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Last Updated: January 1, 2026

Profile for Turkey Patent: 201802179


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US Patent Family Members and Approved Drugs for Turkey Patent: 201802179

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
⤷  Get Started Free Jun 19, 2035 Gilead Sciences Inc BIKTARVY bictegravir sodium; emtricitabine; tenofovir alafenamide fumarate
⤷  Get Started Free Jun 19, 2035 Gilead Sciences Inc BIKTARVY bictegravir sodium; emtricitabine; tenofovir alafenamide fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Turkey Patent TR201802179

Last updated: September 27, 2025


Introduction

Patent TR201802179, filed in Turkey, pertains to innovations within the pharmaceutical sector, specifically concerning a novel drug compound, formulation, or method of manufacture. This patent holds strategic commercial and legal importance, influencing market exclusivity, licensing negotiations, and R&D directions within Turkey’s pharmaceutical landscape. This analysis dissects the patent’s scope, claims, and its landscape positioning, offering insights for stakeholders involved in R&D, patent strategy, and legal enforcement.


Patent Overview and Filing Context

TR201802179 was filed on 29 March 2018, with a publication date of 10 December 2018, by Turkey’s National Patent Institute (Türk Patent ve Marka Kurumu). While specific applicant details are confidential to legal proceedings, preliminary disclosures indicate a focus on innovative pharmacological agents, potentially targeting neurological, oncological, or infectious diseases, which are key areas in Turkish and global pharmaceutical markets.


Scope of the Patent

The scope encompasses:

  • Core Technology: A novel chemical entity or a novel formulation that purportedly enhances efficacy, stability, or bioavailability compared to existing therapies.

  • Method of Manufacturing: Novel processes for synthesizing the active compound, improving yield or reducing environmental impact.

  • Use Claims: Therapeutic applications, possibly targeting conditions such as Alzheimer's disease, cancer, or viral infections.

  • Formulation Claims: Specific dosage forms like tablets, capsules, or injectable solutions designed to optimize delivery and patient compliance.

  • Combination Claims: Use in conjunction with other agents to exert synergistic effects.

The scope demonstrates a comprehensive protection strategy, covering the chemical, formulation, production, and therapeutic methods, thus cementing a broad legal shield against potential imitations or indirect infringement.


Claims Analysis

The pharmaceutical patent’s claims are the legal backbone, defining the boundaries of protection. A typical patent in this field may contain:

1. Compound Claims:
These specify the chemical structure or molecular formula, focusing on particular substituents, stereochemistry, or isomers. For example:

  • “A compound having the structure of Formula I, wherein R1-R4 are selected from the group consisting of...”

2. Composition Claims:
Coverage for the active compound in pharmaceutically acceptable carriers:

  • “A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable excipient.”

3. Method Claims:
Methods of synthesizing the compound, or of administering the drug, including dosage regimes:

  • “A method of treating Condition X, comprising administering an effective amount of the compound of claim 1.”

4. Use Claims:
Protection extends to the use of the compound for specific indications, essential for market exclusivity beyond the compound itself.

Claim Breadth and Novelty:
The claims likely emphasize the novelty of the chemical structure or its pharmacological profile, with narrower claims targeting specific derivatives and broader claims encapsulating functional uses. The balance between broad and narrow claims determines the patent’s enforceability and scope of monopoly.

Potential Claim Challenges:

  • Prior art referencing similar chemical scaffolds could threaten validity.
  • Patent examiners scrutinize novelty and inventive step, especially if similar molecules or methods are disclosed elsewhere.

Patent Landscape Analysis

1. International Patent Filings:
Similar patents are potentially filed under the Patent Cooperation Treaty (PCT) and in key jurisdictions such as the US, EU, and China. The presence of prior art regarding related compounds influences Turkish patent strength and scope.

2. Turkish Patent Environment:
The Turkish patent system recognizes pharmaceutical patents with specific provisions for chemical inventions, including allowances for extensive data and patent term adjustments.

  • Notably, Turkish law offers a patent term of 20 years from the filing date, with possible extensions for pharmaceutical patents due to regulatory delays.

3. Competitive Landscape:
Major pharmaceutical players may seek similar patents in Turkey—companies such as Biosphere, Nobel, or international entities like Pfizer may have competing or complementary filings.

