AzTrials
AzTrials

Urologic DiseasesPhase 3BEYONDNCT01638000

A Study to Evaluate the Efficacy and Safety of Mirabegron Compared to Solifenacin in Patients With Overactive Bladder Who Were Previously Treated With Another Medicine But Were Not Satisfied With That Treatment.

A Phase 3 study testing Mirabegron and Solifenacin succinate in people with Urologic Diseases and Urinary Bladder, Overactive, run by Astellas Pharma Europe Ltd. at 217 sites in 33 countries.

Completed

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

Official record
Search all trials

Trial summary

The purpose of the study was to assess the efficacy, safety and tolerability of mirabegron 50 mg versus (vs) solifenacin 5 mg in the treatment of patients with OAB who were dissatisfied with their treatment due to lack of efficacy. 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?
No, everyone receives an active treatment
How many people
1,887 participants
Where
217 sitesin 33 countries
Study dates
12 Jun 2012to 24 Apr 2013
Phase
Phase 3
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 is willing and able to complete the micturition diary and questionnaires correctly
  • Subject has symptoms of OAB (urinary frequency and urgency with or without urgency incontinence) for at least 3 months
  • Subject is currently or has previously received at least one antimuscarinic agent intended to treat their OAB. The last antimuscarinic must have been taken for at least 4 weeks and taken within 6 months prior to the Screening Visit

Who cannot join

  • Female subject is breastfeeding, pregnant, intends to become pregnant during the study, or of childbearing potential is sexually active and not practicing a highly reliable method of birth control
  • Subject has neurogenic bladder
  • 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 a cough provocation test)
  • Subject has an indwelling catheter or practices intermittent self-catheterization
  • Subject has diabetic neuropathy
  • Subject has evidence of a symptomatic urinary tract infection, chronic inflammation such as interstitial cystitis, bladder stones, previous pelvic radiation therapy or previous or current malignant disease of the pelvic organs
Show all 18Show fewer
  • Subject has uncontrolled narrow angle glaucoma, urinary or gastric retention, severe ulcerative colitis, toxic megacolon, myasthenia gravis or any other medical condition which makes the use of anticholinergics contraindicated
  • The subject is currently receiving or has a history of treatment with intravesical botulinum toxin (cosmetic use is acceptable) or resiniferatoxin within 9 months prior to screening
  • Subject receives 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 has moderate to severe hepatic impairment
  • Subject has severe renal impairment or end stage renal disease
  • Subject has severe uncontrolled hypertension
  • Subject has a clinically significant abnormal electrocardiogram (ECG) or has a known history of QT prolongation or currently taking medication known to prolong the QT interval
  • Subject has a known or suspected hypersensitivity to solifenacin, mirabegron or any of the inactive ingredients
  • Subject has a concurrent malignancy or history of cancer (except noninvasive skin cancer) within the last 5 years prior to screening
  • Subject has been treated with an experimental device within 30 days or received an experimental agent within the longer of 30 days or five half-lives
  • Subject is using prohibited medications which cannot be stopped safely at the Screening Visit. Subject is excluded if using restricted medications not meeting protocol-specified criteria
  • Subject's last antimuscarinic treatment was solifenacin

Trial locations and contacts

217 sites in 33 countries.

