by James Russell, MD; Joel Raskin, MD; Curtis Wiltse, PhD; Daniel Walker, PhD; and Olga Brawman-Mintzer, MD
Drs. Russell, Wiltse, and Walker are with Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana; Dr. Raskin is with Lilly Research Laboratories, Eli Lilly Canada, Toronto, Ontario, Canada; and Dr. Brawman-Mintzer is with the Medical University of South Carolina, Charleston, South Carolina.
Financial support: This work was sponsored by Eli Lilly and Company and Boehringer Ingelheim GmbH.
Clinical trial registry number for this study: NCT00062673 at www.clinicaltrials.gov. First patient enrolled in this study (assigned to therapy): 18 March 2003. Last patient completed: 22 July 2004.
Disclosures: Drs. Russell, Raskin, Wiltse, and Walker are employees of Eli Lilly and Company; Dr. Brawman-Mintzer is on the speakers bureau of AstraZeneca, Forest Pharmaceuticals, Pfizer Inc., Eli Lilly, and Janssen Pharmaceutica, has received grant/research support from Pfizer, Forest Pharmaceuticals, AstraZeneca, Janssen Pharmaceutica, Biovail, UCB Pharma, Eli Lilly, Novartiz, and Sanofi-Aventis, and is a consultant to Pfizer, UCB Pharma, Janssen Pharmaceutica, AstraZeneca, Solvay.
Key Words: duloxetine, anxiety, major depressive disorder, elderly, placebo
ABSTRACT
Objective: To compare the efficacy and tolerability of duloxetine 60mg/day versus placebo in treating elderly patients with major depressive disorder (MDD) and concurrent anxiety symptoms.
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