Urologic DiseasesPhase 2SymphonyNCT01340027
A Study to Evaluate the Efficacy, Safety and Tolerability of Mirabegron and Solifenacin Succinate Alone and in Combination for the Treatment of Overactive Bladder
A Phase 2 study testing Mirabegron and Solifenacin succinate in people with Urologic Diseases and Urinary Bladder Diseases, run by Astellas Pharma Europe B.V. at 133 sites in 20 countries.
Trial summary
The purpose of this study is to examine how well two medicines in combination (solifenacin succinate and mirabegron) work in the treatment of bladder problems over a 12-week period. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Urologic Diseases, Urinary Bladder Diseases, Urological Manifestations
- What is being tested?
- Mirabegron and Solifenacin succinate
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 1,307 participants
- Where
- 133 sitesin 20 countries
- Study dates
- 29 Mar 2011to 28 Jun 2012
- Phase
- Phase 2
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Subject has a Body Mass Index (BMI) of between 18 and 35 kg/m^2 and a total body weight between 50 and 95 kg;
- Subject is willing and able to complete the micturition diary and questionnaires correctly and is willing and able to measure his/her vital signs at home at stipulated time points, using the device provided by the study personnel, and to adequately record the readings;
- Subject has symptoms of overactive bladder (OAB; urinary frequency, urgency and/or urgency incontinence) for at least 3 months.
- Subject has experienced frequency of micturition on average ≥ 8 times per 24-hour period during the 3-day micturition diary period (incontinence episode should not be counted as a micturition);
- Subject must experience at least 1 episode of urgency (grade 3 or 4) per 24-hour period (with or without urgency incontinence) during the 3 day micturition diary period.
Who cannot join
- Subject is breastfeeding, pregnant or intends to become pregnant during the study. The pregnancy test (Beta Human Chorionic Gonadotropin in serum) at Screening must be negative in women of childbearing potential;
- Female subjects of childbearing potential and not using a highly effective method of birth control during the study and for 30 days after final study drug administration.
- Male subjects (unless surgically sterile) with female spouses/partners who are of childbearing potential, and not using a barrier method of contraception during the study and for 30 days after final study drug administration. In addition, female spouses/partners of male subjects and who are of childbearing potential should also use a highly effective method of birth control during the study and for 30 days after final study drug administration. Highly effective methods of birth control are defined as those, alone or in combination, that result in a low failure rate (i.e. less than 1% per year) when used consistently and correctly.
- Subject has significant post-void residual (PVR) volume (> 150 mL);
- Subject has significant stress incontinence or mixed stress/urgency incontinence where stress is the predominant factor as determined by the Investigator (for female subjects confirmed by the cough provocation test);
- Subject has a neurological cause for detrusor overactivity;
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- Subject has an indwelling catheter or practices intermittent self-catheterization;
- Subject has diabetic neuropathy;
- Subject has chronic inflammation such as interstitial cystitis, bladder stones, previous pelvic radiation therapy or previous or current malignant disease of the pelvic organs;
- Subject has had previous lower urinary tract or pelvic floor surgery (except cystoscopy);
- Subject has had intravesical treatment in the past 12 months with e.g., botulinum toxin, resiniferatoxin, capsaicin;
- Subject has uncontrolled narrow angle glaucoma, urinary or gastric retention, severe ulcerative colitis or Crohn's Disease, toxic megacolon, myasthenia gravis or any other condition which makes the use of anticholinergics contraindicated;
- Subject has clinically significant cardiovascular or cerebrovascular diseases within 6 months prior to Screening, such as myocardial infarction, uncontrolled angina, significant ventricular arrhythmias, heart failure and stroke;
- Subject is receiving current non-drug treatment including electro-stimulation therapy (with the exception of a bladder training program or pelvic floor exercises which started more than 30 days prior to Screening);
- Subject is using medications intended to treat OAB or prohibited medications.
- Subject has known or suspected hypersensitivity to solifenacin succinate, mirabegron or any of their excipients;
- Subject has any significant neurological disease or defect affecting bladder function (e.g., neurogenic bladder, systemic or central neurological disease such as multiple sclerosis [MS] and Parkinson's disease);
- Subject has severe hypertension which is defined as a sitting average systolic blood pressure ≥ 180 mmHg and/or an average diastolic blood pressure ≥ 110 mmHg;
- Subject has evidence of a urinary tract infection (UTI) (urine culture containing > 100,000 cfu/mL). The subject can be enrolled into the study after successful treatment of the UTI (confirmed by a laboratory result of negative urine culture). However, the subject must be re screened if the initial screening visit was > 28 days;
- Subject has a QT interval > 450 ms or is at risk of QT prolongation (e.g., family history of long QT syndrome, hypokalaemia) or is on drug treatment known to be associated with QT prolongation;
- Subject has clinically significant abnormalities on the 12 lead electrocardiogram (ECG);
- Subject has serum creatinine > 150 µmol/L, aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) > 2x upper limit of normal (ULN), gamma-glutamyltransferase (γ-GT) > 3x ULN, or total bilirubin > 2x ULN, as assessed in Screening samples;
- Subject had an average total daily urine volume > 3000 mL as recorded in the micturition diary period;
- Subject has severe hypertension which is defined as a sitting average systolic blood pressure ≥ 180 mmHg and/or an average diastolic blood pressure ≥ 110 mmHg.
