Pharmacokinetics and Pharmacodynamics of Tolvaptan in Autosomal Dominant Polycystic Kidney Disease: Phase 2 Trials for Dose Selection in the Pivotal Phase 3 Trial
Author:
Affiliation:
1. Otsuka Pharmaceutical Development & Commercialization; Rockville MD, USA
2. Division of Nephrology; Emory University School of Medicine; Atlanta GA, USA
3. Division of Nephrology and Hypertension; Mayo Clinic; Rochester MN, USA
Funder
Otsuka America Pharmaceutical
Publisher
Wiley
Subject
Pharmacology (medical),Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jcph.880/fullpdf
Reference21 articles.
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2. Tolvaptan, a selective oral vasopressin V2-receptor antagonist, for hyponatremia;Schrier;N Engl J Med,2006
3. Dissociation between urine osmolality and urinary excretion of aquaporin-2 in healthy volunteers;Baumgarten;Nephrol Dial Transplant,2000
4. Prediction of creatinine clearance from serum creatinine;Cockcroft;Nephron,1976
5. Rationale and design of the TEMPO (Tolvaptan Efficacy and Safety in Management of Autosomal Dominant Polycystic Kidney Disease and its Outcomes) 3-4 Study;Torres;Am J Kidney Dis,2011
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3. Comparing Effects of Tolvaptan and Instruction to Increase Water Consumption in ADPKD: Post Hoc Analysis of TEMPO 3:4;Kidney360;2023-11-21
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