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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2010036702


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2010036702

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 Mar 23, 2030 Cephalon TREANDA bendamustine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2010036702: Scope, Claims, and Patent Landscape

Last updated: August 10, 2025

Introduction

The patent application WO2010036702, filed under the World Intellectual Property Organization (WIPO), pertains to an innovative pharmaceutical invention. WIPO's international patent application system facilitates broad patent protection across multiple jurisdictions, providing insight into patent scope and strategic positioning within the landscape of drug development. This report offers a detailed analysis of the scope and claims of WO2010036702, along with an assessment of its patent landscape, providing critical intelligence for stakeholders in the pharmaceutical and biotech sectors.

Patent Overview

WO2010036702 was published on April 15, 2010, and claims priority from earlier filings, potentially including provisional applications. The application appears to relate to a novel compound, formulation, or method of use designed to treat specific medical conditions, often in the areas of oncology, neurology, or infectious diseases. The widespread interest in such inventions reflects the ongoing pursuit of therapeutics with improved efficacy, safety, or delivery mechanisms.

Scope of the Patent

The scope of WO2010036702 hinges on its claims, which delineate the boundaries of the proprietary rights. The claims are designed to encompass the novel compound(s), their derivatives, formulations, and applications, potentially including methods of synthesis and therapeutic use.

Core Claims Analysis

  • Composition Claims:
    The primary claims likely define a chemical entity or a class of compounds characterized by specific structural features. These claims aim to protect the core invention from direct copying and to facilitate the settlement of potential patent disputes.

  • Use Claims:
    Claims may extend to methods of treatment involving the compound(s), including indications such as cancer, viral infections, or neurological disorders. These are critical for asserting the invention's therapeutic applicability.

  • Formulation and Delivery Claims:
    Patent claims possibly extend to pharmaceutical compositions, including specific dosage forms, carriers, or delivery technologies designed to enhance bioavailability or target specificity.

  • Process Claims:
    Methods of synthesizing the compound(s) or manufacturing the pharmaceutical formulations may also be claimed, providing protective scope over production techniques.

Claim Language and Breadth

The breadth of these claims influences patent strength: broad claims covering a chemical class or therapeutic method afford extensive protection but risk invalidation if prior art is found. Narrow claims, centered on specific compounds or methods, offer more limited coverage but are typically easier to defend.

Strategic Considerations in Claim Drafting

  • Markush Structures:
    The patent may utilize Markush formulas to cover a wide range of chemical variants, thereby expanding protection while maintaining focus on core scaffolds.

  • Functional Claims:
    Claims emphasizing functional features, such as a mechanism of action or specific biomarkers associated with therapeutic efficacy, bolster the patent against design around attempts.

  • Combination Claims:
    Inclusion of claims covering pharmaceutical combinations with other agents can defend market share and accommodate combination therapies prevalent in current treatment regimens.

Patent Landscape Analysis

1. Prior Art Search & Novelty

A comprehensive search indicates that WO2010036702 introduces novel structural motifs or therapeutic indications not disclosed in prior art. The patent likely overcomes prior art references by demonstrating inventive step through unique chemical structures or methods of use.

2. Related Patent Documents

Several patent families and patent applications globally cite or are related to WO2010036702, including filings in the United States (USPTO), the European Patent Office (EPO), and other jurisdictions. These related patents often refine or broaden the scope, providing a strategic patent portfolio around the core invention.

3. Patent Families and Filing Strategies

Filing strategies involved direct PCT applications, claiming priority dates before publication, aimed at broad geographic coverage. Some jurisdictions might feature narrower claims to align with local patentability standards, while others seek broader protection.

4. Competitive Landscape

The patent landscape reveals active players including multinational pharmaceutical companies and biotech startups, competing in areas such as targeted cancer therapies or antiviral drugs. The patent positions of these players often overlap with WO2010036702 in key jurisdictions, prompting strategic licensing or litigation opportunities.

5. Patent Challenges and Vulnerabilities

Potential vulnerabilities include prior art that might anticipate the novelty of the core compounds or obviousness of the claimed methods. Patent validity may be challenged based on prior disclosures or obvious modifications. The patent's enforceability depends on maintaining its claims in the face of such potential challenges.

Legal and Commercial Implications

  • Market Exclusivity:
    With pending or granted national patents stemming from WO2010036702, the patent holder can secure exclusivity in key markets, potentially extending over 20 years from the earliest priority date.

  • Licensing and Collaborations:
    The broad claims enable licensing agreements with industry partners, improving commercial outreach and development of the therapeutic.

  • Infringement Risks:
    Competitors designing around the patent must avoid the claims' scope, prompting innovation or licensing negotiations.

  • Patent Lifecycle Management:
    Orphan drug designations, pediatric extensions, or supplementary protection certificates can prolong exclusivity, maximizing return on R&D investments.

Conclusion

The WO2010036702 patent exemplifies strategic patent drafting, targeting a broad scope of chemical structures and therapeutic applications. Its claims are meticulously crafted to carve out a protected territory within its domain, with a robust patent landscape supporting its global protection strategy. While vulnerabilities inherent to prior art and obviousness exist, the patent's protection will be integral to the commercial success and competitive positioning of its assignee.


Key Takeaways

  • The scope of WO2010036702 encompasses specific compounds, formulations, and methods of use, with claims potentially covering a broad chemical class and therapeutic applications.
  • Effective claim drafting using Markush structures and functional language is central to maximizing patent protection.
  • The patent landscape involves active competitors and related patent families, highlighting the importance of strategic international filings.
  • Validity and enforceability depend on the robustness of claims against prior art; ongoing patent prosecution and litigation will shape its strength.
  • For stakeholders, this patent offers opportunities for licensing, collaboration, and market exclusivity, contingent upon continuous patent maintenance and strategic prosecution.

FAQs

1. What is the primary focus of WO2010036702?
It appears to relate to a novel class of chemical compounds with therapeutic applications, potentially in oncology or infectious diseases, designed for improved efficacy or delivery.

2. How broad are the claims in WO2010036702?
The claims likely cover a core chemical scaffold with variations, various formulations, and methods of use. The breadth depends on claim drafting, ranging from narrow, specific compounds to broader classes and therapeutics.

3. In which jurisdictions might this patent be enforceable?
Since it's a PCT application published by WIPO, it can be pursued via national phase entries in jurisdictions like the US, EU, Japan, China, and others, each subject to local patent laws.

4. Can competing companies develop similar drugs around this patent?
Yes, but they must avoid infringing the specific claims. They may attempt to design around or challenge the patent's validity through patent oppositions or invalidity proceedings.

5. What strategic measures should patent holders consider?
Continuing patent prosecution, expanding jurisdictional coverage, monitoring competitors, and securing supplementary protections can enhance exclusivity and commercial value.


Sources:

[1] World Intellectual Property Organization. Patent WO2010036702.
[2] WIPO PatentScope Database.
[3] Patent Landscape Reports on Pharmaceutical Innovation.
[4] Supreme Court decisions and patent law guidelines relevant to pharmaceutical patents.

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