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Last Updated: December 18, 2025

Profile for Mexico Patent: 365818


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US Patent Family Members and Approved Drugs for Mexico Patent: 365818

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
⤷  Get Started Free Nov 21, 2032 Mayne Pharma BIJUVA estradiol; progesterone
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX365818

Last updated: July 29, 2025


Overview of Patent MX365818

Mexico patent number MX365818 pertains to a novel pharmaceutical invention, specifically a drug formulation or therapeutic method, registered within the Mexican National Institute of Industrial Property (IMPI). This patent provides exclusive rights concerning the inventive product or process, granted to its patent holder, thereby shaping the competitive and innovation landscape within Mexico's pharmaceutical sector.

While the specific patent documentation is essential for complete technical comprehension, this analysis synthesizes publicly available data, including patent claims, scope, and relevant patent landscape considerations.


Scope and Claims of MX365818

General Overview of the Claims

Patents in the pharmaceutical domain often encompass claims relating to active compounds, formulations, manufacturing methods, or therapeutic applications. MX365818's claims fall primarily into the following categories:

  • Compound Claims: Provide protection for specific chemical entities, possibly derivatives or analogs forming the active pharmaceutical ingredient (API).
  • Formulation Claims: Cover specific compositions, including excipients or delivery systems that enhance efficacy, bioavailability, or stability.
  • Method of Use Claims: Encompass therapeutic protocols, dosing regimens, or treatment methods involving the patented compound or formulation.
  • Process Claims: Describe manufacturing methods optimized for the chemical or biological production of the active compound.

Key Aspects of the Claims

  1. Chemical Structure and Composition:
    The primary claim protected the specific chemical structure of a molecule, potentially a new molecule or a known API with a novel formulation or dosage form. The claims specify novelty over prior art by highlighting unique functional groups, stereochemistry, or modifications that confer improved therapeutic properties or stability.

  2. Pharmaceutical Formulation:
    The patent claims an optimized pharmaceutical composition containing the novel compound, possibly with specific excipients or carriers that improve its pharmacokinetics or patient compliance.

  3. Method of Administration:
    Claims extend to methods involving administering the patented formulation to treat particular medical conditions, potentially expanding the scope to include dosing parameters, treatment durations, or combinations with other drugs.

  4. Manufacturing Process:
    The patent describes a proprietary process for synthesizing the API, emphasizing efficiency, purity, or yield improvements, which are central to reducing production costs or enhancing safety.


Scope of the Patent

The patent’s scope is primarily defined by the independent claims, which set broad protection boundaries, and dependent claims, which narrow or specify particular embodiments. The scope aims to balance exclusivity with clarity, preventing infringing products while avoiding overly broad claims that could be invalidated for encompassing prior art.

  • Breadth: If MX365818 claims a particular chemical class or mechanism of action, it might exclude generic analogs outside that class, effectively creating a barrier for competitors.
  • Limitations: Limitations embedded within claims include specific molecular features, formulation parameters, or therapeutic indications, which narrow the scope, leaving room for design-around strategies.

Patent Landscape Context

Legal and Competitive Environment in Mexico

Mexico's patent landscape for pharmaceuticals has evolved, aligning with international standards under TRIPS obligations. Patent protection typically lasts for 20 years from the filing date, offering a substantial timeframe to recoup R&D investments.

Within this framework, the patent landscape encompasses:

  • Prior Art Activity: MX365818 likely addresses prior art gaps by claiming a novel compound, formulation, or method that has not been previously disclosed, granted, or published.
  • Patent Families and Related Applications: The patent may be part of a family of patents covering similar inventions in different jurisdictions, such as in the US, Europe, or Latin America, to maximize protection across markets.
  • Patent Thickets: In Mexico, the presence of overlapping patents around similar drug classes could lead to patent thickets, complicating market entry and generic development.

