Methods and compositions for prevention of feedlot bovine respiratory disease
US-2018185344-A1 · Jul 5, 2018 · US
US11419876B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11419876-B2 |
| Application number | US-202016947607-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 10, 2020 |
| Priority date | Sep 6, 2019 |
| Publication date | Aug 23, 2022 |
| Grant date | Aug 23, 2022 |
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Methods for preventing feedlot bovine respiratory diseases employing mirtazapine as pre-shipment treatments are disclosed. Compositions are further disclosed. Beneficially, the methods and compositions provide safe and cost-effective management of a costly disease.
Opening claim text (preview).
What is claimed is: 1. A method of preventing bovine respiratory disease (BRD) in a cattle population comprising: administering to a population of cattle in need of BRD prevention from about 0.1 mg/kg to about 10 mg/kg of a therapeutic agent comprising mirtazapine or one of its pharmaceutically acceptable derivatives; wherein the mirtazapine is administered to the cattle before they are shipped and at a frequency and for a duration of time effective to reduce the incidence of BRD by at least 50%. 2. The method of claim 1 , wherein the therapeutic agent is orally-administered. 3. The method of claim 2 , wherein the therapeutic agent is provided directly to the mouth of the animal or into the feed source for the animal and the dosage form is a tablet, powder, capsule, aqueous solution, non-aqueous solution, suspension, syrup, or emulsion. 4. The method of claim 1 , wherein the therapeutic agent is administered by injection. 5. The method of claim 4 , wherein the injection is in the form of a thixotropic liquid. 6. The method of claim 4 , wherein the injection provides an implanted depot to provide modified release of the mirtazapine. 7. The method of claim 1 , wherein the therapeutic agent is dosed at an amount between about 1 mg/kg to about 5 mg/kg. 8. The method of claim 1 , wherein the therapeutic agent is dosed once per day and administered daily for up to 7 days or up to 14 days. 9. The method of claim 1 , wherein the therapeutic agent is dosed by at least one injection either daily or in a single delayed or sustained release injection to provide controlled release of the therapeutic agent. 10. The method of claim 1 , wherein the prevention of BRD results in at least a 50% reduction in antibiotic usage within a facility housing the cattle. 11. The method of claim 10 , wherein the prevention of BRD results in at least a 75% reduction in antibiotic usage within a facility housing the cattle. 12. The method of claim 10 , wherein the incidence of antibiotic resistance is reduced among the population of cattle. 13. The method of claim 1 , wherein the onset of BRD in the cattle is delayed and the mortality is decreased. 14. The method of claim 13 , wherein the cattle having delayed onset of BRD have at least a 50% reduction in antibiotic retreatments. 15. The method of claim 1 , wherein the rectal temperature of the cattle is less than the rectal temperature of a cattle not treated with the therapeutic agent. 16. The method of claim 1 , wherein the therapeutic agent is absent from muscle tissues at three to six weeks post-withdrawal of the drug.
Mouth and digestive tract, i.e. intraoral and peroral administration · CPC title
Solid, semi-solid or solidifying implants, which are implanted or injected in body tissue (compositions for intravenous administration, normal injectable solutions or dispersions for, e.g. subcutaneous administration A61K9/0019; brain implants A61K9/0085; (coated) prostheses, catheters or stents A61L) · CPC title
for ruminants · CPC title
containing two hetero atoms, of which at least one is nitrogen · CPC title
Drugs for disorders of the respiratory system · CPC title
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