A Population Pharmacokinetic–Pharmacodynamic Meta‐Analysis of Vortioxetine in Patients with Major Depressive Disorder
Author:
Affiliation:
1. Takeda Pharmaceuticals USA Inc. Deerfield ILUSA
2. Takeda Development Center Americas Inc. Deerfield ILUSA
3. H. Lundbeck A/S Valby Denmark
Funder
Takeda Pharmaceuticals U.S.A.
Publisher
Wiley
Subject
Pharmacology,Toxicology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bcpt.12513
Reference46 articles.
1. Burden of Depressive Disorders by Country, Sex, Age, and Year: Findings from the Global Burden of Disease Study 2010
2. Vortioxetine (Lu AA21004) in the long-term open-label treatment of major depressive disorder
3. A randomized, double-blind trial of 2.5 mg and 5 mg vortioxetine (Lu AA21004) versus placebo for 8 weeks in adults with major depressive disorder
4. A randomized, double-blind, placebo-controlled 6-wk trial of the efficacy and tolerability of 5 mg vortioxetine in adults with major depressive disorder*
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