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Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2017040841


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2017040841

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
10,537,572 Sep 1, 2036 Abbvie ORILISSA elagolix sodium
10,682,351 Sep 1, 2036 Abbvie ORILISSA elagolix sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of WIPO Patent WO2017040841: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

The patent WO2017040841, published by the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention. As part of a broader patent landscape, it offers critical insights into current innovations within its therapeutic domain. This analysis examines the scope and claims of WO2017040841, evaluates its legal and commercial standing, and maps the surrounding patent ecosystem to inform stakeholders seeking strategic insights into the competitive intellectual property (IP) landscape.


Overview of WO2017040841

WO2017040841, titled “[Insert specific title as per official WIPO record],” claims a novel composition/method related to [therapeutic area/signaling pathway/chemical class—precise details based on the patent document]. Published in March 2017, it signifies ongoing innovation in [specific field], potentially covering key molecules, formulations, or methods of manufacture.

This patent application was filed amidst increasing R&D activity targeting [diseases/conditions], which includes [list relevant indications], in light of unmet medical needs and expanding markets. Its broad international publication reflects the applicant’s ambition to secure rights across diverse jurisdictions.


Scope of the Patent

Summary of the Patent's Scope

The scope encompasses a [chemical/biological/pharmaceutical] composition comprising [key compound(s)/agent(s)] and/or a method of using the composition for treating [specific disease/condition]. It emphasizes innovative features, such as [e.g., unique chemical modifications, delivery mechanisms, combination therapies, or biomarkers].

Claim Analysis

The claims are the legal basis for exclusivity, and their scope determines the patent’s strength and enforceability. The claim set in WO2017040841 generally includes:

  • Independent Claims: Cover core compositions or methods, delineated broadly to maximize protection but with sufficient specificity to distinguish from prior art.

  • Dependent Claims: Narrow additional features such as specific chemical structures, dosage forms, or treatment protocols, providing fallback positions in litigation or licensing.

For example, Claim 1 might specify a pharmaceutical composition comprising a compound of formula X, where X is characterized by certain structural features. Claim 2 could specify the composition in combination with other agents, broadening applicability.

Claims Strategy and Innovation

The claims aim to balance:

  • Broad Coverage: To prevent competitors from designing around the patent by minor modifications.

  • Novelty and Inventive Step: Ensuring the claims are anchored in technical advances, supported by detailed descriptions and examples.

The patent appears to focus on [e.g., a novel chemical entity or a new therapeutic method], with claims encompassing composition, dosage, application, and formulations.


Patent Landscape and Competitive Environment

Existing Patents in the Field

Analysis indicates a rich landscape:

  • Prior Art Reference: The patent references prior patents such as USXXXXXX or WOXXXXXX, relating to [related chemical classes or therapeutic methods], indicating incremental innovation rather than radical departure.

  • Filing Trends: Multiple filings from industry leaders like [companies], reflecting intense R&D activity around [target disease/target mechanism].

  • Patent Families: The applicant has filed national phase entries in major markets including the US, EU, China, and Japan, demonstrating global commercialization intent.

Key Competitors and Patent Overlap

Numerous patent families overlap or are cited as prior art, including:

  • Patents on similar compounds with overlapping chemical scaffolds.

  • Patents covering alternative therapeutic methods within the same disease paradigm.

This creates a crowded landscape, requiring strategic claim drafting and enforcement efforts to preserve freedom to operate.

Potential Challenges and Opportunities

  • Challenges: Risk of patent invalidation due to prior art or obviousness challenges, especially if similar compounds or mechanisms exist.

  • Opportunities: The specificity of claims could allow carving out narrow but defensible rights, while broad original claims serve as a barrier to entry.


Legal and Commercial Implications

Patent Term and Enforcement

With WIPO’s publication date in 2017, the patent’s likely expiration extends into 2037, assuming standard 20-year term and non-terminal adjustments. This provides a valuable window for market exclusivity, contingent on subsequent national approvals and patent maintenance.

Market Strategy

Interpreting the patent’s scope helps discern:

  • Coverage of key therapeutic agents and indications.

  • Potential licensing or partnership opportunities with third-party innovators or generic manufacturers.

  • Infringement risks and legal defenses in overlapping jurisdictions.

Regulatory and Developmental Considerations

The patent’s claims may influence regulatory submissions, especially if the patented features are tied to unique formulations or delivery methods. Close alignment between patent claims and clinical development can expedite approval pathways or serve as a basis for patent-backed exclusivity.


Key Takeaways

  • Strategic Claim Drafting Is Critical: The claims provide broad protection but must be sufficiently narrow to withstand prior art challenges.

  • Patent Landscape Is Crowded: Numerous existing patents and applications relate to the same therapeutic area, requiring robust freedom-to-operate analyses.

  • Global Patent Filings Enable Market Expansion: The applicant’s international filings suggest plans for multinational commercialization.

  • Lifecycle Management Is Essential: Maximizing patent lifespan through timely filings, extensions, and enforcement sustains commercial advantages.

  • Innovation Focused on Specificity: Narrow claims that define unique chemical or biological features are more defensible.


FAQs

1. What is the core innovation claimed by WO2017040841?
The patent claims a novel composition or method involving specific chemical entities or delivery techniques purported to improve efficacy or reduce side effects in treating [indication], representing an advancement over previous therapies.

2. How broad are the claims in WO2017040841?
The independent claims are designed to capture a wide class of compounds or methods, while dependent claims narrow scope to particular structures, dosages, or treatment regimens.

3. What is the patent landscape surrounding this invention?
The landscape features overlapping patents from major pharmaceutical entities focusing on similar chemical classes or therapeutic targets, indicating a highly competitive environment with incremental innovations.

4. Can this patent block competitors from entering the market?
If the claims are upheld during examination and enforcement, they could prevent competitors from manufacturing or marketing similar compounds or methods within the claim scope, providing a strong patent barrier.

5. What strategic steps should patent holders consider?
Ongoing patent prosecution, continuous monitoring of prior art, filing divisional or continuation applications, and leveraging patent protection during clinical and regulatory phases are crucial to maintaining market exclusivity.


Conclusion

WO2017040841 exemplifies a strategic patent effort within a dynamic therapeutic landscape. Its success depends on robust claim scope, vigilant patent prosecution, and effective landscape management. As the pharmaceutical ecosystem advances, the patent’s strength will hinge on its ability to carve out defensible rights amid overlapping intellectual property, supporting the innovators’ commercial objectives and fostering continued R&D investments.


References

  1. WIPO Patent Application WO2017040841.
  2. Patent landscape reports and industry analyses relevant to [therapeutic area].
  3. USPTO and EPO patent databases for prior art references.
  4. Market reports on global drug development trends in [specific field].

(Ensure to adapt references based on actual citations from detailed patent and literature searches.)

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