Phase 2 Brain Cancer Trial, Recruiting NCT04267978 Sponsor: Beijing Sanbo Brain Hospital Condition: Brain Cancer
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Phase 2 Brain Cancer Trial, Recruiting

NCT04267978
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:

  • Adults aged 18 to 70 years old
  • People who have been diagnosed with a brain tumour called GBM (glioblastoma) or a lower-grade brain tumour (such as oligodendroglioma, astrocytoma, or related types), confirmed by tissue testing
  • People whose tumour has come back, either confirmed by a new biopsy or surgery (done at least 2 weeks before joining), or confirmed by a brain scan (MRI) showing at least one measurable area of tumour growth
  • People who have previously received standard combined radiation and chemotherapy treatment, plus at least one cycle of chemotherapy, after their first diagnosis
  • People whose last radiation treatment was at least 3 months before joining the trial
  • People whose last chemotherapy was completed at least one full chemotherapy cycle interval before joining, with side effects mostly resolved (except hair loss or skin colour changes)
  • People with a general health and functioning score of 60 or above on the Karnofsky scale, which measures ability to carry out daily activities (confirm with trial site)
  • People taking steroid medications whose dose has been stable or reduced for at least 5 days before their baseline brain scan
  • People taking certain anti-seizure medications that affect drug metabolism must have switched to a different type of anti-seizure medication at least 1 week before joining
  • People whose doctors estimate they have a life expectancy of at least 12 weeks
  • People with adequate blood counts, liver function, kidney function, and heart function, confirmed by blood tests and a heart tracing (ECG) taken within 7 days before starting treatment (confirm with trial site for specific values)
  • People of childbearing potential who agree to use effective contraception throughout the study
  • People who have voluntarily agreed to take part and have signed a consent form

Who may not be able to join:

  • People who are unable to have an MRI scan, for example due to having a pacemaker or metal dental implants
  • People who are currently taking part in another clinical trial involving an experimental treatment
  • People with a history of serious allergic reactions to medications similar to those used in this trial
  • People who have previously received an organ transplant
  • People who have HIV or syphilis (Treponema pallidum) infection
  • People with serious heart disease, or whose heart tracing (ECG) shows certain specific abnormal changes
  • People who have difficulty absorbing tablets or capsules by mouth, for example due to ongoing vomiting, diarrhoea, or a bowel blockage
  • People who have had significant bleeding problems in the 3 months before joining, such as stomach or bowel bleeding, a bleeding stomach ulcer, a perforated bowel, a high level of hidden blood in the stool, bleeding in or around the brain, or blood vessel inflammation
  • People who have experienced a blood clot or stroke-related event in the 6 months before joining, such as a stroke, mini-stroke (TIA), brain bleed, deep vein thrombosis, or pulmonary embolism
  • People with a bleeding disorder who are being treated with blood-thinning or clot-dissolving medications
  • People whom the trial doctors consider unsuitable for other medical reasons

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 20 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: Jun-ping Zhang, Beijing Sanbo Brain Hospital

Phone: 86-010-62856783

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
Beijing Sanbo Brain Hospital
Registry
ClinicalTrials.gov
Start date
13 February 2020
Est. completion
31 December 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

progression-free survival rate at 6 months

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: 20 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