IP Library › Granted Patent US 12,473,554
Granted Patent B2
US 12,473,554 · App. 18/520,449 · Granted Nov 18, 2025

MRNA treatment nanoparticles

Inventors: Samuel Deutsch (Walnut Creek, CA); Daniel Frimannsson (Alameda, CA); Nicole Fay (Alameda, CA); Colin McKinlay (Fremont, CA); Ole Haabeth (Emeryville, CA)
Assignee: Nutcracker Therapeutics, Inc.
C12N15/117A61K9/145A61K39/12A61K45/06A61P35/00C07K16/2818A61K2039/53A61K2039/54A61K2039/55522A61K2039/55538A61K2039/892
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Quick Facts
Patent No.
US 12,473,554
App. No.
18/520,449
Granted
Nov 18, 2025
Kind
B2
Abstract

Provided herein are examples of mRNA treatment nanoparticles and methods of using them to treat a patient. An mRNA treatment nanoparticle may include one or more mRNAs encoding a tumor-specific antigen and an immunomodulatory agent; and a delivery vehicle molecule encapsulating the one or more mRNAs.

Claims (16)

1 . A method comprising administering a therapeutic mRNA composition to a subject in need thereof, wherein the therapeutic mRNA composition comprises:

a first mRNA scaffold comprising a first mRNA coding region encoding HPV16 E6 E7;

a second mRNA scaffold comprising a second mRNA coding region encoding interleukin-12, wherein the second mRNA coding region has a nucleic acid sequence identical to SEQ ID NO:5; and

a third mRNA scaffold comprising a third mRNA coding region encoding tumor necrosis factor superfamily member 14 (TNFSF14) wherein the third mRNA coding region has a nucleic acid sequence identical to SEQ ID NO:11, and

wherein the first mRNA scaffold, the second mRNA scaffold and, the third mRNA scaffold are encapsulated in a delivery vehicle, wherein the delivery vehicle is selected from the group consisting of lipid nanoparticles, polymer-based nanoparticles, cationic lipids, ionizable lipids, amino-lipidated peptoids, amphipathic molecules/nanoparticles, and tertiary amino lipidated cationic peptoids.

2 . The method of claim 1 , wherein the first mRNA scaffold and the second mRNA scaffold are encapsulated in a single delivery vehicle.

3 . The method of claim 1 , wherein the first mRNA scaffold, the second mRNA scaffold, and the third mRNA scaffold are encapsulated in a single delivery vehicle.

4 . The method of claim 1 , wherein the interleukin-12 has an amino acid sequence identical to SEQ ID NO:6.

5 . The method of claim 1 , wherein the TNFSF14 has an amino acid sequence identical to SEQ ID NO:12.

6 . The method of claim 1 , wherein the TNFSF14 is wild type TNFSF14.

7 . The method of claim 1 , wherein the therapeutic mRNA composition further comprises an immunostimulator.

8 . The method of claim 7 , wherein the immunostimulator comprises CpG oligodeoxynucleotides.

9 . The method of claim 1 , wherein the therapeutic mRNA composition is administered via injection.

10 . The method of claim 9 , wherein the therapeutic mRNA composition is administered via intratumoral injection.

11 . The method of claim 10 , wherein the intratumoral injection is repeated at least one or more times with a wait between injections, wherein the wait is between about 1 and about 14 days.

12 . The method of claim 1 , wherein the subject is known to have cervical cancer or pre-cancerous cervical indications.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 5, 2026
From: NUTCRACKER THERAPEUTICS, INC.
To: MEDICI THERAPEUTICS, INC.
Reel/Frame 074407/0426 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 7, 2024
From: DEUTSCH, SAMUEL; FAY, NICOLE; FRIMANNSSON, DANIEL; HAABETH, OLE; MCKINLAY, COLIN
To: NUTCRACKER THERAPEUTICS, INC.
Reel/Frame 068519/0905 →
Continuity (4)
Continuation 18048390 · Oct 20, 2022
Continuation PCTUS2021028312 · Apr 21, 2021
Provisional Application 63014074 · Apr 22, 2020
Related Publication 20240158802A1 · May 16, 2024
References Cited (14)
US 20040096835A1 · Dobie · 2004 [cited by applicant]
US 20160016140A1 · Jovanovich et al. · 2016 [cited by applicant]
US 20180311343A1 · Huang et al. · 2018 [cited by applicant]
US 20190142971A1 · Hoge et al. · 2019 [cited by applicant]
US 20190202920A1 · Tuna et al. · 2019 [cited by applicant]
WO 2017193084 · 2017 [cited by applicant]
WO WO2018081459A1 · 2018 [cited by applicant]
PCT, International Preliminary Report of Patentability regarding PCT Application No. PCT/US2021/028312, 14 pages, dated Nov. 3, 2022. [cited by applicant]
PCT, International Search Report regarding PCT Application No. PCT/US2021/028312, dated Sep. 10, 2021, 4 pages. [cited by applicant]
Baiersdorfer, Markus, et al., Molecular Therapy, A Facile Method for the Removal of dsRNA Contaminant from In Vitro-Transcribed mRNA, Molecular Therapy: Nucleic Acids vol. Apr. 15, 2019, 10 pages. [cited by applicant]
Dai et al., “Oncolytic adenovirus encoding Light (TNFSF14) inhibits tumor growth via activating anti-tumor immune responses in 4T1 mouse mammary tumor model in immune competent syngeneic mice”, Cancer Gene Therapy, Dec.… [cited by applicant]
Extended European Search Report for European Patent Application No. 21793753.1, mailed Dec. 3, 2024. [cited by applicant]
Liu et al., “Abstract 5163: Local delivery of mRNA immunotherapy encoding HPV16 antigen, IL-12, and Light/TNFSF14 results in superior immunogenicity and tumor clearance in a murine model of HPV16-driven cancer”. Cancer … [cited by applicant]
Partial Supplementary European Search Report for European Patent Application No. 21793753.1, mailed Sep. 12, 2024. [cited by applicant]