Phase 2 Brain Cancer Trial, Recruiting NCT07145047 Sponsor: Mianyang Central Hospital Condition: Brain Cancer
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Phase 2 Brain Cancer Trial, Recruiting

NCT07145047
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 diagnosed with glioblastoma (a type of brain tumour) that has come back, where the medical team has determined that standard treatments are no longer working
  • People whose returning glioblastoma has been confirmed through a laboratory examination of tumour tissue
  • People whose brain scan (MRI) shows the returning tumour is larger than 1.0 cm at its widest point
  • People who have previously received at least one prior treatment, with enough time having passed since that treatment (for example, more than 28 days since surgery or radiotherapy, or specific waiting periods after certain chemotherapy drugs — confirm exact timing requirements with the trial site)
  • People aged 18 to 70 years old
  • People whose blood counts, kidney function, and liver function are within normal ranges
  • People who are willing to use an approved method of contraception throughout the study and for 180 days after receiving the study treatment
  • People who are able to follow the study procedures and provide written consent to participate

Who may not be able to join:

  • People who have taken part in another drug clinical trial within the past 4 weeks
  • People who have a tendency to bleed easily before surgery, or who are taking blood thinners or other medications that may increase bleeding risk
  • People whose cancer has spread to parts of the body outside the brain
  • People with poorly controlled liver function, including certain liver enzyme or bilirubin levels that are more than twice the normal upper limit
  • People who are currently pregnant or breastfeeding
  • People with an active uncontrolled infection, or conditions affecting the immune system such as autoimmune disease, active hepatitis B, hepatitis C, or active HIV infection
  • People with a history of misusing substances (such as drugs or alcohol) that they have been unable to stop, or people with a diagnosed mental health disorder
  • People with any active autoimmune disease or a history of autoimmune disease
  • People who have used antiviral medications within the past week
  • People who are currently receiving immunosuppressive therapy, chemotherapy, radiation, or biological therapy
  • People who cannot safely have an MRI scan — for example, those with pacemakers, certain metal implants, surgical clips, shrapnel, or metal objects in the eye (confirm specifics with the trial site)
  • People who have received a vaccination within 30 days before starting the study treatment
  • People who have previously received gene therapy or any type of oncolytic virus treatment
  • People with a history of brain or nervous system infections such as encephalitis, multiple sclerosis, or other central nervous system conditions
  • People who are unwilling to use contraception during the study and for 6 months after receiving the treatment
  • People who, in the investigator's judgement, have a serious health condition that could put them at risk or prevent them from completing the study

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 12 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

Phone: +868162247827

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
Mianyang Central Hospital
Registry
ClinicalTrials.gov
Start date
2 November 2023
Est. completion
31 December 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Maximum tolerated dose

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: 12 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