Methods of permeabilizing the blood brain barrier
US-12208066-B2 · Jan 28, 2025 · US
US12514828B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12514828-B2 |
| Application number | US-202418984062-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 17, 2024 |
| Priority date | Feb 8, 2018 |
| Publication date | Jan 6, 2026 |
| Grant date | Jan 6, 2026 |
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The present invention relates to using monoterpene or sesquiterpene to permeabilize the blood brain barrier. The present invention relates to a method of treating a central nervous system (CNS) cancer wherein perillyl alcohol (POH) is administered to a mammal before or concurrently with a therapeutic agent that is a chimeric antigen receptor T-cell (CAR-T cell). The POH and CAR-T cells can be administered by intraarterial injection. The CNS cancer can be a malignant glioma, pilocytic astrocytomas (grade I), meningiomas, metastatic brain tumors, or pituitary adenomas.
Opening claim text (preview).
The invention claimed is: 1 . A method of treating a central nervous system (CNS) cancer, the method comprising administering to a mammal perillyl alcohol (POH) before or concurrently with a therapeutic agent that is a chimeric antigen receptor T-cell (CAR-T cell), wherein the POH and CAR-T cells are administered by intraarterial injection, and wherein the CNS cancer is a malignant glioma, pilocytic astrocytomas (grade I), meningiomas, metastatic brain tumors, or pituitary adenomas. 2 . The method of claim 1 , wherein the perillyl alcohol is administered at a dose ranging from about 0.050 mg/kg to about 500 mg/kg of a body weight of the mammal. 3 . The method of claim 1 , wherein the mammal is a human. 4 . The method of claim 1 , wherein the POH is administered from about 0.2 minutes to about 60 minutes before the CAR-T cell is administered. 5 . The method of claim 1 , wherein the POH is administered from about 1 minute to about 15 minutes before the CAR-T cell is administered. 6 . The method of claim 1 , wherein the POH and the CAR-T cell are administered separately. 7 . The method of claim 1 , wherein the POH and the CAR-T cell are administered concurrently. 8 . The method of claim 1 , wherein the POH and the CAR-T cell are administered together in a pharmaceutical composition. 9 . The method of claim 1 , wherein the CNS cancer is a malignant glioma. 10 . The method of claim 9 , wherein the malignant glioma is a glioblastoma, astrocytoma, or anaplastic astrocytoma. 11 . The method of claim 9 , wherein the malignant glioma is a glioblastoma. 12 . The method of claim 1 , further comprising treating the mammal with radiation. 13 . The method of claim 1 , wherein the CAR-T cell is a CD19 CAR-T cell or a Lym-1 CAR-T cell.
CD19 or B4 · CPC title
Chimeric antigen receptors [CAR] · CPC title
T-cells, e.g. tumour infiltrating lymphocytes [TIL] or regulatory T [Treg] cells; Lymphokine-activated killer [LAK] cells · CPC title
characterised by the dose, timing or administration schedule · CPC title
Blood cells, e.g. leukemia or lymphoma · CPC title
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