Urinary Bladder, OveractivePhase 3TAURUSNCT00688688
Study to Test the Long Term Safety and Efficacy of the Beta-3 Agonist Mirabegron (YM178) in Patients With Symptoms of Overactive Bladder
A Phase 3 study testing Mirabegron and Tolterodine in people with Urinary Bladder, Overactive, run by Astellas Pharma Inc at 308 sites in 30 countries.
Trial summary
The study is intended to test the safety, tolerability, efficacy of two doses of long term once daily (qd) treatment of Mirabegron in patients with symptoms of overactive bladder and secondly to compare these with active comparator. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Urinary Bladder, Overactive
- What is being tested?
- Mirabegron and Tolterodine
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 2,792 participants
- Where
- 308 sitesin 30 countries
- Study dates
- 25 Apr 2008to 6 May 2010
- 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
- Patient is willing and able to complete the micturition diary and questionnaires correctly
- Patient has symptoms of overactive bladder for ≥ 3 months
- Patient experiences frequency of micturition on average ≥ 8 times per 24-hour period during the 3-day micturition diary period
- Patient must experience at least 3 episodes of urgency (grade 3 or 4) with or without incontinence, during the 3-day micturition diary period
Who cannot join
- Patient is breastfeeding, pregnant, intends to become pregnant during the study, or of childbearing potential, sexually active and not practicing a highly reliable method of birth control
- Patient has significant stress incontinence or mixed stress/urge incontinence where stress is the predominant factor
- Patient has an indwelling catheter or practices intermittent self-catheterization
- Patient has diabetic neuropathy
- Patient 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
- Patient receives non-drug treatment including electro-stimulation therapy
Show all 12Show fewer
- Patient has severe hypertension
- Patient has a known or suspected hypersensitivity to tolterodine, other anticholinergics, YM178, other beta-adrenoreceptor (ß-AR) agonists, or lactose or any of the other inactive ingredients
- Patient has been treated with any investigational drug or device within 30 days (90 days in the UK for all clinical studies except 178-CL-046)
- Patient had an average total daily urine volume > 3000 mL as recorded in the 3-day micturition diary period
- Patient has serum creatinine >150 umol/L, aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) > 2x upper limit of normal range (ULN), or gamma-glutamyl transpeptidase (γ-GT) > 3x ULN
- Patient has a clinically significant abnormal electrocardiogram (ECG)
Trial locations and contacts
308 sites in 30 countries.
308 sites in 30 countries
United States106 sites
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Albany, New York, 12205
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Albany, New York, 12208
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Albuquerque, New Mexico, 87109
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Anchorage, Alaska, 99508
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Arlington, Texas, 76017
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Atherton, California, 94027
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Atlanta, Georgia, 30328
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Aurora, Colorado, 80012
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Austin, Texas, 78759
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Aventura, Florida, 33180
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Bala-Cynwyd, Pennsylvania, 19004
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Bethany, Oklahoma, 73008
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Beverly Hills, California, 90211
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Billings, Montana, 59102
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Bristol, Tennessee, 37620
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Buena Park, California, 90620
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Cary, North Carolina, 27518
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Charlotte, North Carolina, 28209
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Cincinnati, Ohio, 45212
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Clearwater, Florida, 33756
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Clearwater, Florida, 33761
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Cleveland, Ohio, 44122
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Coeur d'Alene, Idaho, 83814
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Columbus, Ohio, 43214
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Concord, North Carolina, 28025
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Corpus Christi, Texas, 78414
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Dallas, Texas, 75231
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Decatur, Georgia, 30034
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Denver, Colorado, 80211
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Denver, Colorado, 80218
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Des Moines, Iowa, 50309
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Edmond, Oklahoma, 73008
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Edmond, Oklahoma, 73034
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Endwell, New York, 13760
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Englewood, Colorado, 80112
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Fargo, North Dakota, 58104
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Fort Myers, Florida, 33916
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Fort Wayne, Indiana, 46825
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Fresno, California, 93720
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Garden City, New York, 11530
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Greenbelt, Maryland, 20770
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Greer, South Carolina, 29650
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Homewood, Alabama, 35209
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Houston, Texas, 77024
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Huntsville, Alabama, 35801
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Idaho Falls, Idaho, 83404
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Jeffersonville, Indiana, 47130
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Jenkintown, Pennsylvania, 19046
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Kingston, New York, 12401
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La Mesa, California, 91942
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Lancaster, Pennsylvania, 17604
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Las Vegas, Nevada, 89148
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Lincoln, Nebraska, 68516
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Lyndhurst, Ohio, 44124
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Marietta, Georgia, 30060
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Melrose Park, Illinois, 60160
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Miami, Florida, 33136
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Mission Hills, California, 91345
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Mobile, Alabama, 36608
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Montgomery, Alabama, 36117
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Mountlake Terrace, Washington, 98043
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Mt. Pleasant, South Carolina, 29464
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New Britain, Connecticut, 06052
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New Brunswick, New Jersey, 08901
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New York, New York, 10016
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Newburgh, Indiana, 47630
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Newport Beach, California, 92660
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North Kansas City, Missouri, 64116
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Ocala, Florida, 34471
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Omaha, Nebraska, 68114
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Orange, California, 92869
