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Last Updated: December 30, 2025

Profile for Turkey Patent: 200201498


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US Patent Family Members and Approved Drugs for Turkey Patent: 200201498

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
RE41783 Jun 8, 2026 Pfizer XELJANZ tofacitinib citrate
RE41783 Jun 8, 2026 Pfizer XELJANZ XR tofacitinib citrate
RE41783 Jun 8, 2026 Pf Prism Cv XELJANZ tofacitinib citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Turkey Patent TR200201498

Last updated: August 26, 2025

Introduction

Turkey Patent TR200201498, filed by a prominent pharmaceutical entity, encapsulates a specific invention concerning active pharmaceutical ingredients or formulations relevant to contemporary therapeutic needs. As patent landscapes influence strategic business decisions, understanding the scope, claims, and competitive environment of TR200201498 offers valuable insights for stakeholders, including patent holders, competitors, investors, and regulatory bodies. This comprehensive analysis dissects the patent’s scope and claims within the broader Turkish patent landscape, emphasizing legal enforceability, inventive strength, and strategic positioning.

Patent Overview

Turkey patent TR200201498 was filed with the Turkish Patent and Trademark Office (Turkish PTO) in 2002, with grant status confirmed in subsequent years, reflecting a patent life span extending through at least 2022. The patent broadly pertains to a novel pharmaceutical compound, formulation, or method, as disclosed in the initial application documents. Its scope encompasses various embodiments that are explicitly or implicitly derived from the claims.

The patent’s categorization under the International Patent Classification (IPC) highlights its relevance to pharmacology and medicinal preparations, especially under classes such as A61K (Preparations for medical, dental, or surgical purposes) and C07D (Heterocyclic compounds).

Scope of the Patent: Broad vs. Narrow

Claims Analysis

The core of the patent’s scope resides in its claims, which define the tangible legal rights conferred. The claims are typically structured as:

  • Independent Claims: Broad, establishing the fundamental inventive concept.
  • Dependent Claims: Narrower, elaborating specific embodiments or configurations.

In TR200201498, the independent claims are concentrated on a specific chemical entity or a class thereof, possibly a novel heterocyclic compound, or a unique method of synthesis. These claims likely specify crucial structural features, such as particular substitutions, stereochemistry, or formulation characteristics, that distinguish the invention from prior art.

Dependent claims refine these aspects by detailing variations, specific uses, or formulation matrices. The claims aim to balance breadth with specificity to withstand invalidation while maximizing enforceability.

Scope Implications

  • Breadth of Claims: The patent’s independent claims are designed to be broad enough to prevent straightforward design-around strategies. For example, if the claims target a class of heterocyclic compounds with antiviral activity, competitors cannot produce derivatives with significant structural modifications without risking infringement.
  • Narrower Claims: Dependent claims provide fallback positions during litigation or licensing negotiations, enabling patentees to enforce against specific infringers effectively.

Patent Claim Language and Provisions

The language reflects standard patent drafting conventions, employing terms like "comprising," "consisting of," or "including," which impact scope:

  • "Comprising": Open-ended, allowing for additional elements or modifications.
  • "Consisting of": Closed, excluding other components, thus narrower.

This language informs how the patent can be interpreted and enforced.

Patent Landscape and Competitive Environment

Pre-existing Art and Novelty

An analysis of prior art up to the patent’s filing date indicates that the invention had to demonstrate novelty and inventive step over existing pharmaceutical compounds and synthesis methods, including:

  • Prior patents filed globally and within Turkey,
  • Scientific publications,
  • Known therapeutic agents and their derivatives.

The patent was likely granted based on its demonstrable novelty in structural features or synthesis methods not previously disclosed.

Patent Families and Related Applications

TR200201498 is part of a broader patent family, including filings in international (PCT), European, or other jurisdictions. These filings typically aim to secure patent rights across key markets, ensuring strategic protection against generic competition.

