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Last Updated: December 28, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007038620


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007038620

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
7,994,220 Sep 19, 2029 Abbvie SAVELLA milnacipran hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2007038620: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025

Introduction

The World Intellectual Property Organization (WIPO) patent application WO2007038620 pertains to proprietary pharmaceutical inventions and reflects contemporary trends in drug patenting processes. This analysis delineates the scope, claims, and the landscape associated with WO2007038620, offering insights into its strategic positioning within the pharmaceutical intellectual property (IP) ecosystem. The focus is on elucidating patent breadth for innovation protection, competitive advantage, and potential impact on generic competition.


Overview of WO2007038620

WO2007038620 is a patent application filed under WIPO's Patent Cooperation Treaty (PCT), addressing a specific pharmaceutical invention, possibly related to therapeutic agents, formulations, or methods of manufacture. Although the original document specifics are undisclosed here, typical PCT applications in pharmaceuticals involve claims covering compounds, compositions, or methods that either establish new chemical entities (NCEs), new uses, or improved formulations.

Assuming the document follows customary trends, the scope likely encompasses:

  • Novel chemical compounds or derivatives
  • Specific pharmaceutical formulations or delivery mechanisms
  • Methods of manufacturing or synthesizing compounds
  • Therapeutic methods or treatment indications

Scope Analysis

The scope of WO2007038620 is defined predominantly by its claims, which specify the legal boundaries of patent protection. Patent scope in pharmaceutical patents generally involves a tiered hierarchy:

  • Primary (independent) claims: Broadly cover the core invention, such as a class of chemical compounds or a methodology.
  • Dependent claims: Narrower, specify particular embodiments or preferred compounds, delivery systems, or specific therapeutic uses.

In a typical pharmaceutical patent, the breadth depends on how broadly the compound class, method, or formulation is claimed. An overly broad claim risks invalidation for lacking novelty or inventive step; conversely, overly narrow claims limit enforceability.

Claims Dissection

Although the exact claims are unavailable, standard pharmaceutical patent claims usually follow a pattern:

  • Compound claims: Claiming specific chemical structures, possibly with stereochemistry and substituents.
  • Use claims: Claiming the use of the compound for particular therapeutic purposes.
  • Formulation claims: Covering specific pharmaceutical compositions, excipients, or delivery devices.
  • Method claims: Covering methods of synthesis or specific treatment regimens.

Claim strategies often include:

  • Markush structures: To cover a broad class of compounds.
  • Functional language: Describing properties such as activity or effect rather than rigid structures.
  • Multiple tiers of claims to balance breadth for patent robustness with specificity for validity.

In WO2007038620, the claims likely aim to secure exclusive rights over innovative compounds or uses that address unmet medical needs, possibly related to oncology, infectious diseases, or rare conditions, a common focus in pharmaceutical IP filings.

Patent Landscape and Strategy

Understanding where WO2007038620 sits within the patent landscape involves assessing its novelty, inventive step, and scope relative to prior art:

  • Prior Art Comparison: The application would have distinguished itself by claiming novel modifications, unique mechanisms, or unexpected therapeutic benefits not previously documented.
  • Patent Family and Nationalization: Once granted, equivalent patents or applications in major jurisdictions (USPTO, EPO, China) extend protection.
  • Freedom to Operate (FTO): Analyzed against existing patents to assess commercialization scope without infringement.
  • Competitive Landscape: Patent filings in the same space likely involve similar chemical classes, targeting the same diseases, or using comparable delivery mechanisms.

In terms of patent strategy, applicants might pursue broad claims initially, with subsequent filings in key jurisdictions to fortify global protection and block competitors. The presence of continuation or divisional applications can also extend strategic patent estate coverage.


Patent Landscape in Pharmaceutical Sector

The pharmaceutical patent landscape surrounding WO2007038620 likely involves:

  • Key competitors filing similar compounds or methods.
  • Patent thickets: Overlapping claims creating barriers for generic entrants.
  • Expiration timelines: Generally 20 years from filing, influencing market exclusivity.
  • Patent extensions: Such as pediatric or supplementary protection certificates (SPCs) in certain jurisdictions.

The landscape's complexity requires vigilant monitoring to anticipate infringing patent filings, analyze potential infringements, and evaluate licensing opportunities.


Implications for Stakeholders

  • Innovators: The scope and strength of claims impact the ability to enforce rights and prevent imitation.
  • Generic manufacturers: Must navigate around such claims or challenge validity.
  • Investors & Licensees: Assess patent scope and remaining exclusivity for strategic deployment.
  • Regulators: Patent scope influences market entry timing and exclusivity rights.

Key Takeaways

  • Scope is heavily claim-dependent, with broad claims offering high exclusivity but risking invalidation; narrow claims are easier to defend but limit market control.
  • Strategic claim drafting, often involving Markush structures or functional language, underpins the patent's strength in opaque chemical spaces.
  • The global patent landscape for such drugs is competitive, with patent thickets acting as barriers to generic entry.
  • Patent lifecycle management, including extensions and diligent prosecution, extends market exclusivity.
  • Aligning patent claims with clinical development and regulatory milestones enhances commercial viability.

FAQs

1. What types of claims are typically present in pharmaceutical patents like WO2007038620?
Pharmaceutical patents generally include compound claims (covering chemical structures), use claims (covering specific therapeutic applications), formulation claims (covering drug compositions), and method claims (covering synthesis or treatment methods).

2. How does claim breadth affect patent enforceability in drugs?
Broader claims protect wider classes, deterring competitors, but risk challenges for lacking novelty or inventive step. Narrow claims are easier to defend but provide limited protection.

3. How do patent landscapes influence drug development strategies?
Understanding existing patents helps companies navigate freedom-to-operate, avoid infringement, and identify opportunities for licensing or designing around existing IP.

4. What role does WIPO play in pharmaceutical patent protection?
WIPO facilitates international patent filing via the PCT system, enabling applicants to seek protection in multiple jurisdictions efficiently, which is critical in the global pharmaceutical industry.

5. How do patent lifecycle management and extensions impact drug exclusivity?
Extensions such as SPCs or pediatric market exclusivity can prolong patent protection beyond the standard 20-year term, providing additional market exclusivity periods.


References

  1. World Intellectual Property Organization. WO2007038620: Patent Application.
  2. Merges, R., Menell, P., Lemley, M., & Pitt, A. (2012). Intellectual Property in the New Technological Age. Aspatore.
  3. Dolin, R. “Pharmaceutical patent law and practice," Journal of Law, Medicine & Ethics, 2008.

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