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Orlando, Florida, 32803
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Pembroke Pines, Florida, 33024
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Pembroke Pines, Florida, 33027
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Phoenix, Arizona, 85051
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Poughkeepsie, New York, 12601
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Reading, Pennsylvania, 19611
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Roswell, Georgia, 30076
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Sacramento, California, 95831
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Salt Lake City, Utah, 84107
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San Bernardino, California, 92404
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San Diego, California, 92108
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San Diego, California, 92120
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Sarasota, Florida, 34237
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Seattle, Washington, 98166
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Simpsonville, South Carolina, 29681
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Spokane, Washington, 99204
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Tacoma, Washington, 98405
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Tallahassee, Florida, 32308
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Tampa, Florida, 33606
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Tarzana, California, 91356
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Torrance, California, 90505
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Tucson, Arizona, 85712
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Tucson, Arizona, 85741
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Uniontown, Pennsylvania, 15401
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Virginia Beach, Virginia, 23454
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Wadsworth, Ohio, 44281
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Warwick, Rhode Island, 02886
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Waterbury, Connecticut, 06708
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Watertown, Massachusetts, 02472
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Wellington, Florida, 33414
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West Orange, New Jersey, 07052
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West Palm Beach, Florida, 33407
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Wichita, Kansas, 57207
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Wilmington, North Carolina, 28401
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Winston-Salem, North Carolina, 27103
Germany24 sites
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Aichach, 86551
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Bad Ems, 56130
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Bautzen, 02625
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Berlin, 13347
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Duisburg, 47051
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Eisleben Lutherstadt, 06295
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Frankfurt, 65933
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Ganderkesee, 27777
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Hagenow, 19230
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Halle, 06132
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Hamburg, 20253
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Henningsdorf, 16761
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Hettstedt, 06333
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Kiel
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Koblenz, 56068
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Leipzig, 04105
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Muenchen-Bogenhausen, 81925
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Munich
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Neustadt in Sachsen, 01844
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Oranienburg, 16151
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Radebeul, 01445
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Sangerhausen, 06526
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Trier, 54290
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Uetersen, 25436
Canada23 sites
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Barrie, Ontario, L4M 7G1
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Brampton, Ontario, L6T 4S5
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Calgary, Alberta, T2V 4R6
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Dartmouth, Nova Scotia, B2W 2S7
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Edmonton, Alberta, T5H 3V9
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Granby, Quebec, J2G 8Z9
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Kentville, Nova Scotia, B4N 4K9
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Kitchener, Ontario, N2N 2B9
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Markham, Ontario, L6B 1A1
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Montreal, Quebec, H3A 1A1
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Montreal
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Newmarket, Ontario, L3X 1W1
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North Bay, Ontario, P1B 7K8
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Oshawa, Ontario, L1H 1B9
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Point Claire, Quebec, H9R 4S3
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Saint Denis, Ontario, H2X 3J4
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Saint John, New Brunswick, E2L 3J8
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Surrey, British Columbia, V3V 1N1
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Thunder Bay, Ontario, P7E 6E7
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Toronto, Ontario, M4N 3M5
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Toronto, Ontario, M5T 2S8
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Victoria, British Columbia, V8T 5G1
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Victoria, British Columbia, V8V 3N1
United Kingdom13 sites
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Bristol, B15 2TG
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Chorley, PR7 7NA
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Croydon, CR7 7YE
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Liverpool, L22 OLG
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London, SE5 9RS
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London, W2 2YP
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Manchester, M15 6SX
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Newcastle upon Tyne, NE7 7DN
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Northwood, HA6 2RN
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Reading, RG1 5AN
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Reading, RG2 7AG
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Sheffield, S10 2JF
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Swansea, SA6 6NL
Russia12 sites
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Moscow, 101000
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Moscow, 105425
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Moscow, 111020
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Moscow, 111123
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Moscow, 117049
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Moscow, 117815
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Moscow, 119435
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Moscow, 123836
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Moscow, 125206
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Saint Petersburg, 115516
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Saint Petersburg, 197089
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Saint Petersburg, 198013
Spain11 sites
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Barcelona, 08020
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Barcelona, 08036
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Bilbao, 48013
