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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT00994292




Registration number
NCT00994292
Ethics application status
Date submitted
13/10/2009
Date registered
14/10/2009
Date last updated
19/10/2015

Titles & IDs
Public title
Study Evaluating Safety, Tolerability and Efficacy of YM150 in Subjects With Acute Coronary Syndromes
Scientific title
A Randomized, Double-Blind, Placebo Controlled Multi-Center and Parallel Group Study of the Safety, Tolerability and Efficacy of YM150 in Combination With Standard Treatment in Secondary Prevention of Ischemic Vascular Events in Subjects With Acute Coronary Syndromes
Secondary ID [1] 0 0
2008-005972-29
Secondary ID [2] 0 0
150-CL-201
Universal Trial Number (UTN)
Trial acronym
RUBY-1
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Acute Coronary Syndrome 0 0
Condition category
Condition code
Cardiovascular 0 0 0 0
Coronary heart disease
Other 0 0 0 0
Research that is not of generic health relevance and not applicable to specific health categories listed above

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - YM150
Treatment: Drugs - Placebo

Experimental: 1. YM150 Dose V, twice daily -

Experimental: 2. YM150 Dose W, once daily -

Experimental: 3. YM150 Dose X, twice daily -

Experimental: 4. YM150 Dose Y, once daily -

Experimental: 5. YM150 Dose Y, twice daily -

Experimental: 6. YM150 Dose Z, once daily -

Placebo comparator: 7. Placebo -


Treatment: Drugs: YM150
oral

Treatment: Drugs: Placebo
oral
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Incidence of Major and Clinically Relevant Non Major bleeding events according to International Society of Thrombosis and Hemostasis (ISTH) definition
Timepoint [1] 0 0
6 Months
Secondary outcome [1] 0 0
Incidence of Major and Clinically Relevant Non Major bleeding events
Timepoint [1] 0 0
30 Days

Eligibility
Key inclusion criteria
* has a diagnosis of STE-ACS, NSTE-ACS as index event according to accepted guidelines such as the ESC or AHA guidelines
* has elevated cardiac biomarkers
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* is planned for myocardial revascularization (e.g., Coronary Artery Bypass Graft (CABG) or elective or staged PCI) or any other invasive procedure with increased risk for bleeding (i.e. elective surgical procedures) within 60 days after randomization
* has had recent stroke or TIA = 12 months prior to index event
* has persistent BP of 160 mmHg systolic or higher and/or 100 mmHg diastolic or higher at baseline with or without medication
* has participated in another clinical trial of an investigational drug (including placebo) or device within 30 days (or the limit set by national law, whichever is longer) of signing informed consent for the present study
* has participated in any YM150 clinical trials
* requires ongoing parenteral or oral anticoagulant therapy
* has active bleeding or is in the opinion of the investigator at high risk of bleeding during the study

Study design
Purpose of the study
Prevention
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s

