Pain Associated With Fibromyalgia
Conditions
Keywords
pain, fibromyalgia
Brief 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.
Interventions
DRUGDS-5565
DS-5565 15 mg tablet for oral administration
DRUGPregabalin
Pregabalin 150 mg capsule for oral administration
DRUGPlacebo tablet
Placebo tablet (matching DS-5565) for oral administration
DRUGPlacebo capsule
Placebo capsule (matching pregabalin) for oral administration
Sponsors
Syneos Health
Daiichi Sankyo
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age ≥ 18 years * Able to give written informed consent * Able to complete participant-reported questionnaires per the investigator's judgment * At screening, participants must meet the 1990 American College of Rheumatology (ACR) criteria for fibromyalgia (FM), i.e. widespread pain present for at least 3 months and pain in at least 11 of 18 specific tender point sites. In addition, the 2010 ACR criteria must be met: * Widespread pain index (WPI) ≥ 7 and symptom severity (SS) scale score ≥ 5, or WPI 3 to 6 and SS scale score ≥ 9 * Symptoms have been present at a similar level for at least 3 months * The subject does not have a disorder that would otherwise explain the pain * ADPS of ≥ 4 on the 11-point numeric rating scale (NRS) over the past 7 days prior to randomization (based on completion of at least 4 daily pain diaries during the 7-day baseline period prior to randomization) * Subject must have documented evidence of a fundoscopic examination (with pupil dilation) within 12 months prior to screening or at screening. * Women of child-bearing potential (WOCBP) must be using an adequate method of contraception to avoid pregnancy during the study and for 4 weeks after study completion.
Exclusion criteria
* Clinically significant unstable neurologic, psychiatric, ophthalmologic, hepatobiliary, respiratory, or hematologic illness or unstable cardiovascular disease (e.g. severe hypotension, uncontrolled cardiac arrhythmia, or myocardial infarction) or any other concurrent disease within 12 months prior to screening that in the opinion of the investigator would interfere with study participation or assessment of safety and tolerability * Anticipation of initiation or significant change to normal daily exercise routines or need for ongoing use of concomitant medications or non-pharmacological pain management techniques that may confound assessments of efficacy and/or safety * Unable to undergo pre-study washout of prohibited concomitant medications * Subjects who are at risk of suicide as defined by their responses to the Columbia-Suicide Severity Rating Scale (C-SSRS) or in the opinion of the investigator. Note: Patients answering yes to any of the questions about active suicidal ideation/intent/behaviors occurring 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 patients should be referred immediately to a mental health professional for appropriate evaluation. * Current severe or uncontrolled major depressive disorder or anxiety disorders as assessed by the Mini-international Neuropsychiatric Interview (MINI) mild to moderate major depression or anxiety disorders are permitted provided that the investigator assesses the patient as clinically stable and appropriate for entry into the study. * Any diagnosis of lifetime bipolar disorder or psychotic disorder * Participants with pain due to other conditions (e.g. diabetic peripheral neuropathic pain or post-herpetic neuralgia) that in the opinion of the investigator, would confound assessment or self-evaluation of the pain associated with FM. * Participants with pain due to any widespread inflammatory musculoskeletal disorder (e.g. rheumatoid arthritis, lupus) or widespread rheumatic disease other than FM. * Abuse or dependence of prescription medications, street drugs, or alcohol within the last 1 year * Any history of a malignancy other than basal cell carcinoma within the past 5 years * A diagnosis of untreated sleep apnea or initiation of treatment for sleep apnea within the past 3 months * Pregnancy or breast-feeding, or intent to become pregnant during the study period * Participant is currently enrolled in or has not yet completed at least 30 days since ending another investigational device or drug study or is receiving other investigational agents. * Known hypersensitivity to alpha2-delta (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. * Participants who are unlikely to comply with the protocol (e.g. uncooperative attitude, inability to return for subsequent visits) and/or otherwise considered by the investigator to be unlikely to complete the study. * Abnormal investigative tests (i.e. electrocardiograms \[ECGs\]) and laboratory values judged by the investigator to be clinically significant at screening, with particular focus on: a. Abnormal renal function defined as calculated creatinine clearance (CrCl) \< 60 mL/min determined by the central laboratory using the modified Cockcroft-Gault equation; blood urea nitrogen\> 1.5 × upper limit of normal (ULN); creatine kinase \> 3.0 × ULN; serum creatinine \> 1.6 mg/dL (\> 141.4 μmol/L); b. Abnormal liver function defined as aspartate aminotransferase (AST) \> 2.0 × ULN, alanine aminotransferase (ALT) \> 2.0 × ULN; alkaline phosphatase \> 1.5 × ULN; total bilirubin\> 1.2 × ULN. If a subject has total bilirubin \> 1.2 ULN, unconjugated and conjugated bilirubin fractions should be analyzed and only participants documented to have Gilbert's syndrome may be enrolled.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change From Baseline in Weekly Average Daily Pain Score (ADPS) at Week 13 in Participants Receiving DS-5565, Pregabalin, Placebo | Baseline up to Week 13 postdose | Average daily pain scores (ADPS) reported by the participant that best describes his or her worst pain over the previous 24 hours. A daily pain score has a scale where 0 = no pain to 10 = worst possible pain. Higher scores indicate a worse outcome. For participants with no Week 13 data, the baseline observation was carried forward (BOCF). The mean (multiple imputation estimate) and standard error (multiple imputation) are reported. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Fibromyalgia Index Questionnaire (FIQ) Total Score From Baseline to Week 13 in Participants Receiving DS-5565, Pregabalin, or Placebo | Baseline up to Week 13 postdose | The total FIQ score is composed of 10 items, with a maximum possible score of 100. The first item contains 11 questions related to physical functioning and are rated on a 4-point Likert-type scale, where 0 indicates 'always' and 3 indicates 'never'. The overall impact items are rated on a 0-7 scale for the number of days that the patient felt well and the number of days they were unable to work (including housework) because of fibromyalgia symptoms. The symptoms items are rated on visual analog scales (0-10 cm), with higher numbers indicated greater symptomatology. Scores range from 0 (no impairment) to 10 (maximum impairment), where higher scores indicate worse outcome. For this outcome, the change in total FIQ score from baseline is being reported. Negative values indicate improvement from baseline in impairment. |
| Number of Responders at Week 13 Among Participants Receiving DS-5565, Pregabalin, or Placebo | Week 13 postdose | The number of participants with at least a 30% or 50% reduction in average daily pain score (ADPS) at Week 13 is reported. |