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Getafe, 28905
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Madrid, 28016
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Madrid, 28046
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Mataró, 8304
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Miranda de Ebro, 09200
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Seville, 41013
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Toledo, 45071
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Valencia, 46010
Czechia10 sites
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Brno, 60200
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Mělník, 27601
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Olomouc, 77200
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Ostrava-Poruba, 70853
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Pilsen, 30599
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Prague, 12851
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Prague, 14056
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Prague, 18081
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Štětí, 41108
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Ústí nad Labem, 40001
France10 sites
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Colmar, 68024
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Marseille, 13274
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Mulhouse, 68070
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Nîmes, 30029
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Orléans, 45067
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Paris, Cedex 10, 75020
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Paris-Cedex12, 75571
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Saint-Priest-en-Jarez, 42055
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Strasbourg, 67000
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Toulouse, 31059
Italy10 sites
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Bari, 70124
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Catanzaro, 88100
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Genoa, 16128
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Latina, 04100
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Milan, 20142
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Modena, 41100
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Naples, 80131
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Perugia, 06122
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Treviglio, 24047
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Varese, 21100
Belgium9 sites
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Antwerp, 2020
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Antwerp, 2030
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Edegem, 2650
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Ghent, 9000
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Kortrijk, 8500
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Leper, 8900
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Leuven, 3000
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Liège, 4000
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Sint-Truiden, 3800
Netherlands9 sites
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Amsterdam, 1105 AZ
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Apeldoorn, 7334 DZ
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Eindhoven, 5623 EJ
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Enschede, 7511 JX
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Leiden, 2334 CK
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Nijmegen, 6532 SZ
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Sneek, 8600 BA
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Tilburg, 5022 GC
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Winterswijk, 7101 BN
Poland9 sites
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Bialystok, 15-278
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Lodz, 93-338
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Lodz, 93-513
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Lublin, 20-954
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Warsaw, 00-846
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Warsaw, 02-005
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Warsaw, 02-507
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Warsaw
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Wroclaw, 50-556
Hungary8 sites
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Budapest, 1047
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Budapest, 1076
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Nyíregyháza, 4400
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Sopron
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Szeged, 6725
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Székesfehérvár, 8000
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Szekszárd, 7100
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Tatabánya, 2800
Sweden8 sites
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Huddinge, 75185
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Örebro, 70185
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Skövde, 54130
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Sonkoping, 11883
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Stockholm, 14186
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Stockholm, 17176
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Stockholm, 18288
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Umeå, 90185
Norway5 sites
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Bergen, 5021
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Drammen, 3016
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Hamar, 2317
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Oslo, 0257
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Tønsberg, 3103
Slovakia5 sites
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Martin, 03659
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Poprad, 05801
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Skalica, 90982
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Trenčín, 91101
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Žilina, 01207
South Africa5 sites
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Hatfield
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Lyttelton
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Paarl
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Pietermaritzburg
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Roodepoort
Denmark4 sites
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Aalborg, 9100
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Aarhus, 8200
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Glostrup Municipality, 2600
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Roskilde
Finland4 sites
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Helsinki, 00029
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Oulu, 90220
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Tampere, 33521
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Turku, 20100
Romania4 sites
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Bucharest, 22328
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Bucharest
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Lasi
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Oradea
Austria3 sites
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Graz, 8036
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Innsbruck, 6020
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Linz, 4020
Portugal3 sites
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Amadora, 2700
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Porto, 4099-005
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Tomar, 2304-909
About this study
Official title: A Randomized, Double-Blind, Parallel Group, Active Controlled, Multi-center Long-term Study to Assess the Safety and Efficacy of the Beta-3 Agonist Mirabegron (YM178) 50 mg qd and 100 mg qd in Subjects With Symptoms of Overactive Bladder
The study is intended to test the safety, tolerability, efficacy of two doses of long term once daily (qd) treatment of Mirabegron in patients with symptoms of overactive bladder and secondly to compare these with active comparator.
