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Trial registered on ANZCTR
Registration number
ACTRN12615000038594
Ethics application status
Approved
Date submitted
30/09/2014
Date registered
19/01/2015
Date last updated
27/04/2017
Type of registration
Retrospectively registered
Titles & IDs
Public title
A multi-centre study investigating the pharmacokinetics of treosulfan in children undergoing stem cell transplantation.
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Scientific title
Using blood treosulfan concentrations to reduce toxicity and improve outcome in children undergoing stem cell transplantation.
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Secondary ID [1]
285421
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Nil
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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:
immunodeficiency
293258
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CD40 ligand deficiency
293259
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mucopolysaccharidosis
293260
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infantile malignant osteoporosis
293261
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Condition category
Condition code
Human Genetics and Inherited Disorders
293449
293449
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0
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Other human genetics and inherited disorders
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Cancer
293560
293560
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0
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Children's - Other
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
This is a multi-centre prospective evaluation of the pharmacokinetics of treosulfan and metabolites after intravenous administration prior to blood or marrow transplantation. The exact dose, dosing schedule and infusion duration of treosulfan will be as specified in the protocol by which the patient is being treated. This is an observational study with no control group. Patients will be followed for up to 5 years post transplant.
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Intervention code [1]
290339
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Not applicable
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
293266
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We will establish the pharmacokinetics of treosulfan in a large population of 60 children. Total exposure to treosulfan and metabolites (area-under-the-concentration-versus-time curve, AUC) and other pharmacokinetic parameters will be determined for each individual using the blood concentrations.
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Assessment method [1]
293266
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Timepoint [1]
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Measured after a single dose.
The time points for children less than 20 kg are prior to the infusion start, then at 5 min, 30min, 3h, 5h and 7h after the infusion end. The time points for children greater than 20kg are prior to the infusion then at 5 min, 30 min, 1h, 2h, 4h, 6h, 8h and 10 h after the infusion end.
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Primary outcome [2]
293267
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Data about the patient (e.g. age, weight, height, surface area, renal function, liver function, laboratory values, concomitant medications, diagnosis) will be collected to allow an assessment of the factors that contribute to the variability in treosulfan pharmacokinetics.
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Assessment method [2]
293267
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Timepoint [2]
293267
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Collected prior to the treosulfan dose, on study enrolment.
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Primary outcome [3]
293268
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We will examine the association between exposure to treosulfan (AUC) and the incidence of Grade 3+ transplant-related toxicities.
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Assessment method [3]
293268
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Timepoint [3]
293268
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Toxicities (e.g. renal dysfunction, liver dysfunction, gastrointestinal toxicity, mucositis, haematological toxicity), Graft versus Host Disease) will be followed up to 100 days post transplant.
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Secondary outcome [1]
310696
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Primary outcome 4. We will examine the association between exposure to treosulfan (AUC) and transplant outcome, including survival, relapse and engraftment.
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Assessment method [1]
310696
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Timepoint [1]
310696
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Survival, engraftment and disease response will be followed until five years post transplant.
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Eligibility
Key inclusion criteria
1. Children and adolescents with any diagnosis who are scheduled to receive tresosulfan-based conditioning prior to blood or marrow transplantation.
2. Parental informed consent.
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Minimum age
No limit
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Maximum age
18
Years
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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
Unable to obtain parental informed consent.
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Both
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
3/10/2013
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Actual
5/10/2013
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Date of last participant enrolment
Anticipated
16/10/2018
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Actual
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Date of last data collection
Anticipated
16/10/2023
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Actual
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Sample size
Target
60
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW,QLD
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Recruitment hospital [1]
3029
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The Children's Hospital at Westmead - Westmead
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Recruitment hospital [2]
3030
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Sydney Children's Hospital - Randwick
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Recruitment hospital [3]
3031
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Royal Children's Hospital - Herston
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Funding & Sponsors
Funding source category [1]
290025
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Government body
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Name [1]
290025
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Kids Cancer Alliance (Cancer Institute NSW)
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Address [1]
290025
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Australian Technology Park,
Level 9, 8 Central Ave
Eveleigh, NSW, 2015,
Australia
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Country [1]
290025
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Australia
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Primary sponsor type
Hospital
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Name
The Children's Hospital at Westmead
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Address
Hawkesbury Rd., Westmead, NSW, 2145
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Country
Australia
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Secondary sponsor category [1]
288776
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None
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Name [1]
288776
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Address [1]
288776
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Country [1]
288776
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
291734
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Sydney Children's Hospital Human Research Ethics Committee
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Ethics committee address [1]
291734
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Research and Development Office, Ethics and Governance, Locked Bag 4001, Westmead NSW, 2145.
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Ethics committee country [1]
291734
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Australia
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Date submitted for ethics approval [1]
291734
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Approval date [1]
291734
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05/07/2013
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Ethics approval number [1]
291734
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HREC/13/SCHN/24
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Summary
Brief summary
This study involves measuring the blood levels of the medication, treosulfan, to improve the way we adjust the dose in children. Who is it for? Children and adolescents with either malignant or non malignant (genetic) diseases can join this study if they are receiving the medication, treosulfan, prior to undergoing blood or marrow transplantation. Trial details A series of blood levels will be collected after the treosulfan dose to see how well their body breaks down and gets rid of the medication. This study does not replace other studies, but simply investigates key medication widely used in the treatment of children's cancer. Participants will be studied for several years after the study to monitor their health. This study will define the best way to adjust the dose of the drug, treosulfan, a key medication in blood or marrow transplantation conditioning regimens. Too much causes toxicity and too little risks the disease being more likely to return.
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Trial website
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Trial related presentations / publications
SR. Koyyalamudi, U Kuzhiumparambil, CE Nath, J A. Byrne, CJ. Fraser, TA O’Brien, JW Earl, PJ Shaw. Development and Validation of High pressure liquid chromatography-UV Method for the Determination of Treosulfan and its Epoxy Metabolites in Human Plasma and its Application in Pharmacokinetic Studies. J. Chromatogr.Sci. 2016 54: 326 – 333.
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Public notes
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Contacts
Principal investigator
Name
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Dr Christa Nath
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Address
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Department of Biochemistry,
The Children's Hospital at Westmead,
Locked Bag 4001,
Westmead, NSW, 2145
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Country
51790
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Australia
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Phone
51790
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61-2-98453287
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Fax
51790
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61-2-98453332
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Email
51790
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[email protected]
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Contact person for public queries
Name
51791
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Christa Nath
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Address
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Department of Biochemistry,
The Children's Hospital at Westmead,
Locked Bag 4001,
Westmead, NSW, 2145
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Country
51791
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Australia
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Phone
51791
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61-2-98453287
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Fax
51791
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61-2-98453332
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Email
51791
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[email protected]
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Contact person for scientific queries
Name
51792
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Christa Nath
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Address
51792
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Department of Biochemistry,
The Children's Hospital at Westmead,
Locked Bag 4001,
Westmead, NSW, 2145
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Country
51792
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Australia
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Phone
51792
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61-2-98453287
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Fax
51792
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61-2-98453332
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Email
51792
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[email protected]
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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
Documents added manually
Type
Is Peer Reviewed?
DOI
Citations or Other Details
Attachment
Study results article
Yes
Koyyalamudi SR, Kuzhiumparambil U, Nath CE, Byrne ...
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Documents added automatically
No additional documents have been identified.
Download to PDF