Methods for treatment of cancer with an anti-tigit antagonist antibody
US-2024424092-A1 · Dec 26, 2024 · US
US2017196833A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017196833-A1 |
| Application number | US-201715413257-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jan 23, 2017 |
| Priority date | Oct 1, 2012 |
| Publication date | Jul 13, 2017 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Described are nanoparticle complexes comprising paclitaxel, albumin and anti-HER2 antibody. The nanoparticle complexes are suitable for the treatment of cancer, in particular cancer that expresses VEGF.
Opening claim text (preview).
1 . (canceled) 2 . An antibody-albumin nanoparticle complex comprising albumin, bevacizumab, and a therapeutically effective amount of paclitaxel, wherein the nanoparticle complex has been pre-formed in vitro by mixing an aqueous albumin-paclitaxel nanoparticle with bevacizumab under conditions to form the nanoparticle complex, such that bevacizumab retains anti-VEGF binding specificity, said complex having a diameter of less than 1 μm. 3 . The antibody-albumin nanoparticle complex of claim 2 , wherein the antibody binds an antigen expressed by a tumor cell. 4 . The antibody-albumin nanoparticle complex of claim 3 , wherein the tumor cell is a solid tumor cell. 5 . The antibody-albumin nanoparticle complex of claim 3 , wherein the tumor cell is derived from a colorectal cancer, a lung cancer, a glioblastoma, a kidney cancer, a cervical cancer, or an ovarian cancer. 6 . The antibody-albumin nanoparticle complex of claim 1 , wherein said nanoparticle complex comprises an alkylating agent. 7 . The antibody-albumin nanoparticle complex of claim 6 , wherein said alkylating agent is a platinum compound. 8 . The antibody-albumin nanoparticle complex of claim 7 , wherein said platinum compound is carboplatin. 9 . A pharmaceutical composition comprising a pharmaceutically acceptable carrier and an effective amount of antibody-albumin nanoparticle complexes, wherein said antibody-albumin nanoparticle complexes comprise albumin, bevacizumab, and a therapeutically effective amount of paclitaxel, wherein the nanoparticle complexes have been pre-formed in vitro by mixing albumin-paclitaxel nanoparticles with bevacizumab under conditions to form the nanoparticle complexes, such that bevacizumab retains anti-VEGF binding specificity, wherein the average diameter of at least 90 percent of said complexes is less than 1 μm. 10 . The pharmaceutical composition of claim 9 , wherein the antibody binds an antigen expressed by a tumor cell. 11 . The pharmaceutical composition of claim 10 , wherein the tumor cell is derived from a colorectal cancer, a lung cancer, a renal cell carcinoma, a cervical cancer, a skin cancer, or an ovarian cancer. 12 . The pharmaceutical composition of claim 9 , wherein said composition or said nanoparticle complexes comprise an alkylating agent. 13 . The pharmaceutical composition of claim 12 , wherein said alkylating agent is a platinum compound. 14 . The pharmaceutical composition of claim 13 , wherein said platinum compound is carboplatin.
Antineoplastic agents · CPC title
the antibody targeting a determinant of a tumour cell · CPC title
having four-membered rings, e.g. taxol · CPC title
against CD52 · CPC title
the tumour determinant being from a cell of a blood cancer · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.