This phase I trial tests the safety and effectiveness of administering a single intracerebral (within the brain) dose of D2C7-IT and 2141-V11 in residual disease (within tumor margins) after surgery, followed by repeated injections of 2141-V11 under the skin (subcutaneous area) around the lymph nodes (perilymphatic) of the head and neck for adults newly diagnosed with a type of cancerous brain tumor called glioblastoma (MGMT promoter unmethylated). MGMT promoter is a type of enzyme (substance produced by the body to break down chemicals) that is found in brain tumors. It is known that patients who have a glioblastoma that is MGMT promoter unmethylated do not benefit as much from the standard treatment in comparison to patients with MGMT promoter methylation. D2C7-IT is an immunotoxin, which is a human-made protein that consists of a targeting portion linked to a toxin. The toxin is based on a portion of a common bacteria that the immune system cells will recognize. D2C7-IT is engineered to recognize two receptors that are expressed in many malignant glioma cells. 2141-V11 is a monoclonal antibody that promotes or stimulates immune cells by binding to a protein called CD40 on “antigen-presenting cells” to recognize and attack tumor cells. An antigen is something present in the body that causes the immune system to create a response to fight it off. Combining D2C7-IT with a monoclonal antibody that stimulates immune cells, such as 2141-V11, may be effective against newly diagnosed MGMT unmethylated glioblastoma.
Additional locations may be listed on ClinicalTrials.gov for NCT05734560.
Locations matching your search criteria
United States
North Carolina
Durham
Duke University Medical CenterStatus: Active
Contact: Annick Desjardins
Phone: 919-684-5301
PRIMARY OBJECTIVE:
I. Describe the overall survival (OS) of adult patients with newly diagnosed, MGMT unmethylated glioblastoma (GBM), treated with the combination of immunotoxin D2C7-(scdsFv)-PE38KDEL (D2C7-IT) and Fc-engineered anti-CD40 agonist antibody 2141-V11 (2141-V11) administered in the residual disease via convection enhanced delivery (CED), followed by 3-6 weeks of radiation therapy, followed by cervical perilymphatic injections 1 and 3 weeks after completion of radiation therapy and every 3 weeks for a year.
SECONDARY OBJECTIVES:
I. Assess the safety of treating patients with the combination of D2C7-IT and 2141-V11 administered in the residual disease via CED.
II. Describe progression-free survival (PFS) of adult patients with newly diagnosed, MGMT unmethylated GBM, treated with the combination of D2C7-IT and 2141-V11 administered in the residual disease via CED, followed by cervical perilymphatic subcutaneous injections of 2141-V11 and radiation therapy.
EXPLORATORY OBJECTIVES:
I. Describe patient-reported quality of life outcomes (PROs).
II. Assess circulating antibodies to D2C7-IT and PE-38KDEL.
III. Assess immunologic responses in tumor, peripheral blood, plasma and serum of patients treated with D2C7-IT + 2141-V11.
IV. Identify genetic predictors of response or failure of response to treatment with D2C7-IT+2141-V11.
OUTLINE:
Within 3-5 weeks of surgical resection, patients undergo surgical insertion of a catheter in the area of the tumor margins as well as a tumor biopsy. One to two days after catheter insertion and biopsy, patients receive D2C7-IT over 72 hours on days 1, 2, and 3 and then i2141-V11 over 7 hours on day 4 via intracerebral infusion administered by CED. One week after infusions and no later than 8 weeks following surgical resection, patients undergo standard of care (SOC) radiation therapy (RT) over 15-30 fractions for 3-6 weeks. One week following completion of RT, patients receive 2141-V11 perilymphatic subcutaneous (SC) injections every 3 weeks for up to 1 year in the absence of disease progression or unacceptable toxicity. Patients may be retreated with D2C7-IT and 2141-V11 if disease progression occurs ≥ 6 months from initial resection. Patients also undergo magnetic resonance imaging (MRI) and collection of blood samples at baseline and on trial, computed tomography (CT) on trial, and buccal swab during screening.
After completion of study treatment, patients are followed up to 30 days and then at the discretion of the treating physician. Patients who withdrawal early from the trial are followed every 3 months until death.
Lead OrganizationDuke University Medical Center
Principal InvestigatorAnnick Desjardins