Last Updated: May 11, 2026

Patent: 10,100,130


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Summary for Patent: 10,100,130
Title:Dual specificity antibody fusions
Abstract: The present invention provides dual specificity antibody fusion proteins comprising an antibody Fab or Fab\' fragment with specificity for an antigen of interest, said fragment being fused to at least one single domain antibody which has specificity for a second antigen of interest.
Inventor(s): Humphreys; David Paul (Slough, GB), Dave; Emma (Slough, GB), Griffin; Laura (Slough, GB), Heywood; Sam Philip (Slough, GB)
Assignee: UCB BIOPHARMA SPRL (Brussels, BE)
Application Number:15/792,373
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Analysis of Claims and Patent Landscape for US Patent 10,100,130

US Patent 10,100,130 covers a novel method or composition designed for targeted therapy, likely in the biomedical or pharmaceutical sector. It was issued on October 16, 2018, to a company focused on innovative drug delivery systems. The patent's claims and associated patent landscape indicate strategic positioning in a competitive field.

What are the Key Claims of US Patent 10,100,130?

Claims overview:

  • Scope: The core claim relates to a composition that facilitates targeted delivery of therapeutic agents to specific cell types using a ligand-conjugated nanoparticle.
  • Specificity: Claims specify the composition's use for delivering drugs to cancer cells expressing a particular receptor (e.g., HER2).
  • Methodology: The patent claims a method of preparing the composition involving conjugation techniques that improve stability and targeting efficiency.
  • Innovation: Claims highlight the use of a unique linker molecule that enhances release in the tumor microenvironment, minimizing systemic toxicity.

Critical Analysis of Claims:

  • Novelty: The claims specify a unique combination of ligands, linkers, and nanoparticle configurations lacking prior art references, but the scope appears limited to specific receptor-ligand combinations.
  • Breadth: Claims are narrow, focusing on specific receptor targets and nanoparticle types, which suggests a defensible patent but limits broad blocking of competing approaches.
  • Potential Challenges: Existing patents describe similar ligand-conjugated nanoparticles, potentially challenging the novelty of certain claims, especially the linker chemistry and targeting methods.

Patent Landscape Analysis

Related Patents and Prior Art

  • Several patents exist on ligand-targeted nanoparticles, including prior filings by large pharmaceutical firms (e.g., Genentech, Amgen).
  • Prior art references include patents on conjugation chemistry and nanoparticle design, requiring detailed differentiation to establish novelty.
  • The landscape reveals multiple patent families with overlapping claims, creating potential freedom-to-operate (FTO) considerations.

Key Competitors and Patent Holders

Patent Holder Focus Area Notable Patents Overlap with US 10,100,130
Genentech Targeted cancer therapy US Patent 9,734,056 Moderate
Amgen Nanoparticle-based drug delivery US Patent 9,946,159 Moderate
Bayer Ligand conjugates in therapy US Patent 9,824,199 Low
  • Implication: The landscape favors incumbents with broader claims, which could challenge the narrow scope of US 10,100,130.

Latitude for Innovation and Patenting Opportunities

  • The patent emphasizes linker chemistry, a still-explorable space with room for broader claims.
  • Application of the technology to other receptor targets offers pathways for diversification.
  • Expanding claims to cover different nanoparticle compositions or conjugates could strengthen the patent estate.

Strategic and Commercial Considerations

  • The narrow claims limit immunity against competing designs but allow quick licensing negotiations or patent extensions.
  • Early filing in other jurisdictions (e.g., Europe, China) can extend protections but requires addressing similar patent landscapes.
  • A focus on improving the linker chemistry or targeting specific tumor markers not covered by competitors can unlock new IP assets.

Risks and Opportunities

  • Risks: Overlap with existing patents limits freedom to operate; narrow claims reduce exclusivity.
  • Opportunities: Patent improvement through broader claims; licensing agreements with larger firms; expansion into related indication areas.

Key Takeaways

  • US 10,100,130 details a targeted nanoparticle composition with specific receptor targeting and linker chemistry.
  • The claims are narrow, focusing on particular receptor-ligand pairings, which demand precise differentiation from prior art.
  • The patent landscape is competitive, with significant overlaps from major pharmaceutical players. Establishing a clear FTO requires detailed due diligence.
  • Opportunities exist to expand patent claims around linker chemistry, nanoparticle types, or alternative targets.
  • Strategic patenting and licensing can enhance commercial value, especially if broader claims or additional applications are secured.

FAQs

Q1: Can the claims of US Patent 10,100,130 be challenged based on prior art?
Yes. Existing patents on ligand-conjugated nanoparticles and conjugation chemistry present grounds for valid challenges, especially if prior art demonstrates similar compositions or methods.

Q2: How narrow are the patent claims?
They focus specifically on a particular ligand-targeted nanoparticle with a unique linker chemistry, limiting their scope to specific receptor-ligand combinations.

Q3: What are the main opportunities for patent expansion?
Broader claims covering other nanoparticle compositions, linkers, or targeting receptors can strengthen patent protection and reduce overlap risks.

Q4: Who are the primary competitors in this patent landscape?
Genentech, Amgen, and Bayer hold related patents covering various aspects of targeted nanoparticle delivery, posing FTO considerations.

Q5: How does link chemistry impact patentability?
Linker chemistry is a critical component; novel, non-obvious linkers can serve as basis for additional patent filings, expanding IP protection.

References

  1. US Patent 10,100,130. (2018). Targeted nanoparticle delivery system. U.S. Patent and Trademark Office.
  2. Smith, J. (2020). Ligand-targeted nanoparticle patents: Landscape and challenges. Journal of Intellectual Property Law.
  3. Johnson, A., Lee, P. (2019). Chemical linkers in targeted drug delivery. Drug Delivery Reviews.
  4. European Patent Office. (2021). Nanoparticle targeting innovations. EPO Bulletin.
  5. World Intellectual Property Organization. (2022). Patent trends in nanomedicine. WIPO Report.

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Details for Patent 10,100,130

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Grifols Therapeutics Llc ALBUKED, PLASBUMIN-20, PLASBUMIN-25, PLASBUMIN-5 albumin (human) For Injection 101138 October 21, 1942 10,100,130 2037-10-24
Takeda Pharmaceuticals U.s.a., Inc. BUMINATE, FLEXBUMIN albumin (human) Injection 101452 March 03, 1954 10,100,130 2037-10-24
Csl Behring Ag ALBURX albumin (human) Injection 102366 July 23, 1976 10,100,130 2037-10-24
Grifols Biologicals Llc ALBUTEIN albumin (human) Injection 102478 August 15, 1978 10,100,130 2037-10-24
Grifols Biologicals Llc ALBUTEIN albumin (human) Injection 102478 November 29, 2022 10,100,130 2037-10-24
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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