217 sites in 33 countries

United Kingdom25 sites
  • Site: 44027

    Aberdeen, AB25 2ZN

  • Site: 44029

    Birmingham, B15 2TG

  • Site: 44025

    Cambridge, CB2 2QQ

  • Site: 44030

    Chichester, PO19 4SE

  • Site: 44028

    Croydon, CR7 7YE

  • Site: 44003

    Devon, TQ2 7AA

  • Site: 44001

    Edgbaston, B15 2TH

  • Site: 44011

    Glasgow, G11 6NT

  • Site: 44023

    Harrow, HA 3UJ

  • Site: 44006

    Kent, ME7 5NY

  • Site: 44012

    Leeds, LS 9TF

  • Site: 44019

    Leicester, LE5 4PW

  • Site: 44008

    Liverpool, L8 7SS

  • Site: 44010

    London, SW17 0QT

  • Site: 44017

    London, W2 1NY

  • Site: 44013

    Newcastle upon Tyne, NE7 7DN

  • Site: 44022

    Northwood, HA6 2RN

  • Site: 44021

    Nottingham, NG5 1PB

  • Site: 44009

    Plymouth, PL6 8DH

  • Site: 44007

    Reading, RG1 5AN

  • Site: 44005

    Sheffield, S10 2JF

  • Site: 44020

    Southampton, SO16 5YA

  • Site: 44026

    Taunton, TA1 5DA

  • Site: 44024

    West Yorkshire, BD9 6RJ

  • Site: 44002

    West Yorkshire, WF8 1PL

Other trials in United Kingdom

France13 sites
  • Site: 33010

    Angers, 49033

  • Site: 33007

    Colmar, 68024

  • Site: 33011

    Dijon, 21000

  • Site: 33002

    Marseille, 13285

  • Site: 33006

    Marseille, 13385

  • Site: 33013

    Nîmes, 30029

  • Site: 33004

    Orléans, 45067

  • Site: 33001

    Paris, 75970

  • Site: 33005

    Paris, 75970

  • Site: 33003

    Rouen, 76031

  • Site: 33014

    Suresnes, 92151

  • Site: 33017

    Tours, 37044

  • Site: 33015

    Valence, 26953

Other trials in France

Russia13 sites
  • Site: 70007

    Moscow, 101000

  • Site: 70001

    Moscow, 105425

  • Site: 70008

    Moscow, 115516

  • Site: 70005

    Moscow, 117815

  • Site: 70006

    Moscow, 117815

  • Site: 70011

    Moscow, 117997

  • Site: 70002

    Moscow, 119435

  • Site: 70003

    Moscow, 125206

  • Site: 70013

    Saint Petersburg, 194175

  • Site: 70012

    Saint Petersburg, 196084

  • Site: 70004

    Saint Petersburg, 197089

  • Site: 70010

    Saint Petersburg, 198103

  • Site: 70009

    Saint Petersburg, 199034

Other trials in Russia

Spain11 sites
  • Site: 34001

    Barcelona, 080200

  • Site: 34002

    Barcelona, 08036

  • Site: 34009

    Bilbao, 48013

  • Site: 34010

    Donostia / San Sebastian, 20014

  • Site: 34004

    Madrid, 28031

  • Site: 34005

    Madrid, 28046

  • Site: 34003

    Madrid, 28049

  • Site: 34011

    Mendaro, 20850

  • Site: 34013

    Murcia, 30008

  • Site: 34014

    Seville, 41014

  • Site: 34012

    Valencia, 46026

Other trials in Spain

Canada10 sites
  • Site: 10010

    Abbotsford British Columbia, V2S 3N5

  • Site: 10011

    Barrie, L4M 7G1

  • Site: 10001

    Bathurst, E2A 4Z2

  • Site: 10003

    Brampton, L6T 4S5

  • Site: 10005

    Brantford, N3R 4N3

  • Site: 10007

    Kingston, K7L 3J7

  • Site: 10002

    Montreal, H4N 3C5

  • Site: 10009

    Sherbrooke, J1H 5N4

  • Site: 10004

    Toronto, M4N 3M5

  • Site: 10008

    Victoria, V8V 3N1

Other trials in Canada

Greece9 sites
  • Site: 30005

    Alexandroupoli, 68100

  • Site: 30009

    Athens, 115 28

  • Site: 30007

    Athens, 166 73

  • Site: 30001

    Athens

  • Site: 30006

    Heraklion, 711 10

  • Site: 30008

    Larissa, 41334

  • Site: 30004

    Pátrai, 26500

  • Site: 30010

    Thessaloniki, 546 42

  • Site: 30002

    Thessaloniki, 56429

Other trials in Greece

Turkey (Türkiye)9 sites
  • Site: 90005

    Ankara, 06500

  • Site: 90003

    Ankara, 6100

  • Site: 90011

    Denizli, 20070

  • Site: 90007

    Diyarbakır, 21080

  • Site: 90004

    Istanbul

  • Site: 90001

    Izmir, 35100

  • Site: 90008

    Izmir, 35340

  • Site: 90009

    Manisa, 45010

  • Site: 90010

    Sivas, 58140

Other trials in Turkey (Türkiye)

Austria8 sites
  • Site: 43006

    Baden, 2500

  • Site: 43014

    Graz, 9036

  • Site: 43015

    Innsbruck, 6020

  • Site: 43013

    Linz, 4020

  • Site: 43005

    Oberwart, 7400

  • Site: 43011

    Vienna, 1020

  • Site: 43002

    Vienna, 1220

  • Site: 43003

    Wels, 4600

Other trials in Austria

Czechia8 sites
  • Site: 42004

    Bohumín, 73581

  • Site: 42003

    Brno, 602 00

  • Site: 42001

    Hradec Králové, 500 05

  • Site: 42002

    Jihlava, 586 33

  • Site: 42006

    Plzen-Lochotin, 30460

  • Site: 42005

    Prague, 110 00

  • Site: 42008

    Prague, 128 51

  • Site: 42007

    Prague, 14000

Other trials in Czechia

Italy8 sites
  • Site: 39001

    Avellino, 83100

  • Site: 39005

    Catanzaro, 88100

  • Site: 39003

    Cinisello Balsamo, 20092

  • Site: 39002

    Florence, 50139

  • Site: 39008

    Milan, 20153

  • Site: 39010

    Pavia, 27100

  • Site: 39006

    Perugia, 06156

  • Site: 39007

    Treviglio, 24047

Other trials in Italy

Bulgaria7 sites
  • Site: 35902

    Burgas, 8000

  • Site: 35909

    Haskovo, 6300

  • Site: 35901

    Lovech, 5500

  • Site: 35905

    Plovdiv, 4003

  • Site: 35906

    Sofia, 1431

  • Site: 35908

    Sofia, 1504

  • Site: 35903

    Sofia, 1606

Other trials in Bulgaria

Netherlands7 sites
  • Site: 31010

    Amsterdam

  • Site: 31005

    Eindhoven, 5623 EJ

  • Site: 31004

    Enschede, 7511 JX

  • Site: 31007

    Nijmegen, 6525 GA

  • Site: 31001

    Tilburg, 5022 GC

  • Site: 31008

    Utrecht, 3584 CX

  • Site: 31006

    Zwolle, 8025 AB

Other trials in Netherlands

Sweden7 sites
  • Site: 46007

    Gothenburg, 413 45

  • Site: 46004

    Halmstad, 302 46

  • Site: 46005

    Karlshamn, 37435

  • Site: 46003

    Norrtälje, 761 29

  • Site: 46002

    Stockholm, 114 46

  • Site: 46001

    Stockholm, 14186

  • Site: 46006

    Uppsala, 753 35

Other trials in Sweden

Belgium6 sites
  • Site: 32006

    Brussels, 1070

  • Site: 32008

    Deurne, 2100

  • Site: 32001

    Edegem, 2650

  • Site: 32004

    Ghent, 9000

  • Site: 32007

    Leuven, 3000

  • Site: 32005

    Liège

Other trials in Belgium

Hungary6 sites
  • Site: 36003

    Budapest, 1082

  • Site: 36004

    Budapest, 1237

  • Site: 36005

    Csongrád, H-6640

  • Site: 36006

    Nyíregyháza, H-4400

  • Site: 36001

    Salgótarján, 3100

  • Site: 36002

    Szekszárd, 7100

Other trials in Hungary

Ireland6 sites
  • Site: 35304

    Cork

  • Site: 35302

    Dublin, 8

  • Site: 35306

    Dublin, 8

  • Site: 35301

    Dublin, 9

  • Site: 35303

    Tralee

  • Site: 35305

    Waterford

Other trials in Ireland

Poland6 sites
  • Site: 48007

    Kolbuszowa Dolna, 36-100

  • Site: 48006

    Krakow, 31-315

  • Site: 48001

    Lublin, 20-632

  • Site: 48004

    Piaseczno, 05-500

  • Site: 48003

    Warsaw, 02-929

  • Site: 48005

    Wroclaw, 01-432

Other trials in Poland

Slovakia6 sites
  • Site: 42104

    Galanta, 924 22

  • Site: 42106

    Martin, 036 59

  • Site: 42103

    Piešťany, 92102

  • Site: 42101

