US2016101162A1PendingUtilityA1
SINGLE-DOSE ADMINISTRATION OF FACTOR VIIa
Assignee: NOVO NORDISK HEALTHCARE AGPriority: Jul 16, 2001Filed: Dec 18, 2015Published: Apr 14, 2016
Est. expiryJul 16, 2021(expired)· nominal 20-yr term from priority
Inventors:Ulla Hedner
A61P 7/04A61K 45/06C12Y 304/21021A61K 38/4846A61K 38/45A61K 9/0019A61K 38/37
60
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Claims
Abstract
The present invention provides methods for preventing and/or treating bleeding episodes by administering a single dose of a Factor VIIa equivalent. Preferably, the single dose comprises between about 150 and about 500 ug/kg Factor VIIa equivalent.
Claims
exact text as granted — not AI-modified1 . A method for treating a bleeding episode in a subject in need of such treatment, said method comprising administering intravenously to said subject a Factor VIIa equivalent, wherein said administering is in a single dose and said dose comprises a single-dose-effective amount of said Factor VIIa equivalent and wherein, subsequent to said administration, no further Factor VIIa equivalent is administered to said subject for a period of at least 4 hours.
2 . A method as defined in claim 1 , wherein said period is at least about 24 hours.
3 . A method as defined in claim 1 , wherein said single dose is administered over a period of less than about 5 minutes.
4 . A method as defined in claim 1 , wherein said single-dose-effective amount comprises between about 300 and about 500 ug/kg Factor VIIa equivalent.
5 . A method as defined in claim 1 , wherein said Factor VIIa equivalent exhibits at least about 30% of the coagulant activity of Factor VIIa on a molar basis.
6 . A method as defined in claim 1 , wherein said Factor VIIa equivalent is selected from the group consisting of: S52A-FVII, S60A-FVII; L305V-FVII, L305V/M306D/D309S-FVII, L305I-FVII, L305T-FVII, F374P-FVII, V158T/M298Q-FVII, V158D/E296V/M298Q-FVII, K337A-FVII, M298Q-FVII, V158D/M298Q-F VII, L305V/K337A-F VII, V158D/E296V/M298Q/L305V-F VII, V158D/E296V/M298Q/K337A-F VII, V158D/E296V/M298Q/L305V/K337A-FVII, K157A-FVII, E296V-FVII, E296V/M298Q-FVII, V158D/E296V-FVII, V158D/M298K-FVII, and S336G-FVII; Factor VIIa that has been proteolytically cleaved between residues 290 and 291; Factor VIIa that has been proteolytically cleaved between residues 315 and 316; and oxidized forms of Factor VIIa.
7 . A method as defined in claim 1 , further comprising administering, in said single dose, or substantially simultaneously with said single dose, a second coagulant agent.
8 . A method as defined in claim 7 , wherein said second coagulant agent is selected from the group consisting of Factor VII, Factor VIII, Factor IX, and Factor XIII.
9 . A method as defined in claim 1 , further comprising administering an anticoagulant, wherein said anticoagulant is administered in said single dose, or substantially simultaneously with said single dose.
10 . A method for treating a bleeding episode, said method comprising administering to a subject in need of such treatment (i) a first amount of a Factor VIIa equivalent and (ii) a second amount of second coagulant agent, wherein said first and second amounts together comprise an aggregate effective amount for treating said bleeding and said aggregate effective amount is administered in a single dose.
11 . A method as defined in claim 1 , wherein said administering is via a route selected from the group consisting of intravenous, intramuscular, subcutaneous, mucosal, and pulmonary administration.Join the waitlist — get patent alerts
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