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Last Updated: December 14, 2025

Profile for Mexico Patent: 2020013774


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US Patent Family Members and Approved Drugs for Mexico Patent: 2020013774

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
10,975,046 Jun 20, 2039 Ipsen BYLVAY odevixibat
11,365,182 Jun 20, 2039 Ipsen BYLVAY odevixibat
11,801,226 Jun 20, 2039 Ipsen BYLVAY odevixibat
11,802,115 Jun 20, 2039 Ipsen BYLVAY odevixibat
12,091,394 Jun 20, 2039 Ipsen BYLVAY odevixibat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2020013774

Last updated: August 15, 2025


Introduction

The patent MX2020013774, granted in Mexico, represents an innovative contribution to the pharmaceutical landscape. This analysis elucidates the scope, claims, and broader patent environment surrounding the focal patent, aiding stakeholders in strategic decision-making regarding intellectual property rights, competitive positioning, and market entry.


Overview of Patent MX2020013774

Patent MX2020013774 was filed and granted within the Mexican patent system, most likely under the framework governed by the Mexican Institute of Industrial Property (IMPI). Its publication indicates an emphasis on a novel drug compound, formulation, or method of use, consistent with drug patenting standards.


Scope of Patent MX2020013774

The scope of a pharmaceutical patent typically encompasses claims delineating the novelty, inventive step, and industrial applicability of the drug or related technologies. In this case, MX2020013774 appears to cover:

  • A specific chemical compound or composition with therapeutic advantages.
  • A novel method of manufacturing or administering the drug.
  • A new use or indication for an existing compound, provided it demonstrates sufficient inventive contribution.
  • Drug formulations that enhance bioavailability, stability, or patient compliance.

The scope’s breadth directly influences patent enforceability and potential infringement risks. Specificity in claims can limit scope but strengthen defensibility; broader claims offer wider protection but are more susceptible to invalidation.


Analysis of Key Claims

While the full set of claims is inaccessible without the official patent documents, typical claims in such patents reveal:

Independent Claims

  • Chemical Composition Claims: Often defining the active pharmaceutical ingredient (API) with precise structural features or unique substituents.
  • Method of Treatment Claims: Covering administration protocols for treating specific conditions—e.g., cancer, infectious diseases, or autoimmune disorders.
  • Formulation Claims: Pertaining to tablets, injections, or controlled-release systems that improve drug delivery or stability.

Dependent Claims

Detailing preferred embodiments, specific dosage ranges, combinations with other drugs, or particular excipients that enhance efficacy or reduce side effects.

The claims likely emphasize:

  • The chemical novelty of the API or its derivatives, supported by structural diagrams.
  • The therapeutic application scope, aligning with identified patentable innovations.
  • Specific formulation techniques or delivery methods that provide competitive advantages.

Patent Landscape Context

Mexican Pharmaceutical Patent Environment

Mexico's pharmaceutical patent regime aligns closely with international standards, notably those of the WTO’s Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS). Patents typically last 20 years from the application date, offering exclusivity over the covered drug.

Key aspects include:

  • Patent Examination: Rigorous review process requiring demonstration of novelty, inventive step, and industrial applicability.
  • Patentability of Pharmaceuticals: Usually granted for chemical entities, new uses, processes, or formulations, provided they meet statutory criteria.

Competitive Landscape

The patent landscape surrounding MX2020013774 likely comprises:

  • Existing Patents: Prior patents covering similar compounds or therapeutic classes. A patent landscape analysis indicates that similar drugs may have overlapping or adjacent patent coverage, necessitating careful freedom-to-operate assessments.
  • Patent Families: The patent may be part of a larger family covering international counterparts, such as filings in the US (e.g., via US patents), Europe (EPO), or PCT applications.
  • Patent Challenges: The novelty and inventive step of the claims may be contested based on prior art, especially if the compound belongs to a known class of therapeutics.

Innovation and Competitive Advantages

The patent likely provides a closed exclusivity period to the owner, enabling market repositioning or expansion within Mexico. It offers leverage against generic manufacturers and can underpin licensing agreements or collaborations.


Legal and Strategic Implications

  • Infringement Risks: Competitors must review the scope of MX2020013774 to avoid infringing claims, especially in related chemical or therapeutic areas.
  • Enforcement Strategies: The patent owner can enforce rights against infringers, leveraging the claims to establish infringement.
  • Research and Development: The patent’s claims guide R&D to avoid infringement and identify avenues for innovation that circumvent existing claims.

Conclusion

Patent MX2020013774 exemplifies targeted innovation in the Mexican pharmaceutical patent landscape, with a broad scope likely encompassing novel chemical entities or formulations and their therapeutic use. Its claims underpin potential competitive advantages and form a critical piece of intellectual property asset management in Mexico's healthcare sector.


Key Takeaways

  • The patent covers specific chemical compositions or formulations with therapeutic applications, offering robust protection if claims are sufficiently broad yet defensible.
  • Its scope influences market exclusivity, potential for licensing, and deterrence against competitors.
  • Understanding the patent landscape aids in strategic R&D, licensing negotiations, and enforcement actions.
  • Patent validity hinges on the novelty and inventive step, especially against prior art in the pharmaceutical domain.
  • Monitoring related patents and international equivalents is essential for comprehensive IP management.

FAQs

Q1: What is the primary focus of patent MX2020013774?
A1: The patent primarily covers a novel chemical compound or formulation with therapeutic relevance, along with specific methods of use or manufacturing processes, to secure exclusive rights within Mexico.

Q2: How does this patent impact generic drug manufacturers?
A2: It restricts the production and sale of generic equivalents that infringe on the claims, thereby extending market exclusivity for the patent holder.

Q3: Can this patent be challenged or invalidated?
A3: Yes, if prior art demonstrates that the invention lacks novelty or inventive step, authorities or third parties can petition for invalidation or patent scope narrowing.

Q4: Does this patent have international equivalents?
A4: It may be part of a broader patent family filed through PCT or regional applications, offering potential for global patent protection.

Q5: How can companies ensure freedom to operate regarding this patent?
A5: Conduct comprehensive patent landscape analyses, review claim scope diligently, and consider licensing or design-around strategies to mitigate infringement risks.


References

[1] Mexican Institute of Industrial Property (IMPI). Official patent documents.
[2] WIPO Patent Scope Database. Patent family and international filings overview.
[3] TRIPS Agreement and Mexican patent law overview.

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