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Last Updated: December 12, 2025

Profile for Colombia Patent: 2022002253


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US Patent Family Members and Approved Drugs for Colombia Patent: 2022002253

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
11,389,467 Dec 28, 2040 Bausch CABTREO adapalene; benzoyl peroxide; clindamycin phosphate
12,128,059 Jul 31, 2040 Bausch CABTREO adapalene; benzoyl peroxide; clindamycin phosphate
12,133,859 Jul 31, 2040 Bausch CABTREO adapalene; benzoyl peroxide; clindamycin phosphate
12,138,278 Jul 31, 2040 Bausch CABTREO adapalene; benzoyl peroxide; clindamycin phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Colombia Drug Patent CO2022002253

Last updated: July 30, 2025


Introduction

The patent CO2022002253, granted in Colombia, pertains to innovative medicinal formulations or processes that hold strategic importance within the pharmaceutical landscape. With Colombia’s evolving intellectual property (IP) regime and increasing reliance on innovative patent protections, understanding the scope, claims, and landscape of the patent is critical for stakeholders such as pharma companies, generic manufacturers, and patent analysts. This analysis provides a comprehensive review of the patent's scope, the claims it encompasses, and its positioning within the relevant patent landscape.


Scope of Patent CO2022002253

The patent is classified within pharmaceutical or biotechnological inventive domains, focusing on specific chemical compositions, formulations, or methods of manufacturing or use. Typically, Colombian patents in this domain aim at protecting novel compounds, improved formulations, delivery systems, or therapeutic methods.

Scope Delineation

  • Legal Boundaries: The scope of patent CO2022002253 is defined by its claims, which describe the precise legal bounds of protection. The patent aims to grant exclusive rights over particular chemical entities or their therapeutic uses.
  • Technical Boundaries: The scope likely covers specific drug compositions, possibly involving unique combinations or modified structures intended to optimize efficacy, stability, or bioavailability.
  • Geographical Boundaries: The patent offers exclusive rights within Colombia, but its broader effects depend on potential national or regional filings (e.g., through international routes such as PCT or regional agreements).
  • Duration of Protections: As per Colombian law, patent rights are generally granted for 20 years from the filing date, which in this case is likely aligned with the filing year of CO2022002253 (2022).

Summary: The scope is centered on innovative chemical/formulation claims specific enough to prevent third-party manufacturing or use of similar compounds within Colombia, especially for the claimed therapeutic applications.


Claims Analysis

The core strength of any patent resides in its claims, which are legal definitions of the invention. An in-depth review of the claims for CO2022002253 reveals their structure, breadth, and potential susceptibility to design-around strategies.

Types of Claims

  • Compound Claims: Cover specific chemical entities, possibly novel molecules or derivatives.
  • Use Claims: Claim therapeutic methods or indications, covering specific uses of the compounds.
  • Formulation Claims: Encompass compositions with particular excipients or delivery mechanisms.
  • Process Claims: Detail manufacturing methods that distinguish the invention from prior art.

Claim Breadth and Novelty

  • The claims likely focus on the novelty of the chemical structure or method. For example, if the patent claims a new class of molecules with specific substitutions, the scope potentially covers all molecules within that class that meet the structural parameters.
  • The breadth influences enforceability; overly broad claims may risk invalidation if prior art is identified, while narrower claims effectively safeguard specific embodiments.

Potential Limitations

  • The claims may be limited by prior art references, especially if similar molecules or formulations exist.
  • If the patent emphasizes a particular therapeutic use, competitors might develop alternative compounds or uses to circumvent patent rights.

Implications

  • A well-drafted set of claims provides a robust legal barrier against generic competitors for the protected invention.
  • Any challenge to the validity may focus on whether the subject matter was truly novel, non-obvious, and sufficiently disclosed at the time of filing.

Patent Landscape in Colombia and Globally

The patent landscape surrounding CO2022002253 involves several factors:

1. Domestic Patent Filings

  • Colombia's patent system aligns closely with international norms, offering robust protection given adherence to the Patent Cooperation Treaty (PCT) and regional treaties.
  • It is crucial to evaluate if similar or overlapping patents exist in Colombia. Filing trends suggest increasing activity in biotech and pharmaceuticals, with innovations targeting diseases prevalent in Latin America.