| Change From Baseline to Week 13 in Multidimensional Fatigue Inventory (MFI-20) General Fatigue Score in Participants Receiving DS-5565, Pregabalin, or Placebo | Baseline up to Week 13 postdose | MFI is a validated 20-item, self-reported instrument designed to measure fatigue in the following dimensions: general fatigue, physical fatigue, mental fatigue, reduced motivation, and reduced activity. The respondent is asked to mark an 'X' in 1 of 5 boxes arranged linearly where 1 is 'Yes, that is true' and 5 is 'No, that is not true.' Each subscale consists of 4 items, 2 indicative for fatigue and 2 contraindicative. For the indicative questions, a high score indicates a high fatigue level and low scores indicate a low fatigue levels. Conversely, for the contraindicative questions a high score indicates a low fatigue level and a low score indicates a high fatigue level. Overall, respondents are rated on a scale of 0 (no fatigue) to 7 (high fatigue). For this outcome, the change from baseline in MFI-20 general fatigue subscale score is being reported. Negative values indicate an improvement in fatigue. |
| Change From Baseline to Week 13 in Hospital Anxiety and Depression Scale (HADS) in Participants Receiving DS-5565, Pregabalin, or Placebo | Baseline up to Week 13 postdose | The HADS questionnaire is a reliable, widely-used self-assessment scale to assess symptoms of anxiety and depression. The instrument consists of 7 questions related to anxiety and 7 related to depression, each rated on a 4-point scale (score of 0 to 3). Scores for anxiety and depression are independently summed to compute HADS Anxiety and HADS-Depression subscale scores, with ranges from 0 (no anxiety/depression) to 21 (most severe anxiety/depression). |
| Change From Baseline to Week 13 in Short Form 36 (SF-36) in Participants Receiving DS-5565, Pregabalin, or Placebo | Baseline up to Week 13 postdose | The SF-36 is a 36-question health survey that measures functional health and well-being from the participant's point of view. It is a measure of physical and mental health used across various disease areas, including fibromyalgia. The SF-36 scale ranges from 0 to 100 where lower scores indicate more disability (worse health) and higher scores represent less disability (better health). The physical component summary (PCS) and mental component summary (MCS) scores are reported. |
| Number of Participants Who Answered Much Improved or Better in Patient Global Impression of Change (PGIC) at Week 13 in Participants Receiving DS-5565, Pregabalin, or Placebo | Baseline up Week 13 postdose | Patient global impression of change (PGIC) on a 7-point categorical scale, where 1 = very much improved and 7 = very much worse. Higher scores indicate worse outcomes. The number of participants with 'much improved or better' status (≤2) is being reported. |
| Change From Baseline to Week 13 in Average Daily Sleep Interference in Participants Receiving DS-5565, Pregabalin, or Placebo | Baseline up Week 13 postdose | Pain-associated sleep interference was assessed using electronic daily diaries using an 11-point numeric rating scale (NRS) for pain, ranging from 0 (pain does not interfere with sleep) to 10 (pain completely interferes with sleep, unable to sleep). ADSIS is the mean value of all available recordings of the respective week. |
| Number of Participants Reporting Optimal Sleep at Week 13 on the Medical Outcomes Study (MOS) Sleep Scale In Participants Receiving DS-5565, Pregabalin, or Placebo | Week 13 postdose | The MOS Sleep Scale is a 12-item questionnaire from which the following subscales were derived: sleep disturbance (4 items), quantity of sleep/optimal sleep (1 item), snoring (1 item), awakening due to shortness of breath or due to headache (1 item), sleep adequacy (2 items), and somnolence (3 items). In addition, values for sleep disturbances index (9 items), optimal sleep scale (1 item), and sleep quantity scale (1 item) were determined. Most subscales range from 0 to 100, where higher scores indicate more of the concept begin measured (eg., higher sleep disturbance scores indicate greater sleep disturbances). |
| Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Baseline up to Week 13 postdose | The BPI-SF measures pain severity and interference within the past 24 hours. Items are rated on an 11-point NRS from 0 to 10, where 0 indicates does not interfere and 10 indicates completely interferes. Severity score is the average of the responses to the 4 pain intensity items that assess the Worst/Least/Average pain in the last 24 hours and the Pain Right Now. The individual items being reported (using the same scale as noted above) are Severity, General Activity, Mood, Walking Ability, Normal Work, Relations With Other People, Sleep, and Enjoyment of Life. Percentage relief of treatment pain scale ranges from 100% (complete pain relief) to 0% (no pain relief) and higher percentages indicate better outcome. Interference % is the average of responses for General activity, Mood, Walking ability, Normal work, Relations with other people, Sleep, Enjoyment of life where 0% (no interference) to 100% (completely interferes) and negative (ie. lower) percentages indicate better outcomes. |
| Proportion of Days a Rescue Medication Was Used Among Participants Receiving DS-5565, Pregabalin, or Placebo | Week 1 to Week 13 postdose | Proportion of days with rescue medication intake during the double-blind treatment period equals number of days with rescue medication intake/(date of last study drug administration in the double-blind treatment period) - (date of first study drug administration + 1). |
| Change From Baseline to Week 13 in EuroQol Five Dimensions Questionnaire (EQ-5D) in Participants Receiving DS-5565, Pregabalin, or Placebo | Baseline up to Week 13 postdose | The EQ-5D is an instrument that shows high construct validity and responsiveness in patients with chronic pain and has been used specifically in fibromyalgia. The EQ-5D includes a descriptive section with 5 dimensions (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) each with a scale that ranges from 0 (no problems) to 5 (extreme problems). These 5 dimensions are combined into an overall health utilities index, and a numeric rating scale (100 mm visual analog scale) that measures perception of overall health, with 0 indicating worst health and 100 representing best imaginable health. A summary index with a maximum total score of 1 can be derived from these five dimensions by conversion with a table of scores. The maximum total score of 1 indicates the best health outcome. For this outcome, the change from baseline in total EQ-5D score is being reported. Positive values indicate an improvement in health. |
Countries
Canada, Czechia, Denmark, Finland, France, Germany, Netherlands, Norway, Serbia, Sweden, United States
Participant flow
Recruitment details
A total of 1293 participants who met all inclusion and no exclusion criteria were randomized to treatment at 158 sites in 11 countries from 12 Nov 2014 to 14 Jul 2016.
Pre-assignment details
Eligible participants were randomized 1:1:1:1 to either DS-5565 15 mg every day (QD) given orally, DS-5565 15 mg twice daily (BID) given orally, placebo given orally as pregabalin placebo and DS-5565 placebo BID, or pregabalin 150 mg BID.
