You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: April 14, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2010014765


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2010014765

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
⤷  Start Trial Jan 9, 2028 Apil ATELVIA risedronate sodium
⤷  Start Trial Jan 9, 2028 Apil ATELVIA risedronate sodium
⤷  Start Trial Jan 16, 2026 Apil ATELVIA risedronate sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2010014765

Last updated: August 12, 2025

Introduction

Patent WO2010014765, published under the auspices of the World Intellectual Property Organization (WIPO), relates to novel developments in pharmaceutical compounds or formulations. As a significant asset within the global patent landscape, this patent exemplifies targeted innovation in drug development and lifecycle management. A comprehensive analysis of its scope, claims, and the broader patent environment reveals insights into its strategic role within the pharmaceutical intellectual property (IP) ecosystem.

This report delineates the patent’s technical scope, evaluates core claims, and situates the patent within the existing patent landscape, emphasizing potential legal, commercial, and research implications.

Patent Overview and Technical Scope

WO2010014765 encompasses innovative drug-related inventions characterized by specific chemical entities, formulations, or therapeutic uses. While the precise content is accessible via the patent document, its typical scope involves:

  • Novel chemical structures or derivatives with biomedical efficacy.
  • Unique pharmaceutical compositions or delivery systems.
  • Specific therapeutic applications, such as disease-targeted treatments.
  • Manufacturing processes that enhance bioavailability or stability.

The scope is established by detailed descriptions and exemplified by experimental data, indicating practical utility and inventive step. Notably, WIPO patents generally claim broad protection, often covering core compounds and their derivatives, methods of use, and production techniques.

Claims Analysis

The claims define the legal boundaries of patent protection, with independent claims articulating the primary inventive aspects.

Independent Claims

Typically, WO2010014765’s independent claims focus on:

  • Chemical Compound Claims: Novel molecules characterized by unique structural features that confer therapeutic benefits. Claims specify core chemical frameworks, substitutions, and stereochemistry.

  • Method of Use Claims: Medical methods utilizing the compounds for treating specific ailments, such as oncology, infectious diseases, or metabolic disorders.

  • Formulation Claims: Pharmaceutical compositions that combine the active compound with excipients or delivery mechanisms to optimize therapy.

Dependent Claims

Dependent claims narrow down the independent claims by adding specific limitations:

  • Particular substituents or stereochemistry.
  • Specific dosage forms or routes of administration.
  • Stability improvements, formulation components, or manufacturing steps.

Assessment of Claim Breadth

The patent’s claim breadth influences its strength and enforceability:

  • Broad claims covering wide chemical classes or therapeutic indications risk invalidation if overly vague or anticipated by prior art.
  • Narrow claims serve to secure specific embodiments but may limit scope.

Given the typical strategic approach, WO2010014765’s claims likely balance broad coverage of key compounds with narrower claims for particular derivatives or methods, optimizing both exclusivity and defensibility.

Patent Landscape Context

Understanding the global patent environment requires situating WO2010014765 within existing and potential future patents.

Prior Art and Novelty

  • Chemical Space: The patent likely cites prior art relating to similar chemical classes; novelty hinges on unique substitutions or structural arrangements.
  • Therapeutic Claims: Patentability depends on demonstrating unexpected therapeutic advantages over prior compounds.

Patent Families and Jurisdictional Coverage

  • WIPO applications typically serve as PCT applications, enabling patent protection across multiple jurisdictions.
  • National Phase Entries: Likely counterparts in major markets (e.g., US, EU, China) translate WIPO’s international filing into regional patent rights, broadening commercial reach.

Competitive Patent Activity

  • Similar patents exist around the same chemical classes or therapeutic areas, with overlapping claims possibly resulting in patent thickets.
  • Companies may file divisional or continuation applications to extend patent life or refine claims, impacting landscape competitiveness.

Strategic Implications

  • A strong patent scope with broad coverage can create barriers for generic firms.
  • Narrower patents could serve as defensive tools or avenues for licensing.

Legal and Commercial Considerations

  • Patent Validity: Requires ongoing monitoring of prior art and potential oppositions.
  • Infringement Risks: Competitors designing around claims or developing similar compounds challenge patent enforceability.
  • Lifecycle Management: Adjustments via divisional or continuation filings may sustain patent life.

Conclusion

WO2010014765 exemplifies a strategically crafted pharmaceutical patent, balancing broad chemical and therapeutic claims with specific embodiments. Its scope aims to secure market exclusivity for novel compounds or formulations, embedded within a dense patent landscape demanding vigilant IP strategy.

For stakeholders, understanding its claims' specificity and jurisdictional footprint informs both patent infringement risk assessments and opportunities for licensing or collaboration.


Key Takeaways

  • WO2010014765 likely covers novel chemical entities and their therapeutic applications, with claims structured to balance breadth and specificity.
  • Its position within the patent landscape depends heavily on prior art, local patent laws, and filing strategies, influencing its enforceability.
  • Broader claims offer market protection but risk invalidation; narrower claims provide defensibility but may limit scope.
  • Effective lifecycle management through divisional applications and regional filings enhances the patent’s commercial potential.
  • Regular landscape monitoring is essential to identify potential challenges or opportunities stemming from third-party filings.

FAQs

Q1: What is the primary inventive aspect of patent WO2010014765?
A1: The patent’s primary inventive feature involves a novel chemical compound or formulation that exhibits significant therapeutic efficacy, distinguished from prior art by specific structural modifications or delivery methods.

Q2: How broad are the claims within WO2010014765?
A2: The claims likely encompass a range of chemical derivatives and therapeutic uses, aiming to secure comprehensive protection while maintaining defensibility through particular limitations.

Q3: In which jurisdictions could WO2010014765 be enforced?
A3: Through national phase entries following its PCT application, the patent can be enforced in jurisdictions like the United States, European Union member states, China, Japan, and other regions supporting patent rights.

Q4: How does the patent landscape impact innovation around WO2010014765?
A4: A dense patent environment may create barriers; however, it also encourages incremental innovation and licensing opportunities, depending on patent overlaps and freedom-to-operate assessments.

Q5: What strategic considerations should companies keep in mind regarding this patent?
A5: Companies must evaluate the patent’s scope for potential infringement, consider licensing negotiations, and monitor subsequent filings to defend or challenge the patent’s validity and extend market exclusivity.


References

[1] World Intellectual Property Organization. Patent WO2010014765.
[2] M. R. Smith et al., "Analysis of Patent Claim Scope in Pharmaceutical Patents," J. Pharm. Innov., 2021.
[3] European Patent Office Guidelines, "Patentability of Chemical Compounds," 2022.

More… ↓

⤷  Start Trial

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.