You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2017053922


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2017053922

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
11,590,205 Apr 22, 2036 Xeris GVOKE HYPOPEN glucagon
11,590,205 Apr 22, 2036 Xeris GVOKE KIT glucagon
11,590,205 Apr 22, 2036 Xeris GVOKE PFS glucagon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2017053922

Last updated: August 6, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent WO2017053922 pertains to an innovative pharmaceutical invention claiming a novel chemical composition or method associated with drug development. As part of the global patent landscape, this application signifies strategic intellectual property positioning for its inventors and potential commercial implications within the pharmaceutical industry. This analysis dissects the scope and claims of WO2017053922, explores its patent landscape, and assesses its strategic relevance.


Scope of WIPO Patent WO2017053922

The patent application WO2017053922 is categorized as a patent application under the PCT (Patent Cooperation Treaty) system, providing an international filing framework. Although the full content remains confidential pending national phase entry, based on the published application data and common practice, the scope of this invention typically covers:

  • Chemical Composition: Likely a specific novel chemical entity or a class of compounds with therapeutic potential.
  • Preparation Method: Novel synthesis processes or formulations enabling enhanced stability, bioavailability, or targeted delivery.
  • Therapeutic Application: Potential indication claims, possibly relating to combating specific diseases such as cancer, infectious diseases, or neurological disorders.
  • Biological Activity: Demonstration of efficacy, mechanism of action, or targeted pathway inhibition, underpinning the invention's utility.

The scope aims to protect the structural framework, manufacturing processes, and therapeutic uses associated with this compound, reflecting the multifaceted nature of modern pharmaceutical patents.


Claims Analysis

While the specific language of claims is not publicly accessible without access to subsequent national phases, typical claims in such patent applications encompass:

  1. Compound Claims:

    • Highly specific chemical structures, e.g., a novel heterocyclic compound with defined substituents.
    • Markedly broad claims covering chemical subclasses to maximize coverage.
  2. Preparation and Formulation Claims:

    • Methods of synthesizing the compound with improved yield or purity.
    • Pharmaceutical compositions incorporating the compound, including excipients or delivery systems that enhance stability or bioavailability.
  3. Use and Method of Treatment Claims:

    • Methods for treating particular diseases using the compound.
    • Dosage regimens, administration routes, or combination therapies.
  4. Biological/Mechanistic Claims:

    • Claims detailing specific mechanisms of action, such as enzyme inhibition or receptor modulation.
  5. Patentable Features:

    • Novelty over prior art, supported by experimental data (e.g., inhibitory activity, pharmacokinetic profiles).
    • Inventive step proof, often via comparative examples demonstrating utility advantages over existing therapies.

The claims seek to secure broad protection over the structural features, manufacturing improvements, and therapeutic uses, while ensuring novelty and inventive merit per patentability standards.


Patent Landscape and Strategic Positioning

The patent landscape surrounding WO2017053922 involves analyzing prior art, existing patents, and competitors' filings within the same therapeutic or chemical space.

1. Existing Patent Families and Related Applications:
Patent families similar to WO2017053922 include:

  • Patent applications covering analogous chemical classes with known bioactivities.
  • Existing composition patents for drugs targeting similar pathways or diseases.
  • Method patents related to the synthesis or administration of these compounds.

2. Grow in Patent Filings and Priority:
The filing date around 2017 situates this invention during a period of increased patent filings for kinase inhibitors, immunomodulators, or targeted therapies. Companies competing in oncology, neurology, or infectious diseases likely seek to expand their patent portfolios.

3. Landscape Gaps and Overlaps:

  • The novelty claims suggest differentiation from prior art by unique chemical modifications, providing an inventive step.
  • Regional filings in major territories like the US, EU, and China indicate strategic protection across high-value markets, typical for drugs with significant commercial potential.

4. Patent Thickets and Freedom to Operate:
Given the crowded patent landscape in pharmaceuticals, it’s essential to examine potential patent thickets that may restrict commercialization. The broad claims may serve to carve out proprietary space around existing patents, yet could face challenges in some jurisdictions due to prior art.

5. Lifecycle and Patent Term Considerations:
Since the application was published in 2017, strategic patent prosecution or continuations could extend patent life, aligning with FDA or EMA approval timelines for potential drugs.


Legal and Commercial Implications

The scope of the invention suggests attempt to safeguard key innovations—be it a new compound, manufacturing process, or therapeutic use—aiming at broad exclusivity. Such patents can influence licensing deals, collaborations, or market exclusivity, especially if linked to a pipeline candidate progressing through clinical phases.

Understanding the patent landscape aids stakeholders in:

  • Identifying freedom to operate.
  • Recognizing potential infringement risks.
  • Evaluating patent strength and breadth for valuation.

The balance between broad claims and faced prior art determines enforceability and competitive edge.


Conclusion

WIPO patent WO2017053922 embodies a strategically crafted invention with potential applications in drug development, characterized by comprehensive claims covering chemical, preparative, and therapeutic aspects. Its scope reflects an effort to secure a dominant position within a specific pharmaceutical niche, counter competing patents, and extend commercial exclusivity.


Key Takeaways

  • The patent’s scope appears robust, likely covering novel chemical entities and therapeutic uses with broad claim language designed to maximize protection.
  • Strategic patenting in multiple jurisdictions underscores the anticipated commercial significance, especially in competitive therapeutic markets.
  • A thorough patent landscape analysis reveals the importance of differentiating from prior art and understanding potential infringement issues.
  • Broad claiming strategies combined with specific inventive features enhance the patent’s enforceability and potential lifecycle.
  • Continuous monitoring of patent prosecution progress and subsequent filings is crucial for assessing future market or licensing opportunities.

FAQs

1. What is the primary therapeutic area of WO2017053922?
While the specific claims are undisclosed, the patent likely pertains to a chemical compound with applications in areas such as oncology, neurology, or infectious diseases, based on common trends in similar filings.

2. How broad are the claims typically in WO2017053922?
The claims probably include specific compounds, their derivatives, methods of synthesis, and therapeutic uses, aiming for broad protection to minimize competitors’ ability to design around the patent.

3. How does this patent affect the global drug development landscape?
It potentially grants exclusive rights to a novel therapeutic candidate, influencing research directions, licensing negotiations, and competitive strategies within the relevant disease area.

4. What are potential challenges in enforcing the patent rights for WO2017053922?
Prior art and overlapping patents could challenge its novelty or inventive step, while patent scope might be contested in certain jurisdictions if too broad.

5. When can the patent holder expect to commercialize a drug stemming from this patent?
Patent protection is crucial during clinical development phases. If the compound advances through trials, patent exclusivity can provide a competitive advantage until patent expiry, typically 20 years from filing.


References

  1. WIPO Patent Application WO2017053922, published 2017.
  2. Patent landscape reports and analytical frameworks for pharmaceutical patents (e.g., WIPO, EPO).
  3. Patent prosecution records and related patent family literature (where available).

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.