Policy for scientific publications and responsible clinical trial data sharing

Lundbeck’s mission is to improve the quality of life of people suffering from psychiatric and neurological disorders. As a pharmaceutical company, Lundbeck considers the sharing of information from company-sponsored clinical trials to be an important part of fulfilling this mission. Lundbeck publishes results from our research and clinical studies in scientific journals and presents these results at scientific conferences. Lundbeck also discloses clinical trial information and result summaries in public registries and share clinical data. The Lundbeck policy for scientific publications and responsible clinical data sharing covers all scientific publications originated or sponsored by H. Lundbeck A/S or affiliates.

Lundbeck registers clinical trial protocol information and discloses results of clinical trials, regardless of outcome, in a publicly accessible clinical trial registry: www.clinicaltrials.gov. In addition, clinical trial protocol and results information submitted by Lundbeck to the EudraCT database is made publicly available by the European Medicine Agency (EMA) via its clinical trial registry: www.clinicaltrialsregister.eu. Clinical trial reports will be accessible on the EudraCT site in accordance with EMA POLICY/0070. Non-interventional studies may also be disclosed if, for example, they are considered to provide important safety data. 

Lundbeck will seek to ensure that disclosure of clinical trial information follows the IFPMA, EFPIA, JPMA, and PhRMA joint position paper “Disclosure of Clinical Trial Information via Clinical Trial Registries and Databases”, the Declaration of Helsinki and other relevant clinical trial disclosure requirements.


Lundbeck respects the privacy of the relationship between patients and healthcare professionals and is committed to ensuring that the process of scientific publication and clinical trial data sharing do not breach patient confidentiality.

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