Approval for the conduct of the trial by the first study site (M1)
Approval by ethical committee and regulatory authorities in countries where suPAR is not already routine
Statistical analysis of data: Writing of manuscripts. Publication in peer reviewed journals and presentations at conferences etc.
HISS will finalize the protocol and the informed consent forms; EudraCT registration; drafting of contracts between investigators and hospital/university administration
Searching for OpenAIRE data...
Author(s): Tariq U. Azam, Husam R. Shadid, Pennelope Blakely, Patrick O’Hayer, Hanna Berlin, Michael Pan, Peiyao Zhao, Lili Zhao, Subramaniam Pennathur, Rodica Pop-Busui, Izzet Altintas, Jens Tingleff, Marius A. Stauning, Ove Andersen, Maria-Evangelia Adami, Nicky Solomonidi, Maria Tsilika, Pinkus Tober-Lau, Eleni Arnaoutoglou, Verena Keitel, Frank Tacke, Athanasios Chalkias, Sven H. Loosen, Evangelos J. G
Published in: Journal of the American Society of Nephrology, Issue 31/11, 2020, Page(s) 2725-2735, ISSN 1046-6673