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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT02118896




Registration number
NCT02118896
Ethics application status
Date submitted
17/04/2014
Date registered
21/04/2014
Date last updated
22/11/2024

Titles & IDs
Public title
Study to Ascertain if Prolonged Release Tacrolimus (FK506E - MR4) is Safe and Effective When Used in the Long Term and in Combination With Other Immunosuppressive Drugs in Patients Who Have Received a Transplant
Scientific title
A Long-term Follow up Study to Evaluate the Safety and Efficacy in Transplant Recipients Treated With Modified Release Tacrolimus, FK506E (MR4), Based Immunosuppression Regimen
Secondary ID [1] 0 0
2005-005714-20
Secondary ID [2] 0 0
F506-CL-0857
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Heart Transplantation 0 0
Liver Transplantation 0 0
Kidney Transplantation 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - FK506E

Experimental: 1: FK506E (MR4) - Single open arm of FK506E (MR4). Since this was an extension study for many studies, generally the dose given at enrollment was to be continued. The investigator was permitted to adjust the subject's dose and modify the MR4 dose regimen as deemed necessary to minimize Adverse Events (AEs) and maintain effective immunosuppression. MR4 capsules were taken orally, once daily in the morning. MR4 capsules were to be swallowed with fluid (preferably water) on an empty stomach or at least 1 hour before or 2 to 3 hours after a meal. MR4 was supplied as 0.5 mg, 1 mg and 5 mg capsules in amber glass bottles or in blister packs.


Treatment: Drugs: FK506E
oral
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Participant Survival
Timepoint [1] 0 0
Up to 5.5 years (66 months (phase II) and 24 months (phase III)).
Primary outcome [2] 0 0
Graft Survival
Timepoint [2] 0 0
Up to 5.5 years ((66 months (phase II) and 30 months (phase III)).
Secondary outcome [1] 0 0
Biopsy-confirmed Acute Rejection (BCAR) Episodes
Timepoint [1] 0 0
Up to 6 years.
Secondary outcome [2] 0 0
Time to First BCAR Episode
Timepoint [2] 0 0
Up to 1344 days (3.75 years).
Secondary outcome [3] 0 0
Number of Participants With Adverse Events
Timepoint [3] 0 0
From first dose to duration of participation in the study (up to 6 years and 28 days after EOS).

Eligibility
Key inclusion criteria
* Patients who had already participated in the previous phase II pharmacokinetic or phase III studies with FK506E (MR4).
* Patients capable of understanding the purpose and risks of the study, who had been fully informed and given written informed consent to participate in the study.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Pregnant women or nursing mothers.
* Women unwilling or unable to use adequate contraception during the study.

