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AN INTERNATIONAL, RANDOMIZED, DOUBLE-BLIND, CONTROLLED STUDY OF RINDOPEPIMUTC/GM-CSF WITH ADJUVANT TEMOZOLOMIDE IN PATIENTS WITH NEWLY DIAGNOSED, SURGICALLY RESECTED, EGFRVIII-POSITIVE GLIOBLASTOMA

AN INTERNATIONAL, RANDOMIZED, DOUBLE-BLIND, CONTROLLED STUDY OF RINDOPEPIMUTC/GM-CSF WITH ADJUVANT TEMOZOLOMIDE IN PATIENTS WITH NEWLY DIAGNOSED, SURGICALLY RESECTED, EGFRVIII-POSITIVE GLIOBLASTOMA

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
REPEC
Registry ID
PER-049-12
Enrollment
25
Registered
2012-11-15
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

RANDOMIZATION WILL OCCUR IN A 1:1 RATIO AND WILL BE STRATIFIED ACCORDING TO MGMT STATUS (METHYLATED/UNMETHYLATED/UNKNOWN), EORTC (ADAPTED) RPA CLASS (III OR IV) (MIRIMANOFF, GORLIA ET AL. 2006) AND GE

Sponsors

Celldex Therapeutics, Inc.,
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) HISTOLOGICALLY CONFIRMED, NEWLY DIAGNOSED, DE NOVO GLIOBLASTOMA INCLUDING THE FOLLOWING RECOGNIZED VARIANTS OF GLIOBLASTOMA: SMALL CELL GLIOBLASTOMA, GIANT CELL GLIOBLASTOMA, GLIOSARCOMA AND GLIOBLASTOMA WITH OLIGODENDROGLIAL COMPONENT (CENTRAL PATHOLOGIC REVIEW WILL BE PERFORMED AND HISTOLOGIC CONFIRMATION WILL BE REQUIRED PRIOR TO STUDY ENTRY). 2) ATTEMPTED SURGICAL RESECTION FOLLOWED BY CONVENTIONAL CHEMORADIATION, CONSISTING OF RADIOTHERAPY AT A MINIMALLY ACCEPTABLE TOTAL DOSE OF AT LEAST 90% OF THE PLANNED DOSE (APPROXIMATELY 60 GY) OF ABSORBED RADIATION, CONCURRENT WITH TEMOZOLOMIDE AT A TARGETED DOSE OF 75 MG/M2 BODY SURFACE AREA PER DAY. PATIENTS WHO RECEIVED AN INCOMPLETE COURSE OFTEMOZOLOMIDE MAY BE ELIGIBLE, PROVIDED INCLUSION CRITERION 7 IS MET. 3) TUMOR TISSUE SPECIMENS (PARAFFIN-EMBEDDED) FROM SURGICAL RESECTION MUST BE AVAILABLE FOR CENTRAL PATHOLOGY REVIEW, MGMT STATUS DETERMINATION AND ANALYSIS OF EGFRVIII STATUS. 4) DOCUMENTED EGFRVIII POSITIVE TUMOR STATUS, DETERMINED BY POLYMERASE CHAIN REACTION (PCR) ASSAY ON TUMOR TISSUE, PERFORMED AT A SPONSOR-DESIGNATED CENTRAL LABORATORY .

Exclusion criteria

Exclusion criteria: 1) STEREOTACTIC BIOPSY ONLY (WITHOUT FURTHER SURGICAL RESECTION) 2) PRESENCE OF DIFFUSE LEPTOMENINGEAL DISEASE OR GLIOMATOSIS CEREBRI 3) HISTORY, PRESENCE, OR SUSPICION OF METASTATIC DISEASE 4) PATIENTS WHO HAVE RECEIVED ANY ADDITIONAL TREATMENT FOR GLIOBLASTOMA, ASIDE FROM SURGICAL RESECTION AND CHEMORADIATION WITH TEMOZOLOMIDE. AGENTS USED FOR DIAGNOSIS, IMAGING OR VISUALIZATION, EVEN IF INVESTIGATIONAL, ARE NOT EXCLUSIONARY. EXCLUSIONARY TREATMENTS WOULD INCLUDE, BUT ARE NOT LIMITED TO: STEREOTACTIC RADIOSURGERY, PLACEMENT OF GLIADEL® (CARMUSTINE; BCNU) WAFERS, ANY OTHER ANY OTHER INTRATUMORAL OR INTRACAVITY TREATMENT, RECEIPT OF OTHER CHEMOTHERAPIES, BEVACIZUMAB, OR INVESTIGATIONAL AGENTS. 5) ACTIVE SYSTEMIC INFECTION REQUIRING TREATMENT. A PATIENT WITH AN INFECTION CONTROLLED BY THERAPY WILL NOT BE EXCLUDED PROVIDED IT IS NOT CONSISTENT WITH EXCLUSION CRITERION 7. 6) HISTORY OF ANY MALIGNANCY (OTHER THAN GLIOBLASTOMA) DURING THE LAST THREE YEARS EXCEPT NON-MELANOMA SKIN CANCER, IN SITU CERVICAL CANCER, TREATED SUPERFICIAL BLADDER CANCER OR CURED, EARLY-STAGE PROSTATE CANCER IN A PATIENT WITH PSA LEVEL LESS THAN ULN.

Countries

Australia, Brazil, Canada, Colombia, Czech Republic, Greece, Hungary, India, Mexico, New Zealand, Taiwan, Thailand, United States

Contacts

Public ContactSheily Torres

INTRIALS-PERU INVESTIGACIONES CLINICAS S.R.L.

sheily.torres@intrials.com.br988539878 / 3495168

Outcome results

None listed

Source: REPEC (via WHO ICTRP)