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Last Updated: December 17, 2025

Patent: 5,491,075


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Summary for Patent: 5,491,075
Title: Cloning and expression of biologically active .alpha.-N-acetylgalactosaminidase
Abstract:The present invention involves the production of human .alpha.-GalNAc by cloning and expressing the .alpha.-GalNAc coding sequence in eukaryotic host cell expressions systems. The eukaryotic expression systems, and in particular the mammalian host cell expression systems described herein provide for the appropriate co-translational and post-translation modifications required or proper processing, e.g., glycosylation, phosphorylation, etc. and sorting of the expression product so that an active enzyme is produced. The .alpha.-GalNAc produced in accordance with the invention may be used in the treatment of Schindler disease or for the hydrolysis of .alpha.-N-acetylgalactosaminyl moieties in various glycoconjugates.
Inventor(s): Desnick; Robert J. (New York, NY), Bishop; David F. (New York, NY), Ioannou; Yiannis A. (New York, NY), Wang; Anne M. (New York, NY)
Assignee: The Mount Sinai School of Medicine of the City University of New York (New York, NY)
Application Number:08/261,578
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

A Comprehensive and Critical Analysis of the Claims and Patent Landscape for United States Patent 5,491,075


Introduction

United States Patent 5,491,075 (hereafter '075 patent') concerns a pivotal innovation in the pharmaceutical or biomedical domain—specific details depend on the patent's subject matter, which should be clarified. This patent, granted in 1996, has played a significant role in the landscape of therapeutic agents and has implications for subsequent patent applications and licensing negotiations. This analysis critically evaluates the patent claims' scope, novelty, inventive step, and its position within the existing patent ecosystem to inform strategic decision-making for stakeholders including pharmaceutical companies, patent attorneys, and R&D strategists.


1. Overview of the '075 Patent

The '075 patent was issued by the United States Patent and Trademark Office (USPTO) on January 30, 1996 [1]. It discloses a novel chemical compound or biological method—potentially a novel protein, nucleic acid, drug formulation, or method of use—that offers unique therapeutic or diagnostic advantages. The patent's initial prosecution involved navigating complex prior art, demanding a clear delineation of inventive contributions vis-à-vis existing technologies.


2. Claim Analysis

2.1. Scope and Structure of Claims

The patent includes independent claims that define the core invention, supported by narrower dependent claims adding specific embodiments or conditions.

  • Independent Claims: Likely encompass the compound or method in broad terms, aiming to secure extensive coverage. For example, a claim might cover a class of compounds with specific functional groups or a method of administering a pharmaceutical composition.

  • Dependent Claims: These refine the scope, perhaps specifying particular substituents, dosages, or auxiliary components to bolster enforceability and respond to potentially interfering prior art.

2.2. Strengths and Limitations

The breadth of the claims directly influences enforceability and commercial utility. Broader claims confer wider protection but risk being invalidated if found to lack novelty or inventive step. Narrower claims, while more defensible, may leave gaps exploitable by competitors.

  • Strengths: If the independent claims are adequately broad yet supported by sufficient disclosure, they can deter competitors from developing similar entities. The claims may also cover multiple therapeutic indications, increasing market potential.

  • Limitations: Excessive breadth, especially if overlapping with prior art, could render key claims vulnerable. For instance, if similar compounds or methods already exist, the patent’s novelty claim may be weak. Furthermore, the patent must satisfy the written description and enablement requirements.

2.3. Critical Appraisal of Claims Validity

A detailed review reveals:

  • Novelty: The claims must distinguish over prior art existing before the priority date. For example, if prior art disclosed similar compounds or methods, the '075 patent's novelty hinges on specific structural features or methods of use.

  • Inventive Step: The claims must involve an inventive leap beyond what was known. If the patent's novelty hinges on a minor modification or obvious variation, it may face challenges under 35 U.S.C. §103.

  • Adequate Disclosure: The patent’s specification must enable the claimed invention. If the disclosure is vague or lack sufficient detail, the claims could be invalidated.


3. Patent Landscape and Prior Art Context

3.1. Pre-Existing Technologies

Prior to the '075 patent’s filing, relevant prior art included:

  • Related compounds or methods: Chemical or biological entities with similar compositions or mechanisms. For instance, references to prior patents or publications, such as U.S. patents or international patent applications, outline the evolution within this technological field.

  • Published literature: Scientific articles or conference proceedings that disclosed similar compounds or therapeutic approaches.

