Non-interventional study for the generation of long term safety and efficacy data of pasireotide s.c. in patients with Cushing’s disease (Post-Authorization Safety Study)

First published 10/12/2012

Last updated 16/07/2024

EU PAS number:

EUPAS3199

Study

Finalised

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Documents

Study protocol

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Study results

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Study report

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The use of the ENCePP Seal has been discontinued since February 2025. The ENCePP Seal fields are retained in the display mode for transparency but are no longer maintained.

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Non-interventional study for the generation of long term safety and efficacy data of pasireotide s.c. in patients with Cushing’s disease (Post-Authorization Safety Study)

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