IP Library Granted Patent US 11,643,464
Granted Patent B2
US 11,643,464 · App. 16/728,587 · Granted May 9, 2023

Reducing systemic regulatory T cell levels or activity for treatment of a retinal degeneration disorder

Inventors: Michal Eisenbach-Schwartz (Rehovot, IL); Kuti Baruch (Rehovot, IL); Neta Rosenzweig (Rehovot, IL)
Assignee: Yeda Research and Develpment & Co. Ltd
C07K16/2818A61K31/404A61K31/4155A61K31/7068A61K33/36A61K39/395A61K39/39541A61K45/06C07K16/2803C07K16/2827A61K2039/505A61K2039/507A61K2039/545A61K2039/572C07K2317/21C07K2317/24C07K2317/76
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Quick Facts
Patent No.
US 11,643,464
App. No.
16/728,587
Granted
May 9, 2023
Kind
B2
Abstract

The present specification discloses a pharmaceutical composition comprising an active agent that causes reduction of the level of systemic immunosuppression in an individual for use in treating a disease, disorder, condition or injury of the CNS. The pharmaceutical composition is administered by a dosage regimen comprising at least one course of therapy, each course of therapy comprising in sequence a treatment session followed by an interval session of non-treatment.

Claims (17)

1. A method of treating a retinal degeneration disorder in an individual in need thereof, the method comprising administering to the individual a composition comprising an anti-PD-1 antibody, an anti-PD-L1 antibody, an anti-TIM-3 antibody, or any combination thereof.

2. The method according to claim 1 , wherein the administration of the composition is a single administration.

3. The method according to claim 1 , wherein the administration of the composition is a repeated administration.

4. The method according to claim 1 , wherein the administration is a local administration.

5. The method according to claim 4 , wherein the local administration is to at least one eye of the individual.

6. The method according to claim 5 , wherein the local administration is an intravitreal administration.

7. The method according to claim 1 , wherein the administration is a systemic administration.

8. The method according to claim 1 , wherein the composition is administered by a dosage regime comprising at least two courses of therapy, each course of therapy comprising in sequence a treatment session where the composition is administered to the individual followed by a non-treatment period where the composition is not administered to the individual.

9. The method according to claim 8 , wherein the non-treatment period is longer than the treatment session.

10. The method according to claim 8 , wherein the administration of the composition is a single administration.

11. The method according to claim 8 , wherein the administration of the composition is a repeated administration.

12. The method according to claim 11 , wherein the non-treatment period is longer than the period between repeated administrations during the treatment session.

13. The method according to claim 1 , wherein the anti-PD-1 antibody is a neutralizing anti-PD-1 antibody, the anti-PD-L1 antibody is a neutralizing anti-PD-L1 antibody and/or the anti-TIM-3 antibody is a neutralizing anti-TIM-3 antibody.

14. The method according to claim 13 , wherein the anti-PD-1 antibody is a human neutralizing anti-PD-1 antibody or a humanized, neutralizing anti-PD-1 antibody.

15. The method according to claim 13 , wherein the anti-PD-L1 antibody is a human neutralizing anti-PD-L1 antibody or a humanized, neutralizing anti-PD-L1 antibody.

16. The method according to claim 13 , wherein the anti-TIM-3 antibody is a human neutralizing anti-TIM-3 antibody or a humanized, neutralizing anti-TIM-3 antibody.

17. The method according to claim 1 , wherein the retinal degeneration disorder is wet Age-Related Macular Degeneration, dry Age-Related Macular Degeneration, Retinitis Pigmentosa, Choroideremia, Cone-Rod Retinal Dystrophy, Gyrate Atrophy, Juvenile Retinoschisis, Vitelliform Macular Dystrophy (Best's Disease), Abetalipoproteinemia (Bassen-Kornzweig Disease), Bardet-Biedl Syndrome, Blue Cone Monochromatism Disease, Dominant Drusen, Goldman-Favre Vitreoretinal Dystrophy (Enhanced S-cone Syndrome), Kearns-Sayre Syndrome, Laurence-Moon Syndrome, Leber's Congenital Amaurosis, Leber's Refsum disease, Oguchi Disease, Peripapillary (pericentral) Choroidal Dystrophy, Pigment Pattern Dystrophy, Sorsby Macular Dystrophy, Stargardt's Disease, Stickler's Syndrome, Usher Syndrome or Wagner's Vitreoretinal Dystrophy.

Assignments (2)
SECURITY INTEREST Recorded Feb 17, 2026
From: IMMUNOBRAIN CHECKPOINT, INC.
To: RVIBC LENDER LLC
Reel/Frame 074878/0973 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 17, 2020
From: EISENBACH-SCHWARTZ, MICHAL; BARUCH, KUTI; ROSENZWEIG, NETA
To: YEDA RESEARCH AND DEVELOPMENT CO., LTD.
Reel/Frame 051832/0889 →
Continuity (11)
Division 15261945 · Sep 10, 2016
Continuation In Part PCTIL2016050750 · Jul 13, 2016
Continuation In Part 14850794 · Sep 10, 2015
Continuation In Part 14797894 · Jul 13, 2015
Continuation In Part PCTIL2015050265 · Mar 12, 2015
Provisional Application 62358530 · Jul 5, 2016
Provisional Application 62353549 · Jun 22, 2016
Provisional Application 62279622 · Jan 15, 2016
Provisional Application 62030164 · Jul 29, 2014
Provisional Application 61951783 · Mar 12, 2014
Related Publication 20200140553A1 · May 7, 2020