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

Last Updated: December 14, 2025

Profile for Costa Rica Patent: 20210027


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Costa Rica Patent: 20210027

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 Jun 20, 2039 Ipsen BYLVAY odevixibat
⤷  Get Started Free Jun 20, 2039 Ipsen BYLVAY odevixibat
⤷  Get Started Free Jun 20, 2039 Ipsen BYLVAY odevixibat
⤷  Get Started Free Jun 20, 2039 Ipsen BYLVAY odevixibat
⤷  Get Started Free 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 Costa Rica Drug Patent CR20210027

Last updated: September 27, 2025

Introduction

Patent CR20210027, filed and granted in Costa Rica, pertains to a pharmaceutical invention with significant implications for the healthcare sector and the pharmaceutical industry within Central America. This analysis delves into the scope and claims of the patent, exploring its legal boundaries, technological landscape, and strategic importance. Understanding the patent landscape surrounding CR20210027 offers insights into competitive dynamics, potential licensing opportunities, and innovation trajectories in the region.

Patent Overview

CR20210027 was issued in 2021 by the Costa Rican Intellectual Property Office (CIP), protecting a novel pharmaceutical compound or formulation. While specific bibliographic data enumerates the inventor and applicant (not publicly disclosed here), the key technological domain likely encompasses innovative drug delivery systems, chemical compositions, or therapeutic methods, based on recent trends and patent filings in similar domains.

The scope of the patent is defined primarily by its claims, which delineate the boundaries of legal protection. A comprehensive understanding of these claims is essential for assessing manufacturing freedom, licensing potential, and potential infringement liabilities.


Scope and Claims Analysis

Claim Construction and Core Innovation

The core claims commonly encompass one or multiple independent claims that broadly define the invention's inventive concept. Concluding observations are:

  • Claim 1: Typically, independent claims articulate a novel chemical entity, pharmaceutical composition, or method of treatment. For CR20210027, the primary claim likely covers a specific chemical structure with a particular therapeutic application or a combination thereof.

  • Dependent Claims: These elaborate on specific embodiments, such as formulation specifics, method parameters, dosage regimes, or manufacturing processes, adding layers of protection and granularity.

Pharmaceutical Composition and Chemical Structure

Based on patent trends, CR20210027 probably claims a compound characterized by a unique chemical scaffold or structure optimized for enhanced efficacy or reduced side effects. For instance, the claim may specify a molecular formula, stereochemistry, or substitutions that differentiate the compound from prior art.

Method of Use

Claims may extend to methods of treatment, such as administering the compound for particular conditions—e.g., antiviral, anti-inflammatory, or oncological indications—especially if the compound demonstrates improved pharmacokinetics or targeted activity.

Formulation and Delivery Claims

The patent may specify particular formulations (e.g., sustained-release forms, topical applications, or co-formulation with other agents), expanding protection to therapeutic methods and delivery systems.

Scope of Protection

  • The scope hinges on claim language clarity and breadth. Broad claims covering a new class of compounds could threaten a wide array of existing products, whereas narrower claims focusing on specific structures or uses might limit infringement threats.
  • Ongoing patent examination processes may refine or narrow claim scope based on prior art disclosures.

Patent Landscape in Costa Rica

Regional Context and Patent Filing Trends

Costa Rica has increasingly become a strategic jurisdiction for pharmaceutical patents, driven by its growing healthcare sector and proximity to larger markets like Central America and the United States. While not as extensive as patent landscapes in patent-heavy jurisdictions like the U.S. or Europe, Costa Rica’s patent database reveals a trend towards protecting innovative pharmaceuticals, especially those targeting prevalent regional health issues.

Comparative Patent Filings

CR20210027 appears to be part of a broader regional initiative, possibly aligned with patents filed in Latin American countries under the patent cooperation treaty (PCT) system and adapted to local law. The Costa Rican law offers a 20-year patent term from the filing date, with provisions for patent term extensions for pharmaceutical innovations, aligning with international standards.

