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Spots Global Cancer Trial Database for Pharmacokinetics of Dactinomycin in Young Patients With Cancer

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Trial Identification

Brief Title: Pharmacokinetics of Dactinomycin in Young Patients With Cancer

Official Title: Pharmacokinetics of Actinomycin D in Children With Cancer

Study ID: NCT00900354

Study Description

Brief Summary: RATIONALE: Studying samples of blood in the laboratory from patients with cancer receiving dactinomycin may help doctors learn how dactinomycin works in the body and how patients will respond to treatment. PURPOSE: This laboratory study is evaluating the pharmacokinetics of dactinomycin in young patients with cancer.

Detailed Description: OBJECTIVES: * Determine the pharmacokinetics (PKs) of dactinomycin in pediatric patients with cancer. * Determine the degree of interpatient variation in the PKs of this drug. * Determine the influence of characteristics such as age, tumor type, and concurrent therapy on drug PKs in these patients. * Correlate drug PKs with clinical response and toxicity observed in these patients, focusing particularly on the incidence of severe liver toxicity or veno-occlusive disease. * Correlate pharmacogenetic variability with clinical and PK data. OUTLINE: This is a multicenter study. Patients undergo blood collection for pharmacokinetic sampling of dactinomycin at baseline (prior to the initiation of dactinomycin) and periodically during course 1 of chemotherapy. An additional blood sample is obtained before or after treatment for the collection of peripheral blood lymphocytes. DNA from these cells is isolated and investigated for genetic variation in genes relevant to the pharmacology of dactinomycin. Plasma concentrations of dactinomycin are determined by liquid chromatography mass spectrometry analysis. Patients are followed for 2 years. PROJECTED ACCRUAL: A total of 50 patients will be accrued for this study.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Our Lady's Hospital for Sick Children Crumlin, Dublin, , Ireland

Birmingham Children's Hospital, Birmingham, England, United Kingdom

Institute of Child Health at University of Bristol, Bristol, England, United Kingdom

Addenbrooke's Hospital, Cambridge, England, United Kingdom

Leeds Cancer Centre at St. James's University Hospital, Leeds, England, United Kingdom

Leicester Royal Infirmary, Leicester, England, United Kingdom

Royal Liverpool Children's Hospital, Alder Hey, Liverpool, England, United Kingdom

Middlesex Hospital, London, England, United Kingdom

Great Ormond Street Hospital for Children, London, England, United Kingdom

Royal Manchester Children's Hospital, Manchester, England, United Kingdom

Sir James Spence Institute of Child Health at Royal Victoria Infirmary, Newcastle-Upon-Tyne, England, United Kingdom

University of Newcastle-Upon-Tyne Northern Institute for Cancer Research, Newcastle-Upon-Tyne, England, United Kingdom

Queen's Medical Centre, Nottingham, England, United Kingdom

Oxford Radcliffe Hospital, Oxford, England, United Kingdom

Children's Hospital - Sheffield, Sheffield, England, United Kingdom

Southampton General Hospital, Southampton, England, United Kingdom

Royal Marsden - Surrey, Sutton, England, United Kingdom

Royal Belfast Hospital for Sick Children, Belfast, Northern Ireland, United Kingdom

Royal Aberdeen Children's Hospital, Aberdeen, Scotland, United Kingdom

Royal Hospital for Sick Children, Edinburgh, Scotland, United Kingdom

Royal Hospital for Sick Children, Glasgow, Scotland, United Kingdom

Childrens Hospital for Wales, Cardiff, Wales, United Kingdom

Contact Details

Name: Gareth Veal

Affiliation: University of Newcastle Upon-Tyne

Role: STUDY_CHAIR

Name: Alan Boddy, PhD

Affiliation: University of Newcastle Upon-Tyne

Role:

Useful links and downloads for this trial

Clinicaltrials.gov

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