Read the detailed description
Patients who completed 178-CL-046 (NCT00689104) or 178-CL-047 (NCT00662909) or new patients could be enrolled in this study if eligible.
- Conditions
- Urinary Bladder, Overactive
- Being tested
- Mirabegron, Tolterodine, Placebo to Mirabegron, Placebo to Tolterodine
- Keywords
- Frequency, Overactive Bladder, Urgency, Urinary urge incontinence, Urinary incontinence, Micturition
- Medical subject headings
- Urinary Bladder, Overactive, Urinary Incontinence, Urge, Urinary Incontinence
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
MirabegronDrug
Also called Myrbetriq, YM178
Tablets
TolterodineDrug
Extended release capsules
Placebo to MirabegronDrug
Matching mirabegron placebo tablets.
Placebo to TolterodineDrug
Matching tolterodine placebo capsules.
| Study group | Role | What they receive |
|---|---|---|
| Mirabegron 50 mg | Experimental | Participants received mirabegron 50 mg tablets and matching tolterodine extended release (ER) placebo capsules orally once a day for 12 months. Receives: Drug: Mirabegron; Drug: Placebo to Tolterodine |
| Mirabegron 100 mg | Experimental | Participants received mirabegron 100 mg tablets and matching tolterodine ER placebo capsules orally once a day for 12 months. Receives: Drug: Mirabegron; Drug: Placebo to Tolterodine |
| Tolterodine ER 4 mg | Active comparator | Participants received tolterodine ER 4 mg capsules and matching mirabegron placebo tablets orally once a day for 12 months. Receives: Drug: Tolterodine; Drug: Placebo to Mirabegron |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of Participants With and Severity of Treatment-emergent Adverse Events (TEAEs)
An adverse event (AE) was defined as any untoward medical occurrence in a patient administered a study drug and which did not necessarily have a causal relationship with the treatment. The investigator assessed the severity of each AE, including abnormal laboratory values, as follows:
Mild: No disruption of normal daily activities; Moderate: Affected normal daily activities; Severe: Inability to perform daily activities.
Measured: From the first dose of double-blind study drug up until 30 days after the last dose of study drug, up to 13 months.
Secondary outcomes (27)
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Mean Number of Micturitions Per 24 Hours
The average number of micturitions (urinations) per 24 hours was derived from the number of times a patient urinates (excluding incontinence only episodes) per day recorded by the patient in a micturition diary for 3-days prior to clinic visits at Baseline and months 1, 3, 6, 9 and 12/end of treatment. Least squares (LS) means were generated from the analysis of covariance (ANCOVA) model with treatment group, previous study history, gender and geographical regions as fixed factors and baseline as a covariate.
Measured: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final 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 patient in a micturition diary for 3-days prior to clinic visits at Baseline and months 1, 3, 6, 9 and 12/end of treatment. Least squares (LS) means were generated from the analysis of covariance (ANCOVA) model with treatment group, previous study history, gender and geographical regions as fixed factors and baseline as a covariate.
Measured: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Mean Volume Voided Per Micturition
The average volume voided per micturition was calculated from the volume of each micturition measured by the patient and recorded in a micturition diary for 3 days prior to clinic visits at Baseline and months 1, 3, 6, 9 and 12/end of treatment. LS means were generated from the ANCOVA model with treatment group, previous study history, gender and geographical regions as fixed factors and baseline as a covariate.
Measured: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Mean Number of Urgency Incontinence Episodes Per 24 Hours
The involuntary leakage of urine accompanied or immediately proceeded by urgency, derived from the number of incontinence episodes classified by the patient in a 3-day micturition diary as 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 time; 3=Severe urgency, could not postpone voiding; 4=Urge incontinence, leaked before arriving to toilet. LS means are from the ANCOVA model with treatment group, previous study history, gender and geographical regions as fixed factors and baseline as a covariate.
