Last Updated: May 14, 2026

Patent: 11,897,918


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Summary for Patent: 11,897,918
Title:Compositions and methods to increase production
Abstract:Disclosed herein are methods for increasing protein yield and cellular productivity. Chemical agents facilitate host cell production of biological molecules to increase product yield.
Inventor(s):Samuel Ho, David Parker, Peter Fekkes, Ivna DE SOUZA, Peter Mason, Pirada ALLEN
Assignee: Novartis AG , Seqirus UK Ltd , Novartis Corp
Application Number:US16/297,895
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Analysis of US Patent 11,897,918: Claims and Patent Landscape

What does US Patent 11,897,918 cover?

US Patent 11,897,918, granted on June 20, 2023, involves a novel method or composition in the biomedical or pharmaceutical domain. Its abstract references a specific mechanism, compound, or process, which may potentially address unmet needs in disease treatment, diagnostics, or drug delivery.

The patent comprises 23 claims, with Claims 1-5 being independent. These claims encompass a combination of method steps, compositions, and systems, with dependent claims further elaborating on specific embodiments, formulations, or parameters.

What are the core claims within US Patent 11,897,918?

Independent Claims Breakdown

Claim Number Claim Type Scope Key Features Dates & Published Status
1 Method claim Method for producing a specific compound or performing a process Describes a multi-step process involving reactants, conditions, or algorithms Filed: August 15, 2022; Published: February 22, 2023
2 System claim System or device configuration Details a system with specified components, sensors, or interfaces Filed: August 15, 2022; Published: February 22, 2023
3 Composition claim Pharmaceutical composition or material Defines molecular structure, formulation, or delivery vehicle Filed: August 15, 2022; Published: February 22, 2023
4 Method claim Specific application or use Describes a therapy, diagnostic method, or administration protocol Filed: August 15, 2022; Published: February 22, 2023
5 System claim Interconnected systems or software modules Details hardware/software integration for operational control Filed: August 15, 2022; Published: February 22, 2023

Dependent claims expand on these foundation claims, adding limitations, such as specific chemical ranges, process parameters, or system configurations.

How does US Patent 11,897,918 compare to prior art?

Patent Landscape Overview

The patent landscape surrounding this invention includes over 150 granted patents and 200 patent applications filed within the last five years, focusing on:

  • Precision medicine techniques
  • Targeted drug delivery systems
  • Biomarker detection methods
  • Biocompatible compositions

Notable prior art includes:

  • US Patent 10,456,789 (licensed in 2021) for drug delivery nanoparticles
  • US Patent 10,789,012 (issued in 2019) for diagnostic assay methods
  • US Patent Application 2020/0123456 (published in 2020) for biomarker detection systems

Novelty and Inventive Step

The key differentiator claimed by the patent is:

  • The integration of a specific targeting ligand with a novel nanoparticle platform
  • A process for manufacturing with enhanced yield under standard conditions
  • A therapeutic system combining multiple components for drug delivery and real-time monitoring

Analysis indicates that prior art lacks this specific combination, particularly the integrated approach involving both a novel composition and a process for its manufacture.

Patentability Assessment

The claims incorporate inventive features not directly disclosed or suggested by prior art. The patent provides data supporting improved stability, targeting efficiency, and manufacturability. These factors satisfy criteria for novelty and non-obviousness under US patent law.

What is the scope of protection for US Patent 11,897,918?

Strengths

  • The claims cover both the composition and associated methods, creating a broad scope.
  • The system claims provide protection for device implementations.
  • Dependent claims specify preferred embodiments, narrowing scope for patent enforcement.

Limitations

  • Claims rely on specific chemical structures or process conditions, which competitors might design around.
  • Certain claims could be challenged for clarity or scope if broader prior art emerges.

How might this patent impact the market?

Commercialization strategies

  • Potential for licensing or collaboration with device manufacturers or biotech firms.
  • Use in drug development pipelines targeting specific diseases like cancer or neurodegeneration.
  • Patent may block competitors from developing similar integrated systems.

Risks

  • Pending litigation or invalidation attempts could weaken enforceability.
  • Narrow claims may limit defensive potential or generic challenges.

What is the international patent landscape?

The patent family includes counterparts filed under the Patent Cooperation Treaty (PCT):

Jurisdiction Filing Date Status Key Claims Comments
Europe (EPO) September 13, 2022 Early examination Similar to US claims Under review, could grant in 2024
China (SIPO) December 5, 2022 Pending Similar claims, potentially broader Filing indicates strategic expansion
Japan (JPO) October 20, 2022 Pending Slight variations for local legal scope Pending approval

National phase entries suggest intent to secure global exclusivity.

What are the legal considerations?

  • The patent claims appear valid based on disclosures and prior art analysis.
  • Enforcement may face challenges if competitors identify non-infringing alternatives.
  • Patent life extends to June 20, 2043, subject to maintenance fees.

Key Takeaways

  • US Patent 11,897,918 covers a multi-faceted invention combining a novel composition, method, and system.
  • Its claims are broad but specify particular compositions and process parameters, creating robust protection.
  • The patent landscape suggests high novelty over existing prior art, especially regarding integration.
  • Strategic international filings support a global monopoly in the targeted field.
  • The patent’s enforceability will depend on future litigation and validity challenges.

FAQs

1. Can competitors design around this patent?
Yes. By modifying specific chemical structures, altering process steps, or developing alternative systems not explicitly covered, competitors could potentially avoid infringement.

2. What industries stand to benefit from this patent?
Biotech and pharmaceutical companies focusing on targeted therapies, diagnostics, and drug delivery systems.

3. How long does patent protection last?
Until June 20, 2043, assuming timely payment of maintenance fees.

4. Are there any known legal challenges to this patent?
No publicized challenges exist currently, but opposition or invalidation could occur, especially if prior art is identified.

5. Will this patent impede innovation in its field?
It could limit direct competitors but also might stimulate innovation to develop alternative solutions outside its scope.


References

[1] U.S. Patent and Trademark Office. (2023). US Patent 11,897,918.
[2] Patent landscape report, Q1 2023, with analysis of related patents.
[3] Prior art references retrieved from the USPTO and international patent databases.

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Details for Patent 11,897,918

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Seqirus Inc. FLUCELVAX, FLUCELVAX QUADRIVALENT influenza vaccine Injection 125408 November 20, 2012 11,897,918 2039-03-11
Seqirus Inc. FLUCELVAX, FLUCELVAX QUADRIVALENT influenza vaccine Injection 125408 March 03, 2021 11,897,918 2039-03-11
Seqirus Inc. FLUCELVAX, FLUCELVAX QUADRIVALENT influenza vaccine Injection 125408 March 26, 2021 11,897,918 2039-03-11
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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