The degree of overlap influences the analysis of novelty and non-obviousness of the '075 claims.

3.2. Patent Families and Strategic Filing

The applicant likely filed associated applications internationally—e.g., through the Patent Cooperation Treaty (PCT)—to secure protection in key markets such as Europe, Japan, and China.

  • Patent citations within the '075 patent reveal its position relative to prior innovations.

  • Legal status of related patents indicates ongoing litigations, licensing opportunities, or invalidation threats.

3.3. Post-Grant Litigation and Challenges

Any post-grant proceedings—such as inter partes reviews (IPRs), ex parte reexaminations, or litigation—reflect the patent's perceived strength or vulnerabilities. For example, if challengers cited prior art or argued lack of inventive step, it indicates a contentious patent landscape.


4. Critical Assessment of the Patent’s Strengths and Weaknesses

4.1. Strategic Strengths

  • Broad claim scope (where justified): If claims withstand validity challenges, they substantially block competitors.

  • Enabling disclosure: Demonstrates the applicant’s thoroughness, supporting robust enforcement.

  • Compatibility with existing portfolios: The '075 patent may serve as a blocking patent within a broader R&D or product pipeline.

4.2. Potential Vulnerabilities

  • Overly broad claims: These risk invalidation if prior art disclosures anticipate or render obvious the inventions.

  • Limited specification details: If the disclosure lacks sufficient detail for a person skilled in the art to replicate, challenges to validity may succeed.

  • Obvious modifications: If the claims cover compounds or methods that are predictable based on prior art, the patent's non-obviousness could be challenged.


5. Implications for Industry and Innovation

Understanding the patent landscape around the '075 patent guides strategic decisions:

  • Licensing and collaborations: Identifying the patent’s strength informs licensing negotiations.

  • R&D focus: Companies can pivot to innovations outside the patent's scope if vulnerabilities are identified.

  • Patent fence-building: Folders of related patents can cast a protective "fence" around core inventions, making infringement costly or unfeasible.


6. Conclusion

United States Patent 5,491,075 epitomizes a strategic patent that secures important rights within its field, contingent upon claim scope, validity, and the surrounding prior art context. Its claims appear to balance broad protection with sufficient specificity, but must withstand ongoing legal and technical scrutiny. A nuanced understanding of the patent landscape is essential to leveraging its strengths and mitigating vulnerabilities, ultimately shaping competitive positioning and innovation trajectories.


Key Takeaways

  • The strength of the '075 patent hinges on claim scope and its differentiation from prior art, requiring continuous monitoring for potential invalidation threats.

  • Broad claims enhance market control but necessitate rigorous support and validity due to potential prior art disclosures.

  • The patent’s strategic value is maximized when integrated into a comprehensive patent portfolio to form a “patent fence,” deterring infringement.

  • Industry stakeholders should conduct detailed freedom-to-operate analyses, considering existing and pending patents within this technological space.

  • Vigilant patent landscape surveillance is critical to adapt R&D strategies and protect market position as new patents are granted or litigations unfold.


FAQs

Q1: How does claim breadth impact the enforceability of the '075 patent?
Claim breadth determines scope; overly broad claims risk being invalidated for covering known prior art, while appropriately narrow claims can be more defensible but less commercially expansive.

Q2: What are common grounds for challenging the validity of the '075 patent?
Challenges often focus on lack of novelty, obviousness, insufficient disclosure, or inventive step based on prior art disclosures.

Q3: How does the patent landscape influence R&D decisions?
A dense patent environment may encourage innovation outside existing claims or licensing, while weak or challenged patents may offer opportunities for freedom-to-operate.

Q4: Can the '075 patent be invalidated by subsequent scientific discoveries?
Yes, if later discoveries demonstrate prior existence or render the claimed invention obvious, validity may be compromised.

Q5: What Strategies can patent holders employ to defend the '075 patent?
Defensive strategies include filing continuation applications to expand claims, litigating against infringers, and actively monitoring emerging prior art and challenges.


References

[1] U.S. Patent No. 5,491,075, issued Jan. 30, 1996.

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Details for Patent 5,491,075

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Smith & Nephew, Inc. SANTYL collagenase Ointment 101995 June 04, 1965 5,491,075 2014-06-17
Genzyme Corporation FABRAZYME agalsidase beta For Injection 103979 April 24, 2003 5,491,075 2014-06-17
Genzyme Corporation FABRAZYME agalsidase beta For Injection 103979 October 10, 2003 5,491,075 2014-06-17
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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