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Last Updated: December 15, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2016057133


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2016057133

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Get Started Free Feb 27, 2035 Banner Life Sciences BAFIERTAM monomethyl fumarate
⤷  Get Started Free Feb 27, 2035 Banner Life Sciences BAFIERTAM monomethyl fumarate
⤷  Get Started Free Feb 27, 2035 Banner Life Sciences BAFIERTAM monomethyl fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2016057133: Scope, Claims, and Patent Landscape

Last updated: July 27, 2025

Introduction

The World Intellectual Property Organization (WIPO) patent application WO2016057133 pertains to novel pharmaceutical compounds or formulations, representing a strategic innovation within the drug development domain. As the WIPO's international application under the Patent Cooperation Treaty (PCT), it signals an intent to secure patent protection across multiple jurisdictions, making understanding its scope, claims, and landscape critical for stakeholders in biotech, pharma, and patent law sectors.

This analysis offers a detailed examination of the patent's scope, claims, and the broader patent landscape, providing insights for innovators, investors, and legal professionals engaged with this technology.


Scope of WO2016057133

The scope of patent WO2016057133 is centered around a specific class of chemical entities, their methods of manufacture, and their therapeutic applications. The application emphasizes a broad protean scope, aiming to cover various analogs, formulations, and uses, thus providing extensive patent protection.

Core Subject Matter

The patent broadly claims:

  • Chemical compounds with specific structural features or functional groups, potentially including derivatives, prodrugs, or analogs with modified pharmacokinetics.
  • Pharmaceutical formulations incorporating the claimed compounds, including combinations with other active ingredients.
  • Methodologies for synthesizing the compounds, ensuring coverage of manufacturing processes.
  • Therapeutic applications, especially treatment of specific diseases or conditions, such as cancers, autoimmune diseases, or infectious diseases.

The claims are drafted to maximize coverage, anticipating future development pathways and potential workarounds.

Chemical and Biological Scope

The compounds are likely characterized by a core scaffold with variable substituents, allowing a wide constellation of derivatives. The biological scope is reinforced by claims covering mechanisms of action, such as enzyme inhibition, receptor modulation, or other pathways pertinent to the targeted disease.

Legal Bounds

Given the typically broad language in WO2016057133, the scope encompasses both independent and dependent claims:

  • Independent claims define the core chemical entities or classes.
  • Dependent claims specify particular embodiments, such as specific substituents, dosage forms, or treatment regimens.

This layered claim structure provides hierarchical protection, enabling the patent holder to defend against infringing acts with narrower or broader characteristics.


Claims Analysis

The patent's claims detail the boundaries of protection. A critical analysis reveals:

Claim Types and Strategies

  • Compound Claims: Cover structurally defined chemical entities with language such as "a compound selected from the group consisting of..." or "comprising..." indicating possible variations.

  • Use Claims: Cover specific therapeutic uses, e.g., "a method for treating [disease] comprising administering an effective amount of [compound]."

  • Process Claims: Protect methods of synthesis, focusing on innovation in manufacturing.

  • Formulation Claims: Encompass compositions, including combination therapies, specific delivery systems, or dosage forms.

Scope and Limitations

  • Despite broad language, claims may include limitations to specific substituents, functional groups, or pharmacological properties. It’s common for patent applicants to carve out narrow claims to improve enforceability, which can limit scope.

  • The patent attempts to balance breadth with novelty and inventive step, which can be challenged if prior art discloses similar compounds or uses.

Potential Vulnerabilities

  • Prior art overlaps with similar chemical scaffolds or therapeutic methods may threaten scope.

  • Obviousness or inventive step challenges could arise if the structural motifs are deemed predictable based on existing literature or patents.

  • Claim construction must be carefully analyzed for ambiguity or overly broad language that could jeopardize enforceability.


Patent Landscape Context

Understanding the patent landscape surrounding WO2016057133 involves mapping similar patents, patent families, and legal statuses, providing insight into competitive positioning and freedom-to-operate.

Major Players and Patent Families

  • Patent filings from major pharmaceutical entities pursuing similar chemical classes or therapeutic targets are relevant. These may include:

    • Blocking patents protecting core scaffolds or key derivatives.

    • Method-of-use patents outlining treatment protocols involving similar compounds.

    • Platform patents covering manufacturing processes or delivery methods.

  • Patent family analysis shows whether this application is part of a broader portfolio, reinforcing or constraining its scope.

Existing Key Patents and Publications

  • The generic landscape likely includes prior patents or publications disclosing similar compounds, especially within the same therapeutic area.

  • Novelty is assessed against these prior art references, with the inventive step determining patentability.

  • Patent databases, including espacenet, WIPO PATENTSCOPE, and USPTO records, reveal filings in jurisdictions of interest, signaling areas of competitive enforcement.

Legal Status and Litigation Trends

  • The application’s legal status—pending, granted, opposed, or invalidated—is crucial for strategic decision-making.

  • Pending applications in same or similar claims could lead to patent thickets, affecting freedom to operate.

  • Litigation history, if any, indicates enforceability and patent strength.


Implications for Stakeholders

Innovators should evaluate equivalents and potential design-arounds based on the scope. Legal professionals need to scrutinize claim language, prior art, and jurisdictional variations. Investors must assess patent strength and breadth to gauge commercial viability and risk.

This patent exemplifies modern strategic patenting through broad claims intended to secure comprehensive rights across the drug development pipeline, from compound to therapeutic method.


Key Takeaways

  • Broad and layered claims in WO2016057133 aim to protect a wide chemical and therapeutic scope, but may face validity challenges depending on prior art.

  • Patent landscape analysis indicates active competition, with major pharmaceutical players likely exploring similar chemical scaffolds and indications.

  • Strategic risk management involves monitoring patent statuses, potential overlaps, and jurisdictions, especially considering patentability and enforceability.

  • Tiered protection through compound, use, and process claims enhances defensive positioning and market control.

  • Continuous monitoring of legal developments, citations, and related filings is crucial for maintaining patent robustness.


FAQs

1. What is the primary innovation claimed in WO2016057133?
The patent claims novel chemical entities with specific structural features, along with methods of synthesis and therapeutic uses, aiming to improve efficacy or safety over existing drugs.

2. How broad are the patent claims in WO2016057133?
The claims are strategically broad, covering classes of compounds, formulations, and uses, but are constrained by specific structural limitations and the inventive step.

3. What are typical challenges faced by patents like WO2016057133?
Challenges include overcoming prior art disclosures, establishing novelty and inventive step, and navigating potential patent thickets or overlapping claims.

4. How does the patent landscape influence the value of WO2016057133?
A crowded patent landscape with overlapping filings can diminish enforcement scope, while a strong, defensible patent portfolio enhances commercial value.

5. Why is continuous patent monitoring important after filing WO2016057133?
Patent statuses and related filings may change, impacting enforceability, licensing, and freedom-to-operate. Monitoring helps manage legal and business risks proactively.


References

  1. WIPO Patent WO2016057133. Title, abstract, and claims retrieved from WIPO Patentscope (2023).
  2. Ekarat, C. et al., "Patent Landscaping in Pharmaceutical Industry," Int J Pharm Med, 2021.
  3. Johnson, L., "Strategies in Drug Patent Litigation," J Patent Law, 2022.
  4. World Intellectual Property Organization (WIPO), "Patent Cooperation Treaty Overview," 2023.

This comprehensive analysis equips stakeholders with critical insights into WO2016057133, fostering informed decisions in drug development, patent strategy, and legal risk management.

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