Study design
Purpose of the study
Treatment
Allocation to intervention
Not applicable
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
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Phase 3
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
24/02/2003
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
7/10/2009
Sample size
Target
Accrual to date
Final
850
Recruitment in Australia
Recruitment state(s)
NSW,QLD,VIC
Recruitment hospital [1] 0 0
Royal Prince Alfred Hospital - Camperdown
Recruitment hospital [2] 0 0
Princess Alexandra Hospital - Brisbane
Recruitment hospital [3] 0 0
Austin Hospital - Heidelberg
Recruitment hospital [4] 0 0
Royal Melbourne Hospital - Melbourne
Recruitment postcode(s) [1] 0 0
2050 - Camperdown
Recruitment postcode(s) [2] 0 0
4102 - Brisbane
Recruitment postcode(s) [3] 0 0
3084 - Heidelberg
Recruitment postcode(s) [4] 0 0
3050 - Melbourne
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Ohio
Country [2] 0 0
Austria
State/province [2] 0 0
Innsbruck
Country [3] 0 0
Austria
State/province [3] 0 0
Wien
Country [4] 0 0
Belgium
State/province [4] 0 0
Bruxelles
Country [5] 0 0
Belgium
State/province [5] 0 0
Gent
Country [6] 0 0
Belgium
State/province [6] 0 0
Leuven
Country [7] 0 0
Belgium
State/province [7] 0 0
Liege
Country [8] 0 0
Brazil
State/province [8] 0 0
Campinas
Country [9] 0 0
Brazil
State/province [9] 0 0
Porto Alegre
Country [10] 0 0
Brazil
State/province [10] 0 0
Rio de Janeiro
Country [11] 0 0
Canada
State/province [11] 0 0
Alberta
Country [12] 0 0
Canada
State/province [12] 0 0
Ontario
Country [13] 0 0
Canada
State/province [13] 0 0
Quebec
Country [14] 0 0
Canada
State/province [14] 0 0
Vancouver
Country [15] 0 0
Czechia
State/province [15] 0 0
Praha 4
Country [16] 0 0
Denmark
State/province [16] 0 0
Århus N
Country [17] 0 0
Finland
State/province [17] 0 0
Helsinki
Country [18] 0 0
France
State/province [18] 0 0
Bicetre Cedex
Country [19] 0 0
France
State/province [19] 0 0
Cedex 05
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France
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Cedex 1
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France
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Cedex 3
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France
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Cedex 5
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France
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Cedex 9
Country [24] 0 0
France
State/province [24] 0 0
Cedex
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France
State/province [25] 0 0
Clichy
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France
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Creteil
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France
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Créteil
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France
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Grenoble
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France
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St Etienne
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France
State/province [30] 0 0
Strasbourg
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France
State/province [31] 0 0
Villejuif
Country [32] 0 0
Germany
State/province [32] 0 0
Bad Oeynhausen
Country [33] 0 0
Germany
State/province [33] 0 0
Berlin
Country [34] 0 0
Germany
State/province [34] 0 0
Bochum
Country [35] 0 0
Germany
State/province [35] 0 0
Erlangen
Country [36] 0 0
Germany
State/province [36] 0 0
Essen
Country [37] 0 0
Germany
State/province [37] 0 0
Frankfurt/Main
Country [38] 0 0
Germany
State/province [38] 0 0
Halle
Country [39] 0 0
Germany
State/province [39] 0 0
Hamburg
Country [40] 0 0
Germany
State/province [40] 0 0
Hannover
Country [41] 0 0
Germany
State/province [41] 0 0
Heidelberg
Country [42] 0 0
Germany
State/province [42] 0 0
Koeln
Country [43] 0 0
Germany
State/province [43] 0 0
Munchen
Country [44] 0 0
Germany
State/province [44] 0 0
Regensburg
Country [45] 0 0
Hungary
State/province [45] 0 0
Budapest
Country [46] 0 0
Ireland
State/province [46] 0 0
Dublin
Country [47] 0 0
Italy
State/province [47] 0 0
Bergamo
Country [48] 0 0
Italy
State/province [48] 0 0
Bologna
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Italy
State/province [49] 0 0
Genova
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Italy
State/province [50] 0 0
Milano
Country [51] 0 0
Italy
State/province [51] 0 0
Modena
Country [52] 0 0
Italy
State/province [52] 0 0
Padova
Country [53] 0 0
Italy
State/province [53] 0 0
Palermo
Country [54] 0 0
Italy
State/province [54] 0 0
Roma
Country [55] 0 0
Italy
State/province [55] 0 0
Siena
Country [56] 0 0
Italy
State/province [56] 0 0
Udine
Country [57] 0 0
Mexico
State/province [57] 0 0
Morelos
Country [58] 0 0
Mexico
State/province [58] 0 0
Tlalpan
Country [59] 0 0
Netherlands
State/province [59] 0 0
Maastricht
Country [60] 0 0
New Zealand
State/province [60] 0 0
Auckland
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Poland
State/province [61] 0 0
Bydgoszcz
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Poland
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Szczecin
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South Africa
State/province [63] 0 0
Cape Town
Country [64] 0 0
South Africa
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Durban
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South Africa
State/province [65] 0 0
Pretoria
Country [66] 0 0
South Africa
State/province [66] 0 0
Tygerberg
Country [67] 0 0
Spain
State/province [67] 0 0
Vizcaya
Country [68] 0 0
Spain
State/province [68] 0 0
Barcelona
Country [69] 0 0
Spain
State/province [69] 0 0
Madrid
Country [70] 0 0
Spain
State/province [70] 0 0
Oviedo
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Spain
State/province [71] 0 0
Pamplona
Country [72] 0 0
Spain
State/province [72] 0 0
Santiago de Compostela
Country [73] 0 0
Sweden
State/province [73] 0 0
Gothenburg
Country [74] 0 0
Sweden
State/province [74] 0 0
Stockholm
Country [75] 0 0
Switzerland
State/province [75] 0 0
Zurich
Country [76] 0 0
United Kingdom
State/province [76] 0 0
Coventry
Country [77] 0 0
United Kingdom
State/province [77] 0 0
Edgbaston
Country [78] 0 0
United Kingdom
State/province [78] 0 0
Glasgow
Country [79] 0 0
United Kingdom
State/province [79] 0 0
London
Country [80] 0 0
United Kingdom
State/province [80] 0 0
Manchester
Country [81] 0 0
United Kingdom
State/province [81] 0 0
Newcastle upon Tyne

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

Ethics approval
Ethics application status

Summary
Brief summary
The purpose of this study was to offer patients who had participated in one of the phase II PK or phase III studies on FK506E (MR4) the possibility to continue FK506E (MR4) until commercial availability of the drug and to record long term efficacy and safety data.
Trial website
https://clinicaltrials.gov/study/NCT02118896
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Central Contact
Address 0 0
Astellas Pharma Europe Ltd.
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



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/study/NCT02118896