Stopped: Recruitment has been placed on hold to determine evaluability of currently enrolled patients. Recruitment will remain on hold until evaluability is confirmed. If fewer than 48 evaluable patients are achieved, the study will be re-opened to accrual.
This is a single institution Phase I-II study to evaluate the tolerability and Maximum Tolerated Dose (MTD) (Phase I) and efficacy (Phase II) of adding Niacin CRT™ to standard first line treatment (concurrent Radiation Therapy (RT) and Temozolomide (TMZ) following by monthly TMZ - AKA Stupp protocol) in patients with newly diagnosed glioblastoma isocitrate dehydrogenase (IDH) wild type.
Age range
18 Years – 75 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Determining the Maximum Tolerated Dose
Timeframe: Up to 24 weeks after registration onto the study
Evaluating if Niacin CRT Improves Glioblastoma Survival Rates
Timeframe: 6 months after determining the maximum tolerated dose which can last up to 24 weeks after registration onto the study