AzTrials
AzTrials

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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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
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

Other trials in Slovakia

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

Other trials in Czechia

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

Other trials in Germany

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

Other trials in Russia

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

Other trials in Poland

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

Other trials in United Kingdom

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

Other trials in Romania

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

Other trials in Ukraine

France7 sites
  • FR33104

    Colmar, 68024

  • FR33108

    Dijon, 21079

  • FR33103

    Orléans, 45067

  • FR33111

    Paris, 75651

  • FR33112

    Paris, 75970

  • FR33106

    Toulouse, 31059

  • FR33110

    Tours, 37044

Other trials in France

Hungary7 sites
  • HU36108

    Csongrád, 6640

  • HU36101

    Győr, 9024

  • HU36106

    Körmend, 9900

  • HU36110

    Miskolc, 3526

  • HU36104

    Sopron, 9400

  • HU36103

    Szekszárd, 7100

  • HU36107

    Tatabánya, 2800

Other trials in Hungary

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

Other trials in Portugal

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

Other trials in Spain

Sweden5 sites
  • SE46101

    Gothenburg, 41263

  • SE46103

    Karlshamn, 37435

  • SE46104

    Malmö, 21152

  • SE46102

    Stockholm, 14186

  • SE46105

    Tanumshede, 45781

Other trials in Sweden

Belarus4 sites
  • BY37101

    Minsk, 220036

  • BY37102

    Minsk, 220119

  • BY37103

    Minsk, 223010

  • BY37104

    Vitebsk, 210037

Other trials in Belarus

Belgium4 sites
  • BE32102

    Brussels, 1090

  • BE32104

    Edegem, 2650

  • BE32103

    Ghent, 9000

  • BE32101

    Leuven, 3000

Other trials in Belgium

Finland4 sites
  • FI35803

    Helsinki, 00029

  • FI35804

    Kouvola, 45200

  • FI35801

    Oulu, 90220

  • FI35802

    Tampere, 33521

Other trials in Finland

Italy4 sites
  • IT39103

    Avellino, 83100

  • IT39101

    Catanzaro, 88100

  • IT39105

    Florence, 50139

  • IT39102

    Treviglio (BG), 24047

Other trials in Italy

Netherlands4 sites
  • NL31104

    Amsterdam, 1100 AD

  • NL31106

    Maastricht

  • NL31102

    Sneek, 8601 ZK

  • NL31101

    Winterswijk, 7101 BN

Other trials in Netherlands

Denmark3 sites
  • DK45101

    Aarhus N, 8200

  • DK45102

    Herlev, 2730

  • DK45104

    Holstebro, 7500

Other trials in Denmark

Norway2 sites
  • NO47104

    Elverum, 2408

  • NO47102

    Hamar, 2317

Other trials in Norway

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.

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 groups in NCT01340027
Study groupRoleWhat they receive
PlaceboPlacebo comparatorParticipants received matching placebo tablets orally once a day for 12 weeks
Receives: Drug: Placebo
Mirabegron 25 mgActive comparatorParticipants received mirabegron 25 mg tablets orally once a day for 12 weeks
Receives: Drug: Mirabegron
Mirabegron 50 mgActive comparatorParticipants received mirabegron 50 mg tablets orally once a day for 12 weeks
Receives: Drug: Mirabegron
Solifenacin 2.5 mgActive comparatorParticipants received solifenacin 2.5 mg tablets orally once a day for 12 weeks
Receives: Drug: Solifenacin succinate
Solifenacin 5 mgActive comparatorParticipants received solifenacin 5 mg tablets orally once a day for 12 weeks
Receives: Drug: Solifenacin succinate
Solifenacin 10 mgActive comparatorParticipants received solifenacin 10 mg tablets orally once a day for 12 weeks
Receives: Drug: Solifenacin succinate
Solifenacin 2.5 mg and Mirabegron 25 mgExperimentalParticipants 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 mgExperimentalParticipants 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 mgExperimentalParticipants 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 mgExperimentalParticipants 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 mgExperimentalParticipants 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 mgExperimentalParticipants 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.

  1. 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)
  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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

  9. 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

  10. 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

  11. 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

  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

  13. 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

  14. 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

  15. 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

  16. 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

  17. 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

  18. 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

  19. 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

  20. 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

  21. 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

  22. 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

  23. 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

  24. 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

  25. 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

  26. 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

  27. 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

  28. 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

  29. 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.

  1. First posted21 Apr 2011 (estimated)
  2. Study start29 Mar 2011
  3. Primary completion28 Jun 2012
  4. Study completion28 Jun 2012

Resources

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)
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
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 37160401
  • Abrams 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

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.

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