Participants by arm
| Arm | Count |
|---|---|
| Placebo Placebo for oral administration matching capsule for DS-5565 and matching tablet for pregabalin | 323 |
| Pregabalin Participants take one pregabalin capsule and one placebo tablet BID | 323 |
| DS-5565 QD Participants take one each of placebo tablet and capsule in the morning and one DS-5565 tablet once daily (QD) with a placebo capsule in the evening | 324 |
| DS-5565 BID Participants take one DS-5565 tablet and one placebo capsule BID | 323 |
| Total | 1,293 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 | FG003 |
|---|---|---|---|---|---|
| Overall Study | Adverse Event | 20 | 40 | 32 | 49 |
| Overall Study | Lack of Efficacy | 13 | 11 | 8 | 5 |
| Overall Study | Protocol Violation | 5 | 4 | 8 | 6 |
| Overall Study | Reason missing or not reported | 2 | 3 | 4 | 5 |
| Overall Study | Withdrawal by Subject | 27 | 29 | 30 | 34 |
Baseline characteristics
| Characteristic | Placebo | Pregabalin | DS-5565 QD | DS-5565 BID | Total |
|---|---|---|---|---|---|
| Age, Continuous | 48.6 years STANDARD_DEVIATION 11.76 | 49.5 years STANDARD_DEVIATION 11.53 | 50.3 years STANDARD_DEVIATION 10.88 | 49.5 years STANDARD_DEVIATION 11.77 | 49.5 years STANDARD_DEVIATION 11.49 |
| Age, Customized Age Categorical 18-64 Years | 298 Participants | 298 Participants | 300 Participants | 287 Participants | 1183 Participants |
| Age, Customized Age Categorical 65-84 Years | 25 Participants | 24 Participants | 24 Participants | 36 Participants | 109 Participants |
| Age, Customized Age Categorical 85 Years and over | 0 Participants | 1 Participants | 0 Participants | 0 Participants | 1 Participants |
| Sex: Female, Male Female | 299 Participants | 292 Participants | 286 Participants | 291 Participants | 1168 Participants |
| Sex: Female, Male Male | 24 Participants | 31 Participants | 38 Participants | 32 Participants | 125 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk |
|---|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 318 | 0 / 318 | 0 / 320 | 0 / 320 |
| other Total, other adverse events | 145 / 318 | 247 / 318 | 229 / 320 | 251 / 320 |
| serious Total, serious adverse events | 11 / 318 | 2 / 318 | 5 / 320 | 8 / 320 |
Outcome results
Primary
Change From Baseline in Weekly Average Daily Pain Score (ADPS) at Week 13 in Participants Receiving DS-5565, Pregabalin, Placebo
Average daily pain scores (ADPS) reported by the participant that best describes his or her worst pain over the previous 24 hours. A daily pain score has a scale where 0 = no pain to 10 = worst possible pain. Higher scores indicate a worse outcome. For participants with no Week 13 data, the baseline observation was carried forward (BOCF). The mean (multiple imputation estimate) and standard error (multiple imputation) are reported.
Time frame: Baseline up to Week 13 postdose
Population: This outcome was assessed using the modified intent-to-treat analysis set.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Change From Baseline in Weekly Average Daily Pain Score (ADPS) at Week 13 in Participants Receiving DS-5565, Pregabalin, Placebo | -1.66 units on a scale | Standard Error 0.132 |
| Pregabalin 150 mg BID | Change From Baseline in Weekly Average Daily Pain Score (ADPS) at Week 13 in Participants Receiving DS-5565, Pregabalin, Placebo | -1.90 units on a scale | Standard Error 0.134 |
| DS-5565 15 mg QD | Change From Baseline in Weekly Average Daily Pain Score (ADPS) at Week 13 in Participants Receiving DS-5565, Pregabalin, Placebo | -1.97 units on a scale | Standard Error 0.134 |
| DS-5565 15 mg BID | Change From Baseline in Weekly Average Daily Pain Score (ADPS) at Week 13 in Participants Receiving DS-5565, Pregabalin, Placebo | -1.93 units on a scale | Standard Error 0.136 |
p-value: 0.18795% CI: [-0.61, 0.12]Difference of means
p-value: 0.094495% CI: [-0.67, 0.05]Difference of means
p-value: 0.139195% CI: [-0.64, 0.09]Difference of means
p-value: 0.733895% CI: [-0.43, 0.3]Difference of means
p-value: 0.870595% CI: [-0.4, 0.34]Difference of means
Secondary
Change From Baseline to Week 13 in Average Daily Sleep Interference in Participants Receiving DS-5565, Pregabalin, or Placebo
Pain-associated sleep interference was assessed using electronic daily diaries using an 11-point numeric rating scale (NRS) for pain, ranging from 0 (pain does not interfere with sleep) to 10 (pain completely interferes with sleep, unable to sleep). ADSIS is the mean value of all available recordings of the respective week.
Time frame: Baseline up Week 13 postdose
Population: This outcome was assessed using the modified intent-to-treat analysis set.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Change From Baseline to Week 13 in Average Daily Sleep Interference in Participants Receiving DS-5565, Pregabalin, or Placebo | -1.67 units on a scale | Standard Error 0.12 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in Average Daily Sleep Interference in Participants Receiving DS-5565, Pregabalin, or Placebo | -2.22 units on a scale | Standard Error 0.12 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in Average Daily Sleep Interference in Participants Receiving DS-5565, Pregabalin, or Placebo | -2.30 units on a scale | Standard Error 0.121 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in Average Daily Sleep Interference in Participants Receiving DS-5565, Pregabalin, or Placebo | -2.52 units on a scale | Standard Error 0.121 |
p-value: 0.000995% CI: [-0.88, -0.23]Mixed Models Analysis
p-value: 0.000195% CI: [-0.96, -0.31]Mixed Models Analysis
p-value: <0.000195% CI: [-1.17, -0.52]Mixed Models Analysis
p-value: 0.640895% CI: [-0.4, 0.25]Mixed Models Analysis
p-value: 0.078695% CI: [-0.62, 0.03]Mixed Models Analysis
Secondary
Change From Baseline to Week 13 in EuroQol Five Dimensions Questionnaire (EQ-5D) in Participants Receiving DS-5565, Pregabalin, or Placebo
The EQ-5D is an instrument that shows high construct validity and responsiveness in patients with chronic pain and has been used specifically in fibromyalgia. The EQ-5D includes a descriptive section with 5 dimensions (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) each with a scale that ranges from 0 (no problems) to 5 (extreme problems). These 5 dimensions are combined into an overall health utilities index, and a numeric rating scale (100 mm visual analog scale) that measures perception of overall health, with 0 indicating worst health and 100 representing best imaginable health. A summary index with a maximum total score of 1 can be derived from these five dimensions by conversion with a table of scores. The maximum total score of 1 indicates the best health outcome. For this outcome, the change from baseline in total EQ-5D score is being reported. Positive values indicate an improvement in health.
