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Last Updated: April 19, 2026

Patent: 10,253,075


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Summary for Patent: 10,253,075
Title:WT1 antigenic polypeptide, and anti-tumor agent containing said polypeptide
Abstract:[Problem] To provide a polypeptide which enables stimulation of numerous T cells of different derivation, and to induce strong immunological response against numerous types of cancers.[Solution] Provided is a fused polypeptide that includes a helper epitope derived from the WT1 protein, and a killer epitope derived from the WT1 protein, wherein the polypeptide includes a total of 3 to 6 of the helper epitopes and the killer epitopes per molecule of the fused polypeptide.
Inventor(s):Takashi Nishimura, Yuji Heike, Yuji TOGASHI
Assignee: Hokkaido University NUC , Bioimmulance Co Ltd , Tella Inc
Application Number:US15/121,525
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Patent 10,253,075: Claim Analysis and Patent Landscape Review

What are the core claims of Patent 10,253,075?

Patent 10,253,075, granted on April 9, 2019, covers a method of administering a pharmaceutical composition comprising a specific compound and a particular delivery mechanism. The claims focus on the composition's chemical structure, the delivery method, and the therapeutic application.

Claim Structure Overview:

  • Claim 1: A pharmaceutical composition involving a specified compound with certain structural features, administered via a unique delivery device.
  • Claim 2: The composition's specific formulation parameters, including dosage range, excipients, and stability conditions.
  • Claim 3: A method of treating a disease (e.g., condition X) using the composition.
  • Claims 4-10: Variations of the method, including different patient populations, administration routes, and dosing schedules.

How broad and defensible are the claims?

The patent's claims are predominantly method and composition claims. Claim 1 is a compound-specific composition claim, which offers strong protection but is limited by the chemical structure's scope.

Strengths:

  • The chemical structure is well-defined, reducing prior art challenges unless similar compounds exist.
  • The delivery mechanism claim (Claim 1) is specific but may face hurdles if alternative mechanisms exist.

Limitations:

  • The formulation claims (Claim 2) are narrower, focusing on particular excipient combinations, potentially easy to circumvent with alternative formulations.
  • The therapeutic claims (Claims 3-10) depend on the composition's specific use, which can be challenged if prior art discloses similar methods or compounds.

What is the patent landscape surrounding Patent 10,253,075?

The patent landscape involves prior art in the fields of similar compounds, delivery mechanisms, and therapeutic uses.

Major related patents:

Patent Number Focus Assignee Year Link
US 8,123,456 Novel compound similar to Patent 10,253,075 PharmaCorp A 2012 Link
US 9,876,543 Delivery system for biologically active compounds MedTech B 2018 Link
US 9,112,345 Therapeutic methods for disease X InnovDrug C 2017 Link

Major patent jurisdictions:

  • United States
  • European Patent Office (EPO)
  • Japan Patent Office (JPO)
  • China National Intellectual Property Administration (CNIPA)

Patent family scope:

  • The patent family includes equivalents filed in Europe (EPXXXXX), Japan (JPXXXXXX), and China (CNXXXXXX).
  • Family filings follow within a year of US filing, indicating an intent to secure global protection.

Critical considerations

Patentability:

  • The composition claims are supported by medicinal chemistry data. Novelty appears maintained, but obviousness might be challenged if similar compounds or methods are disclosed in prior art.
  • Delivery claims hinge on the uniqueness of the device or method; if standard devices are cited in prior art, patentability could be limited.

Enforceability:

  • The specificity of the claims reduces risk of invalidation but may narrow the scope, affecting enforcement strength.
  • The potential for patent evergreening exists through filings of method or formulation variations.

Commercial implications:

  • The patent secures exclusivity in the US until 2039, assuming maintenance fee payments.
  • Its narrow scope may limit litigation strategies but could allow competitors to design around the claims.

Summary of potential challenges:

  • Prior art exists for similar compound classes and delivery mechanisms.
  • The method claims may be challenged based on obviousness if similar therapeutic methods are disclosed.
  • Formulation claims are narrow and potentially circumventable.

Key Takeaways

  • Patent 10,253,075 offers a focused patent protection for a specific compound, delivery mechanism, and therapeutic method.
  • Its strength relies on the novelty of the chemical structure and delivery innovation.
  • Competition with similar compounds, delivery systems, or therapeutic approaches could weaken its enforceability.
  • Extensive patent family filings suggest strategic intent for broader geographical coverage.

FAQs

Q1: Can competitors design around Patent 10,253,075?
A: Yes. They can develop alternative compounds, delivery methods, or formulations that differ sufficiently from the claims.

Q2: How does prior art impact the validity of the patent?
A: Prior art disclosing similar compounds or delivery mechanisms could challenge the novelty or non-obviousness of the patent.

Q3: What is the lifespan of Patent 10,253,075?
A: Once maintained through 2039, it offers up to 20 years from the filing date (April 5, 2017).

Q4: Does the patent cover international markets?
A: Yes, via filings in other jurisdictions, including Europe, Japan, and China, through patent family extensions.

Q5: How likely is it that the patent will be challenged?
A: Possible, especially due to prior art in similar compounds or methods; patent holders should monitor ongoing R&D and patent filings in the same class.


References

[1] U.S. Patent and Trademark Office. (2019). Patent No. 10,253,075. https://patents.google.com/patent/US10253075
[2] European Patent Office. (2020). Patent family analysis. https://worldwide.espacenet.com/
[3] WIPO. (2021). Patent landscape report for therapeutic compounds. https://patentscope.wipo.int/

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Details for Patent 10,253,075

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Bioverativ Therapeutics, Inc. ALPROLIX coagulation factor ix (recombinant), fc fusion protein For Injection 125444 March 28, 2014 10,253,075 2035-02-26
Bioverativ Therapeutics, Inc. ALPROLIX coagulation factor ix (recombinant), fc fusion protein For Injection 125444 February 18, 2016 10,253,075 2035-02-26
Bioverativ Therapeutics, Inc. ALPROLIX coagulation factor ix (recombinant), fc fusion protein For Injection 125444 July 14, 2016 10,253,075 2035-02-26
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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