IP Library Granted Patent US 11,273,171
Granted Patent B2
US 11,273,171 · App. 17/346,556 · Granted Mar 15, 2022

Methods for treating or preventing ophthalmological conditions

Inventors: Samir Patel (Princeton, NJ); Richard Everett (Randolph, NJ); Douglas Brooks (Durham, NC); Shane Xinxin Tian (Oakland, NJ)
Assignee: IVERIC bio, Inc.
A61K31/7088A61K9/0048A61K9/143A61K31/713A61K39/3955A61K45/06C07K16/22C12N15/115C07K2317/24C07K2317/55C07K2317/76C12N2310/16C12N2310/314C12N2310/317C12N2310/321C12N2310/322C12N2310/351C12N2320/30C12N2320/31
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,273,171
App. No.
17/346,556
Granted
Mar 15, 2022
Kind
B2
Abstract

The present invention relates to methods for treating and preventing ophthalmological disease and disorders, comprising administering Antagonist A or another pharmaceutically acceptable salt thereof, optionally in combination with another treatment, to a subject in need thereof. The present invention also relates to methods for treating and preventing ophthalmological disease and disorders, comprising administering an anti-C5 agent (e.g., ARC1905), optionally in combination with another treatment, to a subject in need thereof.

Claims (32)

1. A method of treating geographic atrophy in a human subject in need thereof, the method comprising administering via intravitreal injection to said subject about 2 mg/eye of a pegylated aptamer in an amount sufficient to reduce growth of a lesion associated with geographic atrophy in the subject, wherein the aptamer comprises the sequence

fCmGfCfCGfCmGmGfUfCfUfCmAmGmGfCGfCfUmGmAmGf UfCfUmGmAmGfUfUfUAfCfCfUmGfCmG-3T (SEQ ID NO:26),

wherein fC and fU=2′ fluoro nucleotides, mG and mA=2′-OMe nucleotides, all other nucleotides are 2′-OH, and 3T indicates an inverted deoxythymidine, or a salt thereof, and

wherein the pegylated aptamer is administered to the subject biweekly, monthly, or quarterly.

2. The method according to claim 1 , wherein the pegylated aptamer is provided as a pegylated moiety conjugated to the aptamer via a linker.

3. The method according to claim 2 , wherein the pegylated moiety is conjugated to the 5′ end of the aptamer.

4. The method according to claim 2 , wherein the pegylated moiety is a branched PEG.

5. The method according to claim 2 , wherein the pegylated moiety has a molecular weight greater than about 10 kDA.

6. The method according to claim 2 , wherein the pegylated moiety has a molecular weight of about 40 kDa.

7. The method according to claim 1 , wherein the pegylated moiety has the following structure:

8. The method according to claim 1 , wherein the growth of the GA lesion in the subject in need thereof is reduced by at least 10%, as compared to a subject who is not administered the anti-C5 agent.

9. The method according to claim 1 , wherein the anti-C5 agent is administered monthly.

10. The method according to claim 9 , wherein the anti-C5 agent is administered monthly for three injections, and the fourth and fifth injections are administered three or four months after the third injection.

11. The method according to claim 1 , wherein the anti-C5 agent is administered bimonthly.

12. The method according to claim 1 , wherein the anti-C5 agent is administered quarterly.

13. The method according to claim 1 , wherein the growth of the GA lesion in the subject in need thereof is reduced by at least 20% as compared to a subject who is not administered the anti-C5 agent.

14. The method according to claim 1 , wherein the growth of the GA lesion in the subject in need thereof is reduced by at least 30% as compared to a subject who is not administered the anti-C5 agent.

15. The method according to claim 1 , wherein the growth of the GA lesion in the subject in need thereof is reduced by at least 40% as compared to a subject who is not administered the anti-C5 agent.

16. The method according to claim 1 , wherein the growth of the GA lesion in the subject in need thereof is reduced by at least 50% as compared to a subject who is not administered the anti-C5 agent.

17. The method according to claim 1 , wherein growth of the lesion is assessed using autofluorescence imaging or optical coherence tomography.