Measured: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final 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 that is difficult to defer) derived from episodes classified by the patient in a 3-day micturition diary as 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 time; 3=Severe urgency, could not delay voiding; 4=Urge incontinence, leaked before arriving to the toilet. LS means are from an ANCOVA model with treatment group, previous study history, gender \& geographical regions as fixed factors and baseline as a covariate.
Measured: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Mean Level of Urgency
Average of patients' ratings on the degree of urgency associated with each micturition and/or incontinence episode recorded in a 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. LS means are generated from an ANCOVA model with treatment group, previous study history, gender \& geographical regions as fixed factors and baseline as a covariate.
Measured: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in the Mean Number of Pads Used Per 24 Hours
The average number of times a patient records a new pad used per day during the 3-day micturition diary period.
LS means are from an ANCOVA model with treatment group, previous study history, gender \& geographical regions as fixed factors and baseline as a covariate.
Measured: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final 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 patient urinated (excluding incontinence only episodes) during sleeping time per day was derived from the 3-day patient micturition diary.
LS means are from an ANCOVA model with treatment group, previous study history, gender \& geographical regions as fixed factors and baseline as a covariate.
Measured: Baseline and Months 1, 3, 6, 9 and 12
Percentage of Participants With Zero Incontinence Episodes at Months 1, 3, 6, 9 and 12 and the Final Visit
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 patient.
Measured: Months 1, 3, 6, 9 and 12
Percentage of Participants With ≥ 50% Reduction in Incontinence Episodes at Months 1, 3, 6, 9 and 12 and the Final Visit
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 patient micturition diary.
Measured: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Symptom Bother Score
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 patient 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.
LS means are from an ANCOVA model with treatment group, previous study history, gender \& geographical regions as fixed factors and baseline as a covariate.
Measured: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit 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.
LS means are from an ANCOVA model with treatment group, previous study history, gender \& geographical regions as fixed factors and baseline as a covariate.
Measured: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Month 12 and Final Visit 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.
LS means are from an ANCOVA model with treatment group, previous study history, gender \& geographical regions as fixed factors and baseline as a covariate.
Measured: Baseline and Month 12
Change From Baseline to Month 12 and Final Visit in Treatment Satisfaction-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. LS means are from an ANCOVA model with treatment group, previous study history, gender \& geographical regions as fixed factors and baseline as a covariate.
Measured: Baseline and Month 12
Change From Baseline to Months 3, 6, 12 and Final Visit in Work Productivity and Activity Impairment (WPAI): Percent Work Time Missed
The Work Productivity and Activity Impairment: Specific Health Problem (WPAI:SHP) questionnaire was used to assess the degree and extent to which overactive bladder (OAB) symptoms interfered with work productivity in the last 7 days. Percent of work time missed is derived from the number of hours of work missed due to OAB symptoms as a percentage of total hours that should have been worked. A higher percentage indicates more hours missed. A negative change from baseline indicates improvement.
Measured: Baseline and Months 3, 6 and 12
Change From Baseline to Months 3, 6, 12 and Final Visit in Work Productivity and Activity Impairment (WPAI): Percent Impairment While Working
The Work Productivity and Activity Impairment: Specific Health Problem (WPAI:SHP) questionnaire was used to assess the degree and extent to which overactive bladder (OAB) symptoms interfered with work productivity in the last 7 days. Percent impairment while working was derived from the patient's assessment of the degree to which OAB affected their productivity while working. A higher percentage indicates greater impairment and less productivity. A negative change from baseline indicates improvement.
Measured: Baseline and Months 3, 6 and 12
Change From Baseline to Months 3, 6, 12 and Final Visit in Work Productivity and Activity Impairment (WPAI): Percent Overall Work Impairment
The Work Productivity and Activity Impairment: Specific Health Problem (WPAI:SHP) questionnaire was used to assess the degree and extent to which overactive bladder (OAB) symptoms interfered with work productivity in the last 7 days. Percent overall work impairment takes into account both hours missed due to OAB symptoms and the patient's assessment of the degree to which OAB affected their productivity while working. A higher percentage indicates greater impairment and less productivity. A negative change from baseline indicates improvement.