Trial locations and contacts
133 sites in 20 countries.
133 sites in 20 countries
Slovakia11 sites
SK42109
Banská Bystrica, 975 01
SK42112
Bratislava, 832 63
SK42107
Košice, 04011
SK42113
Malacky, 90101
SK42104
Nitra, 949 01
SK42105
Pieštany, 921 01
SK42106
Piešťany, 921 01
SK42102
Prešov, 08001
SK42108
Trenčín, 911 01
SK42101
Trenčín, 91101
SK42103
Žilina
Czechia10 sites
CZ42005
Bohumín, 73581
CZ42003
Hradec Králové, 500 02
CZ42011
Ostrava, 700 30
CZ42006
Pilsen, 301 24
CZ42001
Prague, 128 51
CZ42007
Prague, 14000
CZ42009
Prague, 15006
CZ42010
Roudnice nad Labem, 413 01
CZ42012
Sternberk, 78501
CZ42002
Uherské Hradiště, 68608
Germany10 sites
DE49109
Bad Ems, 56130
DE49103
Göttingen, 37075
DE49117
Hagenow, 19230
DE49105
Hettstedt, 06333
DE49108
Leipzig, 04105
DE49110
Neustadt in Sachsen, 01844
DE49118
Reutlingen, 72764
DE49101
Rostock, 18107
DE49111
Sangerhausen, 06526
DE49104
Wismar, 23970
Russia10 sites
RU70112
Kazan', 420012
RU70108
Moscow, 105425
RU70110
Moscow, 115682
RU70102
Saint Petersburg, 191015
RU70103
Saint Petersburg, 194178
RU70106
Saint Petersburg, 197089
RU70101
Saint Petersburg, 197136
RU70107
Saint Petersburg, 198013
RU70109
Saint Petersburg, 198103
RU70113
Ufa, 450096
Poland9 sites
PL48107
Krakow, 31-530
PL48103
Lodz, 90-602
PL48108
Lublin, 20-954
PL48106
Piaseczno, 05-500
PL48104
Puławy, 24-100
PL48101
Warsaw, 02-507
PL48105
Warsaw, 02-929
PL48112
Więcbork, 89-410
PL48111
Wroclaw, 01-432
United Kingdom9 sites
GB44103
Bristol, BS10 5NB
GB44108
Cambridge, CB2 2QQ
GB44106
Garston, WD25 0EA
GB44111
Glasgow, G20 0XA
GB44104
Nantwich, CW5 5NX
GB44110
Northwood, HA6 2RN
GB44107
Plymouth, PL6 8DH
GB44101
Reading, RG1 5AN
GB44105
Sandbach, CW11 1EQ
Romania8 sites
RO40106
Brasov, 500152
RO40102
Bucharest, 042122
RO40104
Bucharest, 050659
RO40103
Bucharest, 200642
RO40108
Bucharest, 22328
RO40101
Craiova, 20116
RO40105
Craiova, 20116
RO40107
Sibiu, 550245
Ukraine8 sites
UA38104
Dnipro, 49005
UA38102
Donetsk, 83003
UA38111
Donetsk, 83114
UA38106
Kiev, 01023
UA38109
Kiev, 04053
UA38107
Lviv, 79044
UA38101
Odesa
UA38103
Zaporizhzhya, 69600
France7 sites
FR33104
Colmar, 68024
FR33108
Dijon, 21079
FR33103
Orléans, 45067
FR33111
Paris, 75651
FR33112
Paris, 75970
FR33106
Toulouse, 31059
FR33110
Tours, 37044
Hungary7 sites
HU36108
Csongrád, 6640
HU36101
Győr, 9024
HU36106
Körmend, 9900
HU36110
Miskolc, 3526
HU36104
Sopron, 9400
HU36103
Szekszárd, 7100
HU36107
Tatabánya, 2800
Portugal7 sites
PT35102
Coimbra, 3000-075
PT35105
Coimbra, 3041-801
PT35104
Lisbon, 1050-199
PT35107
Lisbon, 1649-035
PT35110
Porto, 4099-001
PT35101
Porto, 4200-319
PT35106
Tomar, 2304-909
Spain7 sites
ES34103
Madrid, 28031
ES34101
Madrid, 28041
ES34109
Madrid, 28046
ES34102
Madrid, 28905
ES34105
Pamplona, 31008
ES34104
Sant Joan d'Alacant, 03550
ES34107
Seville, 41014
Sweden5 sites
SE46101
Gothenburg, 41263
SE46103
Karlshamn, 37435
SE46104
Malmö, 21152
SE46102
Stockholm, 14186
SE46105
Tanumshede, 45781
Belarus4 sites
BY37101
Minsk, 220036
BY37102
Minsk, 220119
BY37103
Minsk, 223010
BY37104
Vitebsk, 210037
Belgium4 sites
BE32102
Brussels, 1090
BE32104
Edegem, 2650
BE32103
Ghent, 9000
BE32101
Leuven, 3000
Finland4 sites
FI35803
Helsinki, 00029
FI35804
Kouvola, 45200
FI35801
Oulu, 90220
FI35802
Tampere, 33521
Italy4 sites
IT39103
Avellino, 83100
IT39101
Catanzaro, 88100
IT39105
Florence, 50139
IT39102
Treviglio (BG), 24047
Netherlands4 sites
NL31104
Amsterdam, 1100 AD
NL31106
Maastricht
NL31102
Sneek, 8601 ZK
NL31101
Winterswijk, 7101 BN
Denmark3 sites
DK45101
Aarhus N, 8200
DK45102
Herlev, 2730
DK45104
Holstebro, 7500
About this study
Official title: A Randomized, Double-Blind, Factorial, Parallel-Group, Active and Placebo-Controlled, Multicenter Dose-Ranging Study to Evaluate the Efficacy, Safety and Tolerability of Six Dose Combinations of Solifenacin Succinate and Mirabegron Compared to Mirabegron and Solifenacin Succinate Monotherapies in the Treatment of Overactive Bladder.
