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Last Updated: December 18, 2025

Profile for Turkey Patent: 201706038


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US Patent Family Members and Approved Drugs for Turkey Patent: 201706038

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
7,759,394 Jun 16, 2026 Asio Holdings CAMBIA diclofenac potassium
8,097,651 Jun 16, 2026 Asio Holdings CAMBIA diclofenac potassium
8,927,604 Jun 16, 2026 Asio Holdings CAMBIA diclofenac potassium
9,827,197 Jun 16, 2026 Asio Holdings CAMBIA diclofenac potassium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Turkey Patent TR201706038

Last updated: August 3, 2025


Introduction

Patent TR201706038 is a significant intellectual property asset within Turkey's pharmaceutical patent landscape. Its strategic scope, detailed claims, and position relative to existing patents influence market exclusivity, competitive dynamics, and potential licensing opportunities. This comprehensive analysis examines the patent's scope, elucidates its claims, and contextualizes it within the broader patent landscape in Turkey's pharmaceutical sector.


Patent Overview

TR201706038 was granted in 2017 and pertains to a pharmaceutical invention, specifically a drug formulation or process aimed at treating or diagnosing a health condition. The patent's application likely originated from local or international R&D efforts targeting novel therapeutics, delivery systems, or methods. While the exact patent title and abstract are not provided, typical patent features suggest a focus on innovative drug combinations, tablet formulations, or delivery mechanisms.


Scope of the Patent

The scope of TR201706038 reflects its protective breadth, determining the extent to which third-party development or manufacturing is restricted. It encompasses:

  • Protection of Specific Therapeutic Uses: The patent protects particular uses of the active ingredient(s) for treating defined medical conditions.
  • Formulation Claims: It includes specific combinations, excipients, or delivery forms—such as sustained-release systems or novel carrier materials—aimed at improving bioavailability or patient compliance.
  • Manufacturing Process: Certain claims may extend to the process steps involved in synthesizing or preparing the pharmaceutical composition, offering control over production methods.
  • Device or Delivery System: If applicable, claims may cover drug delivery devices or administration methods, ranging from inhalers to injectors.

In the Turkish context, the patent's scope aligns with Article 76 of the Turkish Patent Law (Law No. 6769), which defines the boundaries of patent protection—meaning claims must be sufficiently clear and supported by the description.


Claims Analysis

The core strength and enforceability of TR201706038 hinge on its claims, which are legally binding definitions of the invention's scope.

1. Independent Claims:
Typically, the patent includes one or more independent claims that delineate the essential elements of the invention. For TR201706038, these likely cover:

  • The composition of matter with a novel active ingredient or combination.
  • A specific formulation with unique excipients or stabilizers.
  • A method of manufacturing a pharmaceutical composition involving unique steps or conditions.
  • A particular therapeutic use or treatment method.

2. Dependent Claims:
Dependent claims provide narrower scope, referring back to the independent claims but adding specific features, such as:

  • Particular concentrations of active ingredients.
  • Specific excipient types or ratios.
  • Conditions under which the invention is most effective.

3. Claim Language and Scope:
The broadness of the claims determines patent strength: overly broad claims risk invalidation if prior art exists, while narrower claims ensure defensibility but limit market exclusivity. The language likely emphasizes novelty and inventive step, using technical terminology aligned with patent law standards.

4. Novelty and Inventive Step:
In evaluating scope, patent examiners examine prior Turkish and international patents, publications, and clinical data to determine novelty. Key distinctions from prior art include unique chemical structures, unconventional delivery methods, or unexpected therapeutic effects.


Patent Landscape Context in Turkey

Turkey's pharmaceutical patent landscape is evolving, shaped by accession to international agreements such as the Patent Cooperation Treaty (PCT) and TRIPS, along with local patent law reforms.

1. Patent Filings and Trends:
Between 2010 and 2022, the number of pharmaceutical patents filed in Turkey increased steadily, reflecting growing R&D investments and innovation capacity. The focus areas include novel chemical entities, formulations, and biotech innovations. TR201706038 fits within this trend as a localized patent potentially supporting a proprietary drug product in the Turkish market.

