Casellas, F.
Calvet, Xavier
Carpio, D.
Vera, I.
Saldaña, R.
Mínguez, M.
Marín, L.
Juliá, B.
,
Funding for this research was provided by:
Merck Sharp and Dohme (funded the study and medical writing assistance)
Article History
Received: 28 December 2020
Accepted: 13 October 2021
First Online: 29 October 2021
Declarations
:
: The study complied with Good Clinical Practice standards and the principles of the latest version of the Helsinki Declaration (Brazil, 2013) and was approved by the Parc Taulí Ethics Committee. Confidentiality and anonymity were guaranteed in accordance with the Spanish Law 15/1999 on personal data protection.The surveys contained an initial written explanation of the purpose of the study and an invitation to anonymously participate if the patient consent to participate.
: Not applicable.
: Xavier Calvet has served as speaker, consultant and advisory member for, or has received research funding from MSD, Abbvie, Pfizer, Kern Pharma, Takeda, Janssen, Ferring, Faes Farma, Shire Pharmaceuticals, Tillotts Pharma, Otsuka Pharmaceutical and Vifor Pharma. Francesc Casellas has served as speaker, consultant and advisory member for, or has received research funding from Merck Sharp & Dohme, Abbvie, Pfizer, Takeda, Janssen, Ferring, Faes Farma, Shire Pharmaceuticals, Tillotts Pharma and Ferrer. Daniel Carpio has served as speaker, consultant and advisory member for, or has received research funding from Merck Sharp & Dohme, Abbvie, Kern Pharma, Takeda, Janssen, Ferring, Shire Pharmaceuticals, Tillotts Pharma, Dr Falk Pharma, Gebro Pharma. Berta Juliá is an employee of Merck Sharp & Dohme, Spain. Maribel Vera has served as speaker, consultant and advisory member and has received funding from MSD, Abbvie, Pfizer, Ferring, Shire Pharmaceuticals, Takeda and Jannsen.