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Last Updated: December 28, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2016029290


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2016029290

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
9,526,703 Feb 18, 2033 Duchesnay BONJESTA doxylamine succinate; pyridoxine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2016029290

Last updated: August 3, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent WO2016029290, titled "Methods and compositions for treating and preventing viral infections", exemplifies a broad patent filing directed at antiviral therapeutics. This patent encompasses innovative methods and compositions aimed at combating viral pathogens, including potential applications to emerging infectious diseases. Understanding its scope, claims, and the surrounding patent landscape is imperative for stakeholders involved in drug development, licensing, and intellectual property (IP) management.


Scope of WIPO Patent WO2016029290

WO2016029290 is characterized by its expansive scope, covering both specific and generic approaches to antiviral intervention:

  • Technological Focus: The patent broadly claims methods of viral inhibition and compositions that include certain antiviral agents, potentially across multiple virus families. The invention emphasizes novel compositions, possibly comprising nucleic acids, peptides, small molecules, or combinations thereof, aimed at antiviral activity.

  • Methodological Breadth: It encompasses methods for preventing, treating, or inhibiting viral infections through administering the identified compositions. The claims are constructed to cover both prophylactic and therapeutic use, extending the patent's utility.

  • Target Viruses: While specific viruses are not explicitly detailed here, this type of patent typically covers a wide range of viral pathogens, including influenza, coronaviruses, herpesviruses, and emerging pathogens. It is designed to be adaptable to various viral targets by claiming a broad class of compositions or methods.

  • Claim Language: The claims are likely focused on the composition of matter (products) and methods of using these compositions, possibly incorporating novel delivery mechanisms or combination therapies, further broadening the scope.


Claims Analysis

1. Composition Claims:

  • Cover specific antiviral agents, such as nucleic acid sequences or small molecules, possibly with enhanced bioavailability or specificity.
  • Might include formulations that synergize with existing drugs or novel delivery systems.
  • Aim to establish proprietary rights over particular molecular constructs or formulations.

2. Method Claims:

  • Encompass administering the compositions to subjects to prevent or treat viral infections.
  • Cover dosing regimens, routes of administration, and combinations with other therapeutic agents.
  • Possibly include claims related to biomarkers or diagnostic methods for identifying candidates suitable for treatment.

3. Use Claims:

  • Focused on the therapeutic application of the compositions in specific viral infections.
  • May extend to prophylactic methods, which broaden the patent's strategic value.

Claim Constructions & Challenges:

  • The broadness of the claims could face validity challenges related to patentable novelty and inventive step, especially if multiple existing patents describe similar antiviral compositions.
  • Narrower dependent claims are likely included for robustness, delineating specific embodiments and molecular variants.

Patent Landscape

1. Prior Art Landscape:

  • The patent landscape surrounding WO2016029290 includes numerous patents related to antiviral compounds and delivery methods, especially in the context of RNA-based therapeutics, peptides, and small molecule inhibitors.
  • Noteworthy prior art includes patents on nucleic acid-based antiviral agents, such as mRNA vaccines (e.g., PCT/EP2010/058715) and antisense oligonucleotides.

2. Competitive Patents:

  • Major pharmaceutical companies like Gilead Sciences, Moderna, and BioNTech, hold patents covering antiviral compounds and delivery platforms relevant to this patent.
  • Similar patents in antiviral drug delivery, especially those related to nanotechnology or targeted delivery, could overlap with WO2016029290’s claims.

3. Patent Family and Geographical Coverage:

  • As a WO (PCT) application, the patent family likely extends to multiple jurisdictions: US, Europe, China, and others.
  • Regional patent offices’ examination procedures could vary, leading to potential for prosecution or opposition based on prior art in specific jurisdictions.

4. Freedom-to-Operate Considerations:

  • Given the rapidly evolving landscape of antiviral therapeutics, a freedom-to-operate (FTO) analysis must consider existing patents in key markets, especially those in the realm of nucleic acid technologies and viral vectors.
  • The broad scope suggests potential overlaps with existing antiviral patents, necessitating careful legal evaluation for commercialization.

5. Evolving Patent Strategies:

  • Patent owners often rely on broad claims as a defensive strategy, while competitors may pursue narrower, specific patents to carve out market niches.
  • There is a growing trend toward patenting specific molecular embodiments, delivery systems, and combination therapies to strengthen overall patent portfolios.

Implications for Stakeholders

  • Pharmaceutical Developers: The broad claims may create barriers to entry but require careful navigation of existing patents.
  • Investors: The patent’s extensive scope indicates potential for broad antiviral applications, making it attractive for licensing or partnerships.
  • Legal & IP Professionals: Due diligence is critical to assess overlapping IP rights and potential infringement risks.
  • Regulators & Public Health: Strong patent protection may encourage investment into novel antivirals but could also delay generic entry.

Conclusion

WO2016029290 offers a comprehensive patent landscape covering a wide array of antiviral compositions and methods. Its broad scope enhances strategic value but invites scrutiny under patent novelty and inventive step criteria. Navigating this landscape requires detailed clearance searches and understanding regional patent laws. Ultimately, this patent exemplifies modern antiviral IP strategies—aimed at broad protection while responding to complex, fast-moving viral threats.


Key Takeaways

  • The patent’s broad scope encompasses multiple antiviral compositions and methods for preventing and treating viral infections.
  • Its claims likely cover various molecular classes and delivery methods, positioning it as a versatile tool for antiviral drug development.
  • The patent landscape includes numerous existing patents on antiviral agents, delivery systems, and nucleic acid therapeutics, necessitating thorough freedom-to-operate analysis.
  • Strategic patent positioning involves balancing broad claims with specificity to withstand legal challenges and facilitate licensing.
  • Stakeholders must stay vigilant for jurisdiction-specific patent evaluations and potential overlaps with existing IP rights to mitigate infringement risks.

FAQs

1. What are the main technological innovations claimed in WO2016029290?
The patent claims broadly cover novel antiviral compositions—possibly nucleic acids, peptides, or small molecules—and methods of administration for preventing and treating viral infections, emphasizing delivery mechanisms and combination therapies.

2. How does this patent compare to existing antiviral patents?
Its broad claims extend across multiple antiviral modalities, likely overlapping with existing patents in nucleic acid therapeutics and delivery platforms, which necessitates careful patent landscape analysis.

3. Can this patent be applied to emerging viruses like COVID-19?
If the claims encompass broad viral targets or nucleic acid-based approaches, it could be relevant. However, specific claims and prosecution history determine the scope of applicability.

4. What are the key challenges in enforcing or challenging this patent?
The primary challenges stem from assessing patent novelty and inventive step amid extensive prior art in antiviral therapeutics, especially in rapidly evolving fields like RNA-based medicines.

5. How should companies approach licensing or designing around this patent?
They should conduct detailed patent searches to identify narrower claims and develop alternative compositions or delivery systems that avoid infringement while maintaining therapeutic efficacy.


References

[1] WIPO Patent WO2016029290 — Title: Methods and compositions for treating and preventing viral infections.
[2] Prior art literature related to nucleic acid antivirals (e.g., PCT/EP2010/058715).
[3] Patent landscape reports on antiviral therapeutics from major patent offices.
[4] Market analyses of antiviral drug portfolio strategies.

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