The purpose of this study is to examine how well two medicines in combination (solifenacin succinate and mirabegron) work in the treatment of bladder problems over a 12-week period.
- Conditions
- Urologic Diseases, Urinary Bladder Diseases, Urological Manifestations, Signs and Symptoms, Urinary Bladder, Overactive
- Being tested
- Mirabegron, Solifenacin succinate, Placebo
- Keywords
- Urinary incontinence, Overactive bladder (OAB), Micturition, Frequency, YM178, Urgency incontinence, Urgency
- Medical subject headings
- Urologic Diseases, Urinary Bladder Diseases, Urological Manifestations, Signs and Symptoms, Urinary Bladder, Overactive, Urinary Incontinence
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
MirabegronDrug
Also called Betmiga, Myrbetric, Myrbetriq, Betanis
oral
Solifenacin succinateDrug
Also called Vesikur, Vesicare
oral
PlaceboDrug
oral
| Study group | Role | What they receive |
|---|---|---|
| Placebo | Placebo comparator | Participants received matching placebo tablets orally once a day for 12 weeks Receives: Drug: Placebo |
| Mirabegron 25 mg | Active comparator | Participants received mirabegron 25 mg tablets orally once a day for 12 weeks Receives: Drug: Mirabegron |
| Mirabegron 50 mg | Active comparator | Participants received mirabegron 50 mg tablets orally once a day for 12 weeks Receives: Drug: Mirabegron |
| Solifenacin 2.5 mg | Active comparator | Participants received solifenacin 2.5 mg tablets orally once a day for 12 weeks Receives: Drug: Solifenacin succinate |
| Solifenacin 5 mg | Active comparator | Participants received solifenacin 5 mg tablets orally once a day for 12 weeks Receives: Drug: Solifenacin succinate |
| Solifenacin 10 mg | Active comparator | Participants received solifenacin 10 mg tablets orally once a day for 12 weeks Receives: Drug: Solifenacin succinate |
| Solifenacin 2.5 mg and Mirabegron 25 mg | Experimental | Participants received solifenacin 2.5 mg and mirabegron 25 mg tablets orally once a day for 12 weeks Receives: Drug: Mirabegron; Drug: Solifenacin succinate |
| Solifenacin 2.5 mg and Mirabegron 50 mg | Experimental | Participants received solifenacin 2.5 mg and mirabegron 50 mg tablets orally once a day for 12 weeks Receives: Drug: Mirabegron; Drug: Solifenacin succinate |
| Solifenacin 5 mg and Mirabegron 25 mg | Experimental | Participants received solifenacin 5 mg and mirabegron 25 mg tablets orally once a day for 12 weeks Receives: Drug: Mirabegron; Drug: Solifenacin succinate |
| Solifenacin 5 mg and Mirabegron 50 mg | Experimental | Participants received solifenacin 5 mg and mirabegron 50 mg tablets orally once a day for 12 weeks Receives: Drug: Mirabegron; Drug: Solifenacin succinate |
| Solifenacin 10 mg and Mirabegron 25 mg | Experimental | Participants received solifenacin 10 mg and mirabegron 25 mg tablets orally once a day for 12 weeks Receives: Drug: Mirabegron; Drug: Solifenacin succinate |
| Solifenacin 10 mg and Mirabegron 50 mg | Experimental | Participants received solifenacin 10 mg and mirabegron 50 mg tablets orally once a day for 12 weeks Receives: Drug: Mirabegron; Drug: Solifenacin succinate |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change From Baseline to End of Treatment (EOT) in Mean Volume Voided Per Micturition
The average volume voided per micturition was calculated from the volume of each micturition measured by the participant and recorded in a micturition diary for 3 days before the Baseline and Week 12 clinic visits.
