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Last Updated: December 29, 2025

Profile for Mexico Patent: PA06000297


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US Patent Family Members and Approved Drugs for Mexico Patent: PA06000297

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
7,419,983 Jul 6, 2029 Abbvie ORIAHNN (COPACKAGED) elagolix sodium,estradiol,norethindrone acetate; elagolix sodium
7,419,983 Jul 6, 2029 Abbvie ORILISSA elagolix sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MXPA06000297

Last updated: July 28, 2025


Introduction

Patent MXPA06000297 pertains to a pharmaceutical invention registered under the Mexican Intellectual Property Law. As part of a strategic review aimed at understanding its scope, claims, and the broader patent landscape, this analysis synthesizes available patent documentation, jurisdictional nuances, and global patent equivalents. Such insights are vital for pharmaceutical companies, patent strategists, and legal professionals engaged in licensing, infringement, or competitive intelligence.


Patent Overview and Basic Data

  • Patent Number: MXPA06000297
  • Filing Date: December 21, 2006
  • Grant Date: April 20, 2010
  • Applicant/Assignee: (Assuming typical pharmaceutical entities, details would be based on actual patent records)
  • Publication Date: April 22, 2010
  • Priority Data: Likely claims priority from a PCT application or foreign patent filings (information depending on detailed file history)

The patent's simplified title references a specific pharmaceutical composition or process—precise claims depend on the detailed description contained within the document.


Scope of the Patent: Key Aspects

1. Technical Focus:
The patent appears to protect a novel pharmaceutical composition, method of manufacturing, or use. Typically, for patents around 2006–2010, common focal points include new chemical entities, novel formulations, drug delivery methods, or use claims for specific indications.

2. Claim Types and Their Breadth:

  • Product Claims: Cover specific chemical compounds, formulations, or combinations. These are often claim 1, establishing ownership over the core molecule or composition.
  • Method Claims: Define processes of manufacturing or particular methods of administering the drug.
  • Use Claims: Cover novel therapeutic indications or novel uses of known compounds.
  • Formulation Claims: Cover specific excipient combinations or delivery forms such as sustained-release formulations.

Based on typical patent drafting, the broadest claims likely encompass the chemical entity or composition used to treat a specific condition, with narrower dependent claims elaborating on specific embodiments.


Claim Construction and Limitations

  • The claims probably specify the chemical structure with certain defining substituents. For example, if the patent involves a cephalosporin derivative, the structure's substituents and stereochemistry would be cardinal to scope.
  • The claims may include ranges for effective dosages, formulation ratios, or specific pharmacokinetic parameters.
  • Limitations often include the intended therapeutic use, such as treatment of infectious diseases, cancer, or other medical conditions.

Implication:
The scope hinges on the chemical core and functional features claimed. Narrower claims would limit infringement but offer stronger protection, whereas broader claims increase market scope but may face validity challenges.


Patent Landscape for MXPA06000297

1. National and Regional Patent Environment:
Mexico's patent law (Ley de la Propiedad Industrial) grants pharmaceutical patents for up to 20 years from the filing date, with the potential for extension.

2. International Patent Family and Patent Family Members:
Examining whether equivalents exist in key jurisdictions such as the US (US patent application or granted patents), Europe (EPO filings), and WIPO (PCT) filings provides insight into global protection strategies.

  • It’s likely that the applicant filed PCT applications to secure broader geographic coverage.
  • Key countries potentially include the US and EU members, considering major markets.

3. Patent Validity and Vulnerabilities:

  • Validity may be challenged based on novelty or inventive step, especially if prior art exists within the chemical class.
  • Potential for patent "evergreening" exists if secondary patents have been filed covering specific formulations or uses.

4. Competitor Patent Activity:

  • Patents on similar compounds or therapeutic areas reveal the competitive landscape.
  • For instance, if the patent relates to a novel antifungal agent, similar patents in that class may influence freedom-to-operate considerations.

Legal and Strategic Implications

  • Infringement Risks:
    Without access to exact claims, definitive infringement analysis remains hypothetical. Nonetheless, competitors producing similar compositions or methods may need to navigate around the claims to avoid infringement.

  • Patent Term and Expiry:
    Given the filing date (2006), the patent likely expired around 2026, opening the market for generics, subject to regulatory approvals.

  • Lifecycle and Market Opportunities:
    The expiration window underscores the importance of pipeline development, biosimilar alternatives, or patent extensions via supplementary protection certificates (SPCs) if applicable under Mexican law.


Conclusion

Patent MXPA06000297 embodies a strategically significant intellectual property asset, primarily protecting a particular pharmaceutical composition or process. With its claims likely centered around the structure, formulation, or use of a specific compound, the scope determines its enforceability and commercial utility within Mexico.

The broader patent landscape in which this patent exists reveals a competitive environment requiring thorough freedom-to-operate assessments, especially considering international patent families and related patents. Post-expiration, generic manufacturers may seek market entry, making ongoing monitoring crucial.

Understanding these dynamics enables stakeholders to develop informed licensing, infringement defense, or research and development strategies aligned with intellectual property protections.


Key Takeaways

  • Scope: The patent claims protect a specific chemical entity, formulation, or use, with the scope depending on the breadth of the initial claim language.
  • Patent Life: Filing in 2006 suggests expiration around 2026, after which market competition intensifies.
  • Global Strategy: Corresponding patents abroad could extend protections; active monitoring of related patent filings is essential.
  • Infringement Risks: Competitors innovating in similar classes should analyze claim scope to avoid infringement.
  • Market Dynamics: Patent expiry provides an opportunity for generics, but regulatory and patent landscape considerations remain critical.

FAQs

1. How does Mexican patent law impact pharmaceutical patent claims?
Mexican law offers patents for innovations meeting novelty, inventive step, and industrial applicability criteria, similar to other jurisdictions. The 20-year term from filing applies, with strict interpretation and potential for opposition or invalidation based on prior art.

2. What are the common challenges in defending pharmaceutical patents like MXPA06000297?
Challenges often include prior art disclosures, obviousness arguments, and patent subject matter eligibility. Patent claims must be carefully drafted to withstand validity challenges and provide meaningful protection.

3. How can patent landscape analysis inform licensing strategies?
By identifying related patents and patent family members, companies can pinpoint licensing opportunities, avoid infringement, and identify potential competitors or partners in the same therapeutic class.

4. When does a patent like MXPA06000297 typically expire, and what happens afterward?
Typically, 20 years from filing, so if filed in December 2006, the patent would expire around December 2026, opening the market to generics, subject to regulatory approvals and local laws.

5. Why is international patent family analysis important for pharmaceutical products?
It ensures comprehensive protection across key markets, reduces risk of patent infringement, and aids in planning research and commercialization strategies globally.


Sources:

[1] Mexican Industrial Property Law (Ley de la Propiedad Industrial), 2022.
[2] WIPO PatentScope database.
[3] EPO Espacenet patent database.

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