INO-5401 and INO-9012 Delivered by Electroporation (EP) in Combination With Cemiplimab (REGN2810) in Newly-Diagnosed Glioblastoma (GBM)
- Conditions
- Glioblastoma
- Interventions
- Radiation: Radiation Therapy
- Registration Number
- NCT03491683
- Lead Sponsor
- Inovio Pharmaceuticals
- Brief Summary
Phase 1/2 trial to evaluate safety, immunogenicity and preliminary efficacy of INO-5401 and INO-9012 in combination with cemiplimab (REGN2810), with radiation and chemotherapy, in subjects with newly-diagnosed glioblastoma (GBM).
- Detailed Description
This is a phase 1/2, open-label, multi-center trial to evaluate safety, immunogenicity and preliminary efficacy of INO-5401 and INO-9012 in combination with cemiplimab in subjects with newly-diagnosed glioblastoma (GBM). INO-5401 and INO-9012 will be delivered by intramuscular (IM) injection followed by electroporation (EP) in combination with cemiplimab and chemoradiation and radiation. There will be 2 cohorts in this trial. Cohort A will be participants with a tumor with an unmethylated O6-methylguanine-deoxyribonucleic acid (DNA) methyltransferase (MGMT) promoter. Cohort B will be participants with a tumor with a MGMT methylated promoter or who have indeterminate MGMT status. Both cohorts will receive INO-5401 and INO-9012 and cemiplimab at the same doses and on the same dosing schedule, and both cohorts will receive radiation and temozolomide (TMZ), if clinically indicated.
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 52
- Newly-diagnosed brain cancer with histopathological diagnosis of GBM;
- Karnofsky Performance Status (KPS) rating of >/=70 at baseline;
- Receive dexamethasone equivalent dose </=2 mg per day, stable or decreased for >/= three days prior to Day 0;
- Recovery from the effects of prior GBM surgery as defined by the Investigator;
- Electrocardiogram (ECG) with no clinically significant findings as assessed by the Investigator;
- Adequate organ function as demonstrated by hematological, renal, hepatic laboratory assessments;
- Agree that during the trial, men will not father a child, and women cannot be or become pregnant. Participants must be of non-child bearing potential or agree to use one highly effective or combined contraceptive methods that result in a failure rate of <1% per year during the treatment period and at least through week 12 after last dose;
- Ability to tolerate magnetic resonance imaging (MRI).
- Presence of greater than 1 cm x 1 cm residual tumor enhancement on postoperative MRI;
- Multifocal disease or leptomeningeal disease (LM) disease on post-operative MRI;
- Not scheduled to start radiation within 42 days of surgical resection of tumor;
- Dexamethasone equivalent dose >2 mg per day;
- Prior treatment with an agent that blocks the PD-1/PD-Ligand 1 pathway;
- Receipt of previous approved or investigative immune modulatory agent within 28 days of receiving the first dose of treatment;
- Prior treatment with idelalisib;
- Past, current or planned treatment with tumor treatment fields; oncolytic viral treatment; or prior exposure to an investigational agent or device within 28 days of receiving the first dose of treatment;
- Allergy or hypersensitivity to cemiplimab or to any of its excipients;
- History of documented allergic reactions or acute hypersensitivity reaction attributed to antibody treatments;
- Ongoing or recent (within 5 years) evidence of autoimmune disease that required treatment with systemic immunosuppressive treatments;
- Diagnosis of immunodeficiency or treatment with systemic immunosuppressive therapy within 28 days prior to the first dose of trial treatment, other than dexamethasone for the underlying disease under investigation, as noted in the inclusion criteria;
- History of clinically significant, medically unstable disease which, in the judgment of the investigator, would jeopardize the safety of the subject, interfere with trial assessments or endpoint evaluation, or otherwise impact the validity of the trial results.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Cohort A: Unmethylated MGMT Promoter INO-5401 Cohort A will include participants with a glioblastoma tumor with an unmethylated MGMT promoter. Participants will receive INO-5401 and INO-9012 and cemiplimab as well as radiation and temozolomide (TMZ; only during radiation therapy), if clinically indicated. Cohort A: Unmethylated MGMT Promoter INO-9012 Cohort A will include participants with a glioblastoma tumor with an unmethylated MGMT promoter. Participants will receive INO-5401 and INO-9012 and cemiplimab as well as radiation and temozolomide (TMZ; only during radiation therapy), if clinically indicated. Cohort A: Unmethylated MGMT Promoter Cemiplimab Cohort A will include participants with a glioblastoma tumor with an unmethylated MGMT promoter. Participants will receive INO-5401 and INO-9012 and cemiplimab as well as radiation and temozolomide (TMZ; only during radiation therapy), if clinically indicated. Cohort A: Unmethylated MGMT Promoter Radiation Therapy Cohort A will include participants with a glioblastoma tumor with an unmethylated MGMT promoter. Participants will receive INO-5401 and INO-9012 and cemiplimab as well as radiation and