Measured: Baseline and Week 12
Secondary outcomes (29)
Change From Baseline to End of Treatment in Mean Number of Micturitions Per 24 Hours
The average number of micturitions (urinations) per 24 hours was derived from the number of urinations (excluding incontinence only episodes) per day recorded by the participant in the micturition diary for 3-days before the Baseline and Week 12 clinic visits.
Measured: Baseline and Week 12
Change From Baseline to End of Treatment in Mean Number of Incontinence Episodes Per 24 Hours
The average number of incontinence episodes (any involuntary leakage of urine) per day was derived from the number of incontinence episodes recorded by the participant in the micturition diary for 3-days before the Baseline and Week 12 clinic visits.
Measured: Baseline and Week 12
Change From Baseline to Each Visit in Mean Volume Voided Per Micturition
The average volume voided per micturition was calculated from the volume of each micturition measured by the participant and recorded in a micturition diary for 3 days before the Baseline and each post-baseline clinic visit.
Measured: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Number of Micturitions Per 24 Hours
The average number of micturitions (urinations) per 24 hours was derived from the number of urinations (excluding incontinence only episodes) per day recorded by the participant in the micturition diary for 3-days before the Baseline and each post-baseline clinic visit.
Measured: Baseline and Weeks 2, 4, 8 and 12
Percentage of Participants With a Micturition Response
A responder is defined as a participant with at most 8 micturitions per 24 hours post-baseline and a negative change (i.e. an improvement) from Baseline.
Measured: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Number of Incontinence Episodes Per 24 Hours
The average number of incontinence episodes (any involuntary leakage of urine) per day was derived from the number of incontinence episodes recorded by the participant in the micturition diary for 3-days before the Baseline and each post-baseline clinic visit.
Measured: Baseline and Weeks 2, 4, 8 and 12
Percentage of Participants With Zero Incontinence Episodes Post-baseline
The percentage of participants with no incontinence episodes for the 3 days prior to each clinic visit derived from the micturition diary recorded by the participant.
Measured: Weeks 2, 4, 8 and 12
Percentage of Participants With 50% Reduction in Incontinence Episodes
The percentage of participants with at least a 50% decrease from Baseline in mean number of incontinence episodes per 24 hours during the 3 days prior to each clinic visit derived from the participant's micturition diary.
Measured: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Number of Urgency Incontinence Episodes Per 24 Hours
Urgency incontinence is the involuntary leakage of urine accompanied by or immediately preceded by urgency, and was derived from the number of incontinence episodes classified by the participant in a 3-day micturition diary as Grade 3 or 4 on the Patient Perception of Intensity of Urgency Scale: 0 = No urgency; 1 = Mild urgency; 2 = Moderate urgency, could postpone voiding a short while; 3 = Severe urgency, could not postpone voiding; 4 = Urge incontinence, leaked before arriving to the toilet.
Measured: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Number of Urgency Episodes (Grade 3 and/or 4) Per 24 Hours
The average number of urgency episodes (the sudden, compelling desire to pass urine, which is difficult to defer), derived from urgency episodes classified by the participant in the 3-day micturition diary as grade 3 or 4 on the Patient Perception of Intensity of Urgency Scale: 0: No urgency; 1: Mild urgency; 2: Moderate urgency, could delay voiding a short while; 3: Severe urgency, could not delay voiding; 4: Urge incontinence, leaked before arriving to the toilet.
Measured: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Level of Urgency
Average of participants' ratings on the degree of urgency associated with each micturition and/or incontinence episode recorded in the 3-day micturition diary according to the Patient Perception of Intensity of Urgency Scale: 0: No urgency; 1: Mild urgency; 2: Moderate urgency, could delay voiding a short while; 3: Severe urgency, could not delay voiding; 4: Urge incontinence, leaked before arriving to the toilet.
Measured: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Number of Pads Used Per 24 Hours
The average number of times a participant recorded a new pad used per day during the 3-day micturition diary period.
Measured: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Number of Nocturia Episodes Per 24-Hours
Nocturia is defined as waking at night one or more times to void. The average number of times a participant urinated (excluding incontinence only episodes) during sleeping time per day was derived from the 3-day micturition diary.
Measured: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to End of Treatment in Patient Perception of Bladder Condition (PPBC)
The PPBC scale is a global assessment tool that asks patients to rate their impression of their current bladder condition on a 6-point scale from 1: 'Does not cause me any problems at all'; 2: 'Causes me some very minor problems'; 3: 'Causes me some minor problems'; 4: 'Causes me (some) moderate problems'; 5: 'Causes me severe problems' and 6: 'Causes me many severe problems'. A negative change from Baseline score indicates improvement.
