Use of ultrarapid acting insulin

US9943571B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9943571-B2
Application numberUS-201314102383-A
CountryUS
Kind codeB2
Filing dateDec 10, 2013
Priority dateAug 11, 2008
Publication dateApr 17, 2018
Grant dateApr 17, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Disclosed herein are improved methods of treating hyperglycemia with a combination of an ultrarapid acting insulin and insulin glargine comprising prandial administration of the ultrarapid insulin, and administration of a first dose of insulin glargine within 6 hours of waking for a day.

First claim

Opening claim text (preview).

What is claimed is: 1. A method of starting treatment with a prandial insulin using an ultrarapid acting insulin (URAI) preparation comprising administering to a patient in need thereof a dose of an ultrarapid acting insulin preparation in proximity to the beginning of a daily meal wherein the dose is up to 90 units of said URAI, wherein the initial dose administered to said patient is up to 12 units of said URAI, wherein said URAI is not administered by subcutaneous injection. 2. The method of claim 1 wherein the initial dosage is 2-4 units. 3. The method of claim 1 wherein the initial dosage is 1-2 units. 4. The method of claim 1 wherein 2-hour post-prandial blood glucose is measured for said daily meal. 5. The method of claim 4 comprising measuring blood glucose at the daily meal on at least three days within one week. 6. The method of claim 5 comprising measuring blood glucose at the daily meal on three consecutive days. 7. The method of claim 5 comprising measuring blood glucose at the daily meal on seven consecutive days. 8. The method of claim 5 further comprising titrating up the dosage of the URAI preparation by increasing the dosage for the daily meal by the amount of the initial dosage if 2-hour post-prandial median glucose is >110. 9. The method of claim 8 wherein the URAI comprises a diketopiperazine. 10. The method of claim 9 wherein the diketopiperazine is at least one of 3,6-di(succinyl-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(maleyl-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(glutaryl-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(malonyl-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(oxalyl-4-aminobutyl)-2, 5-diketopiperazine, and 3,6-di(fumaryl-4-aminobutyl)-2,5-diketopiperazine. 11. The method of claim 10 wherein the diketopiperazine is 3,6-di(fumaryl-4-aminobutyl)-2,5-diketopiperazine. 12. The method of claim 11 wherein the URAI comprises human insulin. 13. The method of claim 12 wherein the URAI is a dry powder. 14. The method of claim 1 wherein the URAI preparation is not administered by injection. 15. The method of claim 14 wherein the URAI preparation is administered by inhalation. 16. The method of claim 15 wherein the URAI preparation is administered by inhalation into the lungs. 17. The method of claim 1 wherein the initial dosage is provided in a unit dose cartridge. 18. The method of claim 17 , wherein the unit dose cartridge comprises 4, 8, or 12 units. 19. The method of claim 18 , wherein the unit dose cartridge comprises 4 units. 20. The method of claim 18 , wherein the unit dose cartridge comprises 8 units. 21. The method of claim 18 , wherein the unit dose cartridge comprises 12 units. 22. The method of claim 1 wherein the URAI preparation is insulin-FDKP. 23. A method of starting treatment with a prandial insulin using an ultrarapid acting insulin (URAI) preparation comprising 3,6-di(fumaryl-4-aminobutyl)-2,5-diketopiperazine and human insulin, said method comprising prandially administering by inhalation to a patient in need thereof an initial dosage of the URAI preparation of 2-4 units.

Assignees

Inventors

Classifications

  • Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

  • for hyperglycaemia, e.g. antidiabetics · CPC title

  • Anorexiants; Antiobesity agents · CPC title

  • Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof {(enzyme inhibitors A61K38/005)} · CPC title

  • Intradermal administration, e.g. through microneedle arrays or needleless injectors · CPC title

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What does patent US9943571B2 cover?
Disclosed herein are improved methods of treating hyperglycemia with a combination of an ultrarapid acting insulin and insulin glargine comprising prandial administration of the ultrarapid insulin, and administration of a first dose of insulin glargine within 6 hours of waking for a day.
Who is the assignee on this patent?
Mannkind Corp
What technology area does this patent fall under?
Primary CPC classification A61K38/28. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Apr 17 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).