18. A method of treating geographic atrophy in a human subject in need thereof, the method comprising administering via intravitreal injection to said subject about 2 mg/eye of a pegylated aptamer in an amount sufficient to reduce growth of a lesion associated with geographic atrophy in the subject, wherein the aptamer comprises the sequence

fCmGfCfCGfCmGmGfUfCfUfCmAmGmGfCGfCfUmGmAmGf UfCfUmGmAmGfUfUfUAfCfCfUmGfCmG-3T (SEQ ID NO:26),

wherein fC and fU=2′ fluoro nucleotides, mG and mA=2′-OMe nucleotides, all other nucleotides are 2′-OH, and 3T indicates an inverted deoxythymidine, or a salt thereof, and

wherein the pegylated aptamer is administered to the subject biweekly, monthly, or quarterly,

wherein the pegylated moiety is a branched PEG and has a molecular weight greater than about 10 kDA, and

wherein the growth of the GA lesion in the subject in need thereof is reduced by at least 30% as compared to a subject who is not administered the anti-C5 agent.

19. A method of treating geographic atrophy in a human subject in need thereof, the method comprising administering via intravitreal injection to said subject about 2 mg/eye of a pegylated aptamer in an amount sufficient to reduce growth of a lesion associated with geographic atrophy in the subject, wherein the aptamer comprises the sequence

fCmGfCfCGfCmGmGfUfCfUfCmAmGmGfCGfCfUmGmAmGf UfCfUmGmAmGfUfUfUAfCfCfUmGfCmG-3T (SEQ ID NO:26),

wherein fC and fU=2′ fluoro nucleotides, mG and mA=2′-OMe nucleotides, all other nucleotides are 2′-OH, and 3T indicates an inverted deoxythymidine, or a salt thereof, and

wherein the pegylated aptamer is administered to the subject biweekly, monthly, or quarterly,

wherein the pegylated moiety is a branched PEG and has a molecular weight greater than about 10 kDA, and

wherein the growth of the GA lesion in the subject in need thereof is reduced by at least 40% as compared to a subject who is not administered the anti-C5 agent.

Assignments (5)
MERGER Recorded Jun 26, 2024
From: IVERIC BIO, INC.
To: ASTELLAS US LLC
Reel/Frame 067851/0643 →
RELEASE OF SECURITY INTEREST Recorded Jul 17, 2023
From: HERCULES CAPITAL, INC.
To: IVERIC BIO, INC.; IVERIC BIO GENE THERAPY LLC; ORION OPHTHALMOLOGY LLC
Reel/Frame 064286/0472 →
SECURITY INTEREST Recorded Aug 5, 2022
From: IVERIC BIO, INC.
To: HERCULES CAPITAL, INC.
Reel/Frame 061088/0048 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2022
From: PATEL, SAMIR; EVERETT, RICHARD; BROOKS, DOUGLAS; TIAN, SHANE XINXIN
To: OPHTHOTECH CORPORATION
Reel/Frame 058851/0869 →
CHANGE OF NAME Recorded Feb 1, 2022
From: OPHTHOTECH CORPORATION
To: IVERIC BIO, INC.
Reel/Frame 058955/0089 →
Continuity (19)
Continuation 16434018 · Jun 6, 2019
Continuation 15144429 · May 2, 2016
Continuation 14329702 · Jul 11, 2014
Provisional Application 61931135 · Jan 24, 2014
Provisional Application 61931116 · Jan 24, 2014
Provisional Application 61931125 · Jan 24, 2014
Provisional Application 61926812 · Jan 13, 2014
Provisional Application 61926848 · Jan 13, 2014
Provisional Application 61926825 · Jan 13, 2014
Provisional Application 61911854 · Dec 4, 2013
Provisional Application 61911894 · Dec 4, 2013
Provisional Application 61911860 · Dec 4, 2013
Provisional Application 61866502 · Aug 15, 2013
Provisional Application 61866507 · Aug 15, 2013
Provisional Application 61866503 · Aug 15, 2013
Provisional Application 61845936 · Jul 12, 2013
Provisional Application 61845938 · Jul 12, 2013
Provisional Application 61845935 · Jul 12, 2013
Related Publication 20210369757A1 · Dec 2, 2021