Phase 2 Leukaemia Trial, Recruiting NCT06356922 Sponsor: Nantes University Hospital Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT06356922
Recruiting Phase 2

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:

  • Adults aged 18 or older
  • People diagnosed with a type of blood cancer called AML or ALL, where more than 5% of abnormal cells (blasts) are found in the bone marrow, with or without the cancer having spread to other parts of the body
  • People whose cancer cells test positive for a specific protein called CXCR4 (at a level more than twice the control measurement) at the time of pre-screening
  • People with AML or ALL who have already received treatment, but whose cancer has come back or stopped responding, and for whom no other standard treatment options are available
  • People who have had at least 15 days pass since their last cancer treatment
  • People who are generally able to carry out daily activities with little or no restriction (as measured by a standard medical scale called ECOG, with a score below 2)
  • People whose kidneys are functioning at an adequate level (confirm specific threshold with trial site)
  • People with liver enzyme levels within a certain range (confirm specific values with trial site — a different threshold may apply if leukaemia is present in the liver)
  • People with bilirubin (a liver-related substance in the blood) at or below a certain level (confirm with trial site)
  • Women who could become pregnant must have a documented negative pregnancy test before enrolling
  • People who are fertile (male or female) and agree to use an effective form of contraception throughout the study
  • People with no significant heart problems, and where the heart is pumping at more than 45% of its normal capacity
  • People whose lungs are functioning above a minimum level on a specific breathing test (confirm with trial site)
  • People who have signed a written consent form agreeing to take part
  • People who are willing and able to attend scheduled visits and follow all study procedures
  • People who are covered by, or are a beneficiary of, the French social security system

Who may not be able to join:

  • People whose cancer has spread to the membranes surrounding the brain and spinal cord
  • People who are HIV positive
  • People with an active Hepatitis B or C infection
  • People who have had an active infection within 7 days before starting treatment
  • People with a current or previous second cancer, except for certain treated and resolved cancers such as a specific type of skin cancer (basal cell carcinoma), cervical cancer treated with curative intent, or another solid cancer with no signs of disease for at least one year
  • People with psychological, family, social, or geographical circumstances that may make it difficult to follow the study schedule and requirements
  • People already participating in another clinical trial involving experimental drugs at the same time
  • People who have medical reasons they cannot receive certain supporting medications used in the study (confirm the specific medications with the trial site)
  • People who have not provided written consent to participate
  • Women who are pregnant or breastfeeding
  • People who are under legal guardianship or trusteeship
  • People who are under judicial protection

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 12 July 2026
Phase 2: approximately ~30% 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

Phone: 02 40 08 39 94

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 2
Registry
ClinicalTrials.gov
Start date
22 October 2024
Est. completion
22 October 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Safety of RLT using one injection of [177Lu]Lu-PentixaTher; Tolerance

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: 12 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