Neoadjuvant Chemoradiotherapy with or without Azeliragon for the Treatment of Newly Diagnosed Glioblastoma
This early phase I trial compares the effect of adding azeliragon to radiation therapy (RT) and temozolomide (TMZ) before surgery (neoadjuvant chemoradiotherapy) versus (vs.) neoadjuvant chemoradiotherapy alone in treating patients with newly diagnosed glioblastoma (GBM). Azeliragon is a drug that may help slow tumor growth and tumor invasion into healthy tissue, as well as reduce certain types of cells that prevent the immune system from responding to the cancer. RT uses high energy x-rays, particles, or radioactive seeds to kill cancer cells and shrink tumors. Temozolomide is in a class of medications called alkylating agents. It works by damaging the cell's deoxyribonucleic acid and may kill tumor cells and slow down or stop tumor growth. Giving azeliragon with standard neoadjuvant chemoradiotherapy may be safe, tolerable, and/or effective in treating patients with newly diagnosed GBM.
Inclusion Criteria
- Histologically proven diagnosis of IDH-wildtype GBM (World Health Organization [WHO] grade 4) according to the 2021 WHO classification (including subtypes such as gliosarcoma)
- Radiographic evidence of residual tumor after initial surgery or biopsy
- Patient is amenable for future surgery (either surgical resection or laser interstitial thermal therapy [LITT]) to sample the residual tumor after completion of chemoradiotherapy
- At least 18 years of age
- Eligible for and planning to receive standard fractionated RT of 60 gray (Gy) with concurrent TMZ
- Recovered from the effects of surgery, postoperative infection, and other complications sufficiently for initiation of chemoradiotherapy, in the opinion of the treating physician
- Karnofsky performance status ≥ 60
- Absolute neutrophil count (ANC) ≥ 1.5 K/cumm
- Platelets ≥ 100 K/cumm
- Hemoglobin > 9.0 g/dL (Note: the use of transfusion or other intervention to achieve hemoglobin [Hgb] > 9.0 g/dL is acceptable)
- Total bilirubin ≤ 1.5 upper limit of normal (ULN)
- Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamic pyruvic transaminase [SGPT]) ≤ 3 x ULN
- Creatinine ≤ 1.5 ULN or creatinine clearance ≥ 60 mL/min
- If there is history of human immunodeficiency virus (HIV) infection, patients must be on effective antiretroviral therapy, and HIV viral load must be undetectable within 6 months of study enrollment
- If there is history of chronic hepatitis B virus (HBV) infection, patients must have either been treated or are on suppressive therapy (as indicated), and HBV viral load must be undetectable
- If there is history of hepatitis C virus (HCV) infection, patients must have been treated, and HCV viral load must be undetectable
- Females of childbearing potential (defined as a female who is non-menopausal or surgically sterilized) and sexually active heterosexual males must be willing to use an acceptable method of birth control (i.e., hormonal contraceptive, intra-uterine device, diaphragm with spermicide, condom with spermicide, or abstinence) during the trial and for 6 months after the last administration of azeliragon. Should a female trial participant or female partner of a male trial participant become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately
- Able to understand and willingness to sign an institutional review board (IRB)-approved written informed consent document. Legally authorized representatives may sign and give informed consent on behalf of study participants
Exclusion Criteria
- Prior cranial RT or RT to the head and neck where potential field overlap may exist
- Leptomeningeal or metastatic involvement
- Known IDH mutation. IDH status could be determined by either immunohistochemistry or sequencing as evaluated per routine clinical care
- Patients receiving CYP 2C8 inhibitors within 2 weeks or 5 half-lives prior to study entry
- Patients with a gastrointestinal condition that could interfere with swallowing or absorption
- Patients with concurrent participation in another interventional clinical trial or use of another investigational agent within 30 days prior to study entry. Patients who are participating in non-interventional clinical trials (e.g., QOL, imaging, observational, follow-up studies, etc.) are eligible, regardless of the timing of participation
- Medical contraindication to MRI (e.g., unsafe foreign metallic implants, incompatible pacemaker, inability to lie still for long periods, severe to end-stage kidney disease or on hemodialysis)
- Pregnant or breastfeeding. Women of childbearing potential must have a negative pregnancy test within 14 days of the first dose of RT (Arm 1) or azeliragon (Arm 2)
- Patients with psychiatric illness/social situations, including alcohol or drug abuse that in the investigator's opinion will prevent administration or completion of protocol therapy
- Non-English speaking, as the cognitive assessments will only be available in English
Additional locations may be listed on ClinicalTrials.gov for NCT06831526.
