Methods for treatment of cancer with an anti-tigit antagonist antibody
US-2024424092-A1 · Dec 26, 2024 · US
US12215152B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12215152-B2 |
| Application number | US-202217578655-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 19, 2022 |
| Priority date | Oct 1, 2015 |
| Publication date | Feb 4, 2025 |
| Grant date | Feb 4, 2025 |
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Herein is reported an antibody that specifically hinds to human CD 19, wherein the antibody comprises (a) HVR-H1 comprising the amino acid sequence of SEQ ID NO: 03, (b) HVR-H2 comprising the amino acid sequence of SEQ ID NO: 11, (c) HVR-H3 comprising the amino acid sequence of SEQ ID NO: 05, (d) HVR-L1 comprising the amino acid sequence of SEQ ID NO: 20 or 28, (e) HVR-L2 comprising the amino acid sequence of SEQ ID NO: 07, and (f) HVR-L3 comprising the amino acid sequence of SEQ ID NO: 08, as well as methods of using the same.
Opening claim text (preview).
The invention claimed is: 1. An antibody that specifically binds to human CD19, wherein the antibody comprises: (a) HVR-H1 comprising the amino acid sequence of SEQ ID NO: 03, (b) HVR-H2 comprising the amino acid sequence of SEQ ID NO: 11, (c) HVR-H3 comprising the amino acid sequence of SEQ ID NO: 05, (d) HVR-L1 comprising the amino acid sequence of SEQ ID NO: 40, (e) HVR-L2 comprising the amino acid sequence of SEQ ID NO: 07, and (f) HVR-L3 comprising the amino acid sequence of SEQ ID NO: 08. 2. The antibody according to claim 1 , wherein the antibody is a monoclonal antibody. 3. The antibody according to claim 1 , wherein the antibody is a human, humanized or chimeric antibody. 4. The antibody according to claim 1 , wherein the antibody is an antibody fragment that specifically binds to human CD19. 5. The antibody according to claim 1 , wherein the antibody comprises: a VH sequence having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 09 and a VL sequence having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 27. 6. A pharmaceutical formulation, comprising the antibody according to claim 1 and a pharmaceutically acceptable carrier. 7. A method of treating an individual having a B-cell cancer, comprising the step of administering to the individual an effective amount of the antibody according to claim 1 . 8. A method of depleting B-cells in an individual in need thereof, comprising the step of administering to the individual an effective amount of the antibody according to claim 1 to deplete B-cells.
Complement-dependent cytotoxicity [CDC] · CPC title
Antibody-dependent cellular cytotoxicity [ADCC] · CPC title
Complementarity determining region [CDR] · CPC title
Stability, e.g. half-life, pH, temperature or enzyme-resistance · CPC title
Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value · CPC title
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