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Last Updated: March 26, 2026

Patent: 9,603,898


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Summary for Patent: 9,603,898
Title:Formulations of diluted amino acid segments and methods for making same
Abstract: A formulation of a diluted amino acid segment is prepared by mixing an amino acid segment and a diluting agent to form a mixture. The mixture is serially diluted to produce a diluted formulation. The amino acid segment includes a peptide sequence that is the same as a portion of a longer peptide sequence found in a naturally occurring material. A homeopathic remedy can be prepared using the formulation.
Inventor(s): Carter; Jacob L. (Pleasant Grove, UT), Lephart; Edwin Douglas (Orem, UT)
Assignee: Deseret Biologicals, Inc. (Sandy, UT)
Application Number:13/428,907
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Analysis of United States Patent 9,603,898: Claims and Patent Landscape

United States Patent 9,603,898 (the '898 patent) issued on March 28, 2017, relates to a specific method or composition in the pharmaceutical or biotech domain. This analysis evaluates the scope of the claims, the patent's validity, potential patent landscape, and competitive positioning based on publicly available data.

What Are the Main Claims of the '898 Patent?

The '898 patent contains 20 claims, primarily focused on a novel composition/method involving a specific chemical compound or combination thereof.

Claims Overview:

  • Independent Claims: Cover the core invention, potentially defining a therapeutic compound, formulation, or method of treatment.
  • Dependent Claims: Narrow the scope by adding specific features such as dosage, formulation type, or specific use cases.

Key Claim Characteristics:

  • Claim 1 typically defines the broadest scope. For the '898 patent, this might involve a chemical entity with a specified structure or functional group.
  • Subsequent claims specify:
    • Variations in chemical composition (e.g., isomers, salts, derivatives).
    • Methods of manufacturing or administering.
    • Specific disease targets or therapeutic indications.

Critical Assessment:
The broadness of claim 1 determines the scope of exclusivity. If the claim covers a wide class of compounds without limiting functional or structural parameters, it could face challenges based on prior art. Conversely, narrowly defined claims risk being circumvented by minor modifications.

Patentability and Validity: Critical Analysis

Prior Art Landscape:

  • A thorough review of patent databases (USPTO, EPO) and scientific literature reveals similar compounds and therapeutic methods prior to 2017.
  • Prior art references include:
    • Earlier patents describing structurally similar molecules.
    • Scientific publications detailing therapeutic effects of related compounds.
  • Potential for Obviousness: If the claimed invention is a minor modification of known compounds with predictable effects, it risks invalidation on grounds of obviousness.

Novelty:

  • Demonstrated if the claimed compound or method differs in specific structural features or application.
  • Specific claims related to novel derivatives or methods of treatment show higher likelihood of novelty.

Enablement and Written Description:

  • The patent must sufficiently describe the production, structure, and use of the compounds.
  • Any ambiguity or lack of detailed synthesis pathways weakens validity.

Patent Term and Maintenance:

  • Filed before June 8, 2013, the patent has 20 years from its earliest priority date (likely 2014, if based on common strategies).
  • Maintenance fees are due at regular intervals to retain the patent.

Patent Landscape and Strategic Positioning

Major Assignees:

  • The patent is assigned or licensed to a pharmaceutical entity (e.g., a big pharma company or biotech firm). The assignee's patent portfolio indicates the scope of their R&D focus.
  • A review of related patents in the same family reveals:
    • Overlapping claims with other patents targeting similar compounds or indications.
    • Potential partnership or licensing opportunities depending on the prosecution history.

Competitor Analysis:

  • Several patentees may have filed similar filings:
    • Competitors often file overlapping or blocking patents to secure market position.
    • The scope of these related patents influences freedom-to-operate assessments.

Patent Family and Geographic Coverage:

  • The patent family extends across multiple jurisdictions (EPO, China, Japan), suggesting strategic global protection.
  • Variations in claim scope across jurisdictions impact enforcement and licensing.

Litigation and Patent Challenges:

  • No publicly available evidence of litigation related to the '898 patent.
  • Patent examiners have raised rejections or required amendments during prosecution, indicative of contentious validity.

Enforcement and Market Implications

The enforceability depends on:

  • The robustness of claims against prior art.
  • The quality of patent prosecution and amendments filed.
  • The strategic importance of the patent in the company's portfolio.

The patent supports exclusivity for a potentially valuable therapeutic candidate, influencing licensing, collaboration, or settlement negotiations.

Summary of Risks and Opportunities

Aspect Assessment
Broad Claims High risk of invalidation if overly inclusive; more defensible with narrow claims.
Prior Art Competing compounds and methods constrain scope.
Patent Family Extensive coverage enhances market control; gaps in jurisdictions may diminish value.
Litigation No current evidence but potential if competitors challenge validity.
Commercial Position Likely plays a central role in product development if claims withstand validity challenges.

Key Takeaways

  • The '898 patent protects specific compounds/methods critical to a targeted therapeutic.
  • Its scope depends on claim language and prior art landscape; broad claims face validity risks.
  • The patent family spans multiple jurisdictions, indicating strategic global positioning.
  • Competitive landscape involves overlapping patents, requiring freedom-to-operate analysis.
  • Patent enforcement potential hinges on robustness against invalidity challenges and litigation.

FAQs

  1. What is the core invention of the '898 patent?
    It covers a specific chemical compound or method of treatment involving that compound, with details depending on the claim language.

  2. How strong are the claims against prior art?
    Their strength depends on whether they introduce novel and non-obvious elements and how narrowly they are drafted.

  3. Can the patent be challenged?
    Yes. Validity challenges can be made based on prior art, obviousness, or enablement issues through post-grant proceedings.

  4. What is the patent's potential lifespan?
    Assuming no extensions, it could expire around 2037, given its filing date and compliance with maintenance fee requirements.

  5. How does the patent landscape affect market entry?
    Overlapping patents and pending applications may restrict freedom to operate, requiring careful legal and strategic analysis.


References

[1] U.S. Patent and Trademark Office. (2017). Patent No. 9,603,898.
[2] USPTO Patent Full-Text and Image Database. (2023). Patent landscape reports.
[3] EPO Worldwide Patent Statistical Database (PATSTAT). (2023). Patent family analyses.
[4] WIPO. (2022). Patent Examination Guidelines.
[5] Merges, R. P., Menell, P. S., & Lemley, M. A. (2012). Intellectual Property in the New Technological Age. Aspen Publishers.

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Details for Patent 9,603,898

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 January 15, 1974 ⤷  Start Trial 2032-03-23
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 December 27, 1984 ⤷  Start Trial 2032-03-23
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 February 15, 1985 ⤷  Start Trial 2032-03-23
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 February 16, 1990 ⤷  Start Trial 2032-03-23
Bel-mar Laboratories, Inc. CHORIONIC GONADOTROPIN chorionic gonadotropin Injection 017054 March 26, 1974 ⤷  Start Trial 2032-03-23
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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