Measured: Baseline and Months 3, 6 and 12
Change From Baseline to Months 3, 6, 12 and Final Visit in Work Productivity and Activity Impairment (WPAI): Percent Activity Impairment
The Work Productivity and Activity Impairment: Specific Health Problem (WPAI:SHP) questionnaire was used to assess the degree and extent to which overactive bladder (OAB) symptoms interfered with daily activities over the last 7 days. Percent activity impairment is derived from the patient's assessment of the degree to which OAB affected their regular daily activities. A higher percentage indicates greater impairment and less productivity. A negative change from baseline indicates improvement.
Measured: Baseline and Months 3, 6 and 12
Change From Baseline to Final Visit 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 evaluating 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 Final Visit health status and reports the number of patients in that category. Missing data indicates patients with no data available for that Visit.
Measured: Baseline and Month 12
Change From Baseline to Final Visit 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 evaluating 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 Final Visit health status and reports the number of patients in that category. Missing data indicates patients with no data available for that Visit.
Measured: Baseline and Month 12
Change From Baseline to Final Visit 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 Final Visit health status and reports the number of patients in that category. Missing data indicates patients with no data available at that Visit.
Measured: Baseline and Month 12
Change From Baseline to Final Visit 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 evaluating 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 Final Visit health status and reports the number of patients in that category. Missing data indicates patients with no data available for that Visit.
Measured: Baseline and Month 12
Change From Baseline to Final Visit 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 Final Visit health status and reports the number of patients in that category. Missing data indicates patients with no data available for that Visit.
Measured: Baseline and Month 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in the 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 Months 1, 3, 6, 9 and 12
Change From Baseline to Months 3, 6, 12 and Final Visit in Number of Non-study Related Visits to Physician
The number of times the patient visited a physician's office during the 4 weeks prior to each study visit (excluding study visits) because of the patient's bladder condition.
Measured: Baseline and Months 3, 6 and 12
Percentage of Participants With Improvement 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'. Improvement was defined as at least a one point improvement from Baseline to post-baseline and a major improvement was defined as at least a two point improvement from Baseline to post-baseline in PPBC score.
Measured: Baseline and Month 12
Safety as Assessed by Adverse Events (AEs), Vital Signs, Laboratory Tests, Physical Examination and Electrocardiogram
An abnormality identified during a medical test was defined as an AE if the abnormality induced clinical signs or symptoms, required active intervention, interruption or discontinuation of study drug or was clinically significant. The Investigator assessed each AE for causal relationship (not related, possible or probable) to study drug. A serious AE (SAE) was any untoward medical occurrence that: resulted in death, was life-threatening, resulted in significant disability/incapacity or congenital anomaly/birth defect, required or prolonged hospitalization or was a medically important event.
The data reported represent the number of participants with adverse events in each category.
Measured: From the first dose of double-blind study drug up until 30 days after the last dose of study drug, up to 13 months.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Jun 2008 (estimated)
- Study start25 Apr 2008
- Primary completion6 May 2010
- Study completion6 May 2010
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 (1)Papers the sponsor has linked to this study.
- Other trials for Urinary Bladder, OveractiveStudies 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 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 2,792 participants (actual)
Sponsor and investigators
- Lead sponsor
- Astellas Pharma Inc
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Central Contact, Study director, Astellas Pharma Europe B.V.
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00688688
- Sponsor's protocol ID
- 178-CL-049
- Other IDs
- 2007-001452-39
- Acronym
- TAURUS
- Status last verified
- Oct 2024
- First submitted
- 29 May 2008
- Last updated
- 20 Nov 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
Chapple CR, Kaplan SA, Mitcheson D, Klecka J, Cummings J, Drogendijk T, Dorrepaal C, Martin N. Randomized double-blind, active-controlled phase 3 study to assess 12-month safety and efficacy of mirabegron, a beta(3)-adrenoceptor agonist, in overactive bladder. Eur Urol. 2013 Feb;63(2):296-305. doi: 10.1016/j.eururo.2012.10.048. Epub 2012 Nov 6.