Measured: Baseline and Week 12
Percentage of Participants With Improvement in PPBC
The PPBC scale is a global assessment tool that asks patients to rate their impression of their current bladder condition on a 6-point scale from 1: 'Does not cause me any problems at all'; 2: 'Causes me some very minor problems'; 3: 'Causes me some minor problems'; 4: 'Causes me (some) moderate problems'; 5: 'Causes me severe problems' and 6: 'Causes me many severe problems'. Improvement was defined as at least a 1-point improvement (decrease) from Baseline in PPBC score.
Measured: Baseline and Week 12
Percentage of Participants With Major Improvement in PPBC
The PPBC scale is a global assessment tool that asks patients to rate their impression of their current bladder condition on a 6-point scale from 1: 'Does not cause me any problems at all'; 2: 'Causes me some very minor problems'; 3: 'Causes me some minor problems'; 4: 'Causes me (some) moderate problems'; 5: 'Causes me severe problems' and 6: 'Causes me many severe problems'. Major improvement was defined as at least a 2-point improvement (decrease) from Baseline in PPBC score.
Measured: Baseline and Week 12
Percentage of Participants With Deterioration in PPBC
The PPBC scale is a global assessment tool that asks patients to rate their impression of their current bladder condition on a 6-point scale from 1: 'Does not cause me any problems at all'; 2: 'Causes me some very minor problems'; 3: 'Causes me some minor problems'; 4: 'Causes me (some) moderate problems'; 5: 'Causes me severe problems' and 6: 'Causes me many severe problems'. Deterioration was defined as at least a 1 point increase from Baseline in PPBC score.
Measured: Baseline and Week 12
Change From Baseline to End of Treatment in Symptom Bother Score as Assessed by the Overactive Bladder Questionnaire (OAB-q)
Overactive bladder symptoms were assessed using the symptom bother scale of the overactive bladder questionnaire. The symptom bother scale consists of 8 questions answered by the participant on a scale from 1-6. The total symptom bother score was calculated from the 8 answers and then transformed to range from 0 to 100, with 100 indicating worst severity. A negative change from Baseline in symptom bother score indicates improvements.
Measured: Baseline and Week 12
Percentage of Participants With a Symptom Bother Response
Overactive bladder symptoms were assessed using the symptom bother scale of the overactive bladder questionnaire. The symptom bother scale consists of 8 questions answered by the participant on a scale from 1-6. The total symptom bother score was calculated from the 8 answers and then transformed to range from 0 to 100, with 100 indicating worst severity. Symptom bother response is defined as improvement (decrease) of at least 10 points from Baseline.
Measured: Baseline and Week 12
Change From Baseline to End of Treatment in Health-related Quality of Life (HRQL) Total Score
Health-related quality of life was assessed by the HRQL subscales (coping, concern, sleep and social interaction) of the overactive bladder questionnaire (OABq). The HRQL total score was calculated by adding the 4 HRQL subscale scores, and transforming to a scale from 0 to 100, with higher scores indicating better quality of life. A positive change from Baseline in HRQL score indicates improvements.
Measured: Baseline and Week 12
Percentage of Participants With a Health-related Quality of Life Total Score Response
Health-related quality of life was assessed by the HRQL subscales (coping, concern, sleep and social interaction) of the overactive bladder questionnaire (OABq). The HRQL total score was calculated by adding the 4 HRQL subscale scores, and transforming to a scale from 0 to 100, with higher scores indicating better quality of life. HRQL response is defined as improvement (decrease) of at least 10 points from Baseline.
Measured: Baseline and Week 12
Change From Baseline in European Quality of Life-5 Dimensions (EQ-5D) Mobility Score
The EQ-5D is an international, standardized, nondisease-specific (i.e., generic) instrument for describing and valuing health status. Participants were asked to indicate which of the following statements best describes their health state:
I have no problems in walking about; I have some problems in walking about; I am confined to bed.
In the table below, each row title lists Baseline health status first followed by End of Treatment health status and reports the number of patients in that category.
Measured: Baseline and Week 12
Change From Baseline in European Quality of Life-5 Dimensions (EQ-5D) Self-care Score
The EQ-5D is an international, standardized, nondisease-specific (i.e., generic) instrument for describing and valuing health status. Participants were asked to indicate which of the following statements best describes their health state:
I have no problems with self-care; I have some problems washing or dressing myself; I am unable to wash or dress myself.
In the table below, each row title lists Baseline health status first followed by End of Treatment health status and reports the number of patients in that category.
Measured: Baseline and Week 12
Change From Baseline in European Quality of Life-5 Dimensions (EQ-5D) Usual Activities Score
The EQ-5D is a standardized, nondisease-specific instrument for describing health status. Participants were asked which statement best describes their health state with regard to usual activities (work, study or leisure): I have no problems performing my usual activities; I have some problems performing my usual activities; I am unable to perform my usual activities.
In the table below, each row title lists Baseline health status first followed by End of Treatment health status and reports the number of patients in that category.
Measured: Baseline and Week 12
Change From Baseline in European Quality of Life-5 Dimensions (EQ-5D) Pain/Discomfort Score
The EQ-5D is an international, standardized, nondisease-specific (i.e., generic) instrument for describing and valuing health status. Participants were asked to indicate which of the following statements best describes their health state:
I have no pain or discomfort; I have moderate pain or discomfort; I have extreme pain or discomfort. In the table below, each row title lists Baseline health status first followed by End of Treatment health status and reports the number of participants in that category.