The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 2
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/09/2009
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/03/2011
Sample size
Target
Accrual to date
Final
1276
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
- Concord
Recruitment hospital [2] 0 0
- Douglas
Recruitment postcode(s) [1] 0 0
2139 - Concord
Recruitment postcode(s) [2] 0 0
4814 - Douglas
Recruitment outside Australia
Country [1] 0 0
Argentina
State/province [1] 0 0
Ciudad Autonoma de Buenos Aires
Country [2] 0 0
Argentina
State/province [2] 0 0
Corrientes
Country [3] 0 0
Argentina
State/province [3] 0 0
Salta
Country [4] 0 0
Belgium
State/province [4] 0 0
Aalst
Country [5] 0 0
Belgium
State/province [5] 0 0
Bonheiden
Country [6] 0 0
Belgium
State/province [6] 0 0
Brussels
Country [7] 0 0
Belgium
State/province [7] 0 0
Genk
Country [8] 0 0
Belgium
State/province [8] 0 0
Leper
Country [9] 0 0
Belgium
State/province [9] 0 0
Ottignies
Country [10] 0 0
Brazil
State/province [10] 0 0
Brasilia
Country [11] 0 0
Brazil
State/province [11] 0 0
Porto Alegre
Country [12] 0 0
Brazil
State/province [12] 0 0
Recife
Country [13] 0 0
Brazil
State/province [13] 0 0
Salvador
Country [14] 0 0
Brazil
State/province [14] 0 0
Sao Jose
Country [15] 0 0
Brazil
State/province [15] 0 0
Sao Paulo
Country [16] 0 0
Brazil
State/province [16] 0 0
Uberlandia
Country [17] 0 0
Canada
State/province [17] 0 0
Cambridge
Country [18] 0 0
Canada
State/province [18] 0 0
Hamilton
Country [19] 0 0
Canada
State/province [19] 0 0
Laval
Country [20] 0 0
Canada
State/province [20] 0 0
Longueuil
Country [21] 0 0
Canada
State/province [21] 0 0
Montreal
Country [22] 0 0
Canada
State/province [22] 0 0
St Jerome
Country [23] 0 0
Colombia
State/province [23] 0 0
Barranquilla
Country [24] 0 0
Colombia
State/province [24] 0 0
Bogota
Country [25] 0 0
Colombia
State/province [25] 0 0
Cartagena
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Colombia
State/province [26] 0 0
Floridablanca
Country [27] 0 0
Czech Republic
State/province [27] 0 0
Beroun
Country [28] 0 0
Czech Republic
State/province [28] 0 0
Brno
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Czech Republic
State/province [29] 0 0
Jihlava
Country [30] 0 0
Czech Republic
State/province [30] 0 0
Kladno
Country [31] 0 0
Czech Republic
State/province [31] 0 0
Liberec
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Czech Republic
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Pardubice
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Czech Republic
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Prague
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Czech Republic
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Sternberk
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Czech Republic
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Vsetin
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Czech Republic
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Zlin
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Denmark
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Copenhagen
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France
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Paris Cedex 18
Country [39] 0 0
Germany
State/province [39] 0 0
Bad Nauheim
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Germany
State/province [40] 0 0
Dresden
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Germany
State/province [41] 0 0
Freiburg
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Germany
State/province [42] 0 0
Kassel
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Germany
State/province [43] 0 0
Neuss
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Hungary
State/province [44] 0 0
Balatonfured
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Hungary
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Budapest
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Hungary
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Debrecen
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Hungary
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Miskolc
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Hungary
State/province [48] 0 0
Nyiregyhaza
Country [49] 0 0
Hungary
State/province [49] 0 0
Szeged
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Hungary
State/province [50] 0 0
Szekesfehervar
Country [51] 0 0
Hungary
State/province [51] 0 0
Zalaegerszeg
Country [52] 0 0
India
State/province [52] 0 0
Ahmedabad
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India
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Hyderabaad
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India
State/province [54] 0 0
Mangalore
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India
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Nagpur
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India
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New Delhi
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India
State/province [57] 0 0
Tamil Nadu
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India
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Tirupati
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Korea, Republic of
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Busan
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Korea, Republic of
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Gwangju
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Korea, Republic of
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Gyeonggi-do
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Korea, Republic of
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Inchon
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Korea, Republic of
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Seoul
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Mexico
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Colonia Burocratas del Estado
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Mexico
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Guadalajara
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Mexico
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Merida
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Mexico
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Morelia
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Mexico
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Zapopan
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Netherlands
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Amsterdam
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Netherlands
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Heerlen
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Netherlands
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Helmond
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Netherlands
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Hertogenbosch
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Netherlands
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Leeuwarden
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Netherlands
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Nijmegen
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Netherlands
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Oss
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Poland
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Bialystok
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Poland
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Elblag
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Poland
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Gdansk
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Poland
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Inowroclaw
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Poland
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Krakow
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Poland
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Przemysl
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Romania
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Baia Mare
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Romania
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Braila
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Romania
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Bucuresti
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Romania
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Craiova
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Romania
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Oradea
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Romania
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Targoviste
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Romania
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Targu Mures
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Russian Federation
State/province [89] 0 0
Chelyabinsk
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Russian Federation
State/province [90] 0 0
Kemerovo
Country [91] 0 0
Russian Federation
State/province [91] 0 0
Moscow
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Russian Federation
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Saratov
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Russian Federation
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Tomsk
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Russian Federation
State/province [94] 0 0
Tyumen
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Russian Federation
State/province [95] 0 0
Yaroslavl
Country [96] 0 0
Slovakia
State/province [96] 0 0
Martin
Country [97] 0 0
Slovakia
State/province [97] 0 0
Nitra
Country [98] 0 0
Slovakia
State/province [98] 0 0
Rimavska Sobota
Country [99] 0 0
Slovakia
State/province [99] 0 0
Ruzomberok
Country [100] 0 0
South Africa
State/province [100] 0 0
George
Country [101] 0 0
South Africa
State/province [101] 0 0
Johannesburg
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South Africa
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Kuilsriver
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South Africa
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Parow
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South Africa
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Pinelands
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South Africa
State/province [105] 0 0
Tongaat
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South Africa
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Umhlanga
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South Africa
State/province [107] 0 0
Western Cape
Country [108] 0 0
South Africa
State/province [108] 0 0
Worcester
Country [109] 0 0
Ukraine
State/province [109] 0 0
Kharkiv
Country [110] 0 0
Ukraine
State/province [110] 0 0
Kyiv
Country [111] 0 0
Ukraine
State/province [111] 0 0
Zaporizhzhya

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Astellas Pharma Europe B.V.
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Use Central Contact
Address 0 0
Astellas Pharma Europe B.V.
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT00994292