Leukaemia Trial, Recruiting NCT06945042 Sponsor: Wake Forest University Health Sciences Condition: Leukaemia
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Leukaemia Trial, Recruiting

NCT06945042
Recruiting Not Applicable

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:

  • People who are able to understand the study and are willing to sign an approved consent form
  • People who are between 18 and 64 years old at the time of signing consent
  • People who have been newly diagnosed with Acute Myeloid Leukemia (AML), a type of blood cancer, confirmed by a bone marrow biopsy
  • People who are planned to receive intensive chemotherapy to treat their AML (it is acceptable if chemotherapy has already started, as long as it began within the last 30 days)
  • People who are able to read and understand English and/or Spanish
  • People who, in the opinion of the study doctor, are able to understand and follow the study procedures for the full duration of the study

Who may not be able to join:

  • People who have been diagnosed with a specific subtype of blood cancer called Acute Promyelocytic Leukemia
  • People who are unwilling to receive intensive chemotherapy for AML
  • People who have previously received treatment for any blood cancer
  • People who have previously had a stem cell transplant using donor cells (allogeneic hematopoietic stem cell transplant)

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 7 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Thomas Knight, MD, Wake Forest University Health Sciences

Phone: (980) 442-2327

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
Not Applicable
Registry
ClinicalTrials.gov
Start date
27 June 2025
Est. completion
1 May 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Self-reported financial toxicity as assessed by the total score of the COmprehensive Score Financial Toxicity (COST) assessment tool at 6 months after enrollment.

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: 7 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