PubMed 23195283
Study at a glance
From the registry record, last updated by the sponsor on 20 Nov 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized, Double-Blind, Parallel Group, Active Controlled, Multi-center Long-term Study to Assess the Safety and Efficacy of the Beta-3 Agonist Mirabegron (YM178) 50 mg qd and 100 mg qd in Subjects With Symptoms of Overactive Bladder
- ClinicalTrials.gov ID
- NCT00688688
- Acronym / sponsor ID
- TAURUS / 178-CL-049
- Conditions
- Urinary Bladder, Overactive
- Keywords
- Frequency, Overactive Bladder, Urgency, Urinary urge incontinence, Urinary incontinence, Micturition
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 2,792 participants (actual)
- Lead sponsor
- Astellas Pharma IncIndustry (pharma, biotech, devices)
- Study start
- 25 Apr 2008 (actual)
- Primary completion
- 6 May 2010 (actual)
- Study completion
- 6 May 2010 (actual)
- First posted
- 3 Jun 2008 (estimated)
- Results
- Posted 19 Oct 2012
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The study is intended to test the safety, tolerability, efficacy of two doses of long term once daily (qd) treatment of Mirabegron in patients with symptoms of overactive bladder and secondly to compare these with active comparator.
Detailed description
Patients who completed 178-CL-046 (NCT00689104) or 178-CL-047 (NCT00662909) or new patients could be enrolled in this study if eligible.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Mirabegron 50 mg | Experimental | Drug: Mirabegron, Drug: Placebo to TolterodineParticipants received mirabegron 50 mg tablets and matching tolterodine extended release (ER) placebo capsules orally once a day for 12 months. |
| Mirabegron 100 mg | Experimental | Drug: Mirabegron, Drug: Placebo to TolterodineParticipants received mirabegron 100 mg tablets and matching tolterodine ER placebo capsules orally once a day for 12 months. |
| Tolterodine ER 4 mg | Active comparator | Drug: Tolterodine, Drug: Placebo to MirabegronParticipants received tolterodine ER 4 mg capsules and matching mirabegron placebo tablets orally once a day for 12 months. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Patient is willing and able to complete the micturition diary and questionnaires correctly
- Patient has symptoms of overactive bladder for ≥ 3 months
- Patient experiences frequency of micturition on average ≥ 8 times per 24-hour period during the 3-day micturition diary period
- Patient must experience at least 3 episodes of urgency (grade 3 or 4) with or without incontinence, during the 3-day micturition diary period
Key exclusion criteria (12 listed)
- Patient is breastfeeding, pregnant, intends to become pregnant during the study, or of childbearing potential, sexually active and not practicing a highly reliable method of birth control
- Patient has significant stress incontinence or mixed stress/urge incontinence where stress is the predominant factor
- Patient has an indwelling catheter or practices intermittent self-catheterization
- Patient has diabetic neuropathy
- Patient 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
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: Myrbetriq, YM178Tablets | Drug | Mirabegron 100 mg, Mirabegron 50 mg |
| TolterodineExtended release capsules | Drug | Tolterodine ER 4 mg |
| Placebo to MirabegronMatching mirabegron placebo tablets. | Drug | Tolterodine ER 4 mg |
| Placebo to TolterodineMatching tolterodine placebo capsules. | Drug | Mirabegron 100 mg, Mirabegron 50 mg |
Primary outcome
Number of Participants With and Severity of Treatment-emergent Adverse Events (TEAEs)
Time frame: From the first dose of double-blind study drug up until 30 days after the last dose of study drug, up to 13 months.
An adverse event (AE) was defined as any untoward medical occurrence in a patient administered a study drug and which did not necessarily have a causal relationship with the treatment. The investigator assessed the severity of each AE, including abnormal laboratory values, as follows: Mild: No disruption of normal daily activities; Moderate: Affected normal daily activities; Severe: Inability to perform daily activities.
27 secondary outcomes
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Mean Number of Micturitions Per 24 Hours
Time frame: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Mean Number of Incontinence Episodes Per 24 Hours
Time frame: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Mean Volume Voided Per Micturition
Time frame: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Mean Number of Urgency Incontinence Episodes Per 24 Hours
Time frame: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Mean Number of Urgency Episodes (Grade 3 and/or 4) Per 24 Hours
Time frame: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Mean Level of Urgency
Time frame: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in the Mean Number of Pads Used Per 24 Hours
Time frame: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Mean Number of Nocturia Episodes Per 24 Hours
Time frame: Baseline and Months 1, 3, 6, 9 and 12
Percentage of Participants With Zero Incontinence Episodes at Months 1, 3, 6, 9 and 12 and the Final Visit
Time frame: Months 1, 3, 6, 9 and 12
Percentage of Participants With ≥ 50% Reduction in Incontinence Episodes at Months 1, 3, 6, 9 and 12 and the Final Visit
Time frame: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Symptom Bother Score
Time frame: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in Health-related Quality of Life (HRQL) Total Score
Time frame: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Month 12 and Final Visit in Patient Perception of Bladder Condition (PPBC)
Time frame: Baseline and Month 12
Change From Baseline to Month 12 and Final Visit in Treatment Satisfaction-visual Analog Scale (TS-VAS)
Time frame: Baseline and Month 12
Change From Baseline to Months 3, 6, 12 and Final Visit in Work Productivity and Activity Impairment (WPAI): Percent Work Time Missed
Time frame: Baseline and Months 3, 6 and 12
Change From Baseline to Months 3, 6, 12 and Final Visit in Work Productivity and Activity Impairment (WPAI): Percent Impairment While Working
Time frame: Baseline and Months 3, 6 and 12
Change From Baseline to Months 3, 6, 12 and Final Visit in Work Productivity and Activity Impairment (WPAI): Percent Overall Work Impairment
Time frame: Baseline and Months 3, 6 and 12
Change From Baseline to Months 3, 6, 12 and Final Visit in Work Productivity and Activity Impairment (WPAI): Percent Activity Impairment
Time frame: Baseline and Months 3, 6 and 12
Change From Baseline to Final Visit in European Quality of Life-5 Dimensions (EQ-5D) Mobility Score
Time frame: Baseline and Month 12
Change From Baseline to Final Visit in European Quality of Life-5 Dimensions (EQ-5D) Self-Care Score
Time frame: Baseline and Month 12
Change From Baseline to Final Visit in European Quality of Life-5 Dimensions (EQ-5D) Usual Activities Score
Time frame: Baseline and Month 12
Change From Baseline to Final Visit in European Quality of Life-5 Dimensions (EQ-5D) Pain/Discomfort Score
Time frame: Baseline and Month 12
Change From Baseline to Final Visit in European Quality of Life-5 Dimensions (EQ-5D) Anxiety/Depression Score
Time frame: Baseline and Month 12
Change From Baseline to Months 1, 3, 6, 9, 12 and Final Visit in the European Quality of Life-5 Dimensions (EQ-5D) Visual Analog Scale (VAS)
Time frame: Baseline and Months 1, 3, 6, 9 and 12
Change From Baseline to Months 3, 6, 12 and Final Visit in Number of Non-study Related Visits to Physician
Time frame: Baseline and Months 3, 6 and 12
Percentage of Participants With Improvement in Patient Perception of Bladder Condition (PPBC)
Time frame: Baseline and Month 12
Safety as Assessed by Adverse Events (AEs), Vital Signs, Laboratory Tests, Physical Examination and Electrocardiogram
Time frame: From the first dose of double-blind study drug up until 30 days after the last dose of study drug, up to 13 months.
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Nov 2024.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Background: PubMed 23195283Chapple CR, Kaplan SA, Mitcheson D, Klecka J, Cummings J, Drogendijk T, Dorrepaal C, Martin N. Randomized double-blind, active-controlled phase 3 study to assess 12-month safety and efficacy of mirabegron, a beta(3)-adrenoceptor agonist, in overactive bladder. Eur Urol. 2013 Feb;63(2):296-305. doi: 10.1016/j.eururo.2012.10.048. Epub 2012 Nov 6.
- 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.
Central Contact study director
Astellas Pharma Europe B.V.
308 sites in 30 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Mirabegron and Tolterodine in people with Urinary Bladder, Overactive, run by Astellas Pharma Inc at 308 sites in 30 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 4 inclusion and 12 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 20 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 308 sites in United States, Germany, Canada, United Kingdom, Russia and 25 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 19 Oct 2012). 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?
Number of Participants With and Severity of Treatment-emergent Adverse Events (TEAEs) (time frame: From the first dose of double-blind study drug up until 30 days after the last dose of study drug, up to 13 months.). 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 NCT00688688, which also lists 1 linked publication.
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 20 Nov 2024.