Phase 2 Leukaemia Trial, Recruiting NCT07165769 Sponsor: Institute of Hematology & Blood Diseases Hospital, China Condition: Leukaemia
Back to Leukaemia

Phase 2 Leukaemia Trial, Recruiting

NCT07165769
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 aged 18 to 80 years, of any sex
  • People who have been diagnosed with SBLPN (a specific type of lymphoma) confirmed by laboratory tissue or cell testing, and who need active treatment
  • People who have not previously received any systemic (whole-body) treatment for SBLPN
  • People with a general health and activity level rated 0 to 2 on a standard medical scale, meaning able to carry out at least some daily activities (confirm with trial site)
  • People with a life expectancy of at least 6 months
  • People whose blood count and organ function test results meet specific minimum levels, including adequate white blood cell counts, platelets, liver function, and kidney function (confirm with trial site for exact values)
  • People who agree to use medically approved contraception throughout the study and for 4 weeks after treatment ends, if there is any possibility of becoming pregnant
  • People who are willing to join the study voluntarily and sign a written consent form

Who may not be able to join:

  • People diagnosed with a central nervous system disorder, including lymphoma affecting the brain or spinal cord, within the past year
  • People who have had another type of cancer in the past 3 years, with some exceptions such as certain treated skin cancers or early-stage cervical conditions (confirm with trial site for full list of exceptions)
  • People who have taken an experimental drug, antibiotic, or participated in another interventional clinical trial within the past 4 weeks
  • People who have had major surgery (other than a lymph node biopsy) within the past 14 days, or who are expected to need major surgery during the study
  • People who have previously used experimental treatments specifically targeting SBLPN
  • People with active immune system conditions, autoimmune diseases, or who have been on higher-dose steroid medications within the past 7 days, or who are on any immune-suppressing treatment
  • People with severe liver problems (such as serious jaundice, brain complications from liver failure, or related conditions), severe malnutrition, multiple organ failure, or severe kidney disease
  • People with significant heart conditions, including serious heart failure, a heart attack within the past 6 months, uncontrolled irregular heartbeat, poorly controlled high blood pressure despite medication, or unstable chest pain
  • People with bleeding disorders or blood clotting problems, or who have had a blood clot event within the past 3 months
  • People with a known allergy or sensitivity to any ingredient in the study medications
  • People who are pregnant, breastfeeding, or who are able to become pregnant but are unwilling or unable to use contraception
  • People the trial doctor considers unsuitable for participation for other safety or practical reasons

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 9 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: Shuhua Yi, Dr, Institute of Hematology & Blood Diseases Hospital, China

Phone: +86-022-23909106

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
Institute of Hematology & Blood Diseases Hospital, China
Registry
ClinicalTrials.gov
Start date
4 September 2025
Est. completion
31 December 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Objective response rate,ORR

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: 9 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