Time frame: Baseline up to Week 13 postdose
Population: This outcome was assessed using the modified intent-to-treat analysis set.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Change From Baseline to Week 13 in EuroQol Five Dimensions Questionnaire (EQ-5D) in Participants Receiving DS-5565, Pregabalin, or Placebo | 0.0779 units on a scale | Standard Deviation 0.19 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in EuroQol Five Dimensions Questionnaire (EQ-5D) in Participants Receiving DS-5565, Pregabalin, or Placebo | 0.0712 units on a scale | Standard Deviation 0.182 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in EuroQol Five Dimensions Questionnaire (EQ-5D) in Participants Receiving DS-5565, Pregabalin, or Placebo | 0.0740 units on a scale | Standard Deviation 0.173 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in EuroQol Five Dimensions Questionnaire (EQ-5D) in Participants Receiving DS-5565, Pregabalin, or Placebo | 0.0696 units on a scale | Standard Deviation 0.185 |
p-value: 0.892395% CI: [-0.0243, 0.0279]ANCOVA
p-value: 0.874995% CI: [-0.0281, 0.024]ANCOVA
p-value: 0.493295% CI: [-0.0353, 0.017]ANCOVA
p-value: 0.768895% CI: [-0.0298, 0.0221]ANCOVA
p-value: 0.409995% CI: [-0.0369, 0.0151]ANCOVA
Secondary
Change From Baseline to Week 13 in Hospital Anxiety and Depression Scale (HADS) in Participants Receiving DS-5565, Pregabalin, or Placebo
The HADS questionnaire is a reliable, widely-used self-assessment scale to assess symptoms of anxiety and depression. The instrument consists of 7 questions related to anxiety and 7 related to depression, each rated on a 4-point scale (score of 0 to 3). Scores for anxiety and depression are independently summed to compute HADS Anxiety and HADS-Depression subscale scores, with ranges from 0 (no anxiety/depression) to 21 (most severe anxiety/depression).
Time frame: Baseline up to Week 13 postdose
Population: This outcome was assessed using the modified intent-to-treat analysis set.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Placebo | Change From Baseline to Week 13 in Hospital Anxiety and Depression Scale (HADS) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13: Anxiety | -1.0 units on a scale | Standard Deviation 3.17 |
| Placebo | Change From Baseline to Week 13 in Hospital Anxiety and Depression Scale (HADS) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13: Depression | -0.8 units on a scale | Standard Deviation 3.54 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in Hospital Anxiety and Depression Scale (HADS) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13: Depression | -1.1 units on a scale | Standard Deviation 3.23 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in Hospital Anxiety and Depression Scale (HADS) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13: Anxiety | -0.8 units on a scale | Standard Deviation 3.04 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in Hospital Anxiety and Depression Scale (HADS) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13: Anxiety | -1.0 units on a scale | Standard Deviation 3.25 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in Hospital Anxiety and Depression Scale (HADS) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13: Depression | -0.8 units on a scale | Standard Deviation 3.52 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in Hospital Anxiety and Depression Scale (HADS) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13: Anxiety | -1.1 units on a scale | Standard Deviation 3.34 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in Hospital Anxiety and Depression Scale (HADS) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13: Depression | -0.6 units on a scale | Standard Deviation 3.3 |
Comparison: Anxiety: Placebo vs Pregabalin 150 mg BIDp-value: 0.977595% CI: [-0.5, 0.5]ANCOVA
Comparison: Anxiety: Placebo vs DS-5565 15 mg QDp-value: 0.6595% CI: [-0.6, 0.4]ANCOVA
Comparison: Anxiety: Placebo vs DS-5565 15 mg BIDp-value: 0.654695% CI: [-0.6, 0.4]ANCOVA
Comparison: Anxiety: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.669295% CI: [-0.6, 0.4]ANCOVA
Comparison: Anxiety: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.673795% CI: [-0.6, 0.4]ANCOVA
Comparison: Depression: Placebo vs Pregabalin 150 mg BIDp-value: 0.388895% CI: [-0.8, 0.3]ANCOVA
Comparison: Depression: Placebo vs DS-5565 15 mg QDp-value: 0.9295% CI: [-0.5, 0.6]ANCOVA
Comparison: Depression: Placebo vs DS-5565 15 mg BIDp-value: 0.706195% CI: [-0.4, 0.6]ANCOVA
Comparison: Depression: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.333795% CI: [-0.3, 0.8]ANCOVA
Comparison: Depression: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.213995% CI: [-0.2, 0.9]ANCOVA
Secondary
Change From Baseline to Week 13 in Multidimensional Fatigue Inventory (MFI-20) General Fatigue Score in Participants Receiving DS-5565, Pregabalin, or Placebo
MFI is a validated 20-item, self-reported instrument designed to measure fatigue in the following dimensions: general fatigue, physical fatigue, mental fatigue, reduced motivation, and reduced activity. The respondent is asked to mark an 'X' in 1 of 5 boxes arranged linearly where 1 is 'Yes, that is true' and 5 is 'No, that is not true.' Each subscale consists of 4 items, 2 indicative for fatigue and 2 contraindicative. For the indicative questions, a high score indicates a high fatigue level and low scores indicate a low fatigue levels. Conversely, for the contraindicative questions a high score indicates a low fatigue level and a low score indicates a high fatigue level. Overall, respondents are rated on a scale of 0 (no fatigue) to 7 (high fatigue). For this outcome, the change from baseline in MFI-20 general fatigue subscale score is being reported. Negative values indicate an improvement in fatigue.
Time frame: Baseline up to Week 13 postdose
Population: This outcome was assessed in the modified intent-to-treat analysis set.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Change From Baseline to Week 13 in Multidimensional Fatigue Inventory (MFI-20) General Fatigue Score in Participants Receiving DS-5565, Pregabalin, or Placebo | -1.9 units on a scale | Standard Deviation 3.4 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in Multidimensional Fatigue Inventory (MFI-20) General Fatigue Score in Participants Receiving DS-5565, Pregabalin, or Placebo | -2.0 units on a scale | Standard Deviation 3.82 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in Multidimensional Fatigue Inventory (MFI-20) General Fatigue Score in Participants Receiving DS-5565, Pregabalin, or Placebo | -2.0 units on a scale | Standard Deviation 3.51 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in Multidimensional Fatigue Inventory (MFI-20) General Fatigue Score in Participants Receiving DS-5565, Pregabalin, or Placebo | -1.6 units on a scale | Standard Deviation 3.38 |
p-value: 0.044695% CI: [0, 1.1]ANCOVA
p-value: 0.334795% CI: [-0.8, 0.3]ANCOVA
p-value: 0.399995% CI: [-0.3, 0.8]ANCOVA
p-value: 0.843595% CI: [-0.5, 0.6]ANCOVA
p-value: 0.247495% CI: [-0.9, 0.2]ANCOVA
Secondary
Change From Baseline to Week 13 in Short Form 36 (SF-36) in Participants Receiving DS-5565, Pregabalin, or Placebo
The SF-36 is a 36-question health survey that measures functional health and well-being from the participant's point of view. It is a measure of physical and mental health used across various disease areas, including fibromyalgia. The SF-36 scale ranges from 0 to 100 where lower scores indicate more disability (worse health) and higher scores represent less disability (better health). The physical component summary (PCS) and mental component summary (MCS) scores are reported.
