Phase 2 Lymphoma Trial, Recruiting NCT06718244 Sponsor: Ruijin Hospital Condition: Lymphoma
Back to Lymphoma

Phase 2 Lymphoma Trial, Recruiting

NCT06718244
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 16 to 70 years at the time of screening, any gender
  • People with a good general health and activity level, as measured by a standard performance scale (ECOG score of 0 or 1)
  • People newly diagnosed with a type of blood cancer called Ph-negative B-cell acute lymphoblastic leukaemia (B-ALL), who are in their first remission after chemotherapy but still have a small detectable amount of leukaemia remaining in the bone marrow (called MRD-positive)
  • People newly diagnosed with a related type called Ph-positive B-ALL, who are also in their first remission but still have a small detectable amount of leukaemia remaining
  • People whose leukaemia cells tested positive for a protein called CD19 at the time of diagnosis
  • People whose liver, kidneys, heart, lungs, and blood clotting function all fall within acceptable ranges as measured by specific blood and other tests
  • People who meet the trial centre's requirements for a blood cell collection procedure (leukapheresis), with no medical reasons preventing this
  • People who are willing to take part and have signed a consent form agreeing to join the study

Who may not be able to join:

  • People who have previously received CAR-T cell therapy
  • People with an inherited bone marrow failure condition or any other known bone marrow failure syndrome
  • People with active autoimmune diseases that currently require treatment
  • People who test positive for certain infections, including active hepatitis B, hepatitis C, syphilis, HIV, or who have detectable levels of Epstein-Barr virus (EBV) or cytomegalovirus (CMV) in their blood
  • People who have an active infection at the time of screening
  • People who have had another type of cancer in the past five years, unless a doctor determines the risk of it returning is very low or the person has been cancer-free for more than five years after curative treatment
  • People with significant heart problems, including severe heart failure, serious irregular heartbeat, uncontrolled high blood pressure or high blood pressure in the lungs, unstable chest pain, a heart attack or heart surgery within the past six months, significant heart valve disease, or other heart conditions a doctor considers unsuitable
  • People with a history of epilepsy, cerebellar disease, or other active disorders affecting the brain or nervous system
  • People with uncontrolled diabetes
  • People who have had a significant blood clot in a vein or in the lungs within the past six months that is not well controlled
  • People with a known allergy or sensitivity to any ingredient in the study treatment
  • People who have received a live vaccine within six weeks before screening
  • People whose life expectancy is less than three months
  • People who have taken part in another clinical trial involving experimental treatments within three months (or within a specified timeframe for approved drugs) before the cell infusion, or who plan to join another trial or receive other cancer treatments during the study
  • People with any other condition that the trial doctor considers makes participation unsuitable

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 19 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: +86 13651996101

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
Registry
ClinicalTrials.gov
Start date
10 December 2024
Est. completion
31 December 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

MRD negativity rate

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: 19 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