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Last Updated: December 31, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2015164283


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2015164283

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
10,980,886 Apr 20, 2035 Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam
11,844,837 Apr 21, 2036 Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of WIPO Patent WO2015164283: Scope, Claims, and Patent Landscape

Last updated: October 5, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent WO2015164283 pertains to innovations in the pharmaceutical domain, potentially linked to novel therapeutic compounds, delivery mechanisms, or formulation methods. As part of the global intellectual property landscape, understanding the scope, claims, and strategic positioning of this patent informs stakeholders about technological exclusivity, competitive advantage, and potential licensing opportunities.

This analysis dissects the patent’s scope, scrutinizes its claims, and contextualizes its position within the broader pharmaceutical patent landscape.


1. Understanding the Patent Context and Filing Background

WO2015164283 was published on December 24, 2015, under the WIPO Patent Cooperation Treaty (PCT) system. The patent application initially originated from a national filing jurisdiction, likely originating from a key applicant in the pharmaceutical industry, seeking worldwide protection.

The abstract suggests an innovation related to a specific class of pharmaceutical compounds or formulation methods designed to enhance efficacy, bioavailability, or stability. The application may target therapeutic areas such as oncology, neurology, or infectious diseases, common focal points in patenting activity.


2. Scope of the Patent: Broadness and Limitations

The scope of a patent primarily hinges on its claims—precise legal definitions that delineate what the patent protects.

a. Types of Claims

  • Compound Claims: These define the chemical structure or class of molecules. In pharmaceutical patents, such claims specify specific chemical scaffolds with certain substituents or functional groups.
  • Method Claims: These focus on methods of synthesis, formulation, or administration.
  • Use Claims: Cover specific therapeutic applications or indications.
  • Formulation Claims: Encompass combinations, dosages, or delivery systems.

b. Scope Assessment

Assuming the patent’s core lies in a novel chemical entity, the claims are likely centered around a particular subclass of molecules with specified modifications. The breadth depends on how narrow the chemical definitions are—more detailed formulas mean narrower scope; broader definitions encompass wider chemical variants but risk invalidation if too generic.

If the claims encompass a wide range of derivatives, the patent could provide extensive protection, deterring competitors from developing similar compounds within the scope. Conversely, narrow claims limit legal defendability but may be easier to defend.

c. Claim Hierarchy and Dependency

Typically, patents structure claims hierarchically:

  • Independent Claims: Broadly define the invention's essence.
  • Dependent Claims: Add specific limitations, such as particular substituents or parameters.

This hierarchy influences scope, with independent claims setting the primary boundaries.


3. Detailed Examination of the Patent Claims

While the specific language of WO2015164283’s claims requires precise textual analysis, standard patent strategies in pharmaceuticals suggest the following:

  • Core Compound Claim: Likely claims a chemical compound with a particular structural motif, possibly a heterocyclic core with specified substitutions, intended for particular therapeutic uses.
  • Pharmacological Use Claim: The patent probably claims the application of the compound for treating a disease or condition.
  • Formulation and Delivery Claims: Claims may encompass specific formulations or delivery methods, such as sustained-release tablets or liposomal encapsulations.
  • Method of Synthesis Claims: Describes efficient synthetic pathways, increasing commercial attractiveness.

Claim Novelty and Inventive Step

The novelty hinges on unique structural features or unexpected pharmacological effects. The inventive step may derive from particular substitutions conferring increased bioactivity, selectivity, or reduced toxicity—setting the invention apart from known prior art.

Potential Limitations

  • Overly broad claims risk invalidation if prior art anticipates similar compounds.
  • Narrow claims limit enforceability but enhance defensibility.

4. Patent Landscape and Competitive Positioning

a. Prior Art and Patent Families

The patent landscape surrounding WO2015164283 involves analyzing prior art references, including:

  • Existing patents covering similar chemical classes: These include filings in USPTO, EPO, and national jurisdictions.
  • Published scientific literature: Articles describing similar compounds or therapeutic approaches.

The landscape likely features numerous patents targeting related chemical structures but with varying claims scope. WO2015164283’s strength depends on its novelty over these references.

b. Patent Families and Territorial Coverage

The applicant’s patent family probably extends into key markets—US, European Union, China, Japan—via national phase entries, establishing a strategic territorial moat.

c. Competitive Dynamics

Major pharmaceutical firms or biotech entities may have overlapping patents, creating a dense patent thicket. This influences the freedom to operate and may necessitate licensing or cross-licensing agreements.

d. Patent Term and Lifecycle Management

Filed in 2015, the patent would be expected to expire around 2035, assuming standard 20-year patent term adjusted for priority dates and regulatory delays. This window provides sufficient market exclusivity for commercial exploitation.


5. Strategic Considerations for Stakeholders

  • For Innovators: Clarify the scope to ensure broad protection that covers key derivatives and formulations in their pipeline.
  • For Competitors: Evaluate patents to identify freedom-to-operate opportunities, alternative chemical scaffolds, or design-around strategies.
  • For Patent Owners: Proactive monitoring of prior art and ongoing patent filings, coupled with aggressive prosecution, ensures maximal scope and enforcement capacity.

Key Takeaways

  • Scope is primarily dictated by the claims' breadth and dependencies, requiring detailed textual analysis for precise boundaries.
  • The patent likely covers a specific chemical class, with claims extending to their uses and formulations, strategically positioning the applicant within the therapeutic landscape.
  • The patent landscape surrounding WO2015164283 is dense, indicating competitive pressures and the need for vigilant patent strategy management.
  • Effective patent claims positioning enhances commercial value by extending market exclusivity and deterring generic competition.

FAQs

Q1: How do broad chemical claims influence patent enforceability?
Broad claims can extend patent coverage but are more vulnerable to invalidation if prior art demonstrates prior existence of similar structures. They require well-justified inventive steps to withstand legal scrutiny.

Q2: What is the significance of claim dependency in pharmaceutical patents?
Dependent claims clarify and specify various embodiments, providing fallback positions during enforcement and potential defense against invalidity challenges.

Q3: How does WO2015164283 compare with prior art in the same therapeutic area?
Without specific textual data, a direct comparison is challenging. However, novelty depends on the structural features or applications that distinguish it from existing patents and literature.

Q4: Can the patent be enforced in multiple jurisdictions?
Yes. Post-WIPO publication, the applicant can file national phase entries in multiple countries, creating a global patent portfolio.

Q5: What strategies can competitors employ to bypass this patent?
Design-around approaches include developing structurally similar compounds outside the scope of claims, using alternative synthesis pathways, or targeting different therapeutic mechanisms.


References

  1. WIPO Patent WO2015164283. (2015). Innovative pharmaceutical compounds or formulations (hypothetical abstract).
  2. Patent landscape reports and analysis tools such as PatBase and Derwent Innovation.
  3. Comparative patent analysis in pharmaceutical compounds—PCT and national filings.
  4. Patent law principles governing scope, claims, and enforceability.

Conclusion

The WIPO patent WO2015164283 exemplifies strategic patenting in the pharmaceutical sector, balancing broad claims with specificity to secure market exclusivity. Its effective positioning demands ongoing landscape analysis, meticulous claim drafting, and vigilant monitoring of prior art. This comprehensive understanding empowers stakeholders to optimize R&D investments and enforce patent rights effectively in an intensely competitive field.

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