Measured: Baseline and Week 12
Change From Baseline in European Quality of Life-5 Dimensions (EQ-5D) Anxiety/Depression Score
The EQ-5D is an international, standardized, nondisease-specific (i.e., generic) instrument for describing and valuing health status. Participants were asked to indicate which of the following statements best describes their health state:
I am not anxious or depressed; I am moderately anxious or depressed; I am extremely anxious or depressed. In the table below, each row title lists Baseline health status first followed by End of Treatment health status and reports the number of patients in that category.
Measured: Baseline and Week 12
Change From Baseline to End of Treatment in European Quality of Life-5 Dimensions (EQ-5D) Visual Analog Scale (VAS)
The EQ-5D is an international, standardized, generic instrument for describing and evaluating health status. Health status is assessed by patients evaluating their health on a vertical, visual analog scale from 0 to 100 where the endpoints are labeled 'Worst imaginable health state' (=0) and 'Best imaginable health state' (=100). On the EQ-5D VAS, a positive change from baseline indicates improvement.
Measured: Baseline and Week 12
Change From Baseline to End of Treatment in Work Productivity and Activity Impairment (WPAI)
This 6-item assessment measures productivity losses during the past 7 days and includes measures on work time missed due to health, impairment while working due to health (the participant's assessment of the degree to which health affected their productivity while working), overall work impairment due to health (takes into account both hours missed due to health and the participant's assessment of the degree to which health affected their productivity while working) and activity impairment due to health (the degree in which health problems affected their ability to do regular daily activities). Scores for each measure are expressed from 0 to 100 with higher numbers indicating greater impairment and less productivity, i.e., worse outcomes. A negative change from baseline indicates improvement.
Measured: Baseline and Week 12
Change From Baseline to End of Treatment in Treatment Satisfaction on Visual Analog Scale (TS-VAS)
The TS-VAS is a visual analog scale (VAS) that asks patients to rate their satisfaction with treatment by placing a vertical mark on a 10 cm line where the endpoints are labeled 'No, not at all' on the left (=0) to 'Yes, completely satisfied' on the right (=10). A positive change from Baseline indicates improvement.
Measured: Baseline and Week 12
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Apr 2011 (estimated)
- Study start29 Mar 2011
- Primary completion28 Jun 2012
- Study completion28 Jun 2012
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Urologic DiseasesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- Triple blind
- Who is masked
- Participant, Care provider, Investigator
- Enrolment
- 1,307 participants (actual)
Sponsor and investigators
- Lead sponsor
- Astellas Pharma Europe B.V.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Study Physician, Study director, Astellas Pharma Europe B.V.Principal Investigator, Principal investigator, Bristol Urological Institute
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01340027
- Sponsor's protocol ID
- 178-CL-100
- Other IDs
- 2010-020601-32
- Acronym
- Symphony
- Status last verified
- Oct 2024
- First submitted
- 20 Apr 2011
- Last updated
- 31 Oct 2024
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- Individual data sharing
- Yes: Access to anonymized individual participant level data collected during the study, in addition to study-related supporting documentation, is planned for studies conducted with approved product indications and formulations, as well as products terminated during development. Studies conducted with product indications or formulations that remain active in development are assessed after study completion to determine if Individual Participant Data can be shared. Further details on Astellas' data sharing policy can be found at https://www.clinicaltrials.astellas.com/transparency/.
Publications
Stoniute A, Madhuvrata P, Still M, Barron-Millar E, Nabi G, Omar MI. Oral anticholinergic drugs versus placebo or no treatment for managing overactive bladder syndrome in adults. Cochrane Database Syst Rev. 2023 May 9;5(5):CD003781. doi: 10.1002/14651858.CD003781.pub3.
PubMed 37160401Abrams P, Kelleher C, Staskin D, Rechberger T, Kay R, Martina R, Newgreen D, Paireddy A, van Maanen R, Ridder A. Combination treatment with mirabegron and solifenacin in patients with overactive bladder: efficacy and safety results from a randomised, double-blind, dose-ranging, phase 2 study (Symphony). Eur Urol. 2015 Mar;67(3):577-88. doi: 10.1016/j.eururo.2014.02.012. Epub 2014 Feb 19.
PubMed 24612659
Study at a glance
From the registry record, last updated by the sponsor on 31 Oct 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized, Double-Blind, Factorial, Parallel-Group, Active and Placebo-Controlled, Multicenter Dose-Ranging Study to Evaluate the Efficacy, Safety and Tolerability of Six Dose Combinations of Solifenacin Succinate and Mirabegron Compared to Mirabegron and Solifenacin Succinate Monotherapies in the Treatment of Overactive Bladder.
