US2019022253A1PendingUtilityA1
Unit dosage of apadenoson
Assignee: UNIV VIRGINIA PATENT FOUNDATIONPriority: Jul 3, 2008Filed: Jul 25, 2018Published: Jan 24, 2019
Est. expiryJul 3, 2028(~1.9 yrs left)· nominal 20-yr term from priority
A61P 9/10A61K 9/0019A61K 47/12A61K 31/519A61K 47/40A61K 47/02A61K 31/7076A61K 49/0004A61K 9/08
56
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Claims
Abstract
The present invention provides a unit dosage of Apadenoson, a pharmacological stress agent, and use of the same as a pharmacologic agent for myocardial perfusion imaging.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . A method of performing myocardial perfusion imaging of a human patient in need thereof comprising:
(a) administering by a single intravenous (iv) bolus a unit dose of Apadenoson of between about 76-175 μg wherein the unit dose is independent of the patient's weight; (b) administering a radionuclide; and (c) performing a technique to detect the presence of coronary artery stenoses in the patient, to assess the severity of coronary artery stenoses in the mammal, or a combination thereof, so as to diagnose myocardial perfusion abnormalities in the mammal.
3 . The method of claim 2 , wherein the unit dose further comprises a pharmaceutically acceptable carrier.
4 . The method of claim 2 , wherein the unit dose is 1 mL in volume.
5 . The method of claim 2 , wherein the unit dose is 2 mL in volume.
6 . The method of claim 2 , wherein the unit dose is 3 mL in volume.
7 . The method of claim 2 , wherein the unit dose is 4 mL in volume.
8 . The method of claim 2 , wherein the unit dose is 5 mL in volume.
9 . The method of claim 2 , wherein the unit dose further contains sodium citrate buffer.
10 . The method of claim 9 , wherein sodium citrate buffer is present in an amount to buffer the unit dose to pH selected from 4.6-5.0.
11 . The method of claim 9 , wherein sodium citrate buffer is present in an amount to buffer the unit dose to pH 4.8.
12 . The method of claim 2 wherein the unit dose is provided as a prefilled syringe.
13 . The method of claim 12 , wherein the dose of Apadenoson is 150 μg.
14 . The method of claim 12 , wherein the dose of Apadenoson is 175 μg.Join the waitlist — get patent alerts
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