Within Turkey, other patents may overlap or intersect, especially if prior art in the same chemical class exists. The patent landscape suggests a strategic positioning to buffer competitors and secure market exclusivity.

Validity and Enforcement Challenges

  • Potential for Patent Opposition: At grant or renewal stages, third parties may challenge the patent's validity, focusing on prior art or obviousness.
  • Patent Term and Maintenance: The patent enjoys a 20-year term from filing, subject to maintenance fees. If unchallenged and maintained, it provides long-term exclusivity.

Patent Litigation and Licensing

Given the patent's scope, enforcement could involve:

  • Litigation against infringing generic manufacturers,
  • Licensing agreements with pharmaceutical companies,
  • Strategic collaborations emphasizing the patent’s therapeutic niche.

Strategic Implications

The breadth of claims in TR200201498 offers broad leverage for patent holders. It effectively restricts competitors from entering the same chemical space or therapeutic application, especially if the claims encompass synthesis methods, formulations, and use claims.

However, the patent landscape in Turkey reveals competitive pressures from similar innovations and possible prior art challenges. Therefore, the patent’s enforceability depends on ongoing vigilance and strategic patent management.

Regulatory and Market Considerations

In Turkey, patent protection influences regulatory strategies, as pharmaceutical approvals often require patent information disclosures. The patent’s status impacts pricing, market entry, and patent expiration planning.

Moreover, local policies favoring generic entry post-patent expiry underscore the importance of extending patent protections through supplementary strategies such as data exclusivity.

Conclusion

Turkey Patent TR200201498 secures a substantial position in the pharmaceutical patent landscape, contingent on its broad claims and strategic claims drafting. Its scope covers specific chemical entities, methods, and formulations that offer robust protection against generic competition, provided validity is maintained. A nuanced understanding of its claims, combined with the landscape analysis, informs licensing dynamics, litigation strategies, and R&D direction in Turkey’s pharmaceutical sector.


Key Takeaways

  • The patent claims a specific chemical compound or class, with indications of broad protective scope based on structural features and synthesis methods.
  • Its enforceability relies on careful claim drafting, strategic patent prosecution, and ongoing validity challenges.
  • The patent landscape in Turkey is competitive, with potential prior art and regional patent filings impacting strength.
  • Effective patent management and strategic licensing are crucial for maximizing return on investment.
  • Understanding local regulatory requirements and market dynamics enhances the patent’s value proposition.

FAQs

Q1: What is the primary therapeutic application covered by Turkey patent TR200201498?
A1: While specific therapeutic claims are detailed in the patent text, the invention likely pertains to a pharmaceutical compound with antiviral, anti-inflammatory, or oncology indications, consistent with classification codes. Exact applications depend on the claims and disclosed embodiments.

Q2: How does the scope of the independent claims influence patent enforceability?
A2: Broad independent claims confer extensive protection but risk invalidation if overly broad or unsupported by the original disclosure. Narrow, well-drafted claims enhance enforceability but may limit the scope of protection.

Q3: Can competitors circumvent this patent by modifying the chemical structure?
A3: If the claims are narrowly focused on specific structural features, competitors may design around by altering the structure to avoid infringement. If claims are broad, such design-arounds become more difficult.

Q4: What role do prior art references play in challenging this patent?
A4: Prior art can undermine patent validity if it shows the invention is not novel or is obvious. Regular patent validity assessments and prior art searches are vital for maintaining enforcement positions.

Q5: How can patent holders extend protection beyond the 20-year term?
A5: Strategies include patent term extensions (available in some jurisdictions), supplementary protections, or developing new inventive formulations or methods to file follow-up patents.


Sources:

  1. Turkish Patent and Trademark Office (Turkish PTO) official publications.
  2. WIPO PatentScope database.
  3. European Patent Office (EPO) legal literature.
  4. Relevant scientific and legal analyses on pharmaceutical patenting.
  5. Industry reports on Turkish pharmaceutical patent landscapes.

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