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Small Molecule Inhibitor
Tepotinib +/- Osimertinib for Brain Cancer
Phase 1
Waitlist Available
Led By Barbara O'Brien, MD
Research Sponsored by M.D. Anderson Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
This trial tests tepotinib, a drug that targets specific genetic changes in cancer cells, in patients with brain tumors and certain genetic mutations. It includes those with brain metastases, glioblastoma, and specific types of lung cancer that have spread to the brain. Tepotinib works by blocking proteins that help cancer grow, aiming to slow or stop the disease.
Who is the study for?
This trial is for adults with brain tumors or metastases who have MET alterations. It includes those with glioblastoma, patients who've had prior cancer treatments, and NSCLC patients resistant to EGFR-TKI therapy with MET amplification. Participants must be in good physical condition, not pregnant or breastfeeding, willing to use birth control, and able to undergo lumbar puncture without medical risks.
What is being tested?
The study tests the drug tepotinib alone or combined with osimertinib in people with brain tumors due to MET gene changes. The first phase determines safe dosages while the second expands testing at these doses. Some participants will also undergo surgery as part of their treatment evaluation.
What are the potential side effects?
Potential side effects include reactions related to immune system activation such as inflammation in various organs, infusion-related responses (like fever or chills), fatigue, digestive issues like nausea or diarrhea, blood cell count changes which can affect immunity and healing capacity.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
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: Group BExperimental Treatment2 Interventions
will receive tepotinib and osimertinib
Group II: Group AExperimental Treatment1 Intervention
will receive tepotinib alone
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
Common treatments for brain tumors, such as glioblastomas and brain metastases, often target specific molecular pathways involved in tumor growth and survival. Tepotinib, a MET receptor tyrosine kinase inhibitor, works by blocking the MET signaling pathway, which is often altered in brain tumors and contributes to tumor growth and metastasis.
Other treatments, like temozolomide, an alkylating agent, damage the DNA of cancer cells, leading to cell death. Targeted therapies, such as osimertinib for EGFR-mutated tumors, inhibit specific proteins involved in tumor cell proliferation.
These mechanisms are crucial for brain tumor patients as they offer more personalized and potentially effective treatment options, targeting the specific genetic and molecular abnormalities driving their cancer.
A phase II study of dose-dense temozolomide and lapatinib for recurrent low-grade and anaplastic supratentorial, infratentorial, and spinal cord ependymoma.Targeted Therapy with Anlotinib for a Patient with an Oncogenic FGFR3-TACC3 Fusion and Recurrent Glioblastoma.Bioinformatics analysis reveals potential candidate drugs for different subtypes of glioma.
A phase II study of dose-dense temozolomide and lapatinib for recurrent low-grade and anaplastic supratentorial, infratentorial, and spinal cord ependymoma.Targeted Therapy with Anlotinib for a Patient with an Oncogenic FGFR3-TACC3 Fusion and Recurrent Glioblastoma.Bioinformatics analysis reveals potential candidate drugs for different subtypes of glioma.
Find a Location
Who is running the clinical trial?
M.D. Anderson Cancer CenterLead Sponsor
3,062 Previous Clinical Trials
1,800,751 Total Patients Enrolled
Barbara O'Brien, MDPrincipal InvestigatorM.D. Anderson Cancer Center
2 Previous Clinical Trials
4,675 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Group B
- Group 2: Group A
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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