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Duloxetine - Eli Lilly and Company

Drug Profile

Duloxetine - Eli Lilly and Company

Alternative Names: Ariclaim; Cymbalta; LY-227942; LY-248686; Xeristar; Yentreve

Latest Information Update: 05 Nov 2023

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At a glance

  • Originator Eli Lilly and Company
  • Developer Eli Lilly and Company; Shionogi
  • Class Antidepressants; Anxiolytics; Naphthalenes; Non-opioid analgesics; Propanolamines; Small molecules; Thiophenes; Urologics
  • Mechanism of Action Adrenergic uptake inhibitors; Serotonin plasma membrane transport protein inhibitors; Serotonin uptake inhibitors
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity Yes

Highest Development Phases

  • Marketed Back pain; Depressive disorders; Diabetic neuropathies; Fibromyalgia; Generalised anxiety disorder; Major depressive disorder; Musculoskeletal pain; Neuropathic pain; Stress incontinence
  • Phase II/III Chronic fatigue syndrome

Most Recent Events

  • 18 Feb 2022 Eli Lilly's data package protection for duloxetine expires in Japan, before February 2022
  • 03 May 2021 Efficacy and adverse events data from a phase III trial in Major depressive disorders presented at the 174th Annual Meeting of the American Psychiatric Association (APA-2021)
  • 05 Aug 2020 Eli Lilly in collaboration with Shionogi terminates a phase III trial in Major depressive disorder (In children, In adolescents) in Japan (PO), due to business decision (NCT03395353)
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