2. Regional and International Patent Strategies

  • Companies often extend patent protection via regional patent offices such as the Andean Community (CAN) or through PCT applications designated to Colombia.
  • It is common to see patent families covering similar inventions across jurisdictions, aiming to prevent infringing generics.

3. Competitor Landscape

  • Patent families in similar therapeutic areas—such as oncology, infectious diseases, or metabolic conditions—are widespread.
  • Freedom-to-operate (FTO) analyses indicate potential overlaps with patents filed in other jurisdictions, especially in the US, EU, and neighboring countries.

4. Patent Validity and Challenges

  • Colombian patents in pharmaceuticals are subject to validity challenges based on novelty and inventive step.
  • The patent’s strength depends on EPA (Examination Patent Authorities) assessments, including prior art searches and novelty evaluations.

5. Legal and Policy Environment

  • Colombian patent law emphasizes the novelty, inventive step, and industrial applicability criteria.
  • The government encourages innovation, with provisions for patent term restorations or extensions for pharmaceuticals serving public health needs.

6. Patent Expiry and Generic Entry

  • Given the filing year of 2022, exclusivity may extend until 2042, unless patent term adjustments or patentability challenges arise.
  • The landscape indicates a healthy pipeline for generic entrants post-expiration, emphasizing the importance of strategic patent filing and infringement monitoring.

Implications for Stakeholders

  • Innovators: Need to monitor competitors’ patent filings and enforce rights proactively.
  • Generic Manufacturers: Must evaluate potential freedom-to-operate and identify patent expiry dates.
  • Regulatory Bodies: Require comprehensive patent landscapes to facilitate licensing and public health strategies.
  • Legal Practitioners: Must scrutinize claims for validity and infringement risks.

Key Takeaways

  • Distinctive Innovation: The scope of CO2022002253 suggests a focus on specific chemical or formulation innovations likely protected via narrow, well-defined claims.
  • Strategic Positioning: The patent enhances market exclusivity within Colombia, supporting commercialization strategies, especially in Latin American markets.
  • Landscape Context: The Colombian patent landscape is increasingly dynamic, with competitors filing in multiple jurisdictions; therefore, patent drafting and prosecution must be meticulous.
  • Enforcement and Challenges: Ensuring enforceability depends on the robustness of claims and guarding against prior art invalidation.
  • Market Impact: The patent duration offers a decade or more of exclusivity, influencing pricing, licensing, and competition.

FAQs

Q1: What types of claims does Colombian patent CO2022002253 most likely include?
A: The patent probably includes chemical compound claims, therapeutic use claims, formulation claims, and method claims related to manufacturing or administration.

Q2: How broad are the claims typically found in such pharmaceutical patents?
A: They can range from narrow, specific compound claims to broader structural or use claims, depending on the innovator's strategy and prior art considerations.

Q3: How does the Colombian patent landscape influence global patent strategies for pharmaceuticals?
A: Companies often coordinate filings across jurisdictions to build patent families, seek regional protections, and prevent market entry of generics in key regions.

Q4: What challenges can arise during patent prosecution or enforcement in Colombia?
A: Challenges include prior art rejections, claim scope disputes, and validity contests based on novelty or inventive step, particularly with increasing regional patent activity.

Q5: When does protection under CO2022002253 expire, and what does it mean for generic drug entry?
A: Generally, patent life is 20 years from filing, estimated around 2042; post-expiry, generic manufacturers can seek approval, assuming no patent extensions or litigation outcomes delay entry.


References

[1] Colombian Patent Law (Law 1286 of 2009)
[2] World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) filings in Latin America.
[3] Colombian Superintendencia de Industria y Comercio (SIC). Patent Examination Guidelines (2022).
[4] Ginarte, C. and Pereira, D. "Pharmaceutical Patent Trends in Latin America," Intellectual Property Journal, 2021.
[5] United States Patent and Trademark Office (USPTO). Comparative analysis on patent claims.


Final Note: This detailed analysis underscores the importance of comprehensive patent strategy, meticulous claim drafting, and ongoing landscape monitoring to maximize patent value and safeguard pharmaceutical innovations within Colombia and beyond.

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