Phase 2 Leukaemia Trial, Recruiting NCT06696183 Sponsor: Technische Universität Dresden Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT06696183
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:

  • People who have been newly diagnosed with a type of blood cancer called AML (acute myeloid leukaemia), where at least 20% of bone marrow cells are abnormal blast cells, but not the specific subtype called APL (acute promyelocytic leukaemia)
  • People whose AML has a specific gene change called a FLT3 mutation, detected at the time of first diagnosis
  • People whose doctor has determined that standard intensive chemotherapy is not suitable for them
  • People who have already received one cycle of a standard treatment combination of two drugs called Venetoclax and Azacitidine before joining the trial

Who may not be able to join:

  • People whose AML has come back after treatment or has stopped responding to treatment (known as relapsed or refractory AML)
  • People who have previously received any treatment for AML, other than a drug called hydroxyurea and/or one cycle of Venetoclax and Azacitidine as standard care
  • People who have previously been treated with a drug called Gilteritinib
  • People who have active involvement of the brain or spinal cord by their leukaemia
  • People who have a specific heart electrical abnormality detected at screening, including a prolonged QTcF interval (above 450 ms) or a condition called Long QT Syndrome (confirm with trial site)
  • People who are currently taking certain strong medications that affect how the body processes drugs, or who are taking a herbal supplement called St. John's Wort

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 26 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: +49 351 458 4190

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
Sponsor
Technische Universität Dresden
Registry
ClinicalTrials.gov
Start date
25 April 2025
Est. completion
1 April 2029

Where this trial is recruiting

🇩🇪 Germany

Primary endpoints

Ratio of dose delivered/dose planned

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: 26 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