Originalsprog | Engelsk |
---|---|
Tidsskrift | Kidney International |
Vol/bind | 99 |
Udgave nummer | 3 |
Sider (fra-til) | 768-770 |
Antal sider | 3 |
ISSN | 0085-2538 |
DOI | |
Status | Udgivet - mar. 2021 |
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Importance of standardizing renal outcomes in clinical trials : illustration by recent sodium glucose cotransporter 2 inhibitor studies. / van Raalte, Daniël H.; Bjornstad, Petter; Heerspink, Hiddo J.L. et al.
I: Kidney International, Bind 99, Nr. 3, 03.2021, s. 768-770.Publikation: Bidrag til tidsskrift › Letter › peer review
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TY - JOUR
T1 - Importance of standardizing renal outcomes in clinical trials
T2 - illustration by recent sodium glucose cotransporter 2 inhibitor studies
AU - van Raalte, Daniël H.
AU - Bjornstad, Petter
AU - Heerspink, Hiddo J.L.
AU - Persson, Frederik
AU - Cherney, David Z.I.
N1 - Funding Information: DHvR has acted as a consultant and received honoraria from Boehringer Ingelheim and Lilly, Merck, Novo Nordisk, Sanofi, and AstraZeneca and has received research operating funds from Boehringer Ingelheim-Lilly Diabetes Alliance, AstraZeneca, and Novo Nordisk; all honoraria are paid to his employer (AUMC, location VUMC). PB reports grants, personal fees, and nonfinancial support from AstraZeneca; personal fees from Bayer; personal fees from Bristol Meyer Squibb; grants and personal fees from Boehringer-Ingelheim; personal fees from Eli-Lilly; grants and personal fees from Novo Nordisk; personal fees and nonfinancial support from Sanofi; personal fees from XORT; and grants and personal fees from Horizon Pharma, all outside the submitted work. HJLH is a consultant for AbbVie, AstraZeneca, Bayer, Boehringer Ingelheim, Chinook, CSL Pharma, Gilead, Janssen, Merck, Mundi Pharma, Mitsubishi Tanabe, Novo Nordisk, and Retrophin; he has received research support from Abbvie, AstraZeneca, Boehringer Ingelheim, and Janssen. FP reports grants, personal fees, and nonfinancial support from Astra Zeneca; grants, personal fees, and nonfinancial support from Novo Nordisk; personal fees from Boehringer Ingelheim; grants and personal fees from Amgen; personal fees from Novartis; personal fees from MSD; personal fees from Sanofi; personal fees from Eli Lilly; and personal fees from Bayer, all outside the submitted work. DZIC has received honoraria from Boehringer Ingelheim-Lilly, Merck, AstraZeneca, Sanofi, Mitsubishi-Tanabe, Abbvie, Janssen, Bayer, Prometic, BMS, Maze, and Novo-Nordisk and has received operational funding for clinical trials from Boehringer Ingelheim-Lilly, Merck, Janssen, Sanofi, AstraZeneca, and Novo-Nordisk. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/3
Y1 - 2021/3
KW - Canagliflozin/adverse effects
KW - Consensus
KW - Diabetes Mellitus, Type 2/drug therapy
KW - Humans
KW - Hypoglycemic Agents
KW - Renal Insufficiency
KW - Sodium-Glucose Transporter 2 Inhibitors/adverse effects
UR - http://www.scopus.com/inward/record.url?scp=85101099327&partnerID=8YFLogxK
U2 - 10.1016/j.kint.2020.12.006
DO - 10.1016/j.kint.2020.12.006
M3 - Letter
C2 - 33637205
AN - SCOPUS:85101099327
VL - 99
SP - 768
EP - 770
JO - Kidney International
JF - Kidney International
SN - 0085-2538
IS - 3
ER -