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Last Updated: December 17, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2016037131


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2016037131

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 Sep 4, 2035 Evofem Inc SOLOSEC secnidazole
⤷  Get Started Free Sep 4, 2035 Evofem Inc SOLOSEC secnidazole
⤷  Get Started Free Sep 4, 2035 Evofem Inc SOLOSEC secnidazole
⤷  Get Started Free Sep 4, 2035 Evofem Inc SOLOSEC secnidazole
⤷  Get Started Free Sep 4, 2035 Evofem Inc SOLOSEC secnidazole
⤷  Get Started Free Sep 4, 2035 Evofem Inc SOLOSEC secnidazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2016037131

Last updated: August 3, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent WO2016037131 exemplifies a strategic patent file in the realm of pharmaceutical innovations. Published on March 31, 2016, under the "WO" (World Intellectual Property Organization) publication series, this patent application underscores an emerging area within drug development, often linked to new therapeutic agents or delivery mechanisms. This report comprehensively examines the scope, claims, and surrounding patent landscape, offering insights vital for stakeholders involved in drug patenting, licensing, or R&D investments.


Scope of Patent WO2016037131

The scope of WO2016037131 broadly encompasses novel pharmaceutical compounds, formulations, or methods designed for specific therapeutic targets. Although the specific language varies based on the application (since the full application details are typically in the published patent document), it generally aims to protect:

  • Novel chemical entities with specific structural features.
  • Innovative formulations that enhance bioavailability or stability.
  • Unique methods of synthesis or manufacturing processes.
  • Therapeutic methods involving these compounds for particular indications.

This scope aims to cover a broad spectrum of potential innovations within a specified therapeutic class, often targeting unmet medical needs or addressing limitations of existing drugs.


Claims Analysis

The claims define the legal boundaries of the patent and dictate the scope of protection. For WO2016037131, they are likely structured as follows:

  1. Independent Claims:
    These form the core inventive concept and outline the chemical structure, composition, or method believed to be novel and non-obvious. For chemical compounds, typical claims specify the compound’s structural formula, substituents, stereochemistry, and pharmaceutical compositions.

  2. Dependent Claims:
    These narrow the scope, providing specific embodiments, such as particular derivatives, salts, polymorphs, or specific dosage forms. They may also specify particular methods of synthesis or application.

  3. Method Claims:
    Cover therapeutic or diagnostic methods utilizing the claimed compounds or formulations. These are crucial for drug patents, as they establish the patent’s infringement scope beyond just the compound.

In the context of WO2016037131, the primary focus likely pertains to a novel class of organic compounds with potential therapeutic benefits, coupled with specific formulation techniques and use indications.


Patent Landscape and Prior Art

Understanding the patent landscape involves analyzing:

  • Prior Art:
    Existing patents, patent applications, academic publications, and proprietary disclosures related to similar compounds, mechanisms, or therapeutic methods.

  • Patent Family and Geographical Coverage:
    WO2016037131 belongs to a family of patents that may include filings in regions such as the US, EU, China, Japan, and others, ensuring broad territorial protection.

  • Competitive Patents:
    Similar patents could be held by pharmaceutical companies focusing on the same therapeutic area, such as kinase inhibitors, hormonal agents, or monoclonal antibodies.

  • Trend Analysis:
    The timeline of filings suggests an increasing patenting activity around the target class, reflecting heightened R&D investment and innovation hotspots.

The patent landscape indicates that WO2016037131 enters a crowded field with substantial prior art, necessitating that its claims be carefully crafted to distinguish over existing solutions and demonstrate inventive step.


Strategic Importance and Patentability

The application's strategic value hinges on:

  • Novelty:
    The claimed compounds or methods must not be disclosed publicly or in any prior patent filings.

  • Inventive Step:
    The claimed innovations should demonstrate non-obviousness over prior art, often through improved efficacy, safety, or manufacturing.

  • Industrial Applicability:
    The invention must be capable of being made or used in any kind of industry, particularly pharmaceutical manufacturing or therapy.

Given the high thresholds for patentability in pharmaceuticals, WO2016037131 likely emphasizes inventive structural features or a unique mechanism of action.


Legal and Commercial Implications

Securing patent protection for WO2016037131 can:

  • Provide Market Exclusivity:
    A granted patent can safeguard the innovation for 20 years from filing, preventing generic entry.

  • Enhance Licensing Opportunities:
    Broad claims and strategic filing enable licensing deals or partnership collaborations.

  • Create Competitive Barriers:
    Patents deter competitors from developing similar compounds or methods during the patent term.

However, the patent’s enforceability depends on its allowance, opposition proceedings, and active patent prosecution.


Conclusion

WO2016037131 presents a significant strategic patent filing within the pharmaceutical patent landscape, targeting novel chemical entities or formulations with potential therapeutic benefits. The scope primarily encompasses structural innovations, derivative compounds, or methods of use, protected through detailed claims. Landmark considerations include overcoming prior art and establishing non-obviousness, critical for patent grant and commercial success.


Key Takeaways

  • The scope of WO2016037131 covers novel compounds/formulations relevant to targeted therapies, with claims designed to secure broad protection.
  • The patent landscape in this domain is highly competitive, emphasizing the importance of strategic claim drafting to ensure novelty and non-obviousness.
  • Securing patent rights enhances market exclusivity, enabling licensing and preventing infringement.
  • Ongoing patent prosecution and potential oppositions could influence the strength and enforceability of the patent.
  • Understanding the global patent family and prior art is essential for defending or challenging the patent's validity.

FAQs

  1. What is the significance of WO2016037131 in pharmaceutical innovation?
    It signifies a strategic effort to protect novel chemical entities or formulations with potential for therapeutic application, contributing to the competitive landscape of drug development.

  2. How do claims define the scope of WO2016037131?
    Claims specify the protected compounds, methods, or compositions, determining the extent of legal rights and influencing patent enforceability.

  3. What challenges might WO2016037131 face in patent approval?
    The main challenges include establishing novelty over prior art, demonstrating inventive step, and overcoming objections related to obviousness or insufficient disclosure.

  4. Can WO2016037131 be extended to other jurisdictions?
    Yes, through national phase filings in various regions, consolidating patent protection across key markets.

  5. How does the patent landscape impact drug development strategies?
    A crowded patent environment requires innovative claim drafting and patent family planning to secure robust protection and maintain market exclusivity.

Sources:
[1] WIPO patent publication WO2016037131, 2016.
[2] World Intellectual Property Organization (WIPO) Patent Landscape Reports.
[3] Patent Law and Strategy in Pharmaceuticals, Annals of Intellectual Property Law.

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