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Virus Therapy
Intra-tumoral MTX110 for Glioblastoma (MAGIC-G1 Trial)
Phase 1
Waitlist Available
Research Sponsored by Biodexa Pharmaceuticals
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Recurrent glioblastoma
Be older than 18 years old
Must not have
Patients with a history of glioblastoma treatment with nitrosoureas
Patients scheduled to undergo or are undergoing re-irradiation for the recurrent tumour
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
No Placebo-Only Group
Summary
This trial tests the safety of MTX110 in patients with recurrent glioblastoma. The drug is delivered directly to the tumor through a catheter to target it more effectively.
Who is the study for?
This trial is for patients with recurrent glioblastoma who are healthy enough for surgery and general anesthesia, have a life expectancy over 3 months, and haven't had certain recent treatments. Excluded are those with specific brain lesions, prior nitrosoureas treatment, inability to undergo MRI, or active treatment for another cancer.
What is being tested?
The study tests the safety of MTX110 when directly administered into the tumor site using a catheter system inserted surgically. The focus is on individuals whose glioblastoma has returned after previous treatments.
What are the potential side effects?
Potential side effects may include complications from surgery or catheter placement, reactions to MTX110 at the tumor site such as inflammation or infection, and general side effects like fatigue or nausea.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My brain cancer has come back after treatment.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have been treated for glioblastoma with nitrosoureas.
Select...
I am scheduled for or currently receiving a second round of radiation for a returning tumor.
Select...
My tumor is located in the back part of my brain.
Select...
My cancer has not spread to my brainstem, cerebellum, or spinal cord and is not actively growing in these areas.
Select...
I haven't had tumor treating fields therapy in the last week.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Safety of MTX110 administered by CED
Secondary study objectives
Best overall response rate
Progression-free survival
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Cohort B: MTX-110 with optional catheter repositioningExperimental Treatment2 Interventions
Weekly dosing of MTX110 via CED until progression. At progression, optional catheter repositioning may occur, followed by continued weekly dosing of MTX110 until next progression/ unacceptable toxicity.
Group II: Cohort A: MTX-110Experimental Treatment2 Interventions
Weekly dosing of MTX110 via CED until progression/ unacceptable toxicity.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Glioblastoma treatments often aim to maximize the direct impact on the tumor while minimizing systemic side effects. MTX110, for instance, is administered directly to the tumor site via a catheter, allowing for high local concentrations of the drug, which can enhance its efficacy and reduce systemic toxicity.
This localized delivery is crucial for Glioblastoma patients because it targets the tumor more precisely, potentially improving outcomes and reducing adverse effects compared to systemic chemotherapy. Other common treatments include surgical resection to remove as much of the tumor as possible, radiation therapy to destroy remaining cancer cells, and systemic chemotherapy agents like temozolomide, which work by damaging the DNA of cancer cells, thereby inhibiting their ability to replicate.
The combination of these treatments aims to control tumor growth, alleviate symptoms, and extend survival.
Find a Location
Who is running the clinical trial?
Biodexa PharmaceuticalsLead Sponsor
Midatech LtdLead Sponsor
Dmitry ZamoryakhinStudy DirectorBiodexa Pharmaceuticals
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I haven't had chemotherapy or certain cancer drugs in the last 4 weeks.I am scheduled for or currently receiving a second round of radiation for a returning tumor.You are unable to have an MRI scan.I have been treated for glioblastoma with nitrosoureas.You are expected to live for at least 3 more months.It has been more than 12 weeks since I completed radiation therapy for my primary tumor.My tumor is located in the back part of my brain.I am not currently receiving treatment for any cancer other than possibly skin cancer or cervical carcinoma in situ.My cancer has not spread to my brainstem, cerebellum, or spinal cord and is not actively growing in these areas.My brain cancer has come back after treatment.I am healthy enough to undergo surgery and anesthesia.I haven't had tumor treating fields therapy in the last week.
Research Study Groups:
This trial has the following groups:- Group 1: Cohort B: MTX-110 with optional catheter repositioning
- Group 2: Cohort A: MTX-110
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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