Phase 2 Brain Cancer Trial, Recruiting NCT07318818 Sponsor: Tasly Pharmaceutical Group Co., Ltd Condition: Brain Cancer
Back to Brain Cancer

Phase 2 Brain Cancer Trial, Recruiting

NCT07318818
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 who have given voluntary written consent to participate
  • Adults aged 18 to 70 years (inclusive), of any sex
  • People with glioblastoma (a type of brain tumour, grade 4, IDH wild-type) that has come back or continued to grow, confirmed through tissue or molecular testing according to the 2021 WHO brain tumour classification guidelines
  • People whose tumour tissue shows a certain level of specific proteins called CD44 or CD133, confirmed by laboratory staining of tumour tissue — this applies only to the Phase II part of the trial (confirm with trial site)
  • People with at least one measurable area of tumour that meets specific imaging criteria and measures 3 cm or less at its longest point
  • People who have already received radiation therapy and/or chemotherapy with temozolomide or bevacizumab
  • People whom the treating doctor has confirmed are suitable for a specific type of brain surgery involving a fluid drainage system and a small device called an Ommaya reservoir implanted under the scalp

Who may not be able to join:

  • People with a history of severe allergies or allergic reactions, including to cell-based products
  • People who have received certain cancer treatments within a specified period before a blood collection procedure — including biological therapies within 6 weeks, radiotherapy or surgery within 4 weeks, chemotherapy or immune-modulating drugs within 2 weeks, or certain traditional Chinese herbal medicines with anticancer properties within 1 week
  • People whose side effects from previous cancer treatments have not sufficiently resolved (side effects must have improved to a mild level or lower, with some exceptions such as hair loss or skin changes)
  • People whose tumour has spread to the brainstem or spinal cord
  • People with serious neurological conditions other than the brain tumour, such as meningitis, encephalitis, uncontrolled epilepsy, myasthenia gravis, or similar conditions
  • People with a primary immune system deficiency, autoimmune diseases requiring ongoing medication (such as Crohn's disease, rheumatoid arthritis, or lupus), or a past history of autoimmune diseases affecting the nervous system (such as multiple sclerosis or Parkinson's disease)
  • People currently receiving or requiring long-term use of immune-suppressing medications, with limited exceptions for low-dose or short-term steroid use
  • People who have previously had a bone marrow or organ transplant, or who are currently waiting for one
  • People with certain active infections, including active hepatitis B, active hepatitis C, syphilis, or HIV
  • People who have previously participated in any gene therapy or cell therapy trial
  • People who are pregnant or currently breastfeeding
  • People with a history of another cancer (other than glioma) within the past 5 years, with some exceptions for certain low-risk, well-treated cancers as determined by the treating 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 27 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: Zhang Wei, Prof., Beijing Tiantan Hospital, Capital Medical University, Beijing, P.R.China

Phone: +8615022490519

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
Tasly Pharmaceutical Group Co., Ltd
Registry
ClinicalTrials.gov
Start date
5 January 2026
Est. completion
29 February 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Dose limiting toxicities (DLTs); Adverse events (AEs); Maximum tolerated dose (MTD)

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: 27 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