Locations matching your search criteria
United States
Missouri
Saint Louis
PRIMARY OBJECTIVE:
I. To evaluate the impact of azeliragon on immune cells within the tumor microenvironment when administered with RT and TMZ in patients with newly diagnosed isocitrate dehydrogenase (IDH)-wildtype GBM.
SECONDARY OBJECTIVES:
I. To evaluate safety and tolerability of combining azeliragon with RT and TMZ in patients with newly diagnosed IDH-wildtype GBM.
II. To determine progression free survival (PFS) and overall survival (OS) of newly diagnosed IDH-wildtype GBM patients treated with the combination of RT, TMZ, and azeliragon.
III. To evaluate the feasibility of performing surgery or laser interstitial thermal therapy (LITT) after neoadjuvant chemoradiotherapy with or without azeliragon.
TERTIARY/EXPLORATORY OBJECTIVES:
I. To assess the effect of azeliragon on the pathological response of GBM to RT and TMZ.
II. To assess changes in neurocognitive function (NCF) one month post-chemoradiotherapy with concurrent azeliragon.
III. To assess changes in resting state-functional magnetic resonance imaging (RS-fMRI) one month post-chemoradiotherapy with concurrent azeliragon.
IV. To evaluate the relationship between changes in RS-fMRI and NCF in GBM patients after chemoradiotherapy.
V. To explore the impact of azeliragon on changes in NCF six months after chemoradiotherapy compared to a historical control of patients treated without azeliragon (NCT04975139).
VI. To explore the impact of azeliragon on changes in RS-fMRI six months after chemoradiotherapy compared to a historical control of patients treated without azeliragon (NCT04975139).
VII. To explore changes of white matter injury as reflected on diffusion tensor imaging (DTI) after chemoradiotherapy with or without azeliragon.
VIII. To evaluate drug concentration of azeliragon in tumor tissue versus plasma.
IX. To evaluate the impact of chemoradiotherapy and azeliragon on quality of life (QOL) of GBM patients.
OUTLINE: Patients are randomized to 1 of 2 arms.
ARM 1:
NEOADJUVANT THERAPY: Patients undergo RT daily (Monday-Friday) for 30 treatments and receive concurrent TMZ orally (PO) once daily (QD) for the duration of RT in the absence of disease progression or unacceptable toxicity. At 4-6 weeks after completion of RT, patients undergo surgical resection or LITT.
ADJUVANT THERAPY: Following recovery from surgery, patients receive azeliragon PO twice daily (BID) on days -6 to -1 of cycle 1 and then QD thereafter starting on day 1 of cycle 1. Patients also receive TMZ PO QD on days 1-28 of each cycle. Cycles repeat every 28 days for up to 6 months in the absence of disease progression or unacceptable toxicity.
ARM 2:
NEOADJUVANT THERAPY: Patients receive azeliragon PO BID on days -6 to -1 and then QD thereafter starting on day 1 and continuing until the day before surgery in the absence of disease progression or unacceptable toxicity. Patients also undergo RT daily (Monday-Friday) for 30 treatments starting on day 1 and receive concurrent TMZ PO QD for the duration of RT. At 4-6 weeks after completion of RT, patients undergo surgical resection or LITT.
ADJUVANT THERAPY: Following recovery from surgery, patients receive azeliragon PO BID on days -6 to -1 of cycle 1 and then QD thereafter starting on day 1 of cycle 1. Patients also receive TMZ PO QD on days 1-28 of each cycle. Cycles repeat every 28 days for up to 6 months in the absence of disease progression or unacceptable toxicity.
Additionally, all patients undergo tissue sample collection on study and magnetic resonance imaging (MRI) and blood sample collection throughout the trial. Patients may also undergo RS-fMRI and DTI throughout the trial.
After completion of study treatment, patients are followed up at 30 days and months 6 and 12.
Trial PhasePhase O
Trial Typetreatment
Lead OrganizationSiteman Cancer Center at Washington University
Principal InvestigatorJiayi Huang
- Primary ID202504190
- Secondary IDsNCI-2025-04723
- ClinicalTrials.gov IDNCT06831526