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Viral and Non-Viral Nanoplasmid Vectors with Improved Production

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Summary

USPTO granted patent US12600984B2 to Aldevron, L.L.C. covering methods for improving replication of covalently closed circular plasmids through replacement of Pol I-dependent origins with Pol III-dependent origins. The patent also claims antibiotic marker free covalently closed circular recombinant DNA molecules. The patent contains 31 claims.

What changed

USPTO issued patent grant US12600984B2 to Aldevron, L.L.C. for methods of improving replication of covalently closed circular plasmids by replacing Pol I-dependent origins of replication with Pol III-dependent origins. The patent also claims antibiotic marker free recombinant DNA molecules and covers structured DNA sequences including inverted repeat sequences, direct repeat sequences, homopolymeric repeat sequences, eukaryotic origins of replication, and eukaryotic promoter enhancer sequences.

Affected parties in the biotechnology and pharmaceutical manufacturing sectors should consider this patent when developing plasmid-based vector products. The patent may affect freedom-to-operate for competitors developing similar nanoplasmid production methods. No compliance deadlines or penalties apply to this IP grant.

What to do next

  1. Monitor for potential licensing opportunities
  2. Review patent claims for freedom-to-operate analysis

Archived snapshot

Apr 15, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← USPTO Patent Grants

Viral and non-viral nanoplasmid vectors with improved production

Grant US12600984B2 Kind: B2 Apr 14, 2026

Assignee

Aldevron, L.L.C.

Inventors

James A. Williams

Abstract

A method for improving the replication of a covalently closed circular plasmid is provided. The method includes providing a covalently closed circular plasmid having a Pol I-dependent origin of replication, and an insert including a structured DNA sequence selected from inverted repeat sequences, direct repeat sequences, homopolymeric repeat sequences, eukaryotic origins of replication or eukaryotic promoter enhancer sequences, wherein the structured DNA sequence is located at a distance of less than 1000 bp from the Pol I-dependent origin of replication in the direction of replication. The method also includes modifying the covalently closed circular recombinant molecule such that the Pol I-dependent origin of replication is replaced with a Pol III-dependent origin of replication, whereby the resultant Pol III-dependent origin of replication covalently closed circular plasmid has improved replication. An antibiotic marker free covalently closed circular recombinant DNA molecule is also provided.

CPC Classifications

C12N 15/85 C12N 15/70 C12N 15/86 C12N 2740/15043 C12N 2740/15052 C12N 2750/14143 C12N 2750/14152 C12N 2800/90 C12N 2820/55 C12N 2800/101 C12N 2800/24

Filing Date

2020-09-18

Application No.

17026101

Claims

31

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Last updated

Classification

Agency
USPTO
Published
April 14th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US12600984B2

Who this affects

Applies to
Drug manufacturers Manufacturers Healthcare providers
Industry sector
3254.1 Biotechnology
Activity scope
Patent examination IP licensing Biotech research
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Pharmaceuticals Medical Devices

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