Phase 2 Leukaemia Trial, Recruiting NCT07188610 Sponsor: PersonGen BioTherapeutics (Suzhou) Co., Ltd. Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT07188610
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 or older, of any gender
  • People with a life expectancy of at least 3 months
  • People with a good general health and activity level, as measured by a standard medical scoring tool called the ECOG scale (score of 0 or 1, meaning fully active or able to carry out light activity)
  • People who have been formally diagnosed with acute T-cell lymphoblastic leukemia or lymphoma (T-ALL/LBL), including a subtype called early T-cell precursor (ETP), according to the latest World Health Organization classification
  • People whose T-ALL/LBL has come back after treatment or has not responded to treatment (including ETP-ALL/LBL)
  • People whose cancer cells test positive for a marker called CD7 during screening
  • People who have tumours outside the bone marrow (extramedullary lesions) must have at least one lesion that can be measured and tracked
  • People whose liver, kidney, heart, and lung function meet the levels required by the trial
  • People who do not have a severe mental health disorder
  • People who are able to understand the trial and are willing to sign a consent form

Who may not be able to join:

  • People with an active or uncontrolled autoimmune disease (a condition where the immune system attacks the body)
  • People who currently have graft-versus-host disease (GvHD), a complication that can occur after a stem cell or bone marrow transplant
  • People who have been diagnosed with another cancer in the past 5 years, with some exceptions — such as certain treated skin cancers, early-stage cervical abnormalities, localised prostate cancer, or breast ductal carcinoma in situ that was fully surgically removed
  • People who test positive for hepatitis B, hepatitis C, syphilis, or similar infections
  • People with serious heart disease
  • People with unstable ongoing health conditions, as determined by the trial doctor
  • People with an active infection or an infection that cannot be controlled without ongoing treatment
  • People who are pregnant or breastfeeding, or people planning to have a child within 2 years after receiving the trial treatment (this applies to both female participants and male participants whose partners are planning a pregnancy)
  • People who have previously received CAR-T therapy or any other type of gene-modified cell therapy
  • People who have participated in another clinical trial involving an unapproved drug within the month before screening
  • People who show signs of the cancer having spread to the central nervous system (brain or spinal cord) at the time of screening
  • People whose situation is considered unsuitable for preparing the cell therapy, as judged by the trial doctor
  • People considered unsuitable for any other reason, as determined by the trial 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 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: +86-13701389625

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
PersonGen BioTherapeutics (Suzhou) Co., Ltd.
Registry
ClinicalTrials.gov
Start date
25 September 2025
Est. completion
1 October 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Efficacy

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