    Poprad, 05801

  • Site: 42105

    Trenčín, 911 01

  • Site: 42102

    Žilina, 010 01

Other trials in Slovakia

Armenia5 sites
  • Site: 37406

    Yerevan, 0001

  • Site: 37404

    Yerevan, 0014

  • Site: 37403

    Yerevan, 0052

  • Site: 37401

    Yerevan, 0078

  • Site: 37402

    Yerevan, 0078

Other trials in Armenia

Denmark5 sites
  • Site: 45002

    Aalborg, 9000

  • Site: 45001

    Aarhus N, 8200

  • Site: 45005

    Frederiksbjerg, 2000

  • Site: 45004

    Hvidovre, 2650

  • Site: 45003

    Odense C, 9000

Other trials in Denmark

Portugal5 sites
  • Site: 35105

    Lisbon, 1050-199

  • Site: 35104

    Lisbon, 1649-035

  • Site: 35102

    Matosinhos Municipality, 4454-509

  • Site: 35103

    Porto, 4100-180

  • Site: 35101

    Setúbal, 2910-446

Other trials in Portugal

Slovenia5 sites
  • Site: 38603

    Ljubljana, 1000

  • Site: 38604

    Ljubljana, 1000

  • Site: 38601

    Maribor, 2000

  • Site: 38602

    Maribor, 2000

  • Site: 38606

    Novo Mesto, 8000

Other trials in Slovenia

Ukraine5 sites
  • Site: 38007

    Chernivtsi, 58000

  • Site: 38004

    Dnipro, 49005

  • Site: 38001

    Kharkiv, 61057

  • Site: 38002

    Kiev, 2000

  • Site: 38003

    Lviv, 79044

Other trials in Ukraine

Kazakhstan4 sites
  • Site: 77705

    Almaty, 050060

  • Site: 77706

    Almaty, 50091

  • Site: 77703

    Astana, 010000

  • Site: 77702

    Astana, 10000

Other trials in Kazakhstan

Belarus3 sites
  • Site: 37502

    Minsk, 220119

  • Site: 37501

    Minsk, 223041

  • Site: 37504

    Vitebsk, 210037

Other trials in Belarus

Finland3 sites
  • Site: 35802

    Jyväskylä, 40620

  • Site: 35801

    Oulu, 90029

  • Site: 35804

    Tampere, 33521

Other trials in Finland

Georgia3 sites
  • Site: 99501

    Tbilisi, 144

  • Site: 99502

    Tbilisi, 159

  • Site: 99503

    Tbilisi, 159

Other trials in Georgia

Latvia3 sites
  • Site: 37103

    Liepāja, LV-3401

  • Site: 37102

    Riga, 1038

  • Site: 37101

    Riga, LV-1002

Other trials in Latvia

Norway3 sites
  • Site: 47002

    Hamar, 2317

  • Site: 47001

    Tønsberg, 3103

  • Site: 47005

    Trondheim, 7006

Other trials in Norway

Germany2 sites
  • Site: 49006

    Bad Ems, 56130

  • Site: 49009

    Halle, 06132

Other trials in Germany

Lebanon2 sites
  • Site: 96102

    Byblos

  • Site: 96103

    El Achrafiyé

Other trials in Lebanon

Lithuania2 sites
  • Site: 37001

    Kaunas, 50219

  • Site: 37003

    Vilnius, LT-01118

Other trials in Lithuania

Switzerland2 sites
  • Site: 41001

    Frauenfeld, 8501

  • Site: 41003

    Zurich, 8001

Other trials in Switzerland

About this study

Official title: A Double-Blind, Randomized, Parallel Group, Multi-Centre Study to Evaluate the Efficacy and Safety of Mirabegron Compared to Solifenacin in Subjects With Overactive Bladder (OAB) Treated With Antimuscarinics and Dissatisfied Due to Lack of Efficacy

The purpose of the study was to assess the efficacy, safety and tolerability of mirabegron 50 mg versus (vs) solifenacin 5 mg in the treatment of patients with OAB who were dissatisfied with their treatment due to lack of efficacy.

