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Last Updated: December 29, 2025

Profile for Colombia Patent: 6801724


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US Patent Family Members and Approved Drugs for Colombia Patent: 6801724

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Detailed Analysis of the Scope, Claims, and Patent Landscape for Colombia Patent CO6801724

Last updated: August 28, 2025

Introduction

Patent CO6801724 pertains to a pharmaceutical invention registered in Colombia, reflecting strategic intellectual property (IP) protection within the country's robust legal framework. The patent primarily targets innovative compositions, formulations, or methods related to a specific therapeutic field. This analysis dissects the patent's scope, claims, and the current patent landscape surrounding it, providing a comprehensive understanding for stakeholders involved in drug development, licensing, or patent strategy.


Patent Overview and Legal Context

Colombia's patent system, governed by the Superintendencia de Industria y Comercio (SIC), grants patents with a maximum term of 20 years from the filing date. The patent environment emphasizes innovation within healthcare, incentivizing pharmaceutical advancements through rigorous examination of novelty, inventive step, and industrial applicability [1].

Patent CO6801724 was filed with a focus on pharmaceutical compositions, possibly targeting a specific disease indication or therapeutic class. The broad claims are designed to establish comprehensive protection over the key inventive aspects, including formulation specifics, methods of manufacturing, and potentially, novel uses or delivery mechanisms.


Scope of Patent CO6801724

Claim Construction

The claims define the legal scope of the patent's protection. In this case, the patent likely features multiple claims categorized into:

  • Independent Claims: Cover broad formulations or methods, establishing core inventive concepts.
  • Dependent Claims: Narrower adjuncts, specifying particular features such as excipient types, dosages, or administration routes.

Typical Scope Elements:

  • Pharmaceutical Composition: The patent might claim a combination of active ingredients with specific carriers, stabilizers, or adjuvants. The scope could encompass a novel ratio or formulation designed to improve bioavailability or stability.
  • Delivery Method: Claims could include innovative administration techniques, such as controlled-release systems, transdermal patches, or injectable formulations.
  • Use Claims: Protecting specific therapeutic indications or methods of using the composition in treating particular diseases.

Claim Language and Limitations

The language of the claims, especially the independent claims, tends to be broad but includes critical limitations to distinguish from prior art. For instance, the patent may specify:

  • The molecular structure of active compounds.
  • Specific concentration ranges.
  • Unique combinations of components with synergistic effects.
  • Manufacturing steps that yield unexpected results.

The scope thus hinges on these technical features, which demarcate protection boundaries, preventing infringement by similar formulations lacking these features.


Patent Landscape and Related IP

National and Regional Patents

  • Colombia and Latin America: The patent landscape indicates significant activity in pharmaceuticals, with many filings concentrated within Colombia, Brazil, Mexico, and Argentina. Companies often seek local protection to secure market exclusivity and leverage regional manufacturing advantages.
  • International Patents: If the applicant pursued PCT or regional filings (e.g., within the Andean Community), similar patents may exist, with comparable or broader claims, strengthening global patent rights.

Competitor and Prior Art Context

An essential part of the landscape analysis involves assessing prior art that could potentially infringe or invalidate CO6801724. Known patents or publications might include:

  • Similar drug formulations with overlapping ingredients.
  • Alternative delivery methods.
  • Known therapeutic uses for the compositions involved.

This highlights the importance of claim specificity to avoid overlaps.

Legal and Market Implications

The protection conferred by CO6801724 enhances the patent holder's market position within Colombia, preventing generic manufacturers from introducing similar products before patent expiry. Furthermore, the patent's strength depends on ongoing patentability and validity challenges, which require regular monitoring of prior art and potential third-party oppositions.


Analysis of Patentability and Innovation Strength

The patent's novelty is supported if the claimed formulation or method demonstrates a technological advance over existing therapies. Inventive step hinges on demonstrating unexpected technical effects arising from the claimed features.

Patent examiners evaluate these aspects based on prior art searches, considering both patents and scientific literature. Any disclosure prior to the filing date that anticipates or renders obvious the invention could threaten patent validity.

In Colombia, the rapid evolution of pharmaceutical technology necessitates continuous patent landscape monitoring. The specificity of claims, particularly regarding active compound ratios, manufacturing steps, or therapeutic uses, significantly influences the patent’s defensibility.


Potential Challenges and Opportunities

Challenges

  • Prior Art Rebuttal: The presence of prior art similar to the claimed invention could lead to claim narrowing or rejection.
  • Patent Lapse Risks: Expiry due to failure to pay annuities or challenge periods.
  • Infringement Risks: The presence of generic competitors or importers could lead to infringement issues.

Opportunities

  • Patent Extensions or Supplementary Protection: Given the lengthy drug development process, opportunities for extensions via supplementary protection certificates exist, where applicable [2].
  • Strategic Licensing: The patent could underpin licensing deals with local or multinational firms.
  • Market Exclusivity: Enabling exclusive marketing rights that incentivize commercialization and investment.

Conclusion and Key Takeaways

  • Scope Precision: Patents like CO6801724 must balance broad protection with detailed claims to withstand legal scrutiny and block competitors effectively.
  • Landscape Vigilance: Continuous monitoring of related patents, scientific publications, and regulatory developments is essential to maintain competitive advantage.
  • Legal Robustness: Well-drafted claims emphasizing inventive step and clear boundaries are fundamental for patent validity and enforcement.
  • Regional Focus: Colombia's active pharmaceutical patent landscape offers opportunities but necessitates strategic IP management tailored to local and regional laws.
  • Innovation Leverage: Protecting novel formulations, delivery systems, or therapeutic methods can significantly enhance market position and investor confidence.

FAQs

Q1. What are the key elements typically covered by pharmaceutical patents like CO6801724?
A1. They usually encompass active pharmaceutical ingredients, specific formulations, manufacturing processes, delivery mechanisms, and therapeutic methods, with claims tailored to distinguish the invention from prior art.

Q2. How does Colombia’s patent system support pharmaceutical innovation?
A2. Colombia provides up to 20 years of patent protection, emphasizing the novelty, inventive step, and industrial applicability of pharmaceutical inventions, thereby incentivizing research and development investments.

Q3. Can similar formulations be developed without infringing on CO6801724?
A3. Yes. Carefully designing around the claims—such as altering components, ratios, or methods—can avoid infringement if the adjustments do not fall within the patent’s scope.

Q4. What are the strategic advantages of securing patent protection in Colombia for pharmaceutical companies?
A4. It grants exclusive market rights, deters generic competition, enhances licensing opportunities, and supports market entry strategies in Latin America.

Q5. How frequently is patent landscape analysis required in the pharmaceutical sector?
A5. Regular surveillance—at least annually—is recommended to monitor new patents, emerging competitors, and evolving legal standards, ensuring sustained strategic positioning.


References

[1] Superintendencia de Industria y Comercio (SIC). Colombian Patent Law Overview. 2022.
[2] World Intellectual Property Organization (WIPO). Patent Term Extensions and Supplementary Protection Certificates. 2021.

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