Boublay, Nawele http://orcid.org/0000-0002-2074-0298
Fédérico, Denis
Pesce, Alain
Verny, Marc
Blanc, Frédéric
Paccalin, Marc
Desmidt, Thomas
Grosmaître, Pierre
Moreaud, Olivier
Relland, Solveig
Bravant, Estelle
Bouet, Romain
Krolak-Salmon, Pierre
Funding for this research was provided by:
National French Program of Hospital Clinical Research (2012)
Article History
Received: 28 August 2017
Accepted: 16 October 2018
First Online: 14 November 2018
Ethics approval and consent to participate
: Written informed consent is obtained from subject and caregiver prior to the initiation of the study. The study is carried out in accordance with the French and European Guidelines for Good Clinical Practice, the latest version of the Declaration of Helsinki (Edinburg 2000, Washington 2002, Tokyo 2005) and ICH (International Conference on Harmonisation) Recommendations and Guidelines for Good Clinical Practice.In accordance with law n° 2004.806 and the ethical body governing biomedical research, the approval of the French ‘Comité de Protection des Personnes’ (CPP) has been submitted to ‘CPP Sud Est III’. CLEM study has been registered in the clinical trials (Current Controlled Trials NCT02052947).
: Not applicable
: The authors declare that Avid Radiopharmaceuticals, a Wholly Owned Subsidiary of Eli Lilly & Company has contributed to the funding of 50 doses of Florbetapir for the PET examination.
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