Safety Study of DS-5565 for Treatment of Fibromyalgia Pain in Subjects With Chronic Kidney Disease

Abbreviations: alanine aminotransferase (ALT), aspartate aminotransferase (AST), creatinine clearance \[(CrCL) determined by the central laboratory using the Cockcroft-Gault equation\], upper limit of normal (ULN), Columbia-Suicide Severity Rating Scale (C-SSRS) Inclusion Criteria: * Age ≥ 18 years * Able to give written informed consent * Able to complete patient-reported questionnaires per the Investigator's judgment * Estimated CrCl between 15-59 mL/min from serum creatinine by the central laboratory using the Cockcroft-Gault equation * Fibromyalgia meeting American College of Rheumatology criteria for FM: * Widespread pain index (WPI) ≥ 7 and symptom severity (SS) scale score ≥ 5 or WPI 3 to 6 and SS scale score ≥ 9, * Pain in at least 11 of 18 specific tender point sites, * Symptoms have been present at a similar level for at least 3 months, and * The subject does not have a disorder that would otherwise explain the pain * Average Daily Pain Score of ≥ 4 on the 11-point numeric rating scale (NRS) over the 7 days prior to randomization (based on completion of at least 4 daily pain assessments during the 7-day baseline period prior to randomization) * Women of child bearing potential (WOCBP) must be using adequate methods of contraception to avoid pregnancy during the study and for 4 weeks after study completion. Exclusion Criteria: * Need for ongoing use of concomitant chronic pain medications or any new non-pharmacological pain management techniques that may confound assessments of efficacy and/or safety, including neurolytic treatments (destruction of nerves by chemicals, heat, cold) or surgery, intrathecal pumps, spinal cord stimulators or psychological support within the previous year. Also excluded: topical capsaicin within 6 months; or systemic corticosteroids within 3 months of baseline period. * Unable to undergo pre-study washout of prohibited concomitant medications * Subjects with recent history (i.e., within 1 year prior to screening) of alcohol abuse or illicit drug use (cocaine, heroin, marijuana \[including medical, prescribed\], etc.) * Use of any selective serotonin reuptake inhibitor (SSRI), unless the subject has been on a stable dose for ≥ 90 days prior to screening and is not anticipated to need any dose adjustment during the course of the study * Subjects with severe or uncontrolled depression that, in the judgment of the Investigator, makes the subject inappropriate for entry into the study * Significant neurological or psychiatric disorder unrelated to neuropathic pain * Other severe pain (eg, sciatica, rheumatoid arthritis) that might impair the assessment of neuropathic pain * CrCl ≥ 60 mL/min estimated from serum creatinine by the central laboratory using the Cockcroft-Gault equation. * Subjects who are on hemodialysis or who require hemodialysis before the follow-up assessment; acute renal failure; history of kidney transplant * Any history of a malignancy other than basal cell carcinoma within the past 5 years * Clinically significant unstable neurologic, ophthalmologic, hepatobiliary, respiratory, or hematologic illness or unstable cardiovascular disease (eg, severe hypotension, uncontrolled cardiac arrhythmia, or myocardial infarction) within 12 months prior to screening * Pregnancy or breast feeding or intent to become pregnant during the study period * Known hypersensitivity to α2δ ligands or other components of the study medications. Note: Prior exposure to DS-5565 is allowed, as long as hypersensitivity to DS-5565 was not observed. * Clinically significant ECG abnormalities at the Screening Visit * Subjects who are at risk of suicide, as defined by their responses to the C-SSRS or in the opinion of the Investigator. Note: Subjects answering "yes" to any of the questions about active suicidal ideation/intent/behaviors that occurred within the past 12 months must be excluded (C-SSRS Suicide Ideation section - Questions 3, 4, or 5; C-SSRS Suicidal Behavior section - any of the suicide behaviors questions). Such subjects should be referred immediately to a mental health professional for appropriate evaluation. * Subjects who are unlikely to comply with the protocol (eg, uncooperative attitude, inability to return for subsequent visits, and/or otherwise considered by the Investigator to be unlikely to complete the study) * Subject is currently enrolled in, or it has been fewer than 30 days since ending, another investigational device or drug study or is receiving another investigational agent. * Subjects who are employees or immediate family of employees of the study site, Sponsor, or contract research organization (CRO) * Screening laboratory values outside the limits listed in the table below: * Hematology * Hemoglobin \< 8 g/dL * Platelet count \< 100,000/mm3 * Absolute neutrophil count \< 1,500/mm3 * Blood chemistry * AST \> 2.0 × ULN * ALT \> 2.0 × ULN * Alkaline phosphatase \> 1.5 × ULN * Total bilirubin \> 1.2 × ULN (If a subject has total bilirubin \>ULN: unconjugated and conjugated bilirubin fractions should be analyzed and only subject documented to have Gilbert's syndrome may be enrolled) * Creatine kinase \> 3.0 × ULN * Calculated CrCl ≥ 60 mL/min