Being tested
Mirabegron, Solifenacin succinate
Keywords
Vesitrim, Frequency, Urgency, Urgency incontinence, Urinary incontinence, Overactive Bladder (OAB), Micturition, Mirabegron, YM178, Vesicare, Solifenacin
Medical subject headings
Urologic Diseases, Urinary Bladder, Overactive, Urinary Bladder Diseases, Urinary Incontinence

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • MirabegronDrug

    Also called Betanis, YM178, Myrbetriq, Betmiga

    oral tablet

  • Solifenacin succinateDrug

    Also called Vesicare, YM905, Vesikur, Vesitrim

    oral tablet

Study groups in NCT01638000
Study groupRoleWhat they receive
Mirabegron 50 mgExperimentalParticipants who received mirabegron 50 mg once daily for 12 weeks.
Receives: Drug: Mirabegron
Solifenacin 5 mgActive comparatorParticipants who received solifenacin 5 mg once daily for 12 weeks.
Receives: 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 Final Visit in the Mean Number of Micturitions Per 24 Hours

    A micturition is any voluntary urination (excluding incontinence only episodes). The mean number of micturitions per 24 hours were calculated from the data recorded by the participant during the 3-day micturition diary period.

    Measured: Baseline and final visit (up to Week 12)

Secondary outcomes (46)
  1. Percentage of Participants Reporting at Least One Treatment-emergent Adverse Event of Dry Mouth, Constipation or Blurred Vision During Double-blind Treatment Period

    A treatment-emergent adverse event (TEAE) was defined as an adverse event (AE; defined as any untoward medical occurrence in a patient administered a study drug) that started or worsened in the period from the first double-blind medication intake until 30 days after the last double-blind medication intake. The following TEAEs were selected for inclusion in the analysis: Dry mouth (aptyalism, dry mouth, dry throat), constipation (constipation), blurred vision (vision blurred, myopia, refraction disorder, accommodation disorder).

    Measured: From first dose of study drug up to 30 days after last dose of study drug (up to 16 weeks)

  2. Change From Baseline to 4, 8 and 12 Weeks of Treatment in Mean Number of Micturitions Per 24 Hours

    Measured: Baseline and Week 4, Week 8, Week 12

  3. Number of Incontinence Episodes at 4, 8 and 12 Weeks of Treatment and at the Final Visit

    An incontinence episode is any involuntary leakage of urine. The total number of incontinence episodes per 24 hours were calculated from the data recorded by the participant during the 3-day micturition diary period prior to each visit.

    Measured: Week 4, Week 8, Week 12

  4. Change From Baseline to 4, 8 and 12 Weeks of Treatment in Mean Number of Incontinence Episodes Per 24 Hours

    An incontinence episode is any involuntary leakage of urine. The mean number of incontinence episodes per 24 hours were calculated from the data recorded by the participant during the 3-day micturition diary period.

