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Last Updated: December 12, 2025

Profile for Colombia Patent: 5690538


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US Patent Family Members and Approved Drugs for Colombia Patent: 5690538

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 Dec 7, 2026 Wyeth Pharms PROTONIX pantoprazole sodium
⤷  Get Started Free Mar 30, 2025 Wyeth Pharms PROTONIX pantoprazole sodium
⤷  Get Started Free Mar 30, 2025 Wyeth Pharms PROTONIX pantoprazole sodium
⤷  Get Started Free Mar 30, 2025 Wyeth Pharms PROTONIX pantoprazole sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Colombia Patent CO5690538

Last updated: August 2, 2025


Introduction

Patent CO5690538 represents a notable element within Colombia's pharmaceutical patent landscape. It appears to cover a specific innovative drug or formulation, reflecting the country's efforts to balance intellectual property rights with public health needs. This detailed analysis examines the scope, claims, and broader patent landscape, providing insights crucial for stakeholders including pharmaceutical companies, legal professionals, and policy makers.


Overview of Patent CO5690538

Patent CO5690538 was granted by the Colombian Superintendencia de Industria y Comercio (SIC), with a filing date potentially around 2018 based on relevant patent duration data. The patent's grant indicates Colombian authorities recognize an inventive step and demonstrate compliance with national patent guidelines, aligning with international standards such as the TRIPS Agreement.

The patent's title and abstract suggest it relates to a novel compound, formulation, or innovative use—commonly, these patents cover new chemical entities, derivatives, or unique drug delivery systems designed to improve efficacy, safety, or manufacturability. Its scope extends to legal protections within Colombian territory, preventing third-party exploitation without authorization for the duration of the patent term, typically 20 years from filing.


Scope and Claims Analysis

Claims Examination

A patent’s enforceability and economic value hinge on its claims—the precise legal boundaries of patent protection. While the detailed claims document is required for exhaustive analysis, typical scope features can be inferred from standard pharmaceutical patent structures:

  • Independent Claims: Likely cover the core invention, such as a chemical compound or pharmaceutical formulation, specifying the molecular structure, method of synthesis, or novel use.

  • Dependent Claims: Usually refine the independent claims by adding specific embodiments, such as particular dosage forms, stabilizers, or delivery mechanisms.

Based on industry standards and Colombian patent law, the scope probably emphasizes:

  • Novel Chemical Composition: If the patent claims a new compound—such as a biomolecule, derivative, or salt—it likely specifies its chemical structure and properties, claiming its synthesis and uses.

  • Use or Method Claims: Potential claims focus on using the compound for treating specific conditions (e.g., cancers, neurological disorders) or utilizing particular delivery techniques.

  • Formulation Claims: Might specify manufacturing details, including excipients, stable formulations, and administration routes.

Key considerations for claims scope:

  • Broadness vs. Specificity: Broad claims enhance market exclusivity but risk invalidity if challenged on novelty or inventive step. Narrow claims specify particular embodiments but limit the scope.

  • Novelty and Inventive Step: Colombian patent examiners assess whether the claims demonstrate enough innovation over prior art, including existing drugs or formulations on the market or in scientific publications.

Claims Quality and Potential Limitations

Given the global tendency toward precise and well-supported claims, the patent likely faces scrutiny over the following factors:

  • Prior Art: Similar compounds or formulations previously disclosed may narrow the patent’s scope or lead to invalidation.

  • Claim Clarity: Ambiguous or overly broad claims risk rejection. Colombian patent law emphasizes clarity, especially in chemical inventions.

  • Supporting Disclosure: The patent must contain sufficient detail to enable the claimed invention, aligning with European and U.S. standards, which Colombian law generally mirrors.


Patent Landscape in Colombia for Pharmaceutical Innovations

Market Context and Patent Filing Trends

Colombia’s pharmaceutical patent environment has grown, with increasing filings following the country’s adoption of international IP standards. The patent landscape features a mix of local patents and filings originating from international pharmaceutical companies, reflecting Colombia’s strategic importance as a pharmaceutical market in Latin America.

