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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT02312960
Registration number
NCT02312960
Ethics application status
Date submitted
5/12/2014
Date registered
9/12/2014
Titles & IDs
Public title
Radium-223 Dichloride Long-term Follow-up Program
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Scientific title
A Phase 4 Long-term Follow-up Study to Define the Safety Profile of Radium-223 Dichloride
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Secondary ID [1]
0
0
2014-002407-25
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Secondary ID [2]
0
0
16996
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Neoplasm Metastasis / Bone and Bones
0
0
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Condition category
Condition code
Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Other interventions - Data Collection
Other: Arm 1 - The subjects previously enrolled in a selected radium-223 dichloride feeder trial, their treating health care professional, or caregiver will be contacted in 6-month intervals for follow up and query.
Other interventions: Data Collection
No study treatment will be provided in this long term follow up study.
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Intervention code [1]
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0
Other interventions
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Incidence of radium-223 dichloride related Adverse Events
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Assessment method [1]
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0
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Timepoint [1]
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Up to 7 years
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Primary outcome [2]
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Severity of radium-223 dichloride related Adverse Events
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Assessment method [2]
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Severity will be measured as per guidelines by Common Terminology Criteria for Adverse Events; Version 4.03 (CTCAE)
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Timepoint [2]
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Up to 7 years
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Primary outcome [3]
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0
Incidence of radium-223 dichloride related Serious Adverse Events
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Assessment method [3]
0
0
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Timepoint [3]
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0
Up to 7 years
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Primary outcome [4]
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0
Incidence of placebo-related Adverse Events
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Assessment method [4]
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0
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Timepoint [4]
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0
Up to 7 years
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Primary outcome [5]
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Severity of placebo-related Adverse Events
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Assessment method [5]
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0
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Timepoint [5]
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0
Up to 7 years
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Primary outcome [6]
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0
Incidence of placebo-related Serious Adverse Events
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Assessment method [6]
0
0
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Timepoint [6]
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Up to 7 years
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Primary outcome [7]
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0
Incidence of leukemia
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Assessment method [7]
0
0
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Timepoint [7]
0
0
Up to 7 years
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Primary outcome [8]
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0
Incidence of myelodysplastic syndrome
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Assessment method [8]
0
0
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Timepoint [8]
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Up to 7 years
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Primary outcome [9]
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0
Incidence of aplastic anemia
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Assessment method [9]
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0
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Timepoint [9]
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Up to 7 years
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Primary outcome [10]
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Incidence of primary bone cancer
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Assessment method [10]
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0
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Timepoint [10]
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Up to 7 years
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Primary outcome [11]
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0
Incidence of any other new primary malignancy
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Assessment method [11]
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0
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Timepoint [11]
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Up to 7 years
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Primary outcome [12]
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Incidence of bone fractures
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Assessment method [12]
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0
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Timepoint [12]
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Up to 7 years
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Primary outcome [13]
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Incidence of bone-associated events
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Assessment method [13]
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Timepoint [13]
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Up to 7 years
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Primary outcome [14]
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Incidence of febrile neutropenia in subjects who receive cytotoxic chemotherapy
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Assessment method [14]
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0
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Timepoint [14]
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Up to 7 years
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Primary outcome [15]
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Incidence of hemorrhage in subjects who receive cytotoxic chemotherapy
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Assessment method [15]
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0
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Timepoint [15]
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Up to 7 years
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Eligibility
Key inclusion criteria
* Subject was previously enrolled in a selected company sponsored feeder trial, and has received at least 1 dose of radium 223 dichloride or placebo in the feeder trial
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Not applicable to this follow up study
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Study design
Purpose of the study
Other
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Allocation to intervention
NA
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 4
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
18/12/2014
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
31/01/2024
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Sample size
Target
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Accrual to date
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Final
255
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Recruitment in Australia
Recruitment state(s)
NSW,VIC
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Recruitment hospital [1]
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- Darlinghurst
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Recruitment hospital [2]
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- Westmead
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Recruitment hospital [3]
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- Fitzroy
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Recruitment hospital [4]
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- Heidelberg
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Recruitment postcode(s) [1]
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2010 - Darlinghurst
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Recruitment postcode(s) [2]
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2145 - Westmead
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Recruitment postcode(s) [3]
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3065 - Fitzroy
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Recruitment postcode(s) [4]
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3084 - Heidelberg
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Recruitment outside Australia
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United States of America
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Alaska
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Nebraska
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South Dakota
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Washington
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Belgium
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Kortrijk
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Belgium
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Leuven
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Brazil
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Rio Grande Do Sul
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Brazil
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Sao Paulo
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Ontario
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Czechia
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Praha 2
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Finland
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Helsinki
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Finland
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Tampere
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France
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Bordeaux Cedex
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France
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Nantes
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France
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Nîmes
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France
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Saint-Cloud
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France
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Tours
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France
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Villejuif
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Germany
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Baden-Württemberg
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Germany
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Bayern
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Germany
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Mecklenburg-Vorpommern
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Germany
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Nordrhein-Westfalen
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Germany
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Rheinland-Pfalz
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Germany
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Sachsen-Anhalt
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Germany
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Sachsen
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Germany
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Thüringen
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Germany
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Berlin
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Germany
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Bremen
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Hong Kong
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Chai Wan
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Israel
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Afula
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Israel
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Haifa
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Israel
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Jerusalem
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Israel
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Petach Tikva
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Israel
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Ramat Gan
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Israel
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Tel Aviv
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Israel
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Zrifin
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Italy
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Emilia-Romagna
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Italy
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Lazio
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Italy
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Lombardia
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Italy
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Trentino-Alto Adige
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Ehime
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Japan
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Hokkaido
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Japan
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Ishikawa
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Japan
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Kanagawa
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Japan
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Okayama
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Japan
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Osaka
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Japan
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Saitama
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Japan
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Tokyo
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Japan
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Fukuoka
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Japan
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Kumamoto
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Japan
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Miyazaki
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Korea, Republic of
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Seoul Teugbyeolsi
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Korea, Republic of
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Daegu
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Korea, Republic of
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Incheon
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Korea, Republic of
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Seoul
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Country [67]
0
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Norway
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Bodø
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0
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Norway
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State/province [68]
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Oslo
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Country [69]
0
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Poland
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State/province [69]
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Bialystok
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Poland
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Gliwice
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Poland
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Warszawa
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0
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Russian Federation
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Obninsk
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0
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Singapore
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Singapore
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Spain
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Barcelona
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Spain
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State/province [75]
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Illes Baleares
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0
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Spain
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A Coruña
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Spain
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Madrid
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Spain
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Málaga
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0
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Spain
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Pamplona
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Spain
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Sevilla
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Sweden
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Umea
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Taiwan
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Kaohsiung
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Taiwan
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Taichung
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Taiwan
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Taipei
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0
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Taiwan
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Taoyuan
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0
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United Kingdom
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Cornwall
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United Kingdom
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Devon
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0
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United Kingdom
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South Yorkshire
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0
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United Kingdom
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Surrey
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United Kingdom
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Warwickshire
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0
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United Kingdom
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Bristol
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0
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United Kingdom
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State/province [92]
0
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Cottingham
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Bayer
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
Patients will be followed up in this study after prior treatment with BAY88-8223 / Radium-223 dichloride / Xofigo .
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Trial website
https://clinicaltrials.gov/study/NCT02312960
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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0
Bayer Study Director
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Address
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Bayer
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Country
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0
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Phone
0
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Fax
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Email
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Contact person for public queries
Name
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Contact person for scientific queries
Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
Availability of this study's data will later be determined according to Bayer's commitment to the EFPIA/PhRMA "Principles for responsible clinical trial data sharing". This pertains to scope, timepoint and process of data access. As such, Bayer commits to sharing upon request from qualified researchers patient-level clinical trial data, study-level clinical trial data, and protocols from clinical trials in patients for medicines and indications approved in the US and EU as necessary for conducting legitimate research. This applies to data on new medicines and indications that have been approved by the EU and US regulatory agencies on or after January 01, 2014.
Interested researchers can use www.vivli.org to request access to anonymized patient-level data and supporting documents from clinical studies to conduct research. Information on the Bayer criteria for listing studies and other relevant information is provided in the member section of the portal.
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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/NCT02312960