Phase 1 Leukaemia Trial, Recruiting NCT06049667 Sponsor: Nanjing Chia-tai Tianqing Pharmaceutical Condition: Leukaemia
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Phase 1 Leukaemia Trial, Recruiting

NCT06049667
Recruiting Phase 1

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 aged 18 or older, of any gender
  • People diagnosed with acute myeloid leukaemia (AML) that has come back or stopped responding to previous treatment
  • People with a general health and activity level rated between 0 and 2 on a standard medical scale (meaning able to carry out at least some daily activities)
  • People whose doctors estimate they have a life expectancy of at least 3 months
  • People with adequate bone marrow function and sufficiently healthy organ function
  • People who are able to understand the study's purpose and risks, and are willing to sign a consent form

Who may not be able to join:

  • People who have received cancer treatments (such as chemotherapy, immunotherapy, targeted therapy, radiation, or hormone therapy) within 2 weeks or 5 half-lives of the treatment — whichever is the longer period — before the trial starts
  • People who have taken part in another clinical trial and received an experimental treatment within 4 weeks before the trial starts
  • People who have had major surgery within 4 weeks before the trial starts, or who are expected to need surgery during the trial
  • People whose AML is a specific subtype, including acute promyelocytic leukaemia, AML arising from a blast crisis of chronic myelogenous leukaemia, or AML that has spread to the central nervous system
  • People with a current or previous separate cancer diagnosis, unless it was a fully cured non-invasive skin cancer, or another cancer that was fully cured more than 5 years ago with no recurrence (confirm with trial site)
  • People with a history of severe heart or brain blood vessel disease
  • People who have taken certain strong medications known to significantly affect how the body processes drugs (strong CYP3A4 or P-gp inhibitors or inducers) within 7 days before the trial starts
  • People who have received a live or weakened live vaccine within 4 weeks before the trial starts, or who plan to receive one during the trial
  • People who still have unresolved significant side effects (grade 2 or higher) from previous AML treatment, other than hair loss or other effects the doctor considers tolerable
  • People who have previously had an allogeneic (donor) stem cell transplant, or who have had an autologous (own cells) stem cell transplant within 3 months before the trial starts
  • People who are unable to swallow tablets, or who have conditions that seriously affect the absorption of medicines through the digestive system
  • People with infections that are not under control, as judged by the treating doctor
  • People with a known infection of hepatitis B, hepatitis C, HIV, or syphilis
  • People with known alcohol or drug dependence
  • People with mental health conditions or who are unlikely to be able to follow the trial requirements
  • People with a history of severe allergic reactions to any medicine or food
  • Women who are pregnant or breastfeeding, and people of any gender (or their partners) who are planning a pregnancy and are not willing to use adequate contraception throughout the trial and for up to 3 months after the last dose
  • People considered unsuitable for the trial for other reasons, as judged by the treating doctor

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 28 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

Phone: 86-025-85109999

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
Nanjing Chia-tai Tianqing Pharmaceutical
Registry
ClinicalTrials.gov
Start date
7 August 2023
Est. completion
1 August 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Maximum tolerance dose (MTD) and dose limiting toxicity (DLT)

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: 28 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