- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05353530
Fase I-undersøgelse af IL-8-receptormodificeret CD70 CAR T-celleterapi i CD70+ og MGMT-umethyleret voksenglioblastom (IMPACT) (IMPACT)
Fase I-undersøgelse - At vurdere sikkerhed og gennemførlighed af IL-8-receptormodificeret patientafledt aktiveret CD70 CAR T-celleterapi i CD70+ og MGMT-umethyleret voksen GBM
This is a phase I study to assess the safety and feasibility of IL-8 receptor modified patient-derived activated CD70 CAR T cell therapy in CD70+ adult glioblastoma
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Newly diagnosed CD70 positive adult GBM patients who have undergone surgery for maximal debulking will be enrolled in this 3+3 design dose-escalation clinical trial and undergo peripheral venipuncture for collection of PBMCs for generation of investigational 8R-70CAR T Cell vaccine. Patients will then undergo standard of care chemoradiation. Immunotherapy will begin 2 weeks (-7/+4 days) after completion of radiation. One single dose of 8R-70CAR T cells will be administered IV. The dose will depend on the enrolling cohort. Dose escalation will follow the traditional 3+3 design.
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 1
Kontakter og lokationer
Studiesteder
-
-
Florida
-
Gainesville, Florida, Forenede Stater, 32608
- University of Florida Health
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria (Adult GBM):
- Age ≥ 18 years
- Newly-diagnosed de novo GBM based on the absence of previous history of brain tumor (WHO Grade IV glioma) by histopathology or molecular studies. (secondary GBM not eligible)
- The tumor must have a supratentorial component
- CD70 positive (≥5%, 1+)
Tumor expression will be scored on a scale of 0 to 3 staining intensity:
0 = Negative
-
= Low level
-
= Moderate level
-
= High level
-
The criteria for inclusion will be at least 5% of the cells scoring 1+ staining intensity (> 5%, 1+).
- Surgical resection of tumors with less than 3cm x 3cm (9 cm2) residual enhancing tumor as a product of longest perpendicular planes by MRI or biopsy only for tumor measuring less than 3cm x 3cm
- Karnofsky Performance Status (KPS) of > 70%
- CBC with differential with adequate bone marrow function as defined below:
-
Absolute neutrophil count (ANC) ≥ 1500 cells/mm3.
-
Platelet count ≥ 100,000 cells/mm3.
-
Hemoglobin ≥ 10 g/dl. (The use of transfusion or other intervention to achieve Hgb ≥ 10 g/dl is acceptable.)
• Adequate renal function as defined below:
-
BUN ≤ 25 mg/dl
-
Creatinine ≤ 1.7 mg/dl
• Adequate hepatic function as defined below:
-
Bilirubin ≤ 2.0 mg/dl
-
ALT ≤ 5 times institutional upper limits of normal for age
-
AST ≤ 5 times institutional upper limits of normal for age
- Signed informed consent. If the patient's mental status precludes his/her giving informed consent, written informed consent may be given by the legally authorized representative.
- For females of childbearing potential, a negative serum pregnancy test at enrollment.
- Women of childbearing potential (WOCBP) must be willing to use an acceptable contraceptive method to avoid pregnancy throughout the study and for at least 24 weeks after the last dose of study drug.
- Males with female partners of childbearing potential must agree to practice adequate contraceptive methods throughout the study and should avoid conceiving children for 24 weeks following the last dose of study drug.
-
Exclusion Criteria (Adult GBM):
- Prior invasive malignancy (except for non-melanomatous skin cancer) unless disease free for ≥ 3years. (In situ cancer are permissible)
- Metastases detected below the tentorium or beyond the cranial vault
- Leptomeningeal disease beyond the cranial vault. (Focal, adjacent and leptomeningeal involvement is allowable at the discretion of the PI).
- Recurrent or multifocal malignant gliomas.
- The patient is not a candidate for cellular therapy as assessed by the study bone marrow transplant physician.
- Known immunosuppressive disease or human immunodeficiency virus (HIV) infection.
Rationale: The need to exclude patients with the immunosuppressive disease or human
-
Severe, active co-morbidity, defined as follows:
- Unstable angina and/or congestive heart failure requiring hospitalization.
- Transmural myocardial infarction within the last 6 months.
- Acute bacterial or fungal infection requiring intravenous antibiotics at the initiation of XRT/TMZ.
- Chronic Obstructive Pulmonary Disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy at the initiation of XRT/TMZ.
- Hepatic insufficiency resulting in clinical jaundice and/or coagulation defects.
- Patients with an autoimmune disease requiring medical management with immunosuppressants.
- Major medical illnesses or psychiatric impairments that, in the investigator's opinion, will prevent administration or completion of protocol therapy.
- Active connective tissue disorders such as lupus or scleroderma that, in the investigator's opinion, place the patient at high risk for radiation toxicity.
-
Pregnant or lactating women, due to possible adverse effects on the developing fetus or infant.
-
Patients treated on any other therapeutic clinical protocols within 30 days prior to enrollment.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: 8R-70CAR T cells
Cohort 1 will receive 1 x 10^6 cells/kg. Cohort 2 will receive 1 x 10^7 cells/kg. Cohort 3 will receive 1 x 10^8 cells/kg. Cohort 4 will receive Cy/Flu + CAR T cells at established maximum tolerated dose. |
Single dose of 8R-70CAR T cells administered IV
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Safety of 8R-70CAR T-cell therapy in adult patients with de novo CD70+ GBM
Tidsramme: 28 days post-infusion
|
Defined as ≤ 1 DLT out of 6 patients is observed at the 1x10^8 cells/Kg dose. Dose-Limiting toxicity (DLT) will be defined as any adverse event attributable (possible, probable, or definite) to the administration of 8R-70CAR T cells and occurring from the time of infusion through 28 days post-infusion. |
28 days post-infusion
|
|
Feasibility of 8R-70CAR T-cell therapy in adult patients with de novo CD70+ GBM
Tidsramme: 10 weeks
|
Feasibility will be defined as the ability to infuse 8R-70CAR T-cell safely in 66.7 % of enrolled patients (patients who signed consent and were deemed eligible for the study). |
10 weeks
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Ashley Ghiaseddin, MD, University of Florida
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Hjernesygdomme
- Sygdomme i centralnervesystemet
- Sygdomme i nervesystemet
- Neoplasmer efter sted
- Neoplasmer
- Neoplasmer efter histologisk type
- Neoplasmer, kirtel og epitel
- Astrocytom
- Gliom
- Neoplasmer, Neuroepithelial
- Neuroektodermale tumorer
- Neoplasmer, kimceller og embryonale
- Neoplasmer, nervevæv
- Neoplasmer i nervesystemet
- Neoplasmer i centralnervesystemet
- Glioblastom
- Neoplasmer i hjernen
- Aminosyrer, peptider og proteiner
- Proteiner
- Receptorer, G-protein-koblet
- Receptorer, celleoverflade
- Membranproteiner
- Receptorer, cytokin
- Receptorer, immunologisk
- Receptorer, interleukin-8
- Receptorer, CXCR
- Receptorer, kemokin
- Receptorer, interleukin
- Receptorer, interleukin-8b
Andre undersøgelses-id-numre
- IRB202200057-A
- OCR41673 (Anden identifikator: University of Florida)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .