Phase 2 Leukaemia Trial, Recruiting NCT06376721 Sponsor: Beijing Tongren Hospital Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT06376721
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 diagnosed with extranodal NK/T-cell lymphoma (a type of lymphoma), confirmed through tissue and laboratory testing using standard diagnostic criteria.
  • People whose lymphoma has come back after initially responding to treatment, has not responded to treatment, or has been newly diagnosed at an advanced stage (stage III or IV).
  • People who have at least one area of disease that can be measured and tracked on a PET/CT scan, CT scan, or MRI.
  • People who are expected to live for more than 3 months.
  • People who are in reasonably good general health, as measured by a standard medical scoring system (ECOG score of 0–2, meaning able to carry out at least some daily activities).
  • People whose recent blood test results (taken within 1 week before joining) show that blood cell counts, kidney function, liver function, and a blood protein called fibrinogen are all within the acceptable ranges set by the trial.
  • People who have signed a form agreeing to take part in the trial.

Who may not be able to join:

  • People whose lymphoma has spread to the brain or spinal cord, or who have another type of cancer.
  • People who have previously received a type of medication called a PI3K inhibitor.
  • People whose general health is too poor (ECOG score of 2 or higher) (confirm with trial site, as this overlaps with an inclusion criterion).
  • People who are pregnant or breastfeeding.
  • People who could potentially have children but are unwilling or unable to use effective contraception during the trial.
  • People who are allergic to any of the medications used in the trial.
  • People who currently have an active infection.
  • People with a history of immune system deficiency, including HIV, other inherited or acquired immune conditions, or a history of organ transplant.
  • People with a history of a lung condition called interstitial pneumonia, or non-infectious pneumonia, or where this condition is strongly suspected.
  • People with a past history of neurological or psychiatric conditions, including epilepsy or dementia.
  • People who, in the treating doctor's judgment, have other health conditions that could seriously affect their safety or their ability to complete the trial.

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: Liang Wang, M.D., Beijing Tongren Hospital

Phone: +861058268442

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
Beijing Tongren Hospital
Registry
ClinicalTrials.gov
Start date
14 April 2024
Est. completion
31 October 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

The best objective response rate(ORR) over 6 treatment cycles

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