Early Phase 1 Brain Cancer Trial, Recruiting NCT04943913 Sponsor: Shanghai Juncell Therapeutics Condition: Brain Cancer
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Early Phase 1 Brain Cancer Trial, Recruiting

NCT04943913
Recruiting Early 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 between 18 and 75 years old
  • People who have been confirmed by tissue testing to have a primary, returned, or spread brain glioma (a type of brain tumour)
  • People whose life expectancy is estimated to be more than 3 months
  • People who have a reasonable level of general physical functioning, as assessed by their doctor using standard scoring tools (confirm with trial site)
  • People whose standard treatment options have not worked, or for whom no standard treatments are available
  • People who have a tumour area that a surgeon can sample or remove, or a body fluid from which immune cells can be collected
  • People who have at least one measurable tumour that can be tracked during the trial
  • People whose recent blood test results (taken within 7 days before joining) show that white blood cells, infection-fighting cells, immune cells, platelets, and haemoglobin are all at or above minimum levels, and that kidney, liver, and blood-clotting results are within acceptable ranges (confirm specific values with trial site)
  • People who have no medical reason preventing them from having a biopsy or surgery
  • People of childbearing potential who are willing to use highly effective contraception from the time of agreeing to join, and for one year after a specific part of the treatment is completed
  • People who have stopped any cancer-targeting treatments — including radiotherapy, chemotherapy, or biological therapies — at least 28 days before immune cells are collected
  • People who are able to understand and sign the consent form
  • People who are able to attend follow-up visits and meet the other requirements of the trial

Who may not be able to join:

  • People who need steroid medications (such as prednisone) at a daily dose above 15mg, or who need immune-suppressing treatment for an autoimmune condition
  • People with significantly reduced lung function, based on specific breathing test measurements (confirm with trial site)
  • People with serious heart conditions, such as severe heart failure, uncontrolled coronary artery disease, very low blood pressure, poor heart pumping function, or significant heart rhythm or electrical conduction problems
  • People who have HIV infection or a positive HIV antibody test, active hepatitis B or C infection, or a syphilis infection
  • People with serious physical or mental health conditions
  • People who have an active infection throughout the body that requires treatment, or who have had a positive blood culture or imaging showing signs of infection
  • People who have received or are currently receiving other medicines, biological therapy, chemotherapy, or radiotherapy within the past month
  • People with a known allergy to substances similar to those used in cell-based therapies
  • People who have previously received immunotherapy and experienced a serious immune-related side effect rated at level 3 or above
  • People who still have significant side effects (above a mild level) from previous cancer treatments that have not resolved
  • People who are pregnant or breastfeeding
  • People who have previously had an organ transplant, a bone marrow or stem cell transplant from a donor, or kidney replacement therapy (such as dialysis)
  • People who, in the opinion of the trial doctor, have other serious health conditions or circumstances that make 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 16 July 2026
Early Phase 1 studies are small, early exploratory studies that come before the main Phase 1 to 3 testing, so a standard phase success rate does not apply.

Contact this trial

Principal Investigator: Qing Lan, Second Affiliated Hospital of Soochow University

Phone: 086-18001759113

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
Early Phase 1
Sponsor
Shanghai Juncell Therapeutics
Registry
ClinicalTrials.gov
Start date
6 May 2021
Est. completion
30 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Adverse Events (AE); Objective Response Rate (ORR); Disease Control Rate (DCR); Duration of Response (DOR); Progression-Free Survival (PFS); Overall Survival (OS)

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: 16 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