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Not yet recruitingNCT07847476Updated Sep 29, 2026

Flubendazole Added to Standard Concurrent Chemoradiotherapy With Temozolomide in Patients With High-Grade Glioma

An interventional study of Flubendazole in Glioma Patients, sponsored by Assiut University. Not yet recruiting. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-09-29.

Sponsored by Assiut University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
122
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
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Study summary

This study To evalute the efficacy and safety of adding flubendazole to standard concurrent chemoradiotherapy with temozolomide in patients with high grade glioma and also to evaluate DFS,OS for those patients in clinical oncology department , Assiut university Hospital .

Read the detailed description

High grade glioma is the most common and lethal primary brain cancer, arising from glial stem cells . It is characterized by rapid growth, and a poor prognosis .Despite an intensive standard-of-care therapeutic approach combining surgical resection, radiotherapy, and chemotherapy with Temozolomide (TMZ) , survival rates remain low, with an almost inevitable recurrence . The median overall survival is only 12 to 15 months after diagnosis .Despite this scenario, no significant therapeutic advances have been recorded in the past 20 years. Innovative approaches such as tumor-treating fields, immunotherapies, and stem cell-based therapies have reached clinical trials, but clinical benefits remain limited . Therefore, there is an urgent need to identify new strategies to overcome the resistance of this type of cancer. A key contributor to treatment failure is the pronounced cellular heterogeneity of glioma, which resembles the complexity of a developing organ and contains cells with stem-like properties.There are a therapeutic agents that inhibit mitochondrial biogenesis also include antibiotics, anthelmintics, and antimycobacterial drugs. Flubendazole (FLU) is a member of the benzimidazole group, a drug commonly used in veterinary and human medicine for its anthelmintic properties. This anthelmintic effect is based on its ability to bind to β-tubulin, which causes inhibition of tubulin polymerization leading to microtubule disruption and loss of function . These effects are thought to be mediated not only via microtubule disruption but also via interference with several signaling pathways, including IL/JAK/STAT3, AKT, NF-κB and others, ultimately to cell cycle arrest, autophagy, apoptosis and/or other types of cell death .

02

Conditions studied

  • Glioma Patients

Keywords

  • Flubendazole
03

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • - Age ≥18 years.
  • Male or female
  • Histologically confirmed high grade glioma (WHO grade 3(III) and grade 4 IV) after surgery.
  • ECOG PS 0-2
  • Fit patient for concurrent chemoradiotherapy.

Exclusion criteria

Exclusion Criteria:

  • Age ≥80 years.
  • presence of another active malignancy .
  • known hypersensitivity to flubendazole.
  • pregnant or breastfeeding women.
  • inability to comply with study requirements.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
122 participants (estimated)

Study arms

  • Active comparator
    Flu

    Flubendazole 100 mg twice daily for 3 day in the week for 6 weeks

    Drug: Flubendazole

  • No intervention
    Pt will receive concurrent chemo radiotherapy with TMZ with placebo

    Pt will receive CCRth with TMZ with placebo

Interventions

  • DrugFlubendazole

    Flubendazole 100 mg twice daily for 3 day in the week for 6 weeks

05

What researchers measure

Primary outcomes

  1. Incidence of treatment-related adverse events

    Treatment-related adverse events will be assessed according to the Common Terminology Criteria for Adverse Events (CTCAE), version 5.0. The number and severity of treatment-related adverse events occurring during concurrent chemoradiotherapy will be recorded

    Time frame: From baseline until 30 days after completion of concurrent chemoradiotherapy

  2. Change in complete blood count (CBC)

    Complete blood count parameters, including hemoglobin, white blood cell count, absolute neutrophil count, and platelet count, will be assessed weekly during concurrent chemoradiotherapy to evaluate hematologic toxicity.

    Time frame: Baseline and weekly during concurrent chemoradiotherapy for 6 weeks

  3. "Mean change in liver function test levels from baseline to end of treatment"

    Liver function tests, including alanine aminotransferase (ALT), aspartate aminotransferase (AST), total bilirubin, and alkaline phosphatase, will be assessed weekly during concurrent chemoradiotherapy to evaluate hepatic toxicity.

    Time frame: Baseline and weekly during concurrent chemoradiotherapy for 6 weeks

Secondary outcomes

  1. * Disease free survival (DFS)

    is calculated from the date of randomization until the date of the first cancer-related event ,second cancer ,or death from. any cause

    Time frame: baseline

06

Study locations

No study locations are listed for this record.

07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07847476
Lead sponsor
Assiut University
Responsible party
Aya Saber Khalifa Mohammed (Assistant lecture, Assiut University) — Principal investigator
First posted
Sep 29, 2026
Start date
Oct 1, 2026 (estimated)
Primary completion
Oct 1, 2028 (estimated)
Completion
Dec 1, 2028 (estimated)
Last update
Sep 29, 2026

Study contacts

Aya Saber Khalifa, MD
Contact
ayasaber66778899@gmail.com
+201143980715
Maha Salah El Naggar, Prof
Contact
maha_elnaggar@aun.edu.eg
+201227433014

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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