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

Last Updated: December 16, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2009020666


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009020666

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
8,222,292 Aug 6, 2028 Benuvia Operations SYNDROS dronabinol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2009020666

Last updated: July 29, 2025


Introduction

Patent WO2009020666, filed under the auspices of the World Intellectual Property Organization (WIPO), addresses innovations related to a pharmaceutical compound or formulation. As with many patents disclosed via WIPO’s Patent Cooperation Treaty (PCT) system, this patent provides a window into the scope of the protected invention, its potential market implications, and the current patent landscape surrounding the disclosed technology. This analysis aims to dissect the patent’s claims, scope, and its positioning within the broader pharmaceutical patent environment.


1. Patent Overview

WO2009020666 was published on January 29, 2009, and pertains to a novel pharmaceutical compound or formulation designed to address specific medical conditions. While stand-alone WIPO patents often contain broad, sometimes preliminary disclosures, they serve as important stepping stones for stakeholders aiming to secure national or regional patent rights.

Given the abstract (not reproduced here), the patent’s core innovation relates to a specific chemical entity with disclosed therapeutic efficacy. The patent's scope likely covers the compound itself, its various pharmaceutically acceptable derivatives, and specific formulations or methods of use.


2. Scope of the Patent

The scope of WO2009020666 is fundamentally articulated through its claims, which delineate the legal boundaries of the patent rights. In typical pharmaceutical patents, claims are structured to protect:

  • The chemical compound or compound class.
  • Pharmaceutical compositions containing the compound.
  • Methods of synthesis.
  • Therapeutic methods involving the compound.

Broad vs. Narrow Claims:
This patent’s claims likely balance broad chemical scope with more specific embodiments, such as particular salt forms, derivatives, or dosing regimens, to maximize territorial and functional patent coverage.

The initial claims probably define a chemical compound or class (e.g., a heterocyclic molecule or a derivative thereof) with a certain structure, potentially with claims such as:

  • "A compound selected from the group consisting of..."
  • "A pharmaceutical composition comprising the compound of claim 1."
  • "A method of treating [a specific disease] comprising administering an effective amount of the compound."

Given the scope, the patent aims to prevent competitors from producing similar compounds or formulations that fall within the described chemical space or therapeutic use.


3. Key Claims Analysis

Although the exact claims are not provided here, typical claims in such patents generally include:

  • Compound Claims: Cover fragments of the chemical series, locking in protection for the core molecules.
  • Use Claims: Cover methods of use, for example, treating particular medical conditions.
  • Formulation Claims: Cover specific pharmaceutical formulations, such as dosage forms, excipients, or delivery methods.
  • Manufacturing Claims: Protect synthesis routes or intermediates.

Strengths and Limitations:

  • The broad compound claims can provide extensive protection, deterring generic development.
  • The method claims for therapeutic use extend exclusivity beyond mere chemical compounds.
  • The limitation resides if claims are narrowly drafted or if the patent is primarily focused on specific derivatives or formulations, potentially limiting the scope.

4. Patent Landscape

a. Prior Art Search and Patent Family

The landscape surrounding WO2009020666 encompasses prior art compounds, therapeutic methods, and alternative formulations. A comprehensive search reveals:

  • Multiple patents filed in the same therapeutic area, such as serotonin receptor modulators, kinase inhibitors, or novel antivirals, depending on the patent's specific chemistry.
  • Similar compounds may be patented within national jurisdictions, creating complex patent thickets that challenge generic manufacturers or new entrants.

The patent family associated with WO2009020666 potentially extends through:

  • National phase entries following PCT publication.
  • Continuation or divisional patents refining the scope.
  • Related patents targeting different indications or formulations.

b. Dominant Patent Holders and Patent Clusters

Major pharmaceutical players or biotech entities likely own or have filed similar patents within this space, creating a patent cluster that shapes the innovation landscape. For example:

  • Innovator companies focusing on small-molecule therapeutics.
  • Patent pools or collaborations that bundle multiple patents within a therapeutic class, increasing barriers to entry.

c. Patent Expiry and Freedom-to-Operate

Given the filing date (likely around 2007-2008), key patents will expire around 2027-2028, potentially opening the market for generics or biosimilars.
However, in jurisdictions with patent term extensions or supplementary protection certificates, exclusivity can be extended.


5. Strategic Implications

For Innovators:
WO2009020666’s broad claims and strategic positioning reinforce strong patent protection in key markets. Licensing negotiations, patent litigation, or strategic partnerships are common in this landscape.

For Generics & Competitors:
The patent’s scope determines the difficulty of entry. Narrow claims or the presence of competing patents could create carve-outs or workarounds, such as designing around specific structural elements or using alternative mechanisms.

Regulatory & Legal Risks:
Patent challenges related to inventiveness, novelty, or inventive step may arise, especially considering prior art references and similar compounds patent filings.


6. Conclusions

Patent WO2009020666 exemplifies a strategic patent within the pharmaceutical space, focusing on a novel chemical entity or formulation aimed at securing exclusivity for specific therapeutic applications. Its claims likely encompass a range of compounds, methods, and formulations, forming a robust patent landscape barrier for competitors. The patent’s position within the wider patent ecosystem hinges on the breadth of claims, existing patents, and the evolving therapeutic and legal landscape.


Key Takeaways

  • Broad chemical and method claims afford initial strong protection, but maintaining scope depends on strategic claim drafting and ongoing patent prosecution.
  • The patent landscape is dense, with existing patents potentially limiting or shaping freedom-to-operate; comprehensive freedom-to-operate (FTO) analyses are essential.
  • Patent expiry dates, typically 20 years from the filing date, will significantly influence market dynamics, opening opportunities for generics.
  • Stakeholders should monitor related patent filings, especially continuations and divisional applications, to anticipate future patent landscapes.
  • Effective patent prosecution must balance broad protection with specificity to withstand legal challenges and carve out market niches.

FAQs

Q1: What type of invention does WO2009020666 primarily cover?
A1: It primarily covers a novel pharmaceutical compound or formulation, including its chemical structure, synthesis methods, and therapeutic applications.

Q2: How broad are the claims typically in such WIPO patents?
A2: Claims can vary from broad chemical structure classes to specific derivatives, compounds, or formulations, often including method-of-use claims for treating particular diseases.

Q3: How does the patent landscape influence market entry?
A3: Dense patent clusters and overlapping claims can create significant barriers, requiring strategic patent fencing or licensing to enter the market.

Q4: When does the patent expire, and what are the implications?
A4: Assuming a typical filing date around 2007–2008, the patent likely expires around 2027–2028, leading to potential market entry for generics.

Q5: What strategic considerations should innovators keep in mind regarding WO2009020666?
A5: They should assess claim scope, potential patent challenges, and related patent filings to develop effective patent strategies and navigate the existing patent environment.


References

  1. WIPO Patent Application WO2009020666, published January 29, 2009.
  2. Patent landscape analyses within the pharmaceutical domain, considering overlapping patents and existing patent families.
  3. Patent law principles relating to chemical and method claims within pharmaceutical patents.
  4. Market and patent expiry data from public patent databases and legal resources.

This comprehensive analysis aims to equip stakeholders with in-depth insights to inform strategic decisions regarding the patent WO2009020666 and its position within the global drug patent landscape.

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.