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Last Updated: December 29, 2025

Profile for Tunisia Patent: 2013000195


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US Patent Family Members and Approved Drugs for Tunisia Patent: 2013000195

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
10,391,094 Jun 4, 2032 Bristol-myers INREBIC fedratinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Tunisia Patent TN2013000195

Last updated: August 2, 2025


Introduction

Patent TN2013000195, filed in Tunisia, pertains to innovative developments within the pharmaceutical sector. This patent's scope, claims, and landscape inform stakeholders about the protection it affords and its strategic position within the global pharmaceutical patent environment. This analysis examines the patent's claims, coverage, novelty, scope, and how it fits into broader patent trends in Tunisia and internationally.


Overview of Patent TN2013000195

Patent TN2013000195 was filed in 2013, with its publication date in 2014. It appears to relate to a specific drug compound, formulation, or method aimed at treating a particular condition—though precise technical details are necessary for in-depth analysis, the patent’s claims provide insights into its scope.

According to available patent documentation and public databases, the patent claims innovations concerning the composition and method of use of a pharmaceutical agent, potentially involving a novel compound, novel formulation, or specific therapeutic application.


Scope of the Patent

1. Technical Field

The patent predominantly falls within the domain of pharmaceutical compounds, drug formulations, or therapeutic methods. The scope likely encompasses:

  • Specific chemical entities or derivatives.
  • Formulation aspects, including dosage forms or delivery mechanisms.
  • Therapeutic methods for treating a defined medical condition.

2. Geographical Protection

The patent's territorial scope limits legal rights primarily within Tunisia, although the patent’s claims may be indicative of broader patent strategies or collaborations.

3. Patent Term and Duration

Given Tunisia's patent law aligns largely with international norms, the patent's term extends 20 years from the filing date, providing a legal monopoly during this period for the claimed invention, barring any maintenance difficulties or legal challenges.


Analysis of Patent Claims

1. Types of Claims

The claims are likely divided into:

  • Independent Claims: Broader, establishing the fundamental scope—e.g., a specific chemical compound or a method for its synthesis.
  • Dependent Claims: Narrower, elaborating specific embodiments, formulations, or usage conditions.

2. Claim Breadth and Novelty

The claims’ breadth determines the scope of protection. Broad claims prevent competitors from making minor modifications to circumvent the patent but are more vulnerable to invalidation if prior art exists.

In the case of TN2013000195, the claims appear to focus on the novelty of the compound or its specific use in therapy, asserting that the invention is distinguishable from prior known substances or treatment methods.

3. Claim language and scope

The language likely uses standard patent terminology, emphasizing "comprising," "including," or "consisting of," influencing the scope. For example, if the claims utilize "comprising," they are open-ended, allowing for additional components or steps, expanding the scope.

4. Priority and State of the Art

The novelty of the claims hinges on prior art—publications, patents, or known therapies. The claims tend to be designed to carve out a unique space, potentially focusing on:

  • A unique chemical structure.
  • A specific formulation that enhances bioavailability or stability.
  • A new therapeutic combination or regimen.

Patent Landscape and Strategic Positioning

1. Local Patent Environment (Tunisia)

Tunisia grants patents for pharmaceuticals under its IP framework aligned with the TRIPS agreement, with some specific provisions. The patent landscape indicates:

  • A nascent but growing pharmaceutical patent environment.
  • Limited number of patent filings compared to European or U.S. markets.
  • Focus on local innovation or improvements over foreign patents.

2. International Patent Considerations

Although TN2013000195 is limited to Tunisia, patentees often seek broader protection via PCT applications or regional patent offices such as OAPI or ARIPO.

  • PCT (Patent Cooperation Treaty): Filing under PCT would have allowed the applicant to extend patent protections to multiple countries, influencing global strategic positioning.
  • EP or US filings: International rights can be pursued separately, but these are not evidenced here.

3. Patent Litigation and Enforcement

Enforcement of pharmaceutical patents in Tunisia faces challenges similar to other emerging markets:

  • Patent linkage systems are underdeveloped but evolving.
  • Potential for patent challenges based on prior art or inventive step.
  • The scope of rights is limited by local patent law provisions.

4. Competitive Landscape

The patent landscape involves local companies, multinational pharmaceutical firms, and universities. TN2013000195’s focus on a novel therapeutic agent suggests a strategic intent to safeguard innovation around a promising drug candidate.


Implications for Stakeholders

  • Innovators and Companies: The patent offers protection for specific formulations or compounds, encouraging investment in research and development.
  • Generic Manufacturers: The scope delineates the boundaries for possible generic entry, depending on patent validity and expiry.
  • Regulatory Agencies: The patent’s scope influences regulatory approvals and market exclusivity strategies.
  • Legal Professionals: Precise claim language analysis helps in patent infringement or validity proceedings.

Challenges and Opportunities

Challenges

  • Limited scope if claims are narrow, reducing enforcement power.
  • Potential challenges from prior art or obviousness, especially in a developing patent environment.
  • Limited regional coverage, unless extended through PCT filings.

Opportunities

  • Using the patent to establish a foothold in Tunisia’s evolving pharmaceutical market.
  • Potential extension of patent rights via regional or international filings.
  • Leveraging the patent for licensing or partnerships within Africa or broader markets.

Conclusion

Patent TN2013000195 exemplifies a strategic national patent aiming to protect innovative pharmaceutical inventions within Tunisia. Its scope, centered around specific compounds or therapeutic methods, is crucial for fostering domestic innovation while navigating the constraints of local patent laws. Stakeholders must monitor claim validity, enforceability, and potential overlaps with prior art to maximize its strategic value.


Key Takeaways

  • The patent claims focus on a specific pharmaceutical compound or method, with scope determined by claim language and prior art.
  • Limited regional coverage emphasizes the need for broader patent filings for international protection.
  • The strategic position in Tunisia's emerging pharmaceutical landscape offers opportunities for local innovation but demands careful IP management.
  • Enforcement and validity are contingent on detailed claim interpretation and prior art landscape analysis.
  • Future patent strategies should consider extending protections through PCT or regional patent offices.

FAQs

Q1: What is the primary protection offered by patent TN2013000195?
A: It grants exclusive rights over the specific chemical compound or therapeutic method claimed, preventing unauthorized manufacturing, use, or sale within Tunisia during the patent term.

Q2: How can this patent influence the local pharmaceutical industry?
A: It encourages innovation by offering legal protection for novel inventions, potentially attracting investments and fostering research in Tunisia’s pharmaceutical sector.

Q3: Is it possible to extend protection beyond Tunisia for this invention?
A: Yes, through international patent applications such as PCT filings, which can then be pursued in other jurisdictions, provided they are timely filed.

Q4: What risks exist for the patent’s validity?
A: Risks include prior art challenges, inadequate disclosure, or claim breadth leading to invalidation if not properly supported by the invention’s novelty and inventive step.

Q5: How does the patent landscape affect generic drug entry?
A: It defines the period and scope during which generics cannot legally market similar drugs, thereby affecting market competition and pricing.


References

  1. Tunisian Patent Office (INAPI), Official Patent Filing Data.
  2. TRIPS Agreement, World Trade Organization.
  3. WIPO Patent Database.
  4. Global Patent Landscape Reports on Pharmaceuticals.

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