Time frame: Baseline up to Week 13 postdose
Population: This outcome was assessed using the modified intent-to-treat analysis set.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Placebo | Change From Baseline to Week 13 in Short Form 36 (SF-36) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13:Physical Component | 8.052 units on a scale | Standard Deviation 19.91 |
| Placebo | Change From Baseline to Week 13 in Short Form 36 (SF-36) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13: Mental Component | 1.506 units on a scale | Standard Deviation 9.25 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in Short Form 36 (SF-36) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13: Mental Component | 1.995 units on a scale | Standard Deviation 8.59 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in Short Form 36 (SF-36) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13:Physical Component | 9.898 units on a scale | Standard Deviation 16.73 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in Short Form 36 (SF-36) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13:Physical Component | 8.598 units on a scale | Standard Deviation 18.62 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in Short Form 36 (SF-36) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13: Mental Component | 1.163 units on a scale | Standard Deviation 9.32 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in Short Form 36 (SF-36) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13:Physical Component | 7.099 units on a scale | Standard Deviation 19.52 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in Short Form 36 (SF-36) in Participants Receiving DS-5565, Pregabalin, or Placebo | Change from baseline to Week 13: Mental Component | 1.286 units on a scale | Standard Deviation 8.85 |
Comparison: Physical Component: Placebo vs Pregabalin 150 mg BIDp-value: 0.141695% CI: [-0.733, 5.126]ANCOVA
Comparison: Physical Component: Placebo vs DS-5565 15 mg QDp-value: 0.867795% CI: [-2.679, 3.176]ANCOVA
Comparison: Physical Component: Placebo vs DS-5565 15 mg BIDp-value: 0.548195% CI: [-3.834, 2.036]ANCOVA
Comparison: Physical Component: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.190695% CI: [-4.866, 0.971]ANCOVA
Comparison: Physical Component: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.037895% CI: [-6.015, -0.175]ANCOVA
Comparison: Mental Component: Placebo vs Pregabalin 150 mg BIDp-value: 0.333795% CI: [-0.683, 2.011]ANCOVA
Comparison: Mental Component: Placebo vs DS-5565 15 mg QDp-value: 0.777895% CI: [-1.54, 1.152]ANCOVA
Comparison: Mental Component: Placebo vs DS-5565 15 mg BIDp-value: 0.899195% CI: [-1.437, 1.262]ANCOVA
Comparison: Mental Component: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.209895% CI: [-2.198, 0.483]ANCOVA
Comparison: Mental Component: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.272595% CI: [-2.093, 0.591]ANCOVA
Secondary
Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo
The BPI-SF measures pain severity and interference within the past 24 hours. Items are rated on an 11-point NRS from 0 to 10, where 0 indicates does not interfere and 10 indicates completely interferes. Severity score is the average of the responses to the 4 pain intensity items that assess the Worst/Least/Average pain in the last 24 hours and the Pain Right Now. The individual items being reported (using the same scale as noted above) are Severity, General Activity, Mood, Walking Ability, Normal Work, Relations With Other People, Sleep, and Enjoyment of Life. Percentage relief of treatment pain scale ranges from 100% (complete pain relief) to 0% (no pain relief) and higher percentages indicate better outcome. Interference % is the average of responses for General activity, Mood, Walking ability, Normal work, Relations with other people, Sleep, Enjoyment of life where 0% (no interference) to 100% (completely interferes) and negative (ie. lower) percentages indicate better outcomes.
Time frame: Baseline up to Week 13 postdose
Population: This outcome was assessed using the modified intent-to-treat analysis set.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|---|
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Mood | -1.1 units on a scale | Standard Error 0.16 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | General activity | -1.5 units on a scale | Standard Error 0.15 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Severity score | -1.4 units on a scale | Standard Error 0.12 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Enjoyment of life | -1.6 units on a scale | Standard Error 0.16 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Interference (%) | -14.04 units on a scale | Standard Error 1.3 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Relief (%) by treatment pain | 15.9 units on a scale | Standard Error 1.78 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Relations with other people | -0.9 units on a scale | Standard Error 0.15 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Worst pain | 6.6 units on a scale | Standard Error 1.41 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Average pain | -1.2 units on a scale | Standard Error 0.12 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Sleep | -2.1 units on a scale | Standard Error 0.17 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Normal work | -1.5 units on a scale | Standard Error 0.15 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Walking ability | -1.1 units on a scale | Standard Error 0.16 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Pain right now | -1.7 units on a scale | Standard Error 0.14 |
| Placebo | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Least pain | -1.2 units on a scale | Standard Error 0.13 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Normal work | -1.8 units on a scale | Standard Error 0.15 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Worst pain | 6.3 units on a scale | Standard Error 1.5 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Least pain | -1.5 units on a scale | Standard Error 0.13 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Average pain | -1.5 units on a scale | Standard Error 0.12 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Pain right now | -1.9 units on a scale | Standard Error 0.14 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Severity score | -1.7 units on a scale | Standard Error 0.12 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Relief (%) by treatment pain | 18.5 units on a scale | Standard Error 1.74 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Interference (%) | -17.91 units on a scale | Standard Error 1.28 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | General activity | -1.9 units on a scale | Standard Error 0.15 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Mood | -1.6 units on a scale | Standard Error 0.15 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Walking ability | -1.5 units on a scale | Standard Error 0.15 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Relations with other people | -1.3 units on a scale | Standard Error 0.15 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Sleep | -2.7 units on a scale | Standard Error 0.17 |
