Organic compounds
US-2015197528-A1 · Jul 16, 2015 · US
US9468637B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9468637-B2 |
| Application number | US-201013319807-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 13, 2010 |
| Priority date | May 13, 2009 |
| Publication date | Oct 18, 2016 |
| Grant date | Oct 18, 2016 |
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 relates to a new use of phosphodiesterase 1 (PDE1) inhibitors for the treatment of psychosis, schizophrenia, schizoaffective disorder, schizophreniform disorder, psychotic disorder, delusional disorder, mania, or bipolar disorder.
Opening claim text (preview).
What is claimed is: 1. A method of treatment for psychosis, schizoaffective disorder, schizophreniform disorder, psychotic disorder, delusional disorder, mania or bipolar disorder comprising administering an effective amount of a PDE 1 inhibitor to a patient in need thereof wherein the PDE 1 inhibitor is: in free or salt form, including its enantiomers, diastereoisomers and racemates. 2. The method according to claim 1 , wherein the compound inhibits phosphodiesterase-mediated hydrolysis of cGMP or cAMP. 3. The method according to claim 1 , wherein the compound is a PDE1B inhibitor. 4. The method according to claim 1 , wherein the method further comprises administering a compound or compounds selected from typical and atypical antipsychotics to a patient in need thereof. 5. The method according to claim 1 , wherein the PDE1 inhibitor is in free or pharmaceutically acceptable salt form, in combination or association with a pharmaceutically acceptable diluent or carrier.
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia · CPC title
Anxiolytics · CPC title
having six-membered rings with two {or more} nitrogen atoms as the only ring heteroatoms, e.g. piperazine {or tetrazines}(A61K31/48 takes precedence {; with three nitrogen atoms A61K31/53}) · CPC title
ortho- or peri-condensed with heterocyclic rings · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.