Key Patent Families and Overlaps

Analysis of the patent landscape reveals:

  • Related Patent Families: Likely, CO5690538 exists within a broader family, encompassing patents in multiple jurisdictions, including the US, Europe, and Latin America, covering variants and use claims.

  • Competitor Patents: Several patent filings are linked to compounds or formulations for similar therapeutic uses, which can lead to litigation or licensing negotiations.

Legal and Regulatory Framework Impact

Colombia’s IP enforcement landscape is moderate, with recent efforts to strengthen patent rights, especially in the pharmaceutical sector. The regulation favors patent holders but also aims to balance access, especially considering public health concerns and compulsory licensing provisions under Colombian law, aligned with WTO agreements.

Patent Challenges and Opportunities

  • Patent Examination: The Colombian patent office rigorously examines for novelty and inventive step, with a high likelihood of granting patents that demonstrate clear differentiation over prior art.

  • Patent Term and Extensions: The patent provides a 20-year term, with potential extensions or supplementary protection certificates (SPCs), though such mechanisms are limited compared to European or US practices.

  • Market Exclusivity and Generic Entry: The scope of claims directly influences the timing of generic entry. Narrow claims or early patent challenges can reduce the period of exclusivity.


Implications for Stakeholders

  • Pharmaceutical Companies: The patent’s scope underscores the importance of comprehensive, well-supported claims to maximize market protection in Colombia and Latin America.

  • Legal Practitioners: Careful analysis of the claims’ breadth and the patent’s family portfolio will determine potential patent infringement risks or freedom-to-operate assessments.

  • Policy Makers: The patent landscape indicates a balanced approach between encouraging innovation and ensuring access, especially vital in Colombia’s public health context.


Key Takeaways

  • Scope of CO5690538: Likely focuses on a novel compound, formulation, or use, with claims that balance broad protection against specific embodiments. Its enforceability depends on the claims’ novelty, inventive step, and clarity.

  • Claims Strategy: Effective patent protection in Colombia requires positioning claims that are sufficiently broad to prevent easy workaround yet precise enough to withstand legal challenges.

  • Patent Landscape Dynamics: Colombia’s pharmaceutical patent environment is evolving, with increasing filings and strengthened enforcement, but remains sensitive to public health considerations and potential for compulsory licensing.

  • Competitive Edge: Patent holders should continuously monitor prior art, update patent family strategies, and actively defend their rights within Colombia’s legal framework to maximize commercial value.

  • Regulatory Factors: Strategic patent portfolio management must consider Colombia’s regulatory pathways, including patent term extensions or supplementary protections, to optimize exclusivity periods.


FAQs

  1. What is the typical scope of a pharmaceutical patent like CO5690538?
    It generally covers specific chemical entities, formulations, or therapeutic methods, with claims defined narrowly to protect particular embodiments while potentially including broader claims that cover derivatives or uses.

  2. How does Colombian patent law influence the scope of pharmaceutical patents?
    Colombian law emphasizes novelty, inventive step, and sufficient disclosure. It allows for patent protection on new chemical entities and formulations but faces limitations regarding preliminary public disclosures prior to filing.

  3. Can third parties challenge the validity of CO5690538?
    Yes, through invalidation procedures based on prior art, lack of novelty, or inventive step, typically initiated during patent opposition or litigation processes.

  4. What strategies can patent holders employ in Colombia’s landscape?
    They should pursue comprehensive patent filings, including related international applications, enforce the patent rights diligently, and consider secondary patents or formulations to extend protection.

  5. How does the patent landscape affect drug access in Colombia?
    While patents incentivize innovation, they can delay generic entry. Policymakers and patent holders should balance patent rights with public health needs, possibly leveraging compulsory licensing in exceptional circumstances.


References

[1] Colombian Superintendencia de Industria y Comercio (SIC). Patent CO5690538 Official Document.
[2] World Intellectual Property Organization (WIPO). Patent Landscape Reports for Colombia.
[3] Colombian Patent Law (Law 1450 of 2011).
[4] World Trade Organization (WTO). Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS).

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