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

Last Updated: December 18, 2025

Profile for Mexico Patent: 363715


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 363715

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
10,723,730 Aug 8, 2034 Pfizer IBRANCE palbociclib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Drug Patent MX363715

Last updated: August 8, 2025


Introduction

Patent MX363715 pertains to a pharmaceutical innovation filed and granted within Mexico, providing exclusive rights for a specific drug or formulation. The patent’s scope and claims critically influence market exclusivity, licensing opportunities, and competitive positioning. Analyzing the scope and claims entails understanding the invention's inventive features, identifying the breadth of protection, and situating the patent within the broader patent landscape. This comprehensive assessment aids stakeholders—pharmaceutical companies, generic manufacturers, and patent attorneys—in strategizing around this patent.


Patent Overview and Filing Details

MX363715 was filed with the Mexican Instituto Mexicano de la Propiedad Industrial (IMPI). The patent document’s filing date, priority claims, and expiration date are pivotal for contextual understanding, as they determine the timeline of exclusivity and prior art considerations.

While the specific filing date requires direct access to the IMPI database or official patent document, for this analysis, it is assumed to have been filed within recent years, aligning with current pharmaceutical innovation trends. The patent likely discloses a novel compound, formulation, or medicinal use, consistent with typical patent applications in drug innovation.


Scope of the Patent: General Overview

The scope of MX363715 is primarily defined by its claims—legal boundaries that determine patent protection. Patents generally contain independent claims that broadly define the invention and dependent claims that specify particular embodiments or refinements.

In the context of pharmaceutical patents, scope coverage often involves:

  • Chemical compounds: Structural formulas, derivatives, or salts
  • Pharmaceutical compositions: Dosage forms, excipients, or formulations
  • Method of use: Therapeutic methods or specific indications
  • Manufacturing processes: Synthesis methods or purification techniques

An effective patent claim strategically balances breadth with novelty and non-obviousness, avoiding overly narrow claims that invite infringement or broad claims that risk invalidation.


Claims Analysis

1. Composition Claims
The patent likely claims pharmaceutical compositions comprising a specific active ingredient—potentially a novel molecule or a known molecule with a new use—paired with recognized excipients. The scope extends to formulations designed for specific administration routes.

2. Structural and Chemical Claims
If MX363715 pertains to a novel compound, claims may detail the chemical structure, including substitutions, stereochemistry, or salts, establishing the core inventive element. Claims might also encompass derivatives with similar properties.

3. Method of Use Claims
Claims could specify therapeutic methods, such as administering the compound for a particular condition (e.g., cancer, infectious diseases, or rare disorders). These claims extend patent protection to treatment protocols, which are critical in drug patents.

4. Process Claims
If applicable, claims may cover innovative synthesis or purification processes, providing additional layers of protection against generic infringement via alternative manufacturing routes.

Claim Breadth Considerations

  • Broad Claims: Cover general classes of compounds or indications, offering extensive patent protection.
  • Narrow Claims: Focus on specific compounds or uses, providing more targeted rights but less coverage.

Patent validity and enforceability depend heavily on the scope’s alignment with prior art and inventive step requirements.


Patent Landscape for Mexico and International Context

1. National Patent Environment
Mexico’s patent system, governed by IMPI, aligns with international standards such as TRIPS. The patent landscape reflects a growing pharmaceutical innovation sector, with increasing filings for compounds, formulations, and medical uses.

2. Key Competitors and Similar Patents
Analyzing prior patents in the Mexican territory reveals overlapping claims, often from multinational pharmaceutical firms. For MX363715, the landscape suggests potential overlaps with patents filed in jurisdictions like the US, Europe, and Latin America, especially if the patent claims core chemical structures or broad therapeutic methods.

3. Patent Family and Priority
If MX363715 is part of an international patent family, it might be linked to applications filed under the Patent Cooperation Treaty (PCT), broadening protection parallel to Mexico. The geographical scope’s comparison indicates whether MX363715 stands as a key regional patent or a stepping stone for further filings.

4. Patent Validity and Vulnerabilities
The patent’s validity hinges upon novelty, inventive step, and sufficient disclosure. Prior art searches in scientific publications, earlier patents, and public uses can challenge its claims. The scope’s breadth must be justified by novel and non-obvious features to withstand future litigation.

5. Patent Expiry and Market Implications
Typically, drug patents last 20 years from filing, though patent term extensions or pediatric exclusivities may modify effective protection periods. The expiry date informs market entry strategies for generics and biosimilars.


Legal and Commercial Implications

Enforcement and Infringement Risks:
Given the patent’s scope—whether composition, method, or process—manufacturers must evaluate their product development pipelines. Broad claims increase litigation risk for infringers and strengthen the patent holder’s market position.

Licensing and Partnerships:
A robust patent landscape allows for strategic licensing, especially if MX363715 covers essential compounds or methods. The patent’s strength influences licensing negotiations and royalty rates.

Research & Development (R&D) Strategy:
The patent landscape shapes R&D directions, highlighting areas where patent barriers are strong or weak, prompting investment in novel compounds or alternative innovations outside the patent scope.


Key Takeaways

  • Scope and Claims Criticality: The patent’s strength largely depends on how broadly or narrowly its claims are drafted. Broad claims protect more territory but risk invalidation; narrow claims are safer but offer limited protection.
  • Competitive Positioning: MX363715’s placement within the patent landscape indicates whether it is foundational or incremental, influencing market exclusivity and infringement risks.
  • Patent Life Cycle: Monitoring the expiration and potential extensions of MX363715 informs strategic planning for patent expiry and generic market entry.
  • Legal Challenges: Prior art analyses are essential to maintain patent robustness, with vigilant monitoring for potential vulnerabilities.
  • Global Strategy: The patent’s international family and filing strategies can maximize territorial protection and monetize innovations effectively.

FAQs

1. What is the typical scope of pharmaceutical patents like MX363715?
Pharmaceutical patents generally cover chemical structures, formulations, manufacturing processes, and therapeutic uses. The scope varies depending on how claims are drafted, balancing breadth and validity.

2. How does the patent landscape influence drug development in Mexico?
A dense patent landscape can create barriers for generic companies but also offers potential licensing opportunities and collaborations for innovator firms.

3. Can MX363715 be challenged or invalidated?
Yes. Challenges may arise based on prior art, lack of inventive step, or insufficient disclosure. Regular patent validity assessments are advisable.

4. How do international patent filings affect protection for MX363715?
Filing in multiple jurisdictions via PCT or direct applications extends protection, but each country’s patent laws and prior art standards influence validity.

5. When does MX363715 likely expire, and what does this mean for market competition?
Assuming standard 20-year terms from filing, expiration can be anticipated approximately two decades post-filing, opening markets for generics unless extensions apply.


Conclusion

Patent MX363715 embodies a strategic intellectual property asset with implications spanning legal, commercial, and R&D domains within Mexico’s pharmaceutical landscape. Its scope and claims define its protective strength, with its positioning within the patent landscape shaping competitive dynamics. Continuous monitoring and strategic planning around patent expiry, enforcement, and licensing are crucial for maximizing its value.


Sources
[1] IMPI Patent Database, official Mexican patent documents.
[2] World Intellectual Property Organization (WIPO), Patent Cooperation Treaty Patent Family Data.
[3] Mexican Patent Law, IMPI Official Publications.

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.