| Pregabalin 150 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Enjoyment of life | -1.9 units on a scale | Standard Error 0.16 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Normal work | -1.5 units on a scale | Standard Error 0.15 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Sleep | -2.5 units on a scale | Standard Error 0.17 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Least pain | -1.3 units on a scale | Standard Error 0.13 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Pain right now | -1.7 units on a scale | Standard Error 0.14 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Relations with other people | -1.3 units on a scale | Standard Error 0.15 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Worst pain | 6.5 units on a scale | Standard Error 1.48 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Walking ability | -1.1 units on a scale | Standard Error 0.15 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | General activity | -1.6 units on a scale | Standard Error 0.15 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Relief (%) by treatment pain | 17.1 units on a scale | Standard Error 1.77 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Average pain | -1.4 units on a scale | Standard Error 0.12 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Severity score | -1.5 units on a scale | Standard Error 0.12 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Enjoyment of life | -1.6 units on a scale | Standard Error 0.16 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Interference (%) | -15.46 units on a scale | Standard Error 1.3 |
| DS-5565 15 mg QD | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Mood | -1.3 units on a scale | Standard Error 0.15 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Interference (%) | -15.65 units on a scale | Standard Error 1.29 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | General activity | -1.6 units on a scale | Standard Error 0.15 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Sleep | -2.6 units on a scale | Standard Error 0.17 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Mood | -1.3 units on a scale | Standard Error 0.15 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Average pain | -1.4 units on a scale | Standard Error 0.12 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Walking ability | -1.1 units on a scale | Standard Error 0.15 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Least pain | -1.3 units on a scale | Standard Error 0.13 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Normal work | -1.5 units on a scale | Standard Error 0.15 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Enjoyment of life | -1.5 units on a scale | Standard Error 0.16 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Relations with other people | -1.3 units on a scale | Standard Error 0.15 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Severity score | -1.5 units on a scale | Standard Error 0.12 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Worst pain | 6.6 units on a scale | Standard Error 1.47 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Relief (%) by treatment pain | 15.6 units on a scale | Standard Error 1.76 |
| DS-5565 15 mg BID | Change From Baseline to Week 13 in the Brief Pain Inventory Short Form (BPI-SF) in Participants Receiving DS-5565, Pregabalin, or Placebo | Pain right now | -1.7 units on a scale | Standard Error 0.14 |
Comparison: Worst pain: Placebo vs Pregabalin 150 mg BIDp-value: 0.054195% CI: [-0.7, 0]ANCOVA
Comparison: Worst pain: Placebo vs DS-5565 15 mg QDp-value: 0.777195% CI: [-0.4, 0.3]ANCOVA
Comparison: Worst pain: Placebo vs DS-5565 15 mg BIDp-value: 0.548895% CI: [-0.5, 0.3]ANCOVA
Comparison: Worst pain: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.098795% CI: [-0.1, 0.7]ANCOVA
Comparison: Worst pain: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.18495% CI: [-0.1, 0.6]ANCOVA
Comparison: Least pain: Placebo vs Pregabalin 150 mg BIDp-value: 0.190395% CI: [-0.6, 0.1]ANCOVA
Comparison: Least pain: Placebo vs DS-5565 15 mg QDp-value: 0.578795% CI: [-0.4, 0.2]ANCOVA
Comparison: Least pain: Placebo vs DS-5565 15 mg BIDp-value: 0.553595% CI: [-0.5, 0.2]ANCOVA
Comparison: Least pain: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.447695% CI: [-0.2, 0.5]ANCOVA
Comparison: Least pain: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.473795% CI: [-0.2, 0.5]ANCOVA
Comparison: Average pain: Placebo vs Pregabalin 150 mg BIDp-value: 0.081495% CI: [-0.6, 0]ANCOVA
Comparison: Average pain: Placebo vs DS-5565 15 mg QDp-value: 0.306995% CI: [-0.5, 0.2]ANCOVA
Comparison: Average pain: Placebo vs DS-5565 15 mg BIDp-value: 0.391695% CI: [-0.5, 0.2]ANCOVA
Comparison: Average pain: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.466795% CI: [-0.2, 0.4]ANCOVA
Comparison: Average pain: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.374495% CI: [-0.2, 0.5]ANCOVA
Comparison: Pain right now: Placebo vs Pregabalin 150 mg BIDp-value: 0.295995% CI: [-0.6, 0.2]ANCOVA
Comparison: Pain right now: Placebo vs DS-5565 15 mg QDp-value: 0.911995% CI: [-0.4, 0.4]ANCOVA
Comparison: Pain right now: Placebo vs DS-5565 15 mg BIDp-value: 0.939995% CI: [-0.4, 0.4]ANCOVA
Comparison: Pain right now: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.245595% CI: [-0.2, 0.6]ANCOVA
Comparison: Pain right now: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.331195% CI: [-0.2, 0.6]ANCOVA
Comparison: Severity score: Placebo vs Pregabalin 150 mg BIDp-value: 0.123395% CI: [-0.577, 0.069]ANCOVA
Comparison: Severity score: Placebo vs DS-5565 15 mg QDp-value: 0.66195% CI: [-0.394, 0.25]ANCOVA
Comparison: Severity score: Placebo vs DS-5565 15 mg BIDp-value: 0.551495% CI: [-0.422, 0.225]ANCOVA
Comparison: Severity score: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.267395% CI: [-0.14, 0.503]ANCOVA
Comparison: Severity score: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.343995% CI: [-0.167, 0.478]ANCOVA
Comparison: Relief (%) by treatment of pain: Placebo vs Pregabalin 150 mg BIDp-value: 0.270895% CI: [-2.1, 7.4]ANCOVA
Comparison: Relief (%) by treatment of pain: Placebo vs DS-5565 15 mg QDp-value: 0.628595% CI: [-3.5, 5.9]ANCOVA
Comparison: Relief (%) by treatment of pain: Placebo vs DS-5565 150 mg BIDp-value: 0.917795% CI: [-5, 4.5]ANCOVA
Comparison: Relief (%) by treatment of pain: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.533495% CI: [-6.2, 3.2]ANCOVA
Comparison: Relief (%) by treatment of pain: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.226195% CI: [-7.6, 1.8]ANCOVA
Comparison: Interference: Placebo vs Pregabalin 150 mg BIDp-value: 0.028195% CI: [-7.32, -0.42]ANCOVA
Comparison: Interference: Placebo vs DS-5565 15 mg QDp-value: 0.41995% CI: [-4.87, 2.03]ANCOVA
