years
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Active, not recruiting NCT03252353 - Efficacy and Safety of Octreotide Capsules (MYCAPSSA) in Acromegaly Phase 3