Testing Personalized Drug Options for Glioblastoma Using Patient Tumor Cells
Tests a lab screen of drugs on a patient's own tumor cells for glioblastoma.
Plain-language title generated from the registry record
Registry title: Personalized Targeted Glioblastoma Therapies by ex Vivo Drug Screening
Key facts
- Where
- Vienna, AustriaSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 75 years old?
- Has your doctor told you that the MGMT gene in your tumour is "methylated" or "unmethylated"?
- Has a test on your tumour shown it is "IDH wild-type"?
- Are you pregnant or breastfeeding?
Source: NCT06512311, who can take part
Where in Austria
- AKH Vienna, Department for Internal Medicine I, OncologyVienna, AustriaTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Medical University of Vienna
- Trial code
- NCT06512311
- Record updated
- 14 April 2026
- Original description
Patient derived cell line (PDC) -based drug screening will be applied to formulate a personalized treatment approach.Read full original descriptionShow less
Personalized Targeted Glioblastoma Therapies by ex Vivo Drug Screening: Advanced Brain Tumor TheRApy Clinical Trial (ATTRACT)
Patient derived cell line (PDC) -based drug screening will be applied to formulate a personalized treatment approach.
Inclusion: Age 18-75; ECOG performance status 0-2; Newly diagnosed glioblastoma, IDH wildtype - according to the 2021 WHO classification of Tumors of the Central Nervous System; MGMT promotor unmethylated per local investigator; Tissue available for drug screening (successful PDC establishment from surgical material); Scheduled for concomitant radio-chemotherapy with temozolomide; Written informed consent.
Exclusion: Patients with a concurrent malignancy or malignancy within five years prior of study enrolment except for carcinoma in situ of the cervix, non-melanoma skin carcinoma or stage I uterine cancer within the last 3 years; Current known infection with hepatitis B virus (HBV), or hepatitis C virus (HCV). Patients with past HBV infection or resolved HBV infection (defined as having a negative hepatitis B surface antibody [HBsAg] test and a positive anti-hepatitis B core antibody [HBcAb] test, accompanied by a negative HBV DNA test) are eligible. Patients positive for anti-HCV antibody are eligible only if polymerase chain reaction (PCR) is negative for HCV RNA; Known human immunodeficiency virus (HIV) infection that is not well controlled. All of the following criteria are required to define an HIV infection that is well controlled: undetectable viral RNA, CD4+ count ≥350 cells/mm3 , no history of AIDS-defining opportunistic infection within the past 12 months, and stable for at least 4 weeks on the same anti-HIV medications (meaning there are no expected further changes in that time to the number or type of antiretroviral drugs in the regimen). If an HIV infection meets the above criteria, monitoring of viral RNA load and CD4+ count is recommended; Any of the following co-morbidities:; Pre-existing severe peripheral neuropathy (> CTCAE grade 2); Hepatic impairment (Bilirubin Level >1.5x-3x ULN); Kidney dysfunction (CrCl < 59 mL/min); Cardiac dysfunction with left ventricular ejection fraction <60 %; Any grade of interstitial lung disease; Ongoing or previous history of rhabdomyolysis; Acute pancreatitis; QTcF ≥480 msec; Diabetes mellitus with fasting glucose > 250mg/dl or 13.9 mmol/L; Current participation in another therapeutic clinical trial; Pregnant or lactating women; Participants who are unable or unwilling to comply with the requirements of the protocol as assessed by the investigator.