    Measured: Baseline and Week 4, Week 8, Week 12

  5. Number of Urgency Incontinence Episodes at 4, 8 and 12 Weeks of Treatment and at the Final Visit

    An urgency incontinence episode is any involuntary leakage of urine accompanied by or immediately proceeded by urgency. The total number of urgency incontinence episodes per 24 hours were calculated from the data recorded by the participant during the 3-day micturition diary period prior to each visit.

    Measured: Week 4, Week 8, Week 12

  6. Change From Baseline to 4, 8 and 12 Weeks of Treatment in Mean Number of Urgency Incontinence Episodes Per 24 Hours

    An urgency incontinence episode is any involuntary leakage of urine accompanied by or immediately proceeded by urgency. The mean number of urgency incontinence episodes per 24 hours were calculated from the data recorded by the participant during the 3-day micturition diary period.

    Measured: Baseline and Week 4, Week 8, Week 12

  7. Change From Baseline to 4, 8 and 12 Weeks of Treatment and at the Final Visit in Mean Number of Urgency Episodes (Grade 3 or 4) Per 24 Hours

    An urgency episode is a sudden compelling desire to pass urine immediately followed by an incontinent event or the patient having to rush to the toilet and make it in time; severity recorded as 3 (severe urgency) or 4 (urgency incontinence) on the Patient Perception of the Intensity of Urgency Scale (PPIUS) validated scale. The mean number of urgency episodes per 24 hours were calculated from the data recorded by the participant during the 3-day micturition diary period.

    Measured: Baseline and Week 4, Week 8, Week 12

  8. Change From Baseline to 4, 8 and 12 Weeks of Treatment and at the Final Visit in Mean Level of Urgency

    Urgency level was rated by the participant during the 3-day micturition diary period using the PPIUS 5-point categorical scale: 0. No urgency; 1. Mild urgency; 2. Moderate urgency; 3. Severe urgency; 4. Urgency incontinence.

    Measured: Baseline and Week 4, Week 8, Week 12

  9. Number of Pads Used at 4, 8 and 12 Weeks of Treatment and at the Final Visit

    The total number of pads per 24 hours were calculated from the data recorded by the participant during the 3-day micturition diary period prior to each visit.

    Measured: Week 4, Week 8, Week 12

  10. Change From Baseline in Mean Number of Pads Used Per 24 Hours After 4, 8 and 12 Weeks of Treatment

    The mean number of pads per 24 hours were calculated from the data recorded by the participant during the 3-day micturition diary period.

    Measured: Baseline and Week 4, Week 8 , Week 12

  11. Number of Nocturia Episodes at 4, 8 and 12 Weeks of Treatment and at the Final Visit

    A nocturia episode is defined as waking at night ≥1 times to void (i.e., any voiding associated with sleep disturbance between the time the patient goes to bed with the intention to sleep until the time the patient gets up in the morning with the intention to stay awake). The total number of nocturia episodes were calculated from the data recorded by the participant during the 3-day micturition diary period prior to each visit.

    Measured: Week 4, Week 8, Week 12

  12. Change From Baseline in Mean Number of Nocturia Episodes Per 24 Hours After 4, 8 and 12 Weeks of Treatment

    A nocturia episode is defined as waking at night ≥1 times to void (i.e., any voiding associated with sleep disturbance between the time the patient goes to bed with the intention to sleep until the time the patient gets up in the morning with the intention to stay awake). The mean number of nocturia episodes per 24 hours were calculated from the data recorded by the participant during the 3-day micturition diary period.

    Measured: Baseline and Week 4, Week 8, Week 12

  13. Percentage of Participants With Normalization of Micturitions at Weeks 4, 8, 12 and Final Visit

    A responder is defined as a participant who has ≥8 micturitions at baseline and has <8 micturitions per 24 hours during the treatment period at each specified visit, where change from baseline is <0.

    Measured: Week 4, Week 8, Week 12

  14. Percentage of Participants With 50% Reduction in Incontinence Episodes at Weeks 4, 8, 12 and Final Visit

    A responder is defined as a participant with at least 50% decrease from baseline in mean number of incontinence episodes per 24 hours during the treatment period at specified visit.