- ClinicalTrials.gov ID
- NCT01340027
- Acronym / sponsor ID
- Symphony / 178-CL-100
- Conditions
- Urologic Diseases, Urinary Bladder Diseases, Urological Manifestations, Signs and Symptoms, Urinary Bladder, Overactive
- Keywords
- Urinary incontinence, Overactive bladder (OAB), Micturition, Frequency, YM178, Urgency incontinence, Urgency
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 1,307 participants (actual)
- Lead sponsor
- Astellas Pharma Europe B.V.Industry (pharma, biotech, devices)
- Study start
- 29 Mar 2011 (actual)
- Primary completion
- 28 Jun 2012 (actual)
- Study completion
- 28 Jun 2012 (actual)
- First posted
- 21 Apr 2011 (estimated)
- Results
- Posted 21 Jul 2015
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to examine how well two medicines in combination (solifenacin succinate and mirabegron) work in the treatment of bladder problems over a 12-week period.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 12
| Arm | Type | Receives |
|---|---|---|
| Placebo | Placebo comparator | Drug: PlaceboParticipants received matching placebo tablets orally once a day for 12 weeks |
| Mirabegron 25 mg | Active comparator | Drug: MirabegronParticipants received mirabegron 25 mg tablets orally once a day for 12 weeks |
| Mirabegron 50 mg | Active comparator | Drug: MirabegronParticipants received mirabegron 50 mg tablets orally once a day for 12 weeks |
| Solifenacin 2.5 mg | Active comparator | Drug: Solifenacin succinateParticipants received solifenacin 2.5 mg tablets orally once a day for 12 weeks |
| Solifenacin 5 mg | Active comparator | Drug: Solifenacin succinateParticipants received solifenacin 5 mg tablets orally once a day for 12 weeks |
| Solifenacin 10 mg | Active comparator | Drug: Solifenacin succinateParticipants received solifenacin 10 mg tablets orally once a day for 12 weeks |
| Solifenacin 2.5 mg and Mirabegron 25 mg | Experimental | Drug: Mirabegron, Drug: Solifenacin succinateParticipants received solifenacin 2.5 mg and mirabegron 25 mg tablets orally once a day for 12 weeks |
| Solifenacin 2.5 mg and Mirabegron 50 mg | Experimental | Drug: Mirabegron, Drug: Solifenacin succinateParticipants received solifenacin 2.5 mg and mirabegron 50 mg tablets orally once a day for 12 weeks |
| Solifenacin 5 mg and Mirabegron 25 mg | Experimental | Drug: Mirabegron, Drug: Solifenacin succinateParticipants received solifenacin 5 mg and mirabegron 25 mg tablets orally once a day for 12 weeks |
| Solifenacin 5 mg and Mirabegron 50 mg | Experimental | Drug: Mirabegron, Drug: Solifenacin succinateParticipants received solifenacin 5 mg and mirabegron 50 mg tablets orally once a day for 12 weeks |
| Solifenacin 10 mg and Mirabegron 25 mg | Experimental | Drug: Mirabegron, Drug: Solifenacin succinateParticipants received solifenacin 10 mg and mirabegron 25 mg tablets orally once a day for 12 weeks |
| Solifenacin 10 mg and Mirabegron 50 mg | Experimental | Drug: Mirabegron, Drug: Solifenacin succinateParticipants received solifenacin 10 mg and mirabegron 50 mg tablets orally once a day for 12 weeks |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
Key exclusion criteria (24 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| MirabegronAlso: Betmiga, Myrbetric, Myrbetriq, Betanisoral | Drug | Mirabegron 25 mg, Mirabegron 50 mg, Solifenacin 10 mg and Mirabegron 25 mg, Solifenacin 10 mg and Mirabegron 50 mg, Solifenacin 2.5 mg and Mirabegron 25 mg, Solifenacin 2.5 mg and Mirabegron 50 mg, Solifenacin 5 mg and Mirabegron 25 mg, Solifenacin 5 mg and Mirabegron 50 mg |
| Solifenacin succinateAlso: Vesikur, Vesicareoral | Drug | Solifenacin 10 mg, Solifenacin 10 mg and Mirabegron 25 mg, Solifenacin 10 mg and Mirabegron 50 mg, Solifenacin 2.5 mg, Solifenacin 2.5 mg and Mirabegron 25 mg, Solifenacin 2.5 mg and Mirabegron 50 mg, Solifenacin 5 mg, Solifenacin 5 mg and Mirabegron 25 mg, Solifenacin 5 mg and Mirabegron 50 mg |
| Placebooral | Drug | Placebo |
Primary outcome
Change From Baseline to End of Treatment (EOT) in Mean Volume Voided Per Micturition
Time frame: Baseline and Week 12
The average volume voided per micturition was calculated from the volume of each micturition measured by the participant and recorded in a micturition diary for 3 days before the Baseline and Week 12 clinic visits.
