IP Library Granted Patent US 12692497
Granted Patent B2
US 12692497 · App. 17/969,496 · Granted Jul 28, 2026

Cardiac cell proliferation by administering inhibitors of SAV1, NF2, MOB1 and/or mutant SRF

Inventors: Robert Joel Schwartz (Houston, TX); Nada Bejar (Pearland, TX)
Assignee: Animatus Biosciences, Inc.
C12N15/113C12N5/0657C12N15/88C12N2310/14
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Quick Facts
Patent No.
US 12692497
App. No.
17/969,496
Granted
Jul 28, 2026
Kind
B2
Abstract

Disclosed are DsiRNA inhibitors for the genes encoding SAV1, NF2 and MOB1, which cause proliferation of cardiomyocytes on administration to a mammal. The DsiRNA inhibitors can also be administered with a mutant SRF (153-A3) or an mRNA encoding it, and/or Yap5SA (a Yap mutant) or an encoding mRNA, which enhance the proliferative effect on cardiomyocytes. Mutant SRF (153-A3) with Yap5SA alone also induce myocyte replication.

Claims (8)

1 . A method of inducing replication of cardiac cells in a mammal, comprising:

administering to the mammal one or more of the following complementary DsiRNA pairs wherein the complementary DsiRNA pairs target the Mob1 gene and are selected from the group consisting of:

SEQ ID NOS: 43 & 44; SEQ ID NOS: 45 & 46 and SEQ ID NOS: 47 & 48.

2 . The method of claim 1 wherein the mammal is a human and the complementary DsiRNA pairs are selected from the group consisting of: SEQ ID NOS: 43 & 44; SEQ ID NOS: 45 & 46 and SEQ ID NOS: 47 & 48.

3 . The method of claim 1 wherein the cardiac cells are cardiomyocytes.

4 . The method of claim 1 , wherein the administering is by oral administration, inhalation, subcutaneous administration, intravenous administration, intraperitoneal administration, intramuscular administration, intrathecal injection, intra-articular administration, topical administration, central administration, peripheral administration, aerosol-based administration, nasal administration, transmucosal administration, transdermal administration, parenteral administration, or combinations thereof.

5 . The composition of claim 1 , wherein the composition comprises a delivery vehicle.

6 . The composition of claim 5 , wherein the delivery vehicle comprises liposomes.