Phase 1 Brain Cancer Trial, Recruiting NCT07551336 Sponsor: Beijing Biotech Condition: Brain Cancer
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Phase 1 Brain Cancer Trial, Recruiting

NCT07551336
Recruiting 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 18 to 75 years old at the time of signing consent
  • People who have been diagnosed with glioblastoma (a type of aggressive brain tumour, WHO grade 4) or a related high-grade brain tumour (WHO grade 3 or 4) that has come back or continued to grow after standard treatment
  • People who are scheduled for, or have already had, a surgical procedure to remove or sample their tumour — or who have stored tumour tissue available — so that specific tumour proteins can be tested and a small tube can be placed in or near the tumour
  • People whose tumour shows a high enough level of at least two of these specific proteins: IL13Rα2, EGFR (including a variant called EGFRvIII), or B7-H3 (confirm with trial site for exact thresholds)
  • People with a functional ability score of 60 or above on the Karnofsky Performance Scale, meaning someone still able to care for most of their own needs (confirm with trial site)
  • People whose blood tests show the heart, kidneys, and liver are working at levels that meet the trial's requirements
  • People who are able to have a brain MRI scan with contrast dye, or where an alternative type of scan has been approved by the trial site
  • Women who could become pregnant must have a negative pregnancy test, and all participants must agree to use effective contraception during the study and for a set period afterwards
  • People who are able to understand the study information and are willing to sign a consent form

Who may not be able to join:

  • People who have an active infection that is not under control, such as a bacterial, viral, or fungal infection
  • People with HIV who have a detectable level of the virus in their blood, or people with active hepatitis B or hepatitis C with a detectable viral load (confirm with trial site for any exceptions)
  • People who have a significant autoimmune disease — where the immune system attacks the body — that has required medication to suppress the immune system in the past 6 months
  • People who have needed high doses of steroid medication (such as more than 4 mg per day of dexamethasone or equivalent) in the 7 days before the scheduled treatment (low-dose steroids taken to replace what the body naturally produces may be permitted — confirm with trial site)
  • People who have received a previous gene-modified cell therapy (such as CAR-T or CAR-NK therapy) within the past 6 months, or who have previously had treatment targeting the same tumour proteins this trial focuses on, in a way that could affect safety assessments
  • People whose tumour has spread only to the lining around the brain and spinal cord with no other tumour site, or whose anatomy makes it unsafe to place the required small tube near the tumour (confirm with trial site for any exceptions)
  • People who have seizures that are not controlled even with the best available medication
  • People with serious heart or blood vessel problems — such as a recent heart attack or an irregular heartbeat that is not under control — that would make the treatment procedures too risky
  • People who are pregnant or breastfeeding
  • People who have any other condition that the trial doctor believes would make participation unsafe or would make it difficult to follow the trial's requirements

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 26 July 2026
Phase 1: approximately ~10% 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 13076790030

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 1
Sponsor
Beijing Biotech
Registry
ClinicalTrials.gov
Start date
2 March 2026
Est. completion
14 April 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence of dose-limiting toxicities (DLTs) after CAR-NK infusion (CTCAE v5.0; CRS and ICANS grading).; Determination of recommended phase 2 dose (RP2D)

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: 26 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