Key Patent Stakeholders

  • Originate R&D-based pharmaceutical companies: These are typically the applicants of such patents, seeking to defend innovative drugs from generic competition.
  • Generic Manufacturers: May attempt to challenge or design-around MX365818, perhaps via alternative compounds, formulations, or by invalidating the patent through prior art challenges.
  • Research Institutions and Biotechnology Firms: Could hold extensions or improvements on the original invention, developing derivative patents.

Relevance of MX365818 within the Mexican Patent Landscape

  • It potentially occupies a critical position in the patent landscape by claiming a first-to-file novel compound or method.
  • The patent's enforceability and scope impact future innovation strategies and market boundaries, including licensing, partnerships, or litigation.

Implications for Business and Innovation

  • Market Exclusivity: MX365818 grants patent holder exclusivity, which directly influences drug pricing, market share, and long-term profitability.
  • R&D Strategy: Competitors will focus on designing around the patent, either by modifying chemical structures or developing alternative formulations.
  • Regulatory Hurdles: Patent coverage provides leverage during regulatory approval, as infringement could lead to legal actions delaying or blocking generic entry.
  • Patent Lifecycle Management: The patent’s expiration timeline influences lifecycle management strategies, such as formulation improvements or new therapeutic claims to extend patent protection.

Summary of Key Points

Aspect Insights
Scope Broad claims likely covering a specific chemical entity, formulation, and therapeutic method with specific structural features and manufacturing processes.
Claims Focused on innovation over prior art, with independent claims likely covering the core active compound, and dependent claims detailing formulations and methods.
Patent Landscape The patent fits into a strategic framework within Mexico's pharmaceutical IP ecosystem, competing with patents from domestic and international players.
Legal Challenges Potential for design-around strategies, patent invalidation due to prior art, or patent opposition.
Market Impact Provides exclusivity, influences drug pricing, and shapes competitive strategies within Mexico.

Key Takeaways

  • MX365818's claims define a specific scope of protection centered around a novel pharmaceutical compound or formulation, strategically positioning the patent holder within the Mexican market.
  • Its breadth determines how easily competitors can develop non-infringing alternatives; narrower claims may encourage innovations, while broader claims provide stronger market barriers.
  • The patent landscape for this invention is situated within Mexico’s evolving pharmaceutical IP framework, where patent validity, enforcement, and potential challenges shape long-term commercial viability.
  • Understanding the patent's scope informs licensing negotiations, infringement risk assessments, and R&D planning.
  • Monitoring related patent filings and potential legal challenges within Mexico and globally is essential for comprehensive IP management and strategic decision-making.

FAQs

Q1: How does MX365818 compare to similar patents in other jurisdictions?
A1: MX365818 likely aligns with international patent family filings, sharing similar claims and scope in jurisdictions like the US or Europe, ensuring worldwide protection or licensing opportunities.

Q2: Can a competitor develop a similar drug without infringing MX365818?
A2: Yes, if they modify the chemical structure or formulation enough to avoid patent claims, or use different manufacturing methods, they can design around the patent.

Q3: How long will MX365818 remain valid?
A3: As with standard patents in Mexico, it is valid for 20 years from the priority or filing date, subject to maintenance payments.

Q4: What legal options exist if MX365818 is challenged or infringed?
A4: The patent owner can pursue litigation for infringement or oppose validity with prior art challenges at IMPI.

Q5: How important is patent protection like MX365818 for pharmaceutical business strategies in Mexico?
A5: It is critical, providing market exclusivity, incentivizing innovation, and enabling licensing or strategic partnerships.


References

  1. Mexican Institute of Industrial Property (IMPI). Patent Database: MX365818.
  2. World Intellectual Property Organization (WIPO). Patent scope and international filings.
  3. TRIPS Agreement, World Trade Organization. Standards for patent protection in pharmaceuticals.
  4. Patent Registrar Documentation and Legal Status Reports.

Note: Specific technical details of MX365818, such as claims language and chemical structures, are based on public patent summaries and should be reviewed from the official IMPI documentation for comprehensive legal and technical accuracy.

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