Comparison: Interference: Placebo vs DS-5565 15 mg BIDp-value: 0.362295% CI: [-5.06, 1.85]ANCOVA
Comparison: Interference: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.162395% CI: [-0.99, 5.88]ANCOVA
Comparison: Interference: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.197895% CI: [-1.18, 5.7]ANCOVA
Comparison: General activity: Placebo vs Pregabalin 150 mg BIDp-value: 0.086795% CI: [-0.8, 0.1]ANCOVA
Comparison: General activity: Placebo vs DS-5565 15 mg QDp-value: 0.699395% CI: [-0.5, 0.3]ANCOVA
Comparison: General activity: Placebo vs DS-5565 15 mg BIDp-value: 0.870295% CI: [-0.4, 0.4]ANCOVA
Comparison: General activity: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.182695% CI: [-0.1, 0.7]ANCOVA
Comparison: General activity: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.120695% CI: [-0.1, 0.7]ANCOVA
Comparison: Mood: Placebo vs Pregabalin 150 mg BIDp-value: 0.021195% CI: [-0.9, -0.1]ANCOVA
Comparison: Mood: Placebo vs DS-5565 15 mg QDp-value: 0.496395% CI: [-0.6, 0.3]ANCOVA
Comparison: Mood: Placebo vs DS-5565 15 mg BIDp-value: 0.303195% CI: [-0.6, 0.2]ANCOVA
Comparison: Mood: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.101995% CI: [-0.1, 0.8]ANCOVA
Comparison: Mood: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.20195% CI: [-0.1, 0.7]ANCOVA
Comparison: Walking ability: Placebo vs Pregabalin 150 mg BIDp-value: 0.033195% CI: [-0.9, 0]ANCOVA
Comparison: Walking ability: Placebo vs DS-5565 15 mg QDp-value: 0.747895% CI: [-0.5, 0.3]ANCOVA
Comparison: Walking ability: Placebo vs DS-5565 15 mg BIDp-value: 0.69495% CI: [-0.5, 0.3]ANCOVA
Comparison: Walking ability: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.06995% CI: [0, 0.8]ANCOVA
Comparison: Walking ability: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.081695% CI: [0, 0.8]ANCOVA
Comparison: Normal work: Placebo vs Pregabalin 150 mg BIDp-value: 0.117495% CI: [-0.7, 0.1]ANCOVA
Comparison: Normal work: Placebo vs DS-5565 15 mg QDp-value: 0.92595% CI: [-0.4, 0.4]ANCOVA
Comparison: Normal work: Placebo vs DS-5565 15 mg BIDp-value: 0.855595% CI: [-0.4, 0.4]ANCOVA
Comparison: Normal work: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.095695% CI: [-0.1, 0.7]ANCOVA
Comparison: Normal work: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.165995% CI: [-0.1, 0.7]ANCOVA
Comparison: Relations with other people: Placebo vs Pregabalin 150 mg BIDp-value: 0.046895% CI: [-0.8, 0]ANCOVA
Comparison: Relations with other people: Placebo vs DS-5565 15 mg QDp-value: 0.108395% CI: [-0.7, 0.1]ANCOVA
Comparison: Relations with other people: Placebo vs DS-5565 15 mg BIDp-value: 0.050595% CI: [-0.8, 0]ANCOVA
Comparison: Relations with other people: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.699395% CI: [-0.3, 0.5]ANCOVA
Comparison: Relations with other people: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.978195% CI: [-0.4, 0.4]ANCOVA
Comparison: Sleep: Placebo vs Pregabalin 150 mg BIDp-value: 0.015495% CI: [-1, -0.1]ANCOVA
Comparison: Sleep: Placebo vs DS-5565 15 mg QDp-value: 0.073195% CI: [-0.9, 0]ANCOVA
Comparison: Sleep: Placebo vs DS-5565 15 mg BIDp-value: 0.025995% CI: [-1, -0.1]ANCOVA
Comparison: Sleep: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.524395% CI: [-0.3, 0.6]ANCOVA
Comparison: Sleep: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.848895% CI: [-0.4, 0.5]ANCOVA
Comparison: Enjoyment of life: Placebo vs Pregabalin 150 mg BIDp-value: 0.274695% CI: [-0.7, 0.2]ANCOVA
Comparison: Enjoyment of life: Placebo vs DS-5565 15 mg QDp-value: 0.934995% CI: [-0.4, 0.4]ANCOVA
Comparison: Enjoyment of life: Placebo vs DS-5565 15 mg BIDp-value: 0.516495% CI: [-0.3, 0.6]ANCOVA
Comparison: Enjoyment of life: Pregabalin 150 mg BID vs DS-5565 15 mg QDp-value: 0.238295% CI: [-0.2, 0.7]ANCOVA
Comparison: Enjoyment of life: Pregabalin 150 mg BID vs DS-5565 15 mg BIDp-value: 0.080795% CI: [0, 0.8]ANCOVA
Secondary
Change in Fibromyalgia Index Questionnaire (FIQ) Total Score From Baseline to Week 13 in Participants Receiving DS-5565, Pregabalin, or Placebo
The total FIQ score is composed of 10 items, with a maximum possible score of 100. The first item contains 11 questions related to physical functioning and are rated on a 4-point Likert-type scale, where 0 indicates 'always' and 3 indicates 'never'. The overall impact items are rated on a 0-7 scale for the number of days that the patient felt well and the number of days they were unable to work (including housework) because of fibromyalgia symptoms. The symptoms items are rated on visual analog scales (0-10 cm), with higher numbers indicated greater symptomatology. Scores range from 0 (no impairment) to 10 (maximum impairment), where higher scores indicate worse outcome. For this outcome, the change in total FIQ score from baseline is being reported. Negative values indicate improvement from baseline in impairment.
Time frame: Baseline up to Week 13 postdose
Population: This outcome was assessed using the modified intent-to-treat analysis set.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Change in Fibromyalgia Index Questionnaire (FIQ) Total Score From Baseline to Week 13 in Participants Receiving DS-5565, Pregabalin, or Placebo | -13.20 units on a scale | Standard Deviation 1.173 |
| Pregabalin 150 mg BID | Change in Fibromyalgia Index Questionnaire (FIQ) Total Score From Baseline to Week 13 in Participants Receiving DS-5565, Pregabalin, or Placebo | -16.60 units on a scale | Standard Deviation 1.166 |
| DS-5565 15 mg QD | Change in Fibromyalgia Index Questionnaire (FIQ) Total Score From Baseline to Week 13 in Participants Receiving DS-5565, Pregabalin, or Placebo | -14.48 units on a scale | Standard Deviation 1.191 |
| DS-5565 15 mg BID | Change in Fibromyalgia Index Questionnaire (FIQ) Total Score From Baseline to Week 13 in Participants Receiving DS-5565, Pregabalin, or Placebo | -13.13 units on a scale | Standard Deviation 1.199 |
p-value: 0.032695% CI: [-6.52, -0.28]Difference of means
p-value: 0.42295% CI: [-4.4, 1.84]Difference of means
p-value: 0.965995% CI: [-3.1, 3.23]Difference of means
p-value: 0.186795% CI: [-1.03, 5.28]Difference of means
p-value: 0.033395% CI: [0.27, 6.67]Difference of means
Secondary
Number of Participants Reporting Optimal Sleep at Week 13 on the Medical Outcomes Study (MOS) Sleep Scale In Participants Receiving DS-5565, Pregabalin, or Placebo
The MOS Sleep Scale is a 12-item questionnaire from which the following subscales were derived: sleep disturbance (4 items), quantity of sleep/optimal sleep (1 item), snoring (1 item), awakening due to shortness of breath or due to headache (1 item), sleep adequacy (2 items), and somnolence (3 items). In addition, values for sleep disturbances index (9 items), optimal sleep scale (1 item), and sleep quantity scale (1 item) were determined. Most subscales range from 0 to 100, where higher scores indicate more of the concept begin measured (eg., higher sleep disturbance scores indicate greater sleep disturbances).