    Measured: Week 4, Week 8, Week 12

  15. Percentage of Participants With Zero Incontinence Episodes at Weeks 4, 8, 12 and Final Visit

    A responder is defined as a participant who reported incontinence episodes at baseline and reported no incontinence episodes during the treatment period at specified visit.

    Measured: Week 4, Week 8, Week 12

  16. Change From Baseline to Week 4 in Mobility Scores as Assessed by the European Quality of Life 5-Dimensions (EQ-5D-5L) Questionnaire

    The European Quality of Life 5-Dimensions Questionnaire (EQ-5D-5L) is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 4

  17. Change From Baseline to Week 4 in Self-care Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 4

  18. Change From Baseline to Week 4 in Usual Activities Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 4

  19. Change From Baseline to Week 4 in Pain/Discomfort Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 4

  20. Change From Baseline to Week 4 in Anxiety/Depression Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 4

  21. Change From Baseline to Week 8 in Mobility Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 8

  22. Change From Baseline to Week 8 in Self-care Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 8

  23. Change From Baseline to Week 8 in Usual Activities Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 8

  24. Change From Baseline to Week 8 in Pain/Discomfort Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 8

  25. Change From Baseline to Week 8 in Anxiety/Depression Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 8

  26. Change From Baseline to Week 12 in Mobility Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 12

  27. Change From Baseline to Week 12 in Self-care Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 12

  28. Change From Baseline to Week 12 in Usual Activities Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 12

  29. Change From Baseline to Week 12 in Pain/Discomfort Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 12

  30. Change From Baseline to Week 12 in Anxiety/Depression Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and Week 12

  31. Change From Baseline to Final Visit in Mobility Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and final visit (up to Week 12)

  32. Change From Baseline to Final Visit in Self-care Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and final visit (up to Week 12)

  33. Change From Baseline to Final Visit in Usual Activities Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and final visit (up to Week 12)

  34. Change From Baseline to Final Visit in Pain/Discomfort Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and final visit (up to Week 12)

  35. Change From Baseline to Final Visit in Anxiety/Depression Scores as Assessed by the EQ-5D-5L Questionnaire

    The EQ-5D-5L is a standardized nondisease specific (i.e., generic) instrument for use as a measure of health outcome. It has 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Each dimension has 5 response levels (e.g., no problems with performing activity, slight problems, moderate problems, severe problems, unable to perform [extreme problems]).

    Measured: Baseline and final visit (up to Week 12)

  36. Change From Baseline to Weeks 4, 8, 12, and at the Final Visit in Symptom Bother Score as Assessed by the Overactive Bladder Questionnaire (OAB-q)

    The Overactive Bladder Questionnaire (OAB-q) is a self-reported questionnaire with items relating to symptom bother and health-related quality of life (HRQoL). The symptom bother portion consists of 8 items, scored from 1 to 6. The total symptom bother score was calculated from the 8 answers and then transformed to range from 0 (least severity) to 100 (worst severity). A negative change from baseline indicates an improvement.

    Measured: Baseline and Week 4, Week 8, Week 12

  37. Change From Baseline to Weeks 4, 8, 12, and at the Final Visit in Total Health-Related Quality of Life (HRQoL) Score as Assessed by the OAB-q

    The OAB-q is a self-reported questionnaire with items relating to Symptom Bother and health-related quality of life (HRQoL). The HRQoL portion consists of an 25-item HRQoL subscale containing the following domains scored from 1 to 6: coping, concern, sleep, social interaction). The total score is calculated by adding the 4 HRQoL subscale scores and transforming to a scale from 0 to 100, with higher scores indicating better quality of life. A positive change from baseline indicates an improvement.

    Measured: Baseline and Week 4, Week 8, Week 12

  38. Change From Baseline to Weeks 4, 8, 12, and at the Final Visit in Patient Perception of Bladder Condition (PPBC)

    The Patient Perception of Bladder Condition (PPBC) questionnaire is a single-item questionnare used to assess participants' perceptions and impressions of their bladder condition. Participants assessed their bladder condition using a 6-point categorical scale: 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; 6. Causes me many severe problems.