temozolomide (TMZ; only during radiation therapy), if clinically indicated. Cohort A: Unmethylated MGMT Promoter Temozolomide Cohort A will include participants with a glioblastoma tumor with an unmethylated MGMT promoter. Participants will receive INO-5401 and INO-9012 and cemiplimab as well as radiation and temozolomide (TMZ; only during radiation therapy), if clinically indicated. Cohort B: Methylated MGMT Promoter INO-5401 Cohort B will include participants with a glioblastoma tumor with a methylated MGMT promoter or with indeterminate MGMT status. Participants will receive INO-5401 and INO-9012 and cemiplimab as well as radiation and temozolomide (TMZ), if clinically indicated. Participants will continue to receive TMZ following radiation therapy, for up to six additional cycles, if clinically indicated. Cohort B: Methylated MGMT Promoter INO-9012 Cohort B will include participants with a glioblastoma tumor with a methylated MGMT promoter or with indeterminate MGMT status. Participants will receive INO-5401 and INO-9012 and cemiplimab as well as radiation and temozolomide (TMZ), if clinically indicated. Participants will continue to receive TMZ following radiation therapy, for up to six additional cycles, if clinically indicated. Cohort B: Methylated MGMT Promoter Cemiplimab Cohort B will include participants with a glioblastoma tumor with a methylated MGMT promoter or with indeterminate MGMT status. Participants will receive INO-5401 and INO-9012 and cemiplimab as well as radiation and temozolomide (TMZ), if clinically indicated. Participants will continue to receive TMZ following radiation therapy, for up to six additional cycles, if clinically indicated. Cohort B: Methylated MGMT Promoter Radiation Therapy Cohort B will include participants with a glioblastoma tumor with a methylated MGMT promoter or with indeterminate MGMT status. Participants will receive INO-5401 and INO-9012 and cemiplimab as well as radiation and temozolomide (TMZ), if clinically indicated. Participants will continue to receive TMZ following radiation therapy, for up to six additional cycles, if clinically indicated. Cohort B: Methylated MGMT Promoter Temozolomide Cohort B will include participants with a glioblastoma tumor with a methylated MGMT promoter or with indeterminate MGMT status. Participants will receive INO-5401 and INO-9012 and cemiplimab as well as radiation and temozolomide (TMZ), if clinically indicated. Participants will continue to receive TMZ following radiation therapy, for up to six additional cycles, if clinically indicated.
- Primary Outcome Measures
Name Time Method Percentage of Participants with Adverse Events (AEs) From Day 0 to 30 days after the last dose of study treatment (non-serious AEs) and to 6 months after the last dose of study treatment (immune-related AEs, AEs of special interest and serious AEs) up to approximately 24 months
- Secondary Outcome Measures
Name Time Method Overall survival at 18 months (OS18) At Month 18 Change from Baseline in Interferon-gamma Secreting T Lymphocytes in Peripheral Blood Mononuclear Cells (PBMCs) From Day 0 to last dose of study treatment up to approximately 18 months Change from Baseline in T-Cell Phenotypes in PBMCs From Day 0 to last dose of study treatment up to approximately 18 months Change from Baseline in T Cell Receptor (TCR) Subtypes in PBMCs From Day 0 to last dose of study treatment up to approximately 18 months Change from Baseline in Antigen-Specific Humoral Response From Day 0 to last dose of study treatment up to approximately 18 months
Trial Locations
- Locations (21)
University of Pennsylvania Health System: Penn Medicine
🇺🇸Philadelphia, Pennsylvania, United States
Rutgers University - Cancer Institute of New Jersey
🇺🇸New Brunswick, New Jersey, United States
Baylor College of Medicine
🇺🇸Houston, Texas, United States
University of Miami - Sylvester Comprehensive Cancer Center
🇺🇸Miami, Florida, United States
Dana-Farber Cancer Institute
🇺🇸Boston, Massachusetts, United States
Columbia University Medical Center The Neurological Institute of New York
🇺🇸New York, New York, United States
City of Hope
🇺🇸Duarte, California, United States
Stanford University, School of Medicine
🇺🇸Palo Alto, California, United States
Oregon Health & Science University
🇺🇸Portland, Oregon, United States
Huntsman Cancer Institute
🇺🇸Salt Lake City, Utah, United States
Stephenson Cancer Center
🇺🇸Oklahoma City, Oklahoma, United States
Texas Oncology
🇺🇸Austin, Texas, United States
Icahn School of Medicine at Mount Sinai
🇺🇸New York, New York, United States
Henry Ford Health System
🇺🇸Detroit, Michigan, United States
University of North Carolina School of Medicine
🇺🇸Chapel Hill, North Carolina, United States
New York University Langone Medical Center; Perlmutter Cancer Center
🇺🇸New York, New York, United States
New York-Presbyterian Hospital/Weill Cornell Medical Center
🇺🇸New York, New York, United States
Emory University School of Medicine
🇺🇸Atlanta, Georgia, United States
University of California, San Francisco
🇺🇸San Francisco, California, United States
UPMC Cancer Center Neuro-Oncology; UPMC Cancer Pavilion
🇺🇸Pittsburgh, Pennsylvania, United States
Moffitt Cancer Center
🇺🇸Tampa, Florida, United States