29 secondary outcomes
Change From Baseline to End of Treatment in Mean Number of Micturitions Per 24 Hours
Time frame: Baseline and Week 12
Change From Baseline to End of Treatment in Mean Number of Incontinence Episodes Per 24 Hours
Time frame: Baseline and Week 12
Change From Baseline to Each Visit in Mean Volume Voided Per Micturition
Time frame: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Number of Micturitions Per 24 Hours
Time frame: Baseline and Weeks 2, 4, 8 and 12
Percentage of Participants With a Micturition Response
Time frame: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Number of Incontinence Episodes Per 24 Hours
Time frame: Baseline and Weeks 2, 4, 8 and 12
Percentage of Participants With Zero Incontinence Episodes Post-baseline
Time frame: Weeks 2, 4, 8 and 12
Percentage of Participants With 50% Reduction in Incontinence Episodes
Time frame: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Number of Urgency Incontinence Episodes Per 24 Hours
Time frame: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Number of Urgency Episodes (Grade 3 and/or 4) Per 24 Hours
Time frame: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Level of Urgency
Time frame: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Number of Pads Used Per 24 Hours
Time frame: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to Each Visit in Mean Number of Nocturia Episodes Per 24-Hours
Time frame: Baseline and Weeks 2, 4, 8 and 12
Change From Baseline to End of Treatment in Patient Perception of Bladder Condition (PPBC)
Time frame: Baseline and Week 12
Percentage of Participants With Improvement in PPBC
Time frame: Baseline and Week 12
Percentage of Participants With Major Improvement in PPBC
Time frame: Baseline and Week 12
Percentage of Participants With Deterioration in PPBC
Time frame: Baseline and Week 12
Change From Baseline to End of Treatment in Symptom Bother Score as Assessed by the Overactive Bladder Questionnaire (OAB-q)
Time frame: Baseline and Week 12
Percentage of Participants With a Symptom Bother Response
Time frame: Baseline and Week 12
Change From Baseline to End of Treatment in Health-related Quality of Life (HRQL) Total Score
Time frame: Baseline and Week 12
Percentage of Participants With a Health-related Quality of Life Total Score Response
Time frame: Baseline and Week 12
Change From Baseline in European Quality of Life-5 Dimensions (EQ-5D) Mobility Score
Time frame: Baseline and Week 12
Change From Baseline in European Quality of Life-5 Dimensions (EQ-5D) Self-care Score
Time frame: Baseline and Week 12
Change From Baseline in European Quality of Life-5 Dimensions (EQ-5D) Usual Activities Score
Time frame: Baseline and Week 12
Change From Baseline in European Quality of Life-5 Dimensions (EQ-5D) Pain/Discomfort Score
Time frame: Baseline and Week 12
Change From Baseline in European Quality of Life-5 Dimensions (EQ-5D) Anxiety/Depression Score
Time frame: Baseline and Week 12
Change From Baseline to End of Treatment in European Quality of Life-5 Dimensions (EQ-5D) Visual Analog Scale (VAS)
Time frame: Baseline and Week 12
Change From Baseline to End of Treatment in Work Productivity and Activity Impairment (WPAI)
Time frame: Baseline and Week 12
Change From Baseline to End of Treatment in Treatment Satisfaction on Visual Analog Scale (TS-VAS)
Time frame: Baseline and Week 12
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Oct 2024.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 37160401Stoniute A, Madhuvrata P, Still M, Barron-Millar E, Nabi G, Omar MI. Oral anticholinergic drugs versus placebo or no treatment for managing overactive bladder syndrome in adults. Cochrane Database Syst Rev. 2023 May 9;5(5):CD003781. doi: 10.1002/14651858.CD003781.pub3.
- Derived from this study: PubMed 24612659Abrams P, Kelleher C, Staskin D, Rechberger T, Kay R, Martina R, Newgreen D, Paireddy A, van Maanen R, Ridder A. Combination treatment with mirabegron and solifenacin in patients with overactive bladder: efficacy and safety results from a randomised, double-blind, dose-ranging, phase 2 study (Symphony). Eur Urol. 2015 Mar;67(3):577-88. doi: 10.1016/j.eururo.2014.02.012. Epub 2014 Feb 19.
- Individual participant dataSharing planned: Yes. Access to anonymized individual participant level data collected during the study, in addition to study-related supporting documentation, is planned for studies conducted with approved product indications and formulations, as well as products terminated during development. Studies conducted with product indications or formulations that remain active in development are assessed after study completion to determine if Individual Participant Data can be shared. Further details on Astellas' data sharing policy can be found at https://www.clinicaltrials.astellas.com/transparency/.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Study Physician study director
Astellas Pharma Europe B.V.
Principal Investigator principal investigator
Bristol Urological Institute
133 sites in 20 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Mirabegron and Solifenacin succinate in people with Urologic Diseases and Urinary Bladder Diseases, run by Astellas Pharma Europe B.V. at 133 sites in 20 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 24 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 31 Oct 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 133 sites in Slovakia, Czechia, Germany, Russia, Poland and 15 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 21 Jul 2015). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change From Baseline to End of Treatment (EOT) in Mean Volume Voided Per Micturition (time frame: Baseline and Week 12). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01340027, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Oct 2024.