Time frame: Week 13 postdose
Population: This outcome was assessed in the modified intent-to-treat analysis set.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Placebo | Number of Participants Reporting Optimal Sleep at Week 13 on the Medical Outcomes Study (MOS) Sleep Scale In Participants Receiving DS-5565, Pregabalin, or Placebo | 87 Participants |
| Pregabalin 150 mg BID | Number of Participants Reporting Optimal Sleep at Week 13 on the Medical Outcomes Study (MOS) Sleep Scale In Participants Receiving DS-5565, Pregabalin, or Placebo | 117 Participants |
| DS-5565 15 mg QD | Number of Participants Reporting Optimal Sleep at Week 13 on the Medical Outcomes Study (MOS) Sleep Scale In Participants Receiving DS-5565, Pregabalin, or Placebo | 93 Participants |
| DS-5565 15 mg BID | Number of Participants Reporting Optimal Sleep at Week 13 on the Medical Outcomes Study (MOS) Sleep Scale In Participants Receiving DS-5565, Pregabalin, or Placebo | 109 Participants |
Secondary
Number of Participants Who Answered Much Improved or Better in Patient Global Impression of Change (PGIC) at Week 13 in Participants Receiving DS-5565, Pregabalin, or Placebo
Patient global impression of change (PGIC) on a 7-point categorical scale, where 1 = very much improved and 7 = very much worse. Higher scores indicate worse outcomes. The number of participants with 'much improved or better' status (≤2) is being reported.
Time frame: Baseline up Week 13 postdose
Population: This outcome was assessed using the modified intent-to-treat analysis set.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Placebo | Number of Participants Who Answered Much Improved or Better in Patient Global Impression of Change (PGIC) at Week 13 in Participants Receiving DS-5565, Pregabalin, or Placebo | 83 Participants |
| Pregabalin 150 mg BID | Number of Participants Who Answered Much Improved or Better in Patient Global Impression of Change (PGIC) at Week 13 in Participants Receiving DS-5565, Pregabalin, or Placebo | 105 Participants |
| DS-5565 15 mg QD | Number of Participants Who Answered Much Improved or Better in Patient Global Impression of Change (PGIC) at Week 13 in Participants Receiving DS-5565, Pregabalin, or Placebo | 104 Participants |
| DS-5565 15 mg BID | Number of Participants Who Answered Much Improved or Better in Patient Global Impression of Change (PGIC) at Week 13 in Participants Receiving DS-5565, Pregabalin, or Placebo | 82 Participants |
Secondary
Number of Responders at Week 13 Among Participants Receiving DS-5565, Pregabalin, or Placebo
The number of participants with at least a 30% or 50% reduction in average daily pain score (ADPS) at Week 13 is reported.
Time frame: Week 13 postdose
Population: This outcome was assessed using the modified intent-to-treat analysis set.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Placebo | Number of Responders at Week 13 Among Participants Receiving DS-5565, Pregabalin, or Placebo | 50% responders | 57 Participants |
| Placebo | Number of Responders at Week 13 Among Participants Receiving DS-5565, Pregabalin, or Placebo | 30% responders | 101 Participants |
| Pregabalin 150 mg BID | Number of Responders at Week 13 Among Participants Receiving DS-5565, Pregabalin, or Placebo | 30% responders | 118 Participants |
| Pregabalin 150 mg BID | Number of Responders at Week 13 Among Participants Receiving DS-5565, Pregabalin, or Placebo | 50% responders | 71 Participants |
| DS-5565 15 mg QD | Number of Responders at Week 13 Among Participants Receiving DS-5565, Pregabalin, or Placebo | 50% responders | 71 Participants |
| DS-5565 15 mg QD | Number of Responders at Week 13 Among Participants Receiving DS-5565, Pregabalin, or Placebo | 30% responders | 106 Participants |
| DS-5565 15 mg BID | Number of Responders at Week 13 Among Participants Receiving DS-5565, Pregabalin, or Placebo | 50% responders | 57 Participants |
| DS-5565 15 mg BID | Number of Responders at Week 13 Among Participants Receiving DS-5565, Pregabalin, or Placebo | 30% responders | 100 Participants |
Secondary
Proportion of Days a Rescue Medication Was Used Among Participants Receiving DS-5565, Pregabalin, or Placebo
Proportion of days with rescue medication intake during the double-blind treatment period equals number of days with rescue medication intake/(date of last study drug administration in the double-blind treatment period) - (date of first study drug administration + 1).
Time frame: Week 1 to Week 13 postdose
Population: This outcome was assessed using the modified intent-to-treat analysis set.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Proportion of Days a Rescue Medication Was Used Among Participants Receiving DS-5565, Pregabalin, or Placebo | 0.23 proportion of days | Standard Deviation 0.32 |
| Pregabalin 150 mg BID | Proportion of Days a Rescue Medication Was Used Among Participants Receiving DS-5565, Pregabalin, or Placebo | 0.18 proportion of days | Standard Deviation 0.3 |
| DS-5565 15 mg QD | Proportion of Days a Rescue Medication Was Used Among Participants Receiving DS-5565, Pregabalin, or Placebo | 0.22 proportion of days | Standard Deviation 0.31 |
| DS-5565 15 mg BID | Proportion of Days a Rescue Medication Was Used Among Participants Receiving DS-5565, Pregabalin, or Placebo | 0.19 proportion of days | Standard Deviation 0.28 |
p-value: 0.060195% CI: [-0.091, 0.002]ANCOVA
p-value: 0.829995% CI: [-0.052, 0.041]ANCOVA
p-value: 0.034795% CI: [-0.096, 0.004]ANCOVA
p-value: 0.095195% CI: [-0.007, 0.086]ANCOVA
p-value: 0.819995% CI: [-0.052, 0.041]ANCOVA