Prodrugs of 1,4-benzodiazepinone compounds
US-9273075-B2 · Mar 1, 2016 · US
US12281085B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12281085-B2 |
| Application number | US-202017077857-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 22, 2020 |
| Priority date | May 6, 2018 |
| Publication date | Apr 22, 2025 |
| Grant date | Apr 22, 2025 |
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.
The present invention provides compositions comprising bisfluoroalkyl-1,4-benzodiazepinone compounds, including compounds of Formula (I) or prodrugs thereof;in combination with an additional cancer therapeutic agent, and methods of use thereof for treating diseases and disorders such as cancer.
Opening claim text (preview).
What is claimed is: 1. A composition comprising a compound represented by the structure of Compound (1): and/or at least one salt thereof in combination with a composition comprising a CDK 4 and 6 inhibitor, sorafenib, regorafenib, venetoclax, vorinostat, or a combination thereof. 2. The composition of claim 1 , wherein said CDK 4 and 6 inhibitor comprises palbociclib, ribociclib, or abemaciclib, or a combination thereof. 3. A method of treating, suppressing or inhibiting adenoid cystic carcinoma (ACC) in a subject in need thereof comprising the step of administering to said subject a first composition comprising a compound represented by the structure of Compound (1): and/or at least one salt thereof, and a second composition comprising a CDK 4 and 6 inhibitor, sorafenib, regorafenib, venetoclax, vorinostat, or a combination thereof and wherein the subject has adenoid cystic carcinoma (ACC). 4. The method of claim 3 , wherein said first composition and/or said second composition is intravenously administered to said subject. 5. The method of claim 3 , wherein said first composition and/or said second composition is orally administered to said subject. 6. The method of claim 3 , wherein said first composition and said second composition are administered together. 7. The method of claim 3 , wherein said first composition and said second composition are administered at separate sites or at separate times. 8. The method of claim 7 , wherein said first composition comprising Formula (I) is administered prior to and then again subsequent to the administration of said second composition. 9. The method of claim 3 , wherein the adenoid cystic carcinoma (ACC) comprises a notch-activating mutation. 10. The method of claim 3 , wherein said CDK 4 and 6 inhibitor comprises palbociclib, ribociclib, or abemaciclib, or a combination thereof.
against proteinaceous materials, e.g. enzymes, hormones, lymphokines · CPC title
having a heterocyclic ring, e.g. sulfadiazine · CPC title
1,4-Benzodiazepines, e.g. diazepam {or clozapine} · CPC title
Non condensed pyridines; Hydrogenated derivatives thereof · CPC title
Retinoic acids {; Salts thereof} · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.