Phase 1 Lymphoma Trial, Recruiting NCT06383338 Sponsor: Murdoch Childrens Research Institute Condition: Lymphoma
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Phase 1 Lymphoma Trial, Recruiting

NCT06383338
Recruiting Phase 1 🇦🇺 Australian site

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are between 6 and 25 years old
  • You have recently been diagnosed with Hodgkin Lymphoma or Non-Hodgkin Lymphoma (a new diagnosis)
  • You are able to swallow medications by mouth, or receive them through a feeding tube placed through the nose
  • You (or your parent/guardian if you are a child) are able to give written consent to take part

Who may not be able to join:

  • You are allergic to omeprazole (a common heartburn medicine) or dextromethorphan (a common cough medicine used in the study)
  • You have severe organ problems affecting the liver, kidneys, or digestive system (confirm with trial site)
  • You have had cancer treatment before — this trial is only for people who have not yet been treated for cancer
  • You are very unwell and need intensive care treatment
  • Your cancer treatment needs to start urgently at a time when study staff are not available to explain the trial and get your consent beforehand
  • You (or your parent/guardian) are unable to provide written consent to take part

⚠️ Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Rachel Conyers, MBBS (Hons), Murdoch Childrens Research Institute

Phone: +61393455522

Australian sites

Peter MacCallum Cancer Centre, Melbourne, Victoria

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 1
Sponsor
Murdoch Childrens Research Institute
Registry
ClinicalTrials.gov
Start date
22 July 2025
Est. completion
1 July 2026

Where this trial is recruiting

🇦🇺 Australia

1 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Proportion of patients who consent to study and complete baseline and at least two longitudinal timepoints with successful measurement of probe drug MR (Metabolic ratio)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov