IP Library Granted Patent US 9,770,427
Granted Patent B2
US 9,770,427 · App. 14/313,738 · Granted Sep 26, 2017

Antiviral treatments

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Quick Facts
Patent No.
US 9,770,427
App. No.
14/313,738
Granted
Sep 26, 2017
Kind
B2
Abstract

The invention provides unit dosage forms, kits, and methods and useful for treating viral infections.

Claims (22)

1. A method for treating a viral infection in a human comprising administering in a single intravenous administration per day over a course of treatment an effective anti-viral amount of a compound of formula I:

or a pharmaceutically acceptable salt thereof, to the human, wherein the viral infection is a type A, type B, H3N2, H1N1, H5N1, avian, or seasonal influenza infection.

2. The method of claim 1 , wherein the compound of formula I is a compound of formula Ia:

or a pharmaceutically acceptable salt thereof.

3. The method of claim 1 , wherein the influenza infection is a type A influenza infection.

4. The method of claim 1 , wherein the influenza infection is a seasonal influenza infection.

5. The method of claim 1 , wherein the effective anti-viral amount is up to about 800 mg per day.

6. The method of claim 1 , wherein the effective anti-viral amount is up to about 600 mg per day.

7. The method of claim 1 , wherein the effective anti-viral amount is up to about 300 mg per day.

8. The method of claim 1 , wherein the effective anti-viral amount is up to about 150 mg per day.

9. The method of claim 1 , wherein the plasma concentration of the compound is higher than the IC 50 of the virus causing the viral infection 12 hours following administration of the compound.

10. The method of claim 1 , further comprising orally administering a neuraminidase inhibitor to the human.

11. The method of claim 10 , wherein the neuraminidase inhibitor that is administered orally is oseltamivir carboxylate.

12. The method of claim 10 , wherein the neuraminidase inhibitor that is administered orally is a compound of formula I, II, III, or IV:

or a pharmaceutically acceptable salt thereof.

13. The method of claim 10 , wherein the neuraminidase inhibitor that is administered orally is a compound of formula Ia, IIa, IIIa, or IVa:

or a pharmaceutically acceptable salt thereof.

14. The method of claim 13 , wherein the neuraminidase inhibitor that is administered orally is a compound of formula Ia, or a pharmaceutically acceptable salt thereof.

15. The method of claim 10 , wherein the neuraminidase inhibitor that is administered orally is administered for up to 20 days.

16. The method of claim 10 , wherein the neuraminidase inhibitor that is administered orally is administered for up to 5 days or up to 10 days.

17. The method of claim 1 , wherein the effective anti-viral amount is up to about 1000 mg per day.

18. The method of claim 1 , wherein the effective anti-viral amount is about 200 mg per day.

Assignments (7)
SECURITY INTEREST Recorded Jan 23, 2026
From: BIOCRYST PHARMACEUTICALS, INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 074485/0651 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 28, 2023
From: BABU, YARLAGADDA SUDHAKARA; CHAND, POORAN; BANTIA, SHANTA; ARNOLD, SHANE; KILPATRICK, JOHN MICHAEL
To: BIOCRYST PHARMACEUTICALS, INC.
Reel/Frame 065067/0406 →
RELEASE OF GRANT OF SECURITY INTEREST IN PATENTS Recorded Apr 18, 2023
From: ATHYRIUM OPPORTUNITIES III CO-INVEST 1 LP
To: BIOCRYST PHARMACEUTICALS, INC.
Reel/Frame 063362/0550 →
RELEASE OF SECURITY INTEREST Recorded Apr 6, 2023
From: MIDCAP FINANCIAL TRUST
To: BIOCRYST PHARMACEUTICALS, INC.; MDCP, LLC
Reel/Frame 063348/0762 →
SECURITY INTEREST Recorded Dec 17, 2020
From: BIOCRYST PHARMACEUTICALS, INC.
To: ATHYRIUM OPPORTUNITIES III CO-INVEST 1 LP
Reel/Frame 054800/0634 →
RELEASE OF SECURITY INTEREST Recorded Dec 16, 2020
From: MIDCAP FINANCIAL TRUST, AS AGENT
To: BIOCRYST PHARMACEUTICALS, INC.; MDCP, LLC
Reel/Frame 054774/0446 →
SECURITY INTEREST Recorded Sep 26, 2016
From: BIOCRYST PHARMACEUTICALS, INC.; MDCP, LLC
To: MIDCAP FINANCIAL TRUST, AS AGENT
Reel/Frame 039858/0967 →