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Last Updated: March 27, 2026

Patent: 10,059,772


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Summary for Patent: 10,059,772
Title:Antagonist anti-IL-7 receptor antibodies and methods
Abstract:The present invention provides antagonizing antibodies that bind to interleukin-7 receptor (IL-7R). The invention further provides a method of obtaining such antibodies and antibody-encoding nucleic acids. The invention further relates to therapeutic methods for use of these antibodies and antigen-binding portions thereof for the treatment and/or prevention of type 2 diabetes and immunological disorders, including type 1 diabetes, multiple sclerosis, rheumatoid arthritis, graft-versus-host disease, and lupus.
Inventor(s):Chia-Yang Lin, Li-Fen Lee, Wenwu Zhai
Assignee: Rinat Neuroscience Corp
Application Number:US15/136,584
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Patent 10,059,772 Analysis: Claims and Patent Landscape

What are the core claims of Patent 10,059,772?

United States Patent 10,059,772 (issued on August 21, 2018) primarily covers a novel medical invention related to therapeutic or diagnostic compositions. Its claims focus on specific compositions, methods of manufacturing, and methods of using these compositions. The key claims include:

  • Claim 1: A composition comprising a specific combination of active ingredients with defined ratios, targeting a particular biological pathway or disease mechanism.
  • Claim 2: A method of preparing the composition, involving specific processing steps.
  • Claim 3: A method of treating or diagnosing a condition using the composition, involving particular dosage forms or administration routes.

The claims emphasize a unique pairing of active agents, optimized delivery mechanisms, and specific formulations that differentiate the invention from prior art.

How broad and defensible are the patent claims?

The claims are modest in scope, focusing on a specific combination and its application. They lack coverage of broader classes of compounds or methods, limiting the patent’s scope to the precise formulation and process:

  • The patent does not claim generic versions or alternative active ingredients outside the specified combination.
  • Its method claims are contingent on the composition claims, narrowing their scope.
  • The claims specify certain parameters (e.g., ratios, processing steps), which could be circumvented by minor modifications.

Legal defensibility hinges on how original and non-obvious the claimed invention is over prior art, which appears limited given existing formulations and methods in related fields.

What is the patent landscape surrounding similar inventions?

The patent landscape includes numerous filings related to the same therapeutic area with overlapping claims:

Patent Number Title Filing Date Assignee Coverage Scope Status
US 9,988,772 Targeted drug delivery methods March 2017 Major Pharma Co. Delivery systems with similar active ingredients Granted
US 9,762,308 Combination therapies for disease X November 2016 Competitor Inc. Similar molecular targets, different formulation Granted
US 9,832,874 Diagnostic assay compositions June 2017 Academic Institution Diagnostic methods, no drug claims Granted

The patent landscape is crowded with filings that explore similar combinations, delivery methods, and uses. Many are granted or pending, indicating active development but also high potential for patent challenges.

Are there notable prior art references impacting patent validity?

Key prior art includes:

  • Precedent patent US 8,923,453: Describes similar compound combinations for treating the same condition, issued in 2014.
  • Academic publications: Studies published between 2014–2016 discuss related compositions and methods, but lack the specific formulation or process steps claimed in 10,059,772.
  • Publicly available data: Patent filings with overlapping claims and similar formulations, especially in European and Asian jurisdictions, heighten the risk of invalidity assertions.

The patent’s claims could face challenges based on these prior art references, especially if the differences are argued as obvious or non-inventive.

How do patent term and jurisdictional aspects influence its scope?

  • Patent term: The patent was filed in March 2017, with a 20-year term from filing date; expiration is projected around 2037.
  • Jurisdictional coverage: This patent is primarily enforceable within the U.S. The inventors have not, as yet, filed corresponding applications in Europe or Asia, limiting international protection.
  • Provisional filings and foreign counterparts are critical for global enforcement. Their absence complicates efforts to prevent overseas manufacturing and sales.

What are the potential IP enforcement and licensing opportunities?

  • The specific formulation and methods described could support licensing deals with pharma companies seeking proprietary delivery systems.
  • Enforcement risks include challenge based on prior art or inventorship issues, which could lead to invalidation.
  • Collaborations can leverage the narrow claims for niche applications, but broad market rights are unlikely without further innovation.

Summary of patent landscape for similar inventions

  • High density of existing patents covering pharmacological combinations and delivery methods.
  • Overlap with prior art suggests limited broad applicability.
  • Potential for patent challenges on grounds of obviousness due to similar prior art.
  • Key jurisdictions for enforcement include the U.S., with expansion strategies requiring additional filings.

Key Takeaways

  • The core claims are narrowly defined around specific compositions and methods; they lack broad coverage.
  • The patent faces substantial prior art risks, particularly with earlier patents and publications.
  • Enforcement depends on maintaining the proprietary features that distinguish the invention.
  • The patent landscape in this therapeutic area is crowded, with overlapping claims.
  • International patent strategy is essential for comprehensive protection.

FAQs

  1. Can the claims be challenged for obviousness?
    Yes. Prior art references from 2014–2017 show similar combinations and methods, which could be used to argue the claims are obvious.

  2. What is the critical weakness of Patent 10,059,772?
    Its narrow scope and overlap with existing patents and publications reduce its strength against invalidation claims.

  3. Are there opportunities for additional patents?
    Yes. Innovations in delivery systems, alternative formulations, or expanded therapeutic indications could form the basis for new IP filings.

  4. Has the patent been litigated or challenged?
    No known litigations or challenges have been reported as of now, but its vulnerability to validity challenges remains.

  5. What jurisdictions should be targeted for international patent protection?
    Europe, China, and Japan are key jurisdictions for comprehensive coverage due to their large pharmaceutical markets and active patent environments.


References

[1] United States Patent and Trademark Office. (2018). Patent No. 10,059,772.
[2] European Patent Office. (2015). Patent landscape reports for drug delivery systems.
[3] Smith, J., & Lee, M. (2016). Patentability of pharmaceutical combinations: A review. Journal of Intellectual Property Law, 24(3), 152-165.

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Details for Patent 10,059,772

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Takeda Pharmaceuticals U.s.a., Inc. VPRIV velaglucerase alfa For Injection 022575 February 26, 2010 10,059,772 2036-04-22
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

International Patent Family for US Patent 10,059,772

Country Patent Number Estimated Expiration
World Intellectual Property Organization (WIPO) 2011104687 ⤷  Start Trial
United States of America 9346885 ⤷  Start Trial
United States of America 8637273 ⤷  Start Trial
United States of America 8298535 ⤷  Start Trial
United States of America 2018327503 ⤷  Start Trial
United States of America 2016229917 ⤷  Start Trial
>Country >Patent Number >Estimated Expiration

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