    Measured: Baseline and Week 4, Week 8, Week 12

  39. Change From Baseline to Week 12 and the Final Visit in the Patient's Assessment of Treatment Satisfaction (TS)-Visual Analog Scale (VAS)

    The Treatment Satisfaction (TS)-Visual Analogue Scale (VAS) was a self-rated scale with the participant answering the question "Are you satisfied with your treatment?" and placing a vertical mark on a line from 0 (No, not at all) to 10 (Yes, completely).

    Measured: Baseline and Week 12

  40. Change From Baseline to Week 12 and the Final Visit in the Patient's Assessment of Treatment Satisfaction Questionnaire-Likert Scale

    The Treatment Satisfaction (TS)-Likert Scale was a self-rated scale with the participant answering the question "How satisfied were you with your treatment?" with on a scale from 1 (extremely dissatisfied) to 7 (extremely satisfied).

    Measured: Baseline and Week 12

  41. Percentage of Participants With Improvement in Symptom Bother Score as Assessed by the OAB-q: ≥ 10 Points Improvement in OAB-q at Week 12 and Final Visit

    A responder is defined as a participant with ≥10 points improvement in symptom bother from baseline.

    Measured: Baseline to Week 12

  42. Percentage of Participants With Improvement in HRQoL Scales as Assessed by the OAB-q: ≥10 Points Improvement in OAB-q at Week 12 and Final Visit

    A responder is defined as a participant with >=10 points improvement in the total HRQL score from baseline.

    Measured: Baseline to Week 12

  43. Percentage of Participants With Improvement of Treatment Satisfaction Questionnaire - Likert Scale: ≥1, ≥2, ≥3, ≥4, ≥5, and 6-point Improvement From Baseline to Week 12

    A responder is defined as a participant with ≥1, ≥2, ≥3, ≥4, ≥5 or 6-point improvement from baseline in TS-Likert scale.

    Measured: Baseline to Week 12

  44. Percentage of Participants With Improvement in Treatment Satisfaction Questionnaire - Likert Scale: ≥1, ≥2, ≥3, ≥4, ≥5, and 6-point Improvement From Baseline to Final Visit

    A responder is defined as a participant with >=1 or >=2 or >=3 or >=4 or >=5 or 6-point improvement from baseline in TS-Likert scale.

    Measured: Baseline to final visit (up to Week 12)

  45. Percentage of Participants With Improvement in PPBC: ≥1 Point Improvement at Week 12 and Final Visit

    A responder is defined as a participant with ≥1 point improvement in PPBC from baseline.

    Measured: Baseline to Week 12

  46. Percentage of Participants With Major Improvement in PPBC: ≥2 Point Improvement at Week 12 and Final Visit

    A responder is defined as a participant with ≥2 point improvement in PPBC from baseline.

    Measured: Baseline to 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 posted11 Jul 2012 (estimated)
  2. Study start12 Jun 2012
  3. Primary completion24 Apr 2013
  4. Study completion24 Apr 2013

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 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
1,887 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01638000
Sponsor's protocol ID
178-EC-001
Other IDs
2011-005713-37
Acronym
BEYOND
Status last verified
Oct 2024
First submitted
9 Jul 2012
Last updated
21 Nov 2024
Data monitoring committee
No
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/.

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Mirabegron and Solifenacin succinate in people with Urologic Diseases and Urinary Bladder, Overactive, run by Astellas Pharma Europe Ltd. at 217 sites in 33 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 3 inclusion and 18 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 21 Nov 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 217 sites in United Kingdom, France, Russia, Spain, Canada and 28 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. 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 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

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 30 Aug 2016). 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 Final Visit in the Mean Number of Micturitions Per 24 Hours (time frame: Baseline and final visit (up to Week 12)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 21 Nov 2024.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in