Study of Niacin in Glioblastoma

NCT ID: NCT04677049

Last Updated: 2026-01-02

Basic Information

• Recruitment Status: SUSPENDED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 59 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-03-18
• Study Completion Date: 2026-12-31

Brief Summary

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.

Detailed Description

During the Phase I stage Niacin CRT™ dose will be escalated every 4 weeks until the maximum tolerated dose (MTD) is determined. The MTD dose will be prescribed to patients during the Phase II stage.

During the Phase I study a sample of blood at baseline, at each level dose of Niacin CRT™, and every two months during the maintenance phase while on Niacin CRTTM will be sent to a lab to evaluate the peripheral activity of Niacin CRT™ in innate immune system cells. These samples will be taken at the time of routine standard of care lab work.

Based on prior clinical trials evaluating niacin extended release formulation for the management of dyslipidaemias there is vast experience on dose escalation of niacin. One of the main side effects is flushing that is ameliorated by escalating doses in intervals no shorter than 4 weeks and usually decreases with time.

Following this schema, there is no increase in dose coinciding with TMZ while administered in a 5/28 days schedule (given daily for 5 days of each 28-day cycle). This will not only improve tolerance but also will allow us to differentiate potential adverse events from chemotherapy from the ones from Niacin CRT™.

Conditions

Glioblastoma IDH (Isocitrate Dehydrogenase) Wildtype

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Niacin

Niacin controlled release technology (CRT):

Niacin CRT™ is to be started 7 days before concurrent Radiation Therapy (RT)- Temozolomide (TMZ) treatment.

Chemo/Radiation Therapy:

For all patients, regardless of the phase of the study, concurrent RT and TMZ for 6 weeks followed by 6-12 cycles of monthly TMZ will be given.

Concurrent Temozolomide:

TMZ will be administered from the first to the last day of RT at 75 mg/m2 orally (PO) for a maximum of 49 days.

Monthly Temozolomide:

Cycles of chemotherapy Day 1 to Day 5 every 28 days will start 28 days (+/- 2 days) after the end of RT-TMZ. First cycle of TMZ is administered at 150 mg/m2 Day 1-Day 5 by mouth (PO) and increased to 200 mg/m2 Day 1-Day 5 PO from cycle 2 onwards if well tolerated. While 6 cycles are standard of care, the Neuro-Oncologist may continue up to 12 cycles if clinically appropriate.

Group Type: EXPERIMENTAL

Niacin CRT

Intervention Type: DRUG

A controlled release technology (CRT) tablet of Niacin

Interventions

Niacin CRT

A controlled release technology (CRT) tablet of Niacin

Intervention Type: DRUG

Other Intervention Names

Nicotinic acid; Vitamin B3

Eligibility Criteria

Inclusion Criteria

• Adults, 18 years old to 75 years old inclusive.
• New diagnoses of glioblastoma IDH wild type.
• ECOG 0-2 (Appendix I).
• Candidates for concurrent standard first line treatment according to their Neuro-Oncologist and Radiotherapy Oncologist after maximal safe debulking neurosurgery. Patients that only had biopsy are included as long as pathology confirms the diagnoses and it is considered the maximal safe procedure for that patient.
• Adequate hematological, renal and hepatic function (see details in Section 4.1 of the protocol).
• Absence of known human immunodeficiency virus (HIV) infection, chronic hepatitis B or hepatitis C infection.
• Absence of any other serious medical condition according to the medical judgment of the Qualified Investigator prior to registration.
• Absence of any medical condition, which could interfere with oral medication intake.
• Signed informed consent.
• Patients must be accessible for treatment and follow-up. Patients registered on this trial must be treated and followed at the participating centre.
• Women/men of childbearing potential must have agreed to use a highly effective contraceptive method.

Exclusion Criteria

• Glioblastoma, IDH-mutant.
• Patients with a history of other malignancies, except: adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix, or other solid tumours curatively treated with no evidence of disease for ≥ 5 years. Additionally, any low grade or low risk malignancy not requiring treatment will not exclude a patient from participation in the trial.
• Known hypersensitivity to niacin.
• Inability to provide informed consent.
• Active liver disease or unexplained persistent elevations of serum transaminases.
• Active peptic ulcer or active gastrointestinal bleeding.
• Unstable angina or myocardial infarction within 6 months.
• Symptomatic gout.
• Patients on 3-hydroxy-3-methylglutaryl-coenzyme (HMG-COA reductase) inhibitors that cannot discontinue them at least 2 weeks before starting Niacin CRT™.
• Any prior systemic treatment for glioblastoma (standard, evidence based or experimental) or radiotherapy/radiosurgery.
• Individuals with MRI non-compatible metal in the body, or unable to undergo MRI procedures including allergy to gadolinium.
• Patients unfit for any treatment component, including contraindications for radiotherapy or Connective Tissue Disease.
• Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks of the first dose of treatment.
• Has known psychiatric or substance abuse disorders that would interfere with compliance with the requirements of the trial.
• Pregnant, breast-feeding, unable and/or unwilling to use contraception methods.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Tom Baker Cancer Centre

OTHER

Sponsor Role: collaborator

AHS Cancer Control Alberta

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Gloria Roldan Urgoiti, MD

Role: PRINCIPAL_INVESTIGATOR

Tom Baker Cancer Centre/Arthur J.E. Child Comprehensive Cancer Centre

Locations

Tom Baker Cancer Centre/Arthur J E Child Comprehensive Cancer Centre

Calgary, Alberta, Canada

Countries

Canada

Other Identifiers

NiacinCNS2020

Identifier Type: -

Identifier Source: org_study_id