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Treatment of Pain Associated With Fibromyalgia

NCT02146430 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 1293

Last updated 2020-11-09

Study results available
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Summary

The main objective of this trial is to compare change in weekly average daily pain score (ADPS) from baseline to Week 13 in subjects receiving either dose of DS-5565 versus placebo. Weekly ADPS is based on daily pain scores reported by the participant that best describes his or her worst pain over the previous 24 hours.

Conditions

  • Pain Associated With Fibromyalgia

Interventions

DRUG

DS-5565

DS-5565 15 mg tablet for oral administration

DRUG

Pregabalin

Pregabalin 150 mg capsule for oral administration

DRUG

Placebo tablet

Placebo tablet (matching DS-5565) for oral administration

DRUG

Placebo capsule

Placebo capsule (matching pregabalin) for oral administration

Sponsors & Collaborators

Principal Investigators

  • Global Clinical Leader · Daiichi Sankyo

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-10-27
Primary Completion
2016-07-14
Completion
2016-07-14

Countries

  • United States
  • Canada
  • Czechia
  • Denmark
  • Finland
  • France
  • Germany
  • Netherlands
  • Norway
  • Serbia
  • Sweden

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02146430 on ClinicalTrials.gov