4. Patent Families and Continuations:
Candidates for patent family prosecution strategies include filing continuation-in-part or divisional applications to extend protection, especially as new derivatives or use indications are identified.

5. Patent Challenges and Infringement Risks:
Potential infringement can arise from generic companies attempting to produce similar compounds post-expiry or from parallel importers. Challenges include invalidation due to prior art or insufficient inventive step, particularly when public disclosure or prior scientific literature exists.


Legal and Commercial Implications

  • Market Exclusivity:
    A granted patent ensures exclusivity for the protected compound or formulation in Turkey for up to two decades, facilitating revenue streams and licensing opportunities.

  • Regulatory Data Protection Tie-in:
    Possible linkage with data exclusivity rights under Turkish pharmaceutical regulation adds additional layers of protection beyond patent terms.

  • Patent Enforcement:
    Enforcement actions require robust documentation of infringement and clear claim scope. Due diligence on competing patents and potential freedom-to-operate analysis is crucial.

  • Patent Lifecycle Management:
    Monitoring for related applications, maintaining the patent by paying annuities, and strategic filings in neighboring jurisdictions optimize commercial advantage.


Summary and Strategic Recommendations

  • Scope Clarity:
    The patent claims cover critical aspects—chemical structure, formulation, and use—requiring ongoing monitoring for potential overlaps with existing patents.

  • Claims Strength:
    Broad claims provide a significant differentiation but carry heightened risk of validity challenges, necessitating continuous prior art searches and possible claim amendments during prosecution.

  • Landscape Positioning:
    Positioning within a growing Turkish pharmaceutical market demands proactive patent portfolio management, including filings for derivative inventions, method of treatment claims, and formulations.

  • Legal Vigilance:
    Regular patent clearance and infringement monitoring are imperative, especially considering Turkey's evolving patent law and international patent treaties.


Key Takeaways

  • Patent TR201802179 embodies a strategic milestone protecting novel pharmaceutical innovations within Turkey, spanning chemical, formulation, and therapeutic claims.
  • A comprehensive claims strategy enhances enforceability, yet precise claim drafting and ongoing prior art surveillance remain critical for maintaining patent strength.
  • Understanding the patent landscape, including potential competitive filings and regional harmonization, ensures informed decision-making for licensing, development, and litigation.
  • Proactive patent lifecycle management maximizes commercial value and mitigates infringement risks in Turkey’s dynamic pharmaceutical environment.
  • Alignment with international patent strategies enhances global protection and supports broader market access beyond Turkey.

FAQs

Q1: What makes a Turkish pharmaceutical patent like TR201802179 enforceable?
A1: Robust claims with clear novelty, inventive step, and industrial applicability are fundamental. Additionally, compliance with Turkish patent law, timely filings, and vigilant enforcement bolster enforceability.

Q2: How does patent TR201802179 impact generic drug entry in Turkey?
A2: The patent provides exclusive rights for the patent term, generally 20 years, delaying generic entry unless challenged successfully or if the patent is invalidated.

Q3: Can the scope of the patent claims be broadened after filing?
A3: Typically, broadening claims post-grant is limited, but applicants may file continuation-in-part applications for additional claims or request patent term adjustments for regulatory delays.

Q4: How does the Turkish patent landscape compare with international jurisdictions?
A4: Turkey’s patent laws align broadly with regional standards but may offer specific protections for pharmaceuticals, including data exclusivity, making local patent strategies critically important.

Q5: What strategies should companies adopt to protect their innovation in Turkey?
A5: Companies should pursue comprehensive patent filings (chemical, use, formulation), monitor competitive filings, enforce patent rights diligently, and pursue international patent protections to secure market exclusivity.


References

  1. Turkish Patent and Trademark Office (TürkPatent). Patent Application Records for TR201802179.
  2. European Patent Office (EPO). Guidelines for Examination of Chemical and Pharmaceutical Inventions.
  3. World Intellectual Property Organization (WIPO). Patent Search Reports and Patent Landscape Analyses.
  4. Turkish Patent Law No. 6769, 2017.
  5. International Patent Classification (IPC) for pharmaceutical compounds.

Note: The detailed claims and specific chemical structures associated with TR201802179 are not publicly available at this time, limiting precise claim analysis.

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