Duloxetine

Phase 3Completed
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Interest: 40/100
40
Hype Score

Development Stage

Pre-clinical
Phase 1
Phase 2
4
Phase 3
5
Approved
Indication / Disease

Fibromyalgia

Conditions

Fibromyalgia

Trial Timeline

Jun 1, 2012 → Feb 1, 2014

About Duloxetine

Duloxetine is a phase 3 stage product being developed by Shionogi for Fibromyalgia. The current trial status is completed. This product is registered under clinical trial identifier NCT01621191. Target conditions include Fibromyalgia.

What happened to similar drugs?

11 of 20 similar drugs in Fibromyalgia were approved

Approved (11) Terminated (3) Active (9)
zonisamideEisaiApproved
DuloxetineEli LillyApproved
Duloxetine + PlaceboEli LillyApproved
Eszopiclone + placeboSumitomo PharmaApproved
QuetiapineAstraZenecaApproved
amitriptyline + quetiapineAstraZenecaApproved

Hype Score Breakdown

Clinical
17
Activity
8
Company
15
Novelty
0
Community
0

Clinical Trials (3)

NCT IDPhaseStatus
NCT02335346Phase 3Completed
NCT01914666Phase 3Completed
NCT01621191Phase 3Completed

Competing Products

20 competing products in Fibromyalgia

See all competitors
ProductCompanyStageHype Score
DS-5565 + Pregabalin + Placebo tablet + Placebo capsuleDaiichi SankyoPhase 3
40
DS-5565Daiichi SankyoPhase 3
40
DS-5565 + PlaceboDaiichi SankyoPhase 3
40
DS-5565 + Pregabalin + Placebo tablet + Placebo capsuleDaiichi SankyoPhase 3
40
DS-5565 + Pregabalin + Placebo tablet + Placebo capsuleDaiichi SankyoPhase 3
40
ASP8062 + PlaceboAstellas PharmaPhase 2
35
ASP0819 + PlaceboAstellas PharmaPhase 2
35
Duloxetine 60 mg + PlaceboShionogiPhase 3
40
zonisamideEisaiApproved
35
ONO-1110 + PlaceboOno PharmaceuticalPhase 2
42
DuloxetineEli LillyApproved
35
duloxetine hydrochloride + placeboEli LillyApproved
43
duloxetineEli LillyPhase 3
40
Duloxetine + placeboEli LillyPhase 3
40
Duloxetine + PlaceboEli LillyPhase 3
40
Duloxetine + PlaceboEli LillyApproved
43
Treatment for FibromyalgiaEli LillyPre-clinical
26
Duloxetine + PlaceboEli LillyPhase 3
40
duloxetine + placeboEli LillyPhase 3
40
Eszopiclone + placeboSumitomo PharmaApproved
43