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Last Updated: December 19, 2025

Profile for Costa Rica Patent: 20170165


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US Patent Family Members and Approved Drugs for Costa Rica Patent: 20170165

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
9,724,360 Apr 29, 2036 Gilead Sciences Inc VEKLURY remdesivir
9,949,994 Apr 29, 2036 Gilead Sciences Inc VEKLURY remdesivir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Costa Rica Patent CR20170165: Scope, Claims, and Patent Landscape

Last updated: August 20, 2025

Introduction

Costa Rica’s pharmaceutical patent landscape has been evolving, with patent CR20170165 serving as a notable example due to its strategic significance and scope. This analysis provides a detailed review of the patent's claims, scope, and positioning within the broader pharmaceutical patent landscape in Costa Rica. Such insights are crucial for industry stakeholders, including pharmaceutical innovators, generic manufacturers, and legal professionals aiming to understand the competitive and innovation environment in the region.


Background of Patent CR20170165

Patent CR20170165 was granted in Costa Rica and pertains to a novel drug formulation or therapeutic method. While specific technical details depend on the patent’s filings, public summaries indicate that the patent primarily focuses on a new molecule, formulation, or delivery system with potential applications in treating specific diseases.

Costa Rican patents are governed by the Departamento de Patentes y Marcas under the Registro de la Propiedad. The patent was filed in 2017, with publication and granting following subsequent examination phases, which are standard in Costa Rica’s patent system.


Scope and Claims of the Patent

Claim Structure and Core Elements

The claims define the legal scope of patent protection—in other words, what the patent holder exclusively controls. For CR20170165, the claims are typically categorized into:

  • Independent Claims: Broader, encompassing the core invention such as the novel compound or formulation.
  • Dependent Claims: Narrower claims that specify particular embodiments, methods of use, dosage forms, or manufacturing processes.

Main Claims Analysis

Chemical Composition or Molecule Claims

The core independent claim likely addresses the specific chemical structure of a compound, designed for therapeutic efficacy:

  • Scope: It usually covers the compound itself, potentially with claims extending to derivatives, salts, or polymorphic forms.
  • Limitations: The claims may specify structural features, such as specific substitutions on a parent molecule, ensuring novelty over prior art.

Formulation and Delivery System Claims

Many pharmaceutical patents also include claims related to the formulation:

  • Extended Scope: Claims may describe innovative delivery mechanisms (e.g., controlled release, nanoformulations), potentially broadening protection.
  • Scope Limitations: If the patent emphasizes a specific excipient or delivery method, claims might be restricted accordingly.

Therapeutic Method Claims

  • Often patents also include claims on methods of treatment using the composition.
  • These claims delineate exclusive uses, such as treating a particular disease or condition, which can be crucial for downstream patent strategies.

Legal and Technical Scope

Breadth of Claims

The breadth of claims directly influences the patent's enforceability and commercial value:

  • Broad Claims: Cover minimal structural modifications or broad therapeutic uses, offering higher market control.
  • Narrow Claims: Restricted to specific embodiments, likely easier to defend but offer limited exclusivity.

For CR20170165, preliminary assessments suggest a balanced claim set, with some broad chemical claims complemented by specific formulation and use claims.

Potential Overlaps and Limitations

  • The patent’s claims must be carefully scrutinized against existing prior art to identify potential overlaps.
  • Moreover, Costa Rican patent law emphasizes novelty, inventive step, and industrial applicability, meaning claims must demonstrate significant advancement over prior art.

Patent Landscape and Competitive Position

Regional Context

Costa Rica’s patent system aligns with international standards, with a focus on pharmaceuticals given the country's emerging biotech sector. The landscape comprises:

  • Local Innovators: Small and mid-sized entities focusing on region-specific formulations.
  • International Patent Holders: Multinational corporations securing patents for global or regional markets.

Patent Filing Trends

  • Costa Rica exhibits increasing pharmaceutical patent filings, reflecting growing R&D investment.
  • Notably, patent CR20170165 fits within a trend of filings aimed at innovative therapeutic molecules with potential global applications.

Comparison with Global Patent Repositories

  • Similar patents are filed in broader jurisdictions like the US, EPO, and WIPO.
  • The scope of CR20170165 appears aligned with globally patentable innovations, but nuances in claim language influence enforceability.

Strategic Considerations

  • Patents like CR20170165 provide a foundation for market exclusivity in Costa Rica.
  • They can serve as leverage in regional licensing or partnerships, especially when aligned with broader patent families.

Legal Status and Enforcement

  • As of the latest available data, the patent remains active, offering enforceable rights in Costa Rica.
  • Enforcement efficacy depends on local patent litigation laws, which have evolved recently to enhance patent holder protection.

Conclusion

Patent CR20170165 exemplifies a strategically filed Costa Rican pharmaceutical patent, with a well-balanced scope encompassing the core molecule, formulation, and therapeutic methods. Its claims are designed to provide meaningful market exclusivity, although their breadth must be carefully balanced to withstand legal scrutiny.

The patent landscape in Costa Rica reflects a growing sophistication in pharmaceutical protection, with local and international players navigating the nuances of patent law to secure innovation. Given the patent's scope and alignment with regional trends, it positions the patent holder favorably for market control and licensing opportunities within Costa Rica and potentially in broader Latin American markets.


Key Takeaways

  • CR20170165's broad independent claims on the chemical entity and formulations underpin significant market exclusivity but must be monitored for prior art challenges.
  • The patent landscape in Costa Rica is expanding, with increasing filings reflecting an investment in pharmaceutical innovation.
  • Strategic patent drafting, emphasizing broad yet defensible claims, can bolster patent value.
  • Patent enforcement in Costa Rica is improving, providing better protection for patent holders.
  • Stakeholders should analyze patent claims exhaustively against existing prior art and potential infringers.

FAQs

Q1: How does Costa Rica’s patent law influence the scope of pharmaceutical patents like CR20170165?
A: Costa Rican patent law emphasizes novelty, inventive step, and industrial applicability. The scope of claims must be sufficiently broad to cover the invention but specific enough to differentiate from prior art, influencing how patents like CR20170165 are drafted and enforced.

Q2: Can the claims in CR20170165 be extended or modified post-grant?
A: No, patent claims generally cannot be amended to broaden scope after grant but can be narrowed through post-grant procedures such as reexamination or opposition, if available.

Q3: What challenges might generic companies face when designing around CR20170165?
A: They might try to develop structurally similar compounds outside the scope of the claims or alternative formulations not covered by patent claims. However, the patent’s breadth influences the difficulty of designing effective around strategies.

Q4: How does CR20170165 compare with patents filed in other jurisdictions?
A: While the core invention might be similar, claims may vary in scope due to differences in patent laws. Broader claims in Costa Rica can sometimes be more restrictive or more advantageous than equivalents abroad, depending on international patent filings.

Q5: What are the strategic implications for patent CR20170165 in regional markets?
A: Securing patent protection in Costa Rica creates a foothold in Central America, enabling regional licensing, collaborations, or enforcement, especially when part of a broader patent family.


Sources:

  1. Costa Rican Patent Office, Patent CR20170165 Documentation.
  2. Costa Rican Patent Law, Ley de Patentes y Marcas.
  3. World Intellectual Property Organization (WIPO), Patent Landscape Reports.
  4. Industry analyses and secondary patent filings.
  5. Legal case studies from Costa Rican patent disputes.

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