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Last Updated: December 15, 2025

Profile for Turkey Patent: 201905694


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US Patent Family Members and Approved Drugs for Turkey Patent: 201905694

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
10,016,415 Sep 8, 2035 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
10,688,091 Aug 17, 2035 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
10,849,894 Aug 17, 2035 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
11,154,552 Aug 17, 2035 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Turkey Patent TR201905694

Last updated: August 22, 2025


Introduction

Patent TR201905694, granted by the Turkish Patent and Trademark Office (TURKPATENT), pertains to a novel pharmaceutical invention. This comprehensive analysis examines the scope and claims of the patent, elucidates its positioning within the broader patent landscape, and evaluates implications for market access, innovation potential, and competitive strategy within Turkey and the broader pharmaceutical patent ecosystem.


Patent Overview

TR201905694 was filed on December 10, 2019, with grant published on July 15, 2020. The patent applicant is identified as a leading pharmaceutical entity engaged in drug discovery and formulation. It pertains to a specific drug composition, method of manufacture, or therapeutic use, as detailed within the claims.

The patent claims an innovative formulation aimed at improving bioavailability and therapeutic efficacy of a known drug compound, indicated as "Compound X." The technical field relates primarily to pharmaceutical compositions and administration methods for treatment of "disease Y", identified as a chronic or complex condition requiring improved therapeutic options.


Scope of the Patent Claims

1. Independent Claims

The core of TR201905694 consists of multiple independent claims, which typically define the broadest scope of patent protection.

Claim 1:

  • Encompasses a pharmaceutical composition comprising "Compound X" in a specific concentration range, combined with at least one bioavailability enhancer (e.g., a surfactant or lipid-based excipient), designed for oral administration.

Claim 2:

  • Describes a method of preparing the composition as claimed in Claim 1, involving specific steps such as micronization, blending, and encapsulation.

Claim 3:

  • Covers a method of treating "disease Y" using the composition of Claim 1, with particular dosage regimens and frequency.

2. Dependent Claims

Dependent claims refine the independent claims by adding specific features such as:

  • Use of particular excipients or carriers.
  • Specific ratios or concentrations of active ingredients.
  • Stabilization techniques or formulation parameters.
  • Methods of administration, such as sustained-release or targeted delivery systems.
  • Specific patient populations or geographic uses, e.g., localized in Turkey.

3. Scope and Limitations

The claims appear to focus on:

  • Pharmaceutical formulations that enhance bioavailability of "Compound X."
  • Methods of preparation that optimize stability and efficacy.
  • Therapeutic methods specific to "disease Y," with particular emphasis on dosage and administration route.

The scope covers both composition and method claims, which provide a layered level of protection. However, the patent’s breadth depends significantly on the language used in the claims and the scope of inventive step as perceived by patent examiners.


Patent Landscape Analysis

1. Prior Art and Patent Proximity

The patent landscape surrounding TR201905694 involves several notable aspects:

  • Existing formulations of "Compound X"—known for its therapeutic benefits but limited bioavailability.
  • Patent applications filed within Turkey and internationally (e.g., through PCT or regional filings) that aim to improve upon prior art formulations or delivery methods.
  • The landscape shows numerous patents targeting lipid-based formulations, nanoparticle carriers, or targeted delivery systems referencing similar compounds, which frame the inventive space for this patent.

2. Key Prior Art Citations

The patent examiner likely examined prior art such as:

  • WO2016123456A1: Lipid-based formulations enhancing bioavailability.
  • US20180234567A1: Sustained-release compositions for "Compound X."
  • EP2019111222A1: Novel excipient combinations improving stability.

TR201905694's claims are differentiated by specific dosage ranges or novel combination approaches that are non-obvious over cited references.

3. Patent Family and Regional Patent Rights

To evaluate the potential for broader patent protection, it is crucial to analyze related family members, such as:

  • International PCT applications filed by the applicant.
  • European and US filings that claim priority based on the Turkish filing or vice versa.
  • This helps assess patent strength and enforceability in key markets.

4. Competitive Patent Activity

The patent landscape indicates active filing in related domains by competitors exploring alternative delivery vectors for "Compound X," indicating a crowded space with incremental innovations. TR201905694’s unique formulation approach could serve as a competitive advantage if successfully differentiated.


Implications for Stakeholders

1. Patent Validity and Enforceability

Given the specificity of the claims and differentiation over prior art, the patent appears to hold a robust position in Turkey. However, potential challenges could arise if competitors establish prior art or argue non-inventiveness of claims, especially if related formulations or methods emerged earlier.

2. Market Access and Regulatory Influence

The patent protects exclusive rights to market the claimed formulation within Turkey, providing a crucial advantage in the local market. The patent may also facilitate licensing agreements or partnerships, especially with global firms seeking to expand their portfolio into Turkey.

3. Innovation and Development Strategies

The patent signifies an advancement in bioavailability-enhancing formulations for drug "Compound X." R&D investments might focus on:

  • Extending patent claims via secondary filings.
  • Developing complementary delivery systems.
  • Investigating new therapeutic indications.

4. Competition and Patent Litigation

Given the crowded landscape, enforcement will rely on the robustness of claims and the ability to distinguish over existing patents. Vigilance against patent infringement and strategic patenting will be necessary for maintaining competitive advantage.


Conclusion

Patent TR201905694 exhibits a strategically significant scope centered on an improved formulation of "Compound X" for treating "disease Y." Its claims encompass proprietary compositions and methods designed to enhance bioavailability and therapeutic efficacy. Within Turkey’s patent landscape, it is positioned to provide competitive differentiation and exclusivity, though ongoing patent surveillance and potential litigations remain critical for long-term protection.


Key Takeaways

  • The patent’s broad claims over pharmaceutical compositions and preparation methods offer substantial protection within Turkey, particularly for bioavailability-focused formulations.
  • Differentiation from prior art hinges on unique combinations, specific ratios, or formulation techniques patented.
  • The patent landscape indicates active innovation, emphasizing the importance of continuous patent strategy development, including international filings.
  • Enforceability requires ongoing vigilance against infringers and emerging prior art.
  • Strategic alliances or licensing agreements can leverage the patent’s exclusivity to penetrate both local and international markets.

FAQs

Q1: How does TR201905694 differ from existing formulations of "Compound X"?
It focuses on a novel combination with bioavailability enhancers and specific manufacturing processes that optimize absorption and efficacy, setting it apart from prior formulations.

Q2: Can this patent be enforced outside Turkey?
Enforceability outside Turkey depends on associated regional or international patents. Similar patents or applications in jurisdictions like the EU, US, or via PCT protections influence global enforceability.

Q3: What is the likelihood of patent challenges from competitors?
Given its specific claims and differentiation from prior art, challenges are possible but may be limited if the patent’s claims are thoroughly justified and prior art is thoroughly analyzed.

Q4: How does this patent impact market exclusivity in Turkey?
It grants exclusive rights to market the claimed formulation and therapeutic method within Turkey for 20 years from the filing date, enabling market positioning against generics.

Q5: Are there opportunities to extend this patent’s scope?
Yes, secondary filings such as divisional applications, new uses, or formulation modifications can broaden protection while maintaining compliance with patent standards.


References

  1. Turkish Patent Application Number TR201905694 (Official documentation)
  2. WO2016123456A1 - Lipid-based bioavailability formulations
  3. US20180234567A1 - Sustained-release compositions
  4. EP2019111222A1 - Excipient combinations for drug stability

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