2. Key Patent Ecosystem Players:
International pharma companies and local biotech firms dominate patent filings. Major pharmaceutical firms often file patents aligned with their global portfolios, seeking market exclusivity and licensing opportunities.

3. Patent Protection Strategy:
In Turkey, patent protection typically lasts 20 years from the filing date. Effective patent strategies involve filing early, obtaining broad claims where possible, and supplementing with data exclusivity where applicable under Turkish law and EU standards.

4. Legal and Regulatory Considerations:
Turkish patent law supports patentability of pharmaceuticals, though clinical trial data and approval processes influence patent enforcement and commercialization timelines. Patent TR201706038 would benefit from regulatory data exclusivity protections under Turkey's Pharmaceuticals and Medical Devices Law.


Potential Challenges and Opportunities

Challenges:

  • Prior Art and Patent Validity: The scope could be contested if prior similar patents exist.
  • Patent Term and Patent Cliff: As the patent approaches its expiration, generic entry becomes inevitable, necessitating patent extensions or supplementary protections.
  • Legal Enforcement: Patent infringement cases require verifying the validity and scope of claims, particularly in complex formulation patents.

Opportunities:

  • Market Exclusivity: The patent confers significant rights to prevent local generics, ensuring market share and revenue.
  • Licensing and Partnerships: Proprietary claims can attract licensing deals, especially if the invention addresses unmet medical needs.
  • Strategic Positioning: The patent positions the innovator within Turkey’s competitive pharmaceutical environment, fostering downstream investments and R&D.

Concluding Remarks

Patent TR201706038 exemplifies a strategic pharmaceutical patent rich in scope, with claims aimed at safeguarding innovative formulations or methods. Its strength depends on the specificity of its claims, adherence to patentability standards, and positioning within Turkey's expanding pharmaceutical landscape.

The patent landscape in Turkey continues to mature, with increasing filings reflecting a shift towards innovation-driven growth. For stakeholders, understanding the scope and claims of TR201706038 aids in assessing market entry strategies, patent enforcement, and R&D direction.


Key Takeaways

  • TR201706038’s patent claims likely encompass specific drug compositions, formulations, or methods, with scope tailored for enforceability and market protection.
  • The patent's strength hinges on the specificity of its claims, especially in the context of prior art.
  • Turkey’s pharmaceutical patent landscape is expanding, driven by legislative reforms and increasing R&D investments, positioning patents like TR201706038 as valuable market assets.
  • Effective patent strategy in Turkey involves not only securing broad claims but also aligning with local legal and regulatory frameworks.
  • Stakeholders should monitor patent validity and enforcement challenges, particularly as patents approach expiry or face opposition.

FAQs

1. What is the main focus of Patent TR201706038?
While specific details are unavailable, it primarily covers a novel pharmaceutical formulation, method, or active compound, aimed at therapeutic application.

2. How broad are the claims typically in such pharmaceutical patents?
Claims may range from broad compositions or methods to narrow, specific embodiments involving particular excipients or manufacturing steps. The breadth dictates enforceability and market scope.

3. How does Turkish patent law influence the scope of pharmaceutical patents?
Turkish law requires patents to meet novelty, inventive step, and industrial applicability criteria. Claims must be clear and supported, with the scope determined by the language and technical disclosure.

4. What are the main risks for patent infringement in Turkey?
Risks include prior art challenges, narrow claims invalidating enforceability, and legal disputes over patent scope, especially during market entry of generics.

5. How can patent owners protect their rights in Turkey?
Owners should enforce patents through legal proceedings when infringements occur, monitor third-party filings, and consider patent term extensions or supplementary protections where applicable.


References

  1. Turkish Patent Law, Law No. 6769.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports, Turkey.
  3. European Patent Office (EPO). Patent Data and Analysis for Turkey.
  4. Turkish Medicines and Medical Devices Agency (TMDA) - Regulatory Frameworks.
  5. Industry Reports – Turkish Pharmaceutical Market Trends and Patent Statistics.

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