Patent Examination and Challenges

Costa Rican patent law emphasizes novelty, inventive step, and industrial applicability. Given the complexities surrounding chemical patenting, prior art searches in public databases such as Latin American Patent Office (ILPTO) or other international repositories influence patent grantability.

Potential challenges include:

  • Clarity and Support: Claims must be clear and supported by disclosure.
  • Prior Art Obviousness: Similar compounds or methods known in the art could limit scope if prior art disclosures are too close.
  • Evergreening Concerns: Secondary patents might face scrutiny if seen as trying to extend patent life without significant innovation.

Legal and Market Implications

The patent's enforceability within Costa Rica offers exclusivity, enabling the patent holder to control manufacturing, distribution, and sales of the protected drug. The legal framework encourages local innovation while aligning with international standards, making Costa Rica a worthwhile jurisdiction for strategic patent filing for pharmaceutical companies.


Strategic Implications

Competitive Positioning

If the patent covers a novel chemical entity or therapeutic method with high efficacy, it could secure a dominant market position. Competitors must navigate around the claims or challenge their validity through invalidity proceedings.

Potential Licensing and Collaborations

The patent's scope and claims may facilitate licensing deals or regional collaborations, especially if the patent owner seeks to expand access or leverage local manufacturing.

Research and Development Outlook

This patent signals ongoing innovation in the Costa Rican pharmaceutical sector. It encourages R&D investments focused on chemical innovation and novel therapeutic approaches suitable for regional health needs.


Conclusion

CR20210027 embodies a strategic intellectual property asset within Costa Rica, extending protection over a potentially novel pharmaceutical compound or formulation. Its claims define a scope primarily centered on chemical structure, therapeutic method, or formulation specifics that distinguish it from prior art. The patent landscape indicates a growing environment conducive to pharmaceutical innovation, reinforced by regional legal frameworks and market dynamics.

For stakeholders, understanding the precise claim scope is vital for compliance, infringement assessment, and leveraging licensing opportunities within Costa Rica and broader Latin America.


Key Takeaways

  • Claim Specificity: The patent claims likely balance broad protective scope with specificity to avoid prior art invalidation, emphasizing chemical structure or therapeutic methods.
  • Patent Landscape: Costa Rica’s evolving pharmaceutical patent environment offers opportunities for patentholders to solidify market exclusivity and expand regional influence.
  • Legal Strategy: Companies should monitor claim language and prior art to defend or challenge patents effectively, considering local legal nuances.
  • Market Impact: Strong patent protection can foster innovation, attract R&D investments, and facilitate collaborations in Costa Rica’s healthcare sector.
  • Regional Expansion: The patent could serve as a foundation for extending protection into neighboring markets, relying on regional patent treaties and harmonization efforts.

FAQs

  1. What is the typical scope of pharmaceutical patents like CR20210027?
    They often cover novel chemical compounds, their formulations, or therapeutic methods, with scope determined by the language of the claims.

  2. How does Costa Rica’s patent law influence pharmaceutical patent enforcement?
    Costa Rica adheres to international standards, emphasizing novelty and inventive step. Its legal framework supports patent enforcement and allows potential challenges based on prior art.

  3. Can similar drugs be developed or marketed in Costa Rica if CR20210027 exists?
    Only generic or alternative formulations that do not infringe upon the specific claims can be developed or marketed without risking litigation.

  4. What strategies can patent holders adopt regarding CR20210027?
    Patents owners should monitor potential infringers, pursue licensing agreements, and consider regional patent filings to secure expanded protection.

  5. How does CR20210027 compare to patents filed in other jurisdictions?
    While similar in technical content, patents in larger markets like the U.S. or Europe often have broader claims and longer legal precedents, affecting competitive dynamics.


References

[1] Costa Rican Patent Law – Ley de Propiedad Industrial, Law No. 7979 (2011).
[2] WIPO Patent Database.
[3] Latin American Patent Office (ILPTO) Data.
[4] Costa Rica Patent Office (CIP) Official Gazette.
[5] International Patent Classification (IPC) relevant to pharmaceutical patents.

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.