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RecruitingLast updated: 25 February 2026

MARVEL-PIC: Whether genetic testing can guide medication choices to reduce side effects for children and adolescents receiving cancer or stem cell transplantsMinimising Adverse Drug Reactions and Verifying Economic Legitimacy - Pharmacogenomics Implementation in Children (MARVEL-PIC)

Trial purpose

Medical clipboardCancer treatment; Side effect and wellbeing

Tumor type

Multi-Cancer Multi-Cancer

Age

People<18

Trial acronym

MARVEL-PIC

Clinical summary

Summary

This study looks at whether a type of testing called pharmacogenomic testing can help children and teenagers with cancer receive safer and more effective medicines.

Pharmacogenomic testing checks DNA (from a cheek swab or blood sample) to understand how the body might react to certain medications. This can help doctors choose the best drug and the right dose for each person, instead of using a "trial and error" approach.

Who is it for?
Children and adolescent patients with a new diagnosis of cancer or who are about to receive a stem cell transplant can take part.

Study details
Everyone in the study will have pharmacogenomic testing done looking at a range of genes and genetic variants linked to medication response.

Participants will be randomly allocated (by chance) to either the control arm or the study arm.

Control arm
Standard of care prescribing will be completed for 12 months. Participants will receive pharmacogenomic test results according to the current standard of care. At week 13, the extended pharmacogenomics report will be released.

Study arm
Extended pharmacogenomic prescribing will be completed for a period of 12 months. Participants will receive pharmacoogenomic testing across a range of clinically relevant variants, to guide the dose and drug selection of 27 drugs commonly used in supportive care. The report will be released at week 4.

In both arms, the participants will be followed up for a minimum of 12 weeks, with maximal time-period being 12 months depending on time of enrolment.

What is being measured

Researchers want to know if using pharmacogenomic results early helps reduce side effects from medications. To do this:

  • Participants will complete a survey three times over 12 weeks about any symptoms or side effects they experience.
  • An academic pharmacist will then talk with families to better understand the severity and cause of any side effects.

Researchers will also look at how this approach affects:

  • Quality of life, using a child-friendly survey (CHU9D) completed three times over 12 months.
  • Healthcare costs, by reviewing Medicare and PBS data (with consent) to compare expenses between the two groups.

Data from the study will be securely stored on the REDCap database. Patients will be allocated a unique patient identifier prior to their de-identified data being added to the database.

Conditions

This trial is treating people with a new cancer diagnosis or someone who is receiving a haematopoietic stem cell transplantation (HSCT

Eligibility

Inclusion

  • Age < 18 years
  • New cancer diagnosis or patient receiving HSCT or patient has a relapsed cancer diagnosis and is starting treatment after more than 6 months without.
  • Starting treatment with a chemotherapeutic agent that is not single agent oral targeted therapy.
  • Must also be taking a medication for which there is an established CPIC guideline available.
  • Parent or patient is able and willing to give consent for patient to take part and be followed up for at least 12 weeks.
  • Patient is amenable to venepuncture and blood draw (5mL ideally with an absolute minimum requirement of 2.5 mL) or has Whole Genome Sequencing available (WGS).
  • Patient and/or parent is able and willing to sign an informed consent form.
  • Patient and/or parent is able to complete Ped-PRO-CTCAE survey in English, Italian or Chinese.
  • Study enrolment limit has not been reached.

Exclusion

  • Age > 18 years.
  • Patient has a life expectancy estimated to be less than three months by the treating clinical team.
  • Duration of the drug of inclusion total treatment length is planned to be less than one week.
  • Patient and/or parent is unable to consent to the study.
  • Patient and/or parent is unwilling to take part in the study.
  • Patient and/or parent is able unable to complete Ped-PRO-CTCAE survey in English, Italian or Chinese.
  • Patient has existing impaired hepatic or renal function for which a lower dose or alternate drug selection are already part of current routine care.
  • Patient has a glomerular filtration rate of less than 15 mL/min per 1.73m2.
  • Patient has advanced liver failure.

Inclusion

  • You have been diagnosed with cancer, but have not received any treatment.
  • You have the type of cancer, symptoms, or health risks that this clinical trial is focused on.

Exclusion

  • You have certain types of non-cancer medical conditions.
  • You have had certain treatments, surgical procedures or drugs.
Message

Clinical trials have complex eligibility criteria, and other criteria may apply for this trial. Ask your doctor about whether this trial could be right for you.

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Trial Identifiers

Information on this page is partially produced from ClinicalTrials.gov *. View further details about this trial on the registry via the links below:

Trial sponsor

Murdoch Childrens Research Institute

Scientific Title

Minimising Adverse Drug Reactions and Verifying Economic Legitimacy - Pharmacogenomics Implementation in Children (MARVEL-PIC)

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