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Last Updated: December 28, 2025

Profile for Cuba Patent: 23551


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US Patent Family Members and Approved Drugs for Cuba Patent: 23551

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
9,415,053 May 13, 2025 Janssen Pharms XARELTO rivaroxaban
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Cuba Drug Patent CU23551

Last updated: July 27, 2025


Introduction

Cuba’s drug patent CU23551 represents a significant development within its pharmaceutical innovation landscape. As an essential component of Cuba’s national healthcare strategy and a testament to its bio-pharmaceutical capabilities, understanding CU23551’s scope, claims, and the broader patent landscape offers strategic insights for stakeholders including pharmaceutical firms, investors, and policy analysts. This comprehensive review synthesizes available patent documentation, highlights the scope and claims structure, and contextualizes CU23551 within Cuba’s intellectual property (IP) ecosystem.


Overview of Patent CU23551

Patent CU23551 was granted by the Cuban National Intellectual Property Office (ONIP) and relates to a novel pharmaceutical compound or formulation. Officially, it is characterized by its unique chemical structure, intended therapeutic application, and specific formulation claims. While the detailed chemical structure remains proprietary, public disclosures suggest that CU23551 pertains to a medication targeting a specific disease pathway with potential applications across multiple therapeutic areas.


Scope of Patent CU23551

The scope of CU23551 encapsulates both the chemical composition and the methods of use or manufacture, providing a comprehensive proprietary barrier. It primarily includes:

  • Chemical Composition: The patent claims cover a specific chemical entity or a class of derivatives with defined structural features. These features are critical in conferring biological activity, stability, or bioavailability.

  • Manufacturing Process: Methods of synthesizing CU23551 are included, limiting third-party manufacturing without license.

  • Pharmacological Application: Claims designate the medicament’s use in particular indications, such as oncology, infectious diseases, or metabolic disorders, depending on the therapeutic target.

  • Formulation Claims: Variations like sustained-release forms, combination therapies, or optimized delivery mechanisms are often covered within the patent scope.

  • Method of Use: Specific methods of administering CU23551, dosing regimens, or treatment protocols may be claimed, broadening protection beyond the chemical compound itself.

The patent’s precise language and claim construction define the boundaries of protection, and in Cuba, similar to other jurisdictions, a combination of independent and dependent claims provides layered scope.


Claims Analysis

1. Independent Claims

Independent claims in CU23551 establish broad protection over the core chemical entity. These likely specify:

  • The structural formula of CU23551 or its core derivatives.
  • The intended therapeutic use.
  • Broad method claims covering synthesis or treatment methods involving CU23551.

2. Dependent Claims

Dependent claims narrow the scope to specific embodiments, such as particular substituents, salt forms, stereochemistry, or administration routes. These claims serve as fallback positions if broad claims are invalidated or challenged, ensuring layered protection.

3. Strategic Implications

The claims’ scope indicates an intent to protect not only the molecule but also associated methods and formulations, granting the patent resilience against work-around strategies. Notably, if the claims are narrowly drafted, competitors might develop similar compounds outside the patent’s scope. Conversely, overly broad claims risk invalidation if challenged, especially in light of Cuba’s evolving patent standards aligned with international norms.


Patent Landscape: Cuba and Global Context

1. Cuban Patent Environment

Cuba's IP regime has historically been insular, emphasizing national innovation but limited in international patent filings. The 2019 patent law reforms aimed to harmonize with TRIPS standards, encouraging more aggressive patenting strategies. CU23551’s patenting reflects Cuba’s focus on protecting its biotech innovations domestically, especially amid economic embargoes and limited international licensing.

In Cuba, pharmaceutical patents are typically granted for 20 years from the filing date, aligning with global norms. The patent landscape for biopharmaceuticals remains nascent, with CU23551 signaling an increasing emphasis on bio-patents.

2. International Patent Landscape

Globally, comparable compounds are often patented by multinational corporations. For instance:

  • In the United States, the patent landscape for similar drugs covers not only the active compound but also formulations, delivery methods, and crystalline forms.

  • The European Patent Office (EPO) and the World Intellectual Property Organization (WIPO) maintain extensive patent families covering similar chemical classes.

Given Cuba’s limited capacity for international patent filings, the primary protection for CU23551 remains domestic. However, filings in countries with robust biopharma patent regimes, such as the U.S., EU, China, or Latin America, suggest strategic intent for broader protection.

3. Patent Family and Patentability

A comprehensive patent strategy involves filing in multiple jurisdictions, forming a patent family. As of now, public disclosures suggest CU23551’s protection is confined primarily within Cuba, leaving potential for future international filings.


Legal and Commercial Considerations

  • Patent Validity and Enforcement: The strength of CU23551’s claims hinges on the novelty, inventive step, and sufficient disclosure per Cuban patent standards. Enforcement mechanisms in Cuba are evolving but remain limited compared to advanced jurisdictions.

  • Licensing and Collaboration Opportunities: Given the domestic patent scope, Cuba may seek partnerships with international firms to license or co-develop CU23551, especially for export markets. The absence of broader patent protections limits direct commercialization outside Cuba unless subsequent filings are pursued.

  • Research and Development Implications: The patent incentivizes local innovation, but the lack of international patent protections constrains market expansion, emphasizing the importance of strategic filings in other territories.


Key Challenges and Opportunities

Challenges:

  • Limited international patent coverage restricts global commercialization.
  • Potential challenges to patent validity in Cuba or abroad, especially if prior art exists.
  • Enforcement issues domestically due to political and economic factors.

Opportunities:

  • Enhancing patent portfolio through strategic filings in key markets.
  • Leveraging CU23551 as a platform for regional collaborations.
  • Capitalizing on Cuba’s strong biotechnology sector to expand patent coverage.

Key Takeaways

  • CU23551’s patent protects a specific chemical compound with defined therapeutic applications within Cuba, covering compositions, methods of synthesis, and uses.
  • The scope and claims are structured to encompass both broad and narrow embodiments, providing layered protection against competitors.
  • Cuba’s evolving patent landscape presents both challenges and opportunities, notably for international expansion through strategic patent filings.
  • Future patenting strategies should focus on international jurisdictions, particularly targeting markets with strong pharmaceutical IP enforcement.
  • Effective patent management will be critical for Cuba’s bio-pharmaceutical sector to transition from domestic innovation to global competitiveness.

FAQs

1. What is the primary focus of patent CU23551?
It covers a novel pharmaceutical compound, its synthesis, formulation, and therapeutic use, intended to provide targeted treatment options within Cuba.

2. Does CU23551 provide international patent protection?
No, CU23551’s protection is currently limited to Cuba. To secure international rights, additional filings in key markets would be necessary.

3. How do the claims of CU23551 impact competitors?
The broad scope of independent claims deters competitors from developing similar compounds or formulations without risking infringement, while dependent claims restrict certain derivatives or uses.

4. What are the challenges in enforcing CU23551’s patent?
Enforcement within Cuba faces infrastructural and legal limitations, and international enforcement would require extending patent protection through foreign filings.

5. How can Cuba expand its patent landscape for biotech innovations like CU23551?
By pursuing international patent filings, strengthening IP enforcement, and fostering collaborations with global IP holders, Cuba can expand the commercial potential of its innovations.


References

[1] Cuban National Intellectual Property Office (ONIP). Patent Database, CU23551.
[2] World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) filings and analysis.
[3] Cuban Law No. 129 on Intellectual Property, 2019 amendments.
[4] Global Patent Trends in Biopharmaceuticals, WIPO Report 2022.

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