Cyclic dinucleotide metal compound, and preparation and application thereof
US-2024317792-A1 · Sep 26, 2024 · US
US2018360873A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2018360873-A1 |
| Application number | US-201815954304-A |
| Country | US |
| Kind code | A1 |
| Filing date | Apr 16, 2018 |
| Priority date | Feb 28, 2013 |
| Publication date | Dec 20, 2018 |
| 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.
Disclosed herein are methods for treating acute or chronic heart failure using inorganic nitrite, such as sodium nitrite. Sodium nitrite is a naturally occurring compound that is commonly used as a preservative in meats. Due to its vasodilative properties and involvement in the nitric oxide pathway, drug development companies and researchers are also investigating sodium nitrite as a therapeutic agent.
Opening claim text (preview).
1 . A method for treating heart failure with preserved ejection fraction (HFpEF) comprising administering to a subject in need of treatment a therapeutically effective amount of inorganic nitrite. 2 . The method of claim 1 , wherein the nitrite is administered by inhalation. 3 . The method of claim 2 , wherein the nitrite is nebulized. 4 . The method of claim 3 , wherein the nitrite is administered at an emitted dose of about 90 mg or less. 5 . The method of claim 3 , wherein the nitrite is administered at an emitted dose of about 45 mg to about 90 mg. 6 . The method of claim 3 , wherein the nitrite is administered at an emitted dose of about 25 mg to about 80 mg. 7 . The method of claim 2 , wherein the nitrite is administered in an escalated titrated dose. 8 . The method of claim 7 , wherein the nitrite is administered at one or more doses lower than about 90 mg, followed by one or more doses that escalate to a final emitted dose at about 80 mg to about 90 mg. 9 . The method of claim 2 , wherein the inhaled nitrite is a liquid formulation. 10 . The method of claim 9 , wherein the inhaled nitrite is nebulized. 11 . The method of claim 2 , wherein the inhaled nitrite is a dry powder formulation. 12 . The method of claim 1 , wherein the nitrite is sodium nitrite. 13 . The method of claim 1 , wherein the administration of inorganic nitrite results in a decrease in one or more of right atrial pressure, pulmonary arterial pressure, pulmonary capillary wedge pressure, and pulmonary vascular resistance. 14 . The method of claim 1 , wherein the administration of inorganic nitrite results in an improved cardiac index. 15 . The method of claim 1 , wherein the administration of inorganic nitrite results in increased exercise capacity. 16 . The method of claim 1 , wherein the HFpEF is associated with pulmonary hypertension. 17 . A method of decreasing one or more of pulmonary capillary wedge pressure, right atrial pressure and pulmonary arterial pressure in a subject in need of treatment with a condition that results in one or more of increased pulmonary capillary wedge pressure, right atrial pressure and pulmonary arterial pressure comprising administering a therapeutically effective dose of inorganic nitrite and wherein such administration does not cause a significant drop in blood pressure and increase in heart rate, wherein the subject has a condition selected from one or more of pulmonary hypertension associated with diastolic heart failure, pulmonary hypertension associated with systolic heart failure, interstitial lung disease, pulmonary arterial hypertension including associated pulmonary arterial hypertension, idiopathic pulmonary arterial hypertension; exercise intolerance, and sleep-disordered breathing-related pulmonary hypertension. 18 . (canceled) 19 . (canceled) 20 . (canceled) 21 . (canceled) 22 . (canceled) 23 . (canceled) 24 . (canceled) 25 . (canceled) 26 . (canceled) 27 . (canceled) 28 . (canceled) 29 . (canceled) 30 . The method of claim 1 , wherein the subject is administered a dose of inorganic nitrite at a dose of nitrite that results in a plasma concentration of nitrite of about 4 micromolar to about 15 micromolar nitrite. 31 . The method of claim 1 wherein the inhaled inorganic nitrite is administered at a dose of nitrite that results in a plasma concentration of nitrite of about 4 micromolar to about 15 micromolar nitrite. 32 . (canceled) 33 . (canceled) 34 . (canceled) 35 . (canceled) 36 . (canceled) 37 . (canceled) 38 . (canceled) 39 . (canceled) 40 . (canceled) 41 . (canceled) 42 . (canceled) 43 . (canceled) 44 . (canceled) 45 . (canceled) 46 . (canceled) 47 . (canceled) 48 . (canceled) 49 . The method of claim 15 , wherein the increase in exercise capacity is associated with a decrease in one or more of right atrial pressure, pulmonary capillary wedge pressure, or pulmonary vascular resistance.
Nitro compounds · CPC title
Medicinal preparations containing inorganic active ingredients · CPC title
Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure · CPC title
Pulmonary tract; Aromatherapy · CPC title
Antihypertensives · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.