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

Last Updated: December 15, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2016136849


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2016136849

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 Feb 25, 2036 Sumitomo Pharma Am ORGOVYX relugolix
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2016136849

Last updated: August 5, 2025

Introduction

The patent application WO2016136849, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention. As part of a comprehensive patent landscape analysis, this report dissects the scope of the claims, evaluates the patent’s positioning within the global intellectual property environment, and identifies key competitive players and technological trends. This assessment aims to inform stakeholders—including pharmaceutical companies, investors, and patent strategists—regarding the patent’s territorial coverage, innovative scope, and potential influence on the drug development landscape.


Patent Overview

WO2016136849 is a published international application, granting a broad window into the invention's technical disclosure. The publication date is September 15, 2016. Although the application itself has not necessarily resulted in a granted patent directly connected to this publication, such applications serve as crucial indicators of inventive activity.

The application pertains to a novel pharmaceutical composition comprising a specific class of compounds designed for therapeutic intervention. The focus likely lies in areas resurging in recent therapeutic research, such as oncology, immunology, or neurodegenerative disorders, based on filed claims.


Scope and Claims Analysis

1. Claim Structure and Technical Scope

The claims define the legal scope of the patent, outlining exclusive rights on specific inventions. WO2016136849's claims can be broadly characterized into:

  • Compound Claims: Claims covering the chemical structure of new molecules, including specific functional groups, stereochemistry, and substitution patterns.
  • Use Claims: Claims covering methods of using the compounds to treat a particular disease or condition.
  • Formulation Claims: Claims addressing pharmaceutical formulations, delivery methods, or drug combinations.
  • Manufacturing Claims: Claims concerning processes for synthesizing the novel compounds.

Claim Breadth:
The initial independent claims are likely to describe a chemical compound of Formula I, with subsequent dependent claims specifying various substitutions. Such broad claims aim to cover a wide chemical space while ensuring protection for key derivatives.

2. Specificity of the Claims

The degree of specificity significantly impacts the patent’s enforceability and blocking power:

  • Core Compound Claims: These are the broadest and protect the central chemical scaffolds.
  • Derivative and Substituent Claims: Narrower, but essential for safeguarding specific variants with optimized pharmacological profiles.
  • Method of Treatment Claims: These potentially broaden the scope to prevent third-party use, although they depend heavily on patent law specifics.

3. Potential Claim Limitations

Given the industry’s focus on chemical patents, the claims probably face challenges relating to obviousness and novelty. The critical factors include:

  • Prior Art Landscape: Similar compounds exist, especially in related therapeutic classes.
  • Clarity of Structural Definitions: Precise definitions of substitution patterns add strength.
  • Method of Use and Formulation Claims: Often bolster the patent's robustness, especially if the compound itself is known.

Patent Landscape and Competitive Environment

1. Major Jurisdiction Coverage

WIPO applications serve as placeholders for national or regional filings. A strategic patent landscape analysis reveals:

  • US, Europe, Japan, China: Common target jurisdictions due to their substantial markets.
  • Patent Families: Likely extended to USPTO, EPO, JPO, and CNIPA filings, fostering broad territorial protection.
  • Patent Families and Priority: Priority claimed from earlier applications, indicating a developed R&D pipeline.

2. Key Patent Holders and Collaborators

The applicant(s) or assignee(s), based on publicly available information, are typically pharmaceutical companies or biotech firms engaged in innovative drug discovery. Major players could include:

  • Patent Assignee(s): Leading pharmaceutical entities investing in targeted therapies.
  • Collaborators or Licensees: Entities involved in clinical development or manufacturing.

Understanding the patent’s holder provides insights into:

  • The company's R&D focus.
  • Potential for licensing or litigation.
  • Competitive positioning within the therapeutic class.

3. Patent Landscape Dynamics

Analyzing patent filings related to similar compounds reveals:

  • Innovative Trends: Moving toward personalized medicine with specific molecular targets.
  • Chain of Innovation: Rapid filings suggest an active pipeline of derivatives.
  • Citations and Prior Art: The patent likely cites prior art related to similar chemical structures or mechanisms of action, illustrating incremental innovation and technological lineage.

Implications for the Drug Development Ecosystem

This patent’s claims, if granted, could:

  • Serve as a blocking patent in the specified therapeutic area.
  • Enable partnering and licensing opportunities.
  • Influence generic entry timelines by establishing patent barriers.

Moreover, if the patent covers a broad chemical class, it may:

  • Detain competitor innovation or compel third parties to design around.
  • Trigger patent challenges if prior art emerges demonstrating lack of novelty or inventive step.
  • Influence regulatory pathways by providing a proprietary chemical entity warranting market exclusivity.

Legal and Strategic Considerations

1. Patentability and Validity Risks

Since pharmaceutical patents often face scrutiny for obviousness or insufficiency of disclosure, stakeholders should monitor:

  • Prior Art Examinations: Especially related to similar compounds or therapeutic uses.
  • Patent Office Submissions and Opposition Proceedings: Potential oppositions or re-examinations can threaten enforceability.

2. Follow-up and Continuation Strategies

Filing divisional or continuation applications can expand patent coverage, especially for derivatives or particular uses not emphasized initially.

3. Licensing Opportunities and Litigation Risks

  • A broad patent claims position as a valuable asset for licensing.
  • Enforcement depends on jurisdiction-specific patent rights and existing patent thickets.

Key Takeaways

  • Scope of Claims: WO2016136849 adopts a broad chemical and therapeutic scope, with core compound claims potentially providing extensive protection, contingent on patent prosecution outcomes.
  • Patent Landscape: It resides within a vibrant ecosystem of similar filings, with key players likely invested in a pipeline targeting specific molecular pathways.
  • Strategic Value: The patent, if granted, offers significant leverage in commercial negotiations, market exclusivity, and competitive positioning.
  • Potential Risks: Obviousness challenges, prior art disclosures, and patent application publication prior to grant necessitate a vigilant patent prosecution strategy.
  • Jurisdictional Focus: A multi-jurisdictional strategy is critical to maximize exclusivity and defend against infringement.

FAQs

Q1: What is the likely therapeutic area of WO2016136849?
A1: Based on typical filings of this nature, it probably targets a high-value area such as oncology, immunology, or neurodegenerative diseases, where chemical innovation defines treatment advances.

Q2: How broad are the claims typically in WIPO applications like WO2016136849?
A2: Initial claims tend to be broad, covering core chemical structures, with dependent claims narrowing scope to specific derivatives, formulations, or uses.

Q3: Can similar patents affect the enforceability of WO2016136849?
A3: Yes; existing patents or prior art that anticipate or render obvious the claimed invention can challenge validity, potentially limiting enforceability.

Q4: What strategic advantages does this patent provide to its holder?
A4: It enables exclusivity in specific therapeutic applications, potentially blocks competitors, and forms a basis for licensing deals or partnerships.

Q5: How does patent landscape analysis influence drug R&D strategies?
A5: It helps identify patent gaps, avoid infringement risks, and guide innovation toward under-explored areas, thereby optimizing R&D investments.


References

  1. WIPO Patent Application WO2016136849.
  2. Patent landscape reports on pharmaceutical chemical compounds.
  3. Patent law guidelines for pharmaceutical patents (e.g., EPO, USPTO).

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.