Brain Cancer Trial, Recruiting NCT06740955 Sponsor: The First Hospital of Jilin University Condition: Brain Cancer
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Brain Cancer Trial, Recruiting

NCT06740955
Recruiting Not Applicable

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 been newly diagnosed with glioblastoma (a type of brain tumour), confirmed by laboratory testing of tumour tissue
  • People who have had surgery to remove all or part of the tumour, or to take a small sample (biopsy)
  • People aged 18 to 70 years old at the time of signing the consent form, of any gender
  • People with a general health and functioning score of 60 or above on a standard medical scale called the KPS (confirm with trial site)
  • People whose doctors expect them to live for at least 6 months
  • People who are able to begin radiation therapy within 6 weeks after their surgery
  • People whose blood, kidney, and liver test results fall within acceptable ranges — including adequate white blood cell counts, platelet levels, haemoglobin, kidney function, and liver enzyme levels (confirm with trial site for specific values)
  • People who are able and willing to attend all required study visits and follow-up appointments
  • People of childbearing potential who agree to use reliable contraception throughout the study and for 6 months after treatment ends; women of childbearing potential must also have a negative blood pregnancy test within 72 hours before the first dose
  • People who voluntarily agree to take part and sign a consent form

Who may not be able to join:

  • People who have previously received systemic cancer treatment (such as chemotherapy) targeting the same tumour
  • People who have had radiation therapy to the head before
  • People whose current glioblastoma developed from a previous lower-grade brain tumour
  • People whose glioblastoma is a spread (metastasis) from a glioma that was originally in another part of the body
  • People who are unable to have an MRI scan, or unable to have an MRI scan with contrast dye
  • People who received a drug called bevacizumab or internal radiation treatment within one month before joining
  • People who participated in another clinical trial within one month before joining
  • People who experienced a serious injury or serious infection within one month before joining, including infections that required a hospital stay
  • People with significant heart problems, including certain types of heart muscle disease, uncontrolled irregular heartbeat, severe heart failure, or a weakened pumping function of the heart (confirm with trial site for specific classifications)
  • People who had a major surgical procedure (other than brain tumour surgery) within 4 weeks before joining
  • People with a history of misusing substances such as illicit drugs
  • People who have had another type of cancer within the past 5 years (exceptions may apply if the cancer was fully cured — confirm with trial site)
  • People with HIV, AIDS, active hepatitis B, hepatitis C, or a combination of hepatitis B and C infections
  • People who are allergic to a medicine called temozolomide, or who cannot take temozolomide for any other reason
  • Women who are not breastfeeding but have a positive blood pregnancy test within 7 days before the first treatment; or people (of any gender) who are unwilling to use at least one acceptable form of contraception during the study and for 3 months after the last treatment
  • People whom the trial investigators judge to have other conditions that could increase their risk from participating, or that make participation otherwise 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 6 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 13944152797

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
The First Hospital of Jilin University
Registry
ClinicalTrials.gov
Start date
13 August 2024
Est. completion
30 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall Survival

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: 6 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