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Trials / Completed

CompletedNCT00830128

A Long-Term Study To Evaluate Safety And Efficacy Of Pregabalin In Patients With Fibromyalgia

An Open-Label Extension Safety And Efficacy Study Of Pregabalin (CI-1008) For The Treatment Of Fibromyalgia

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
106 (actual)
Sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study will assess the safety and efficacy of the long-term use of pregabalin at doses up to 450 mg/day in patients with fibromyalgia who have completed 16 weeks of dosing in Study A0081208 (NCT00830167).

Conditions

Interventions

TypeNameDescription
DRUGpregabalin (Lyrica)Dosage: 300-450 mg/day (150-225 mg twice daily), oral administration, Treatment duration: 52 weeks

Timeline

Start date
2009-07-01
Primary completion
2011-02-01
Completion
2011-02-01
First posted
2009-01-27
Last updated
2021-01-25
Results posted
2012-02-14

Locations

19 sites across 1 country: Japan

Source: ClinicalTrials.gov record NCT00830128. Inclusion in this directory is not an endorsement.

A Long-Term Study To Evaluate Safety And Efficacy Of Pregabalin In Patients With Fibromyalgia (NCT00830128) · Clinical Trials Directory