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Last Updated: December 31, 2025

Profile for Colombia Patent: 6321226


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US Patent Family Members and Approved Drugs for Colombia Patent: 6321226

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
7,842,714 Aug 15, 2029 Abbvie ACUVAIL ketorolac tromethamine
9,192,571 Mar 7, 2028 Abbvie ACUVAIL ketorolac tromethamine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Colombia Patent CO6321226

Last updated: August 11, 2025


Introduction

Patent CO6321226 pertains to an innovative pharmaceutical compound or formulation granted within Colombia. Understanding the scope, claims, and broader patent landscape associated with this patent is crucial for pharmaceutical companies, investors, and legal professionals engaged in the Colombian and Latin American markets. This analysis offers a comprehensive overview of the patent's legal scope, claim structure, and its position within the drug patent landscape.


1. Patent Overview and Background

Patent CO6321226 was granted by the Colombian Superintendencia de Industria y Comercio (SIC), reflecting an inventive step in pharmaceutical technology. While specific patent documentation details are essential for exact scope delineation, general patterns in such patents often encompass chemical entities, formulations, methods of use, or manufacturing processes related to a particular drug.

The patent’s strategic importance lies in its potential to protect novel active pharmaceutical ingredients (APIs), improved delivery methods, or compound formulations that confer therapeutic advantages or manufacturing efficiencies.


2. Scope of the Patent

Scope Definition

The scope of CO6321226 is primarily defined by its claims, which specify the extent of legal protection conferred. In pharmaceutical patents, claims can encompass:

  • The underlying chemical compound or molecules, including salts and stereoisomers.
  • Pharmaceutical formulations incorporating the active compound.
  • Specific methods of manufacturing or synthesizing the compound.
  • Therapeutic methods involving the compound.

Given the typical structure and scope of drug patents, it’s likely that the patent claims cover:

  • A novel chemical entity or a family of compounds with specific structural features.
  • A pharmaceutical composition comprising the compound and suitable excipients.
  • Use claims relating to the treatment of particular diseases or conditions.
  • Manufacturing techniques that improve yield, purity, or stability.

Claim Types Analysis

  • Independent claims: Usually define the core invention, such as a new chemical structure or formulation.
  • Dependent claims: Specify particular embodiments, such as specific salts, isomers, dosage forms, or methods of administration.

Example (Hypothetical):

"An isolated chemical compound of formula X, wherein the substituents are as defined herein."

or

"A pharmaceutical composition comprising compound X and a pharmaceutically acceptable excipient."

Legal Implication of Scope

The breadth of claims influences enforcement and potential challenges. Broader claims cover more embodiments but face higher scrutiny for novelty and inventive step. Narrow claims provide specific protection but limit the scope.


3. Patent Claims Analysis

3.1. Claim Breadth and Specificity

The likely claims in CO6321226 are carefully crafted to balance breadth and validity:

  • Core compound claims: Cover novel chemical entities with distinct structures or modifications.
  • Use claims: Protect therapeutic applications, e.g., "use in the treatment of..." or "method of treating..."
  • Formulation claims: Encompass specific delivery forms, such as sustained-release systems.
  • Process claims: Cover manufacturing routes, purification methods, or synthesis pathways.

The patent’s claim set likely aims to prevent third-party manufacturers from producing similar drugs by blocking the use of the protected compound or method for specific indications.

3.2. Claim Limitations

Possible limitations include:

  • Narrow structural variations or specific stereochemistry.
  • Limitation to particular formulations or administration routes.
  • Specific disease indications, especially if the compound demonstrates improved efficacy or safety profiles.

This offshoot of scope is typical in pharmaceutical patents, enabling incremental protection.


4. Patent Landscape and Strategic Position

4.1. Patent Family Context

The Colombian patent CO6321226 is likely part of a broader patent family, with corresponding patents filed in multiple jurisdictions including the US, Europe, and Latin America, to maximize market protection. These counterparts may include:

  • Composition patents.
  • Use patents.
  • Process patents.

The existence of family members enhances enforcement flexibility, enabling the patent holder to confront generic competition effectively across key markets.

4.2. Competitive Landscape

The patent landscape surrounding CO6321226 revolves around:

  • Existing patents for similar chemical classes or indications.
  • Patent expirations that could open pathways for generics.
  • Recent filings for similar compounds in Colombia and Latin America, signaling ongoing innovation activity.

4.3. Patent Validity and Challenges

Patent validity hinges on:

  • Novelty: The compound or formulation must be new.
  • Inventive Step: The invention must demonstrate unexpected advantages over prior art.
  • Industrial Applicability: The claimed subject must be practically applicable.

Third-party challenges could target scope breadth, inventive step, or prior art references, especially if similar compounds or methods exist.

4.4. Regulatory and Market Considerations

In Colombia, pharmaceutical patents are subject to examination standards aligned with international norms, but data exclusivity and supplementary protections influence market dynamics. Patent CO6321226 could effectively delay generic entry if claims are upheld, but challenges or expiry could facilitate market competition.


5. Implications for Stakeholders

For Innovators:

  • Protect a novel compound with broad claims to extend exclusivity.
  • File for key jurisdictions to secure comprehensive protection.

For Generics and Competitors:

  • Conduct thorough patent landscape analyses to identify potential infringement risks.
  • Evaluate possible challenges based on prior art or inventive step issues.

For Legal Professionals:

  • Monitor the scope of claims during patent prosecution and enforcement.
  • Prepare for potential patent challenges or licensing negotiations.

6. Conclusion and Recommendations

Patent CO6321226 appears to provide a strategic monopoly for a novel pharmaceutical compound or formulation in Colombia, with claims likely covering the compound itself, its uses, and manufacturing methods. Its strength depends on the specificity and breadth of its claims, the scope of the patent family, and its validity amid prior art challenges.

Businesses should continuously monitor the patent landscape to adjust R&D and commercialization strategies. For patent holders, broad, well-supported claims are crucial for maximizing market exclusivity and deterring infringement.


Key Takeaways

  • The patent’s scope hinges on its claims, directly affecting enforceability and competitive leverage.
  • Broad claims covering the chemical entity and its therapeutic use offer stronger market protection.
  • The patent landscape, including family members and prior art, influences patent robustness and freedom-to-operate.
  • Continuous surveillance and strategic patent filings are vital to sustain competitive advantage.
  • Legal challenges must target specific claim limitations or prior art to be effective.

FAQs

Q1: How does the scope of patent CO6321226 influence market exclusivity in Colombia?
A1: A broader scope enhances market exclusivity by covering multiple embodiments and formulations, deterring competitors from entering similar markets without infringing.

Q2: Can the claims in CO6321226 be challenged legally?
A2: Yes, challenges can target lack of novelty, inventive step, or insufficient disclosure, especially if prior art demonstrates similar compounds or technology.

Q3: What is the significance of patent family filings for this drug?
A3: Family filings extend the patent’s territorial coverage, ensuring protection across various markets, which is critical for global commercialization strategies.

Q4: How does Colombia’s patent law impact the enforceability of CO6321226?
A4: Colombian law requires patents to meet novelty and inventive step criteria; robust claims and thorough prosecution increase enforceability.

Q5: What strategies should innovators adopt post-grant?
A5: Monitor for potential infringement, defend claims actively, and consider supplementary protections like data exclusivity or supplementary patents for formulations and uses.


References

[1] Superintendencia de Industria y Comercio (SIC). Patent database, Colombia.
[2] WIPO PATENTSCOPE. International patent filings and family data.
[3] World Patent Information. Patent law and pharmaceutical patent strategies.

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