IP Library Granted Patent US 11,098,110
Granted Patent B2
US 11,098,110 · App. 16/018,244 · Granted Aug 24, 2021

Methods for treating ocular diseases with brolucizumab

Inventors: Margarita Gekkieva (Basel, CH); Peter Sallstig (Summit, NJ); Werner Schmidt (Fort Worth, TX); James Warburton (Buckinghamshire, GB); Andreas Weichselberger (Basel, CH)
Assignee: NOVARTIS AG
C07K16/22A61B3/12A61B5/4848A61K9/0048A61K39/3955A61K39/39591A61K2039/54A61K2039/545C07K2317/24C07K2317/52C07K2317/522C07K2317/56C07K2317/565C07K2317/567C07K2317/569C07K2317/622C07K2317/76C07K2317/94
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Quick Facts
Patent No.
US 11,098,110
App. No.
16/018,244
Granted
Aug 24, 2021
Kind
B2
Abstract

A method is provided for reducing the treatment burden for patients who have an intraocular neovascular disorder, the method comprising administering a therapeutically effective amount of VEGF antagonist on a dosing schedule that includes treatment intervals of 8 and/or 12 weeks.

Claims (6)

1. A method for treating neovascular age-related macular degeneration (nAMD) in a patient, the method comprising administering to the patient three individual doses of a VEGF antagonist at 4-week intervals, and thereafter administering to the patient an additional dose every 12 weeks and monitoring the patient's best-corrected visual acuity (BCVA) for a decrease of letters due to nAMD disease activity to determine if the patient should receive a dose more frequently than once every 12 weeks, wherein each dose of the VEGF antagonist is at least 3 mg and the VEGF antagonist is brolucizumab.

2. The method of claim 1 , wherein each dose of the VEGF antagonist is 3 mg.

3. The method of claim 2 , wherein each dose of the VEGF antagonist is administered as a 50 μL intravitreal injection.

4. The method of claim 1 , wherein each dose of the VEGF antagonist is 6 mg.

5. The method of claim 4 , wherein each dose of the VEGF antagonist is administered as a 50 μL intravitreal injection.

6. The method of claim 1 , wherein a 12 week treatment interval is switched to an 8 week treatment interval if the patient's BCVA decreases ≥5 letters due to nAMD disease activity.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE TYPO ON PAGE 1, PARAGRAPH 3, LINE 5, ENTITY ALCON LABORATORIES SHOULD BE NOVARTIS PHARMA AG PREVIOUSLY RECORDED ON REEL 55873 FRAME 427. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Dec 9, 2025
From: GEKKIEVA, MARGARITA; WARBURTON, JAMES; WEICHSELBERGER, ANDREAS
To: NOVARTIS PHARMA AG
Reel/Frame 073978/0202 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2021
From: GEKKIEVA, MARGARITA; WARBURTON, JAMES; WEICHSELBERGER, ANDREAS
To: NOVARTIS PHARMA AG
Reel/Frame 055873/0427 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2021
From: SALLSTIG, PETER; SCHMIDT, WERNER
To: ALCON RESEARCH, LTD.
Reel/Frame 055873/0611 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2021
From: NOVARTIS PHARMA AG
To: NOVARTIS AG
Reel/Frame 055873/0670 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2021
From: ALCON RESEARCH, LTD.
To: NOVARTIS AG
Reel/Frame 055873/0773 →
Cited By (7)
US 1,116,103 US 1,120,314 US 12,274,865 US 12,600,769 US 12,649,031 US 12,649,781 US 12,691,227