The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Sep. 27, 2022

Filed:

Apr. 24, 2020
Applicants:

Opko Ireland Global Holdings, Ltd., Grand Cayman, KY;

Opko Renal, Llc, Miami, FL (US);

Inventors:

Charles W. Bishop, Miami Beach, FL (US);

Keith H. Crawford, Parker, CO (US);

Eric J. Messner, Lake Forest, IL (US);

P. Martin Petkovich, Kingston, CA;

Christian F. Helvig, Markham, CA;

Assignee:

EIRGEN PHARMA LTD., Waterford, IE;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 31/593 (2006.01); A61K 31/59 (2006.01); A61K 31/592 (2006.01); A61K 9/48 (2006.01); A61P 5/18 (2006.01); A61K 9/00 (2006.01);
U.S. Cl.
CPC ...
A61K 31/593 (2013.01); A61K 9/0053 (2013.01); A61K 9/48 (2013.01); A61K 9/4825 (2013.01); A61K 31/59 (2013.01); A61K 31/592 (2013.01); A61P 5/18 (2018.01);
Abstract

The method of treating elevated blood levels of iPTH by increasing or maintaining blood concentrations of both 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D in a patient by administering, as necessary, both Vitamin D repletion and Vitamin D hormone replacement therapies, is disclosed. The blood concentrations of 25-hydroxyvitamin D are increased to and maintained at or above 30 ng/mL, and blood concentrations of 1,25-dihydroxyvitamin D are increased to or maintained within a patient's normal historical physiological range for 1,25-dihydroxyvitamin D without causing substantially increased risk of hypercalcemia, hyperphosphatemia or over suppression of plasma iPTH in the patient. The blood levels of 25-hydroxyvitamin D are maintained at or above 30 ng/mL between doses of Vitamin D repletion therapies, and the blood levels of 1,25-dihydroxyvitamin D are maintained in the patient's normal historical physiological range between doses of Vitamin D hormone replacement therapies. In one aspect, the disclosure includes methods wherein the blood concentration of 25-hydroxyvitamin D during treatment comprises predominantly 25-hydroxyvitamin D, and/or wherein the method includes administering predominantly or solely 25-hydroxyvitamin Dfor 25-hydroxyvitamin D repletion and/or maintenance.


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