Phase 1 Brain Cancer Trial, Recruiting NCT05686798 Sponsor: Henry Ford Health System Condition: Brain Cancer
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Phase 1 Brain Cancer Trial, Recruiting

NCT05686798
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 who have been previously diagnosed with a high-grade brain tumour called glioblastoma or anaplastic astrocytoma, and whose brain scans show signs that the tumour has come back or grown
  • People who are 18 years of age or older and are able to give informed consent and commit to the full requirements of the study
  • People whose tumour has come back at least 3 months after finishing radiation therapy, at least 4 weeks after finishing most types of chemotherapy, or at least 6 weeks after finishing a specific type of chemotherapy called nitrosourea
  • People who have recovered from most side effects of previous treatments (side effects must be mild or resolved)
  • People whose tumour can be partially or fully removed through surgery, as determined by a specialist medical team including neurosurgeons, radiation specialists, and brain tumour doctors
  • People whose surgical cavity after tumour removal is not expected to connect to the fluid-filled spaces in the brain (ventricles)
  • People with a general health and functioning score of 60 or above on a standard medical scale called the Karnofsky Performance Status at the time of surgery
  • People who have not previously had gene therapy, virus therapy, immunotherapy, radiation implants, or chemotherapy implants (such as Gliadel Wafers) used to treat this tumour
  • People with no immune system disorders and who are not on immune-suppressing medications
  • People with blood test results within acceptable ranges, including kidney function, blood cell counts, and liver function, measured within 30 days before starting the study
  • Women who could become pregnant must agree to use contraception throughout treatment and for at least 90 days after surgery; men must use barrier contraception during treatment and for at least 90 days after surgery

Who may not be able to join:

  • People with an active infection (such as a viral, bacterial, or fungal infection) that has required treatment and caused a high fever or significant changes in white blood cell counts
  • People who test positive for HIV antibodies
  • People with a history of liver disease, including autoimmune or viral hepatitis
  • People who test positive for Hepatitis B or Hepatitis C
  • People currently taking immune-suppressing medications (corticosteroids are an exception)
  • People with serious medical or mental health conditions, or who are taking other medications, that the medical team believes could interfere with their ability to participate in or tolerate the trial
  • People with weakened immune systems or who are particularly vulnerable to serious viral infections
  • People who are pregnant or breastfeeding
  • People with known allergies to any product used in this trial
  • People who are unable to have a brain MRI scan
  • People whose tumour cannot be surgically removed

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 9 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

Principal Investigator: Tobias Walbert, MD, PhD, Henry Ford Health System

Phone: 3139162723

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
Henry Ford Health System
Registry
ClinicalTrials.gov
Start date
29 November 2022
Est. completion
1 January 2027

Where this trial is recruiting

🇺🇸 United States

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: 9 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