Phase 2 Leukaemia Trial, Recruiting NCT07604064 Sponsor: Kissei Pharmaceutical Co., Ltd. Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT07604064
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 are Japanese patients and who personally provide written agreement to take part in this clinical trial
  • People who have been diagnosed with a type of blood cancer called AML (Acute Myeloid Leukaemia), as defined by the World Health Organization's 2022 guidelines, but not a specific subtype called acute promyelocytic leukaemia with a particular genetic change (t(15;17))
  • People whose AML has come back after treatment or has not responded to treatment, whether or not a bone marrow or stem cell transplant from a donor has previously been carried out
  • People whose AML has been confirmed, through central laboratory testing, to have a specific genetic change called an IDH1 mutation, detected after the cancer returned or stopped responding to treatment

Who may not be able to join:

  • People who have a different genetic change called an IDH2 mutation, or who have previously been treated with a medicine that targets IDH2
  • People who have had serious problems tolerating medicines that target IDH1
  • People who the trial doctor or their team considers to be unsuitable for the trial for any other reason

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 22 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

Principal Investigator: Yumi Ikezaki, Kissei Pharmaceutical Co., Ltd.

Phone: Email only

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
Kissei Pharmaceutical Co., Ltd.
Registry
ClinicalTrials.gov
Start date
1 June 2026
Est. completion
1 September 2030

Where this trial is recruiting

🇯🇵 Japan

Primary endpoints

Incidence of adverse events and adverse drug reactions

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: 22 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