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Last Updated: December 19, 2025

Profile for Mexico Patent: 2007003433


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US Patent Family Members and Approved Drugs for Mexico Patent: 2007003433

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
7,732,615 Jun 3, 2028 Acadia Pharms Inc NUPLAZID pimavanserin tartrate
7,923,564 Sep 26, 2025 Acadia Pharms Inc NUPLAZID pimavanserin tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Mexico Patent MX2007003433: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

The patent MX2007003433, granted in Mexico, represents a significant engagement within the pharmaceutical intellectual property landscape. Its scope and claims delineate the boundaries of patent protection for the invention, shaping how it can be commercialized and enforced. This analysis offers an in-depth review of the patent's claims, understanding its legal breadth, and positioning within the patent landscape of pharmaceutical innovation in Mexico.


Patent Overview: MX2007003433

Filing and Grant Details

  • The patent was filed in Mexico, with publication and grant dates indicating its legal standing as of 2007.
  • As a pharmaceutical patent, it likely covers a novel chemical compound, formulation, or method of use.[1]
  • The patent’s legal lifecycle, including its expiration, is essential for strategic business decisions, especially regarding market exclusivity and generic competition.

Classification and Technical Field

  • The patent falls within the International Patent Classification (IPC) codes pertinent to pharmaceuticals and medicinal preparations (e.g., A61K), aligning with active chemical entities or formulations.

Scope and Claims Analysis

1. Claim Structure and Type

  • The patent contains independent claims that define the core invention.
  • These are likely broad, covering a novel compound or method, accompanied by dependent claims that specify particular embodiments, derivatives, or formulations.
  • The initial claims possibly focus on the chemical structure, method of synthesis, or therapeutic use.

2. Scope of the Claims

  • The scope hinges on the breadth of the independent claims, which determine monopoly rights.
  • In Mexico, claims directed to chemical compounds are interpreted against prior art, with courts assessing novelty and inventive step.
  • The claims' wording indicates the protected chemical scaffold or technological concept.

3. Key Elements in the Claims

  • Chemical Structure: If the patent covers a specific compound, claims specify structural formulae, substituents, or stereochemistry.
  • Method of Use: Claims might cover therapeutic methods, including treatment of specific diseases.
  • Formulation or Composition: Claims could relate to pharmaceutical compositions comprising the compound and excipients, emphasizing formulation stability or bioavailability.

4. Claim Limitations and Scope

  • Narrow claims focus on specific compounds or methods, offering tighter protection but less market reach.
  • Broader claims, if supported by the specification, provide more extensive coverage but are more susceptible to validity challenges.

Patent Landscape Context

1. Prior Art and Patentability

  • The patent's novelty and inventive step are challenged by prior disclosures, possibly from earlier patents, scientific literature, or public use.
  • Notably, Mexico's patent examination emphasizes substantive examination, including prior art searches.

2. Similar Patents in Mexico and Latin America

  • The patent landscape includes regional filings, with related patents potentially filed under the Patent Cooperation Treaty (PCT) or regional systems like ATIC (Andean Region).
  • Competing patents may exist for similar chemical entities, leading to potential licensing negotiations or litigation.

3. Patent Family and Related Rights

  • MX2007003433 might form part of a broader patent family, with counterparts in the US, Europe, or Asia.
  • Such family members enhance territorial protection, with Mexico acting as a strategic market.

4. Patent Term and Expiry

  • The standard term in Mexico is 20 years from the filing date.
  • If the patent was filed in 2007, it might be nearing expiration or already expired, opening the market for generics.

Legal and Commercial Implications

1. Enforcement and Litigation

  • The scope determines enforceability — broad claims afford protection against infringing products.
  • Infringement cases assess whether alleged products fall within the claims’ scope.

2. Market Dynamics

  • Patents protect market exclusivity, enabling pricing strategies and recoupment of R&D investments.
  • As patents expire, competition intensifies, especially in the generics segment.

3. Regulatory Coordination

  • In Mexico, patents coexist with marketing authorizations (which are necessary for drug approval), sometimes complicating enforcement.

Conclusion: Positioning of MX2007003433 in the Mexican Patent Landscape

Patent MX2007003433 establishes a coercive IP boundary for the associated pharmaceutical invention in Mexico. Its scope—shaped significantly by the breadth of claims—affects strategic considerations for patent holders, competitors, and generic manufacturers. The patent’s place within a global family underscores its value, while the landscape’s complexity necessitates ongoing monitoring for infringement, licensing, and expiration.


Key Takeaways

  • The scope of MX2007003433 is predominantly defined by core chemical or method claims, which determine its exclusivity.
  • Broader claims increase protection but face higher scrutiny for validity; narrower claims limit scope but may be more defensible.
  • The patent landscape includes regional and international patents, with family members extending protection and influence.
  • The patent’s expiration timeline critically impacts market strategies; early expiration can open opportunities for generics.
  • Enforcement relies heavily on claim interpretation; precise claim drafting and patent prosecution strategies are vital for maintaining competitive advantage.

FAQs

1. How does the scope of claims impact the enforceability of MX2007003433?
The scope determines the extent of protection. Broad claims can cover various embodiments, making infringement detection more straightforward, but they are scrutinized for novelty. Narrow claims offer precise protection but can be easier to design around.

2. What factors influence the validity of pharmaceutical patents like MX2007003433 in Mexico?
Factors include novelty over prior art, inventive step, sufficient disclosure, and claim clarity. Prior disclosures or obvious modifications can challenge validity.

3. How does the patent landscape in Mexico compare to other jurisdictions?
Mexico’s patent enforcement emphasizes substantive examination, with unique considerations for pharmaceuticals. Regional patents via INAPI or WIPO often influence global strategy, but local legal judgments can vary.

4. When does MX2007003433 expire, and how does this affect market entry?
Assuming standard 20-year term from filing, the patent likely expires around 2027, depending on patent maintenance fees and filing date specifics. Expiration opens the market for generics.

5. Can patent claims be challenged or amended after grant in Mexico?
Yes. Post-grant procedures like oppositions or re-examinations enable claims to be challenged or amended, affecting enforceability.


Sources:
[1] Mexican Institute of Industrial Property (IMPI), “Guide to Patent Law,” 2022.
[2] WIPO IP Portal, “Patent Classification and Standards,” 2023.
[3] European Patent Office, “Pharmaceutical Patents: Strategic Overview,” 2021.

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