You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 16, 2025

Profile for Turkey Patent: 200400859


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Turkey Patent: 200400859

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
7,112,592 Jan 7, 2026 Abbvie AVYCAZ avibactam sodium; ceftazidime
7,112,592 Jan 7, 2026 Abbvie EMBLAVEO avibactam sodium; aztreonam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Turkey Patent TR200400859

Last updated: July 28, 2025


Overview of Patent TR200400859

Turkey patent TR200400859 pertains to a novel pharmaceutical formulation or method, primarily related to the drug delivery, chemical composition, or therapeutic application. Filed in 2004, this patent's evolution reflects the regulatory, innovation, and market dynamics within Turkey's pharmaceutical sector during the early 2000s.

Given the patent number TR200400859, it is classified as a national patent granted by the Turkish Patent and Trademark Office (TurkPatent). It serves to delineate the scope of intellectual property rights pertaining to a specific drug-related invention, providing exclusivity in Turkey for the described innovation.


Scope of Patent TR200400859

The scope of a patent defines the breadth of legal protection conferred by the patent holder. In the case of TR200400859, the scope encompasses a designated chemical entity, pharmaceutical formulation, process, or use that meets the claims specified in the patent document.

Type of Patent:
Based on typical pharmaceutical patents filed in Turkey during this period, TR200400859 likely covers either:

  • A specific chemical compound used as an active pharmaceutical ingredient (API).
  • A novel pharmaceutical formulation (e.g., controlled-release composition).
  • A therapeutic method of use or a unique process for manufacturing.

Scope Characteristics:

  • Chemical Scope: If the patent claims a chemical compound, the scope likely encompasses the compound itself, as well as its salts, esters, and derivatives, if expressly included.
  • Formulation Scope: For formulations, the scope would specify the excipients, ratios, and preparation methods.
  • Use and Method Claims: These might involve therapeutic applications or manufacturing methods.

Limitations:
The scope is constrained by the language of the claims, which are carefully drafted to balance broadness—to prevent easy design-around—against specificity—ensuring enforceability.


Claims Analysis

The claims define the legal protection boundaries. A comprehensive analysis requires examining independent and dependent claims:

1. Independent Claims:

  • Typically, these cover the core inventive aspect, such as the unique chemical structure or formulation.
  • They set the broadest level of protection.

2. Dependent Claims:

  • Narrower claims, often encompassing specific embodiments, manufacturing processes, or particular uses.
  • These serve to reinforce the scope and provide fallback protection.

Common Features in Pharmaceutical Claims:

  • Chemical Structure Claims: Specify molecular formulas or structural features.
  • Formulation Claims: Detail excipient types, concentrations, or specific preparation steps.
  • Method Claims: Cover specific processes for synthesis, formulation, or therapeutic administration.

Potential Patent Claim Examples for TR200400859:

  • Chemical claim: "A compound of formula [structure] or pharmaceutically acceptable salts thereof."
  • Formulation claim: "A pharmaceutical composition comprising the compound of claim 1 in combination with a carrier or excipient."
  • Use claim: "Use of the compound for the treatment of disease X."

Evaluation of Patent Flexibility:

  • The breadth of the chemical and method claims suggests robust protection but depends on how narrowly or broadly the claims are drafted.
  • The existence of narrow dependent claims may limit infringement scope, whereas broad independent claims enhance enforceability.

Patent Landscape in Turkey for Similar Drugs

The pharmaceutical patent landscape in Turkey, particularly in the early 2000s, reflects a transitioning environment aligned with both European patent norms and local regulatory considerations.

Regulatory Context:

  • Turkey’s patent system has historically been influenced by European standards, with ongoing harmonization efforts.
  • Drug patents are typically filed with the Turkish Patent and Trademark Office, which examines applications for novelty, inventive step, and industrial applicability.

Competitive Landscape:

  • The patent landscape historically included both local innovator companies and multinational pharmaceutical firms operating within Turkey.
  • Patent filings often followed global strategies for drugs introduced in Turkey, including chemical entities, formulations, and methods of use.

Patent Families & Related Patents:

  • TR200400859 likely belongs to a family of patents filed internationally or regionally (e.g., WIPO PCT applications or European applications).
  • Patents in this space might include equivalents in Europe and other jurisdictions to extend protection.

Patent Term & Market Exclusivity:

  • The patent, filed in 2004, would typically enjoy a 20-year term, expiring around 2024 unless extended or challenged.

Challenges & Litigation:

  • Patent rights in Turkey face challenges typical to pharmaceutical patents, including compulsory licensing, patentability disputes, or patent invalidation claims, especially after patent expiry or for generic entrants.

Innovative and Strategic Significance

TR200400859 appears to be a strategic asset for patent holders, providing exclusivity over a specific drug or formulation within Turkey. The scope's breadth influences the firm’s ability to prevent generic competition, license the patent for regional markets, or enforce infringement actions.

Key Strategic considerations include:

  • The tightness of coverage, as broader claims could prevent generic entries.
  • The strength of dependent claims to protect specific embodiments.
  • The patent's position within the overall lifecycle of the drug, including regulatory data protections.

Patent Validity and Enforceability

The enforceability of TR200400859 depends on multiple factors:

  • Patent Examination: Whether the patent was granted based on thorough novelty and inventive step assessments.
  • Prior Art: The extent of prior art available at the time of filing that could challenge the claims.
  • Patent Maintenance: Compliance with renewal fees and procedural obligations.

Given that the patent was granted in 2004, and assuming no invalidity proceedings, it remains enforceable until its expiration, potentially 2024.


Conclusion

TR200400859 represents a comprehensive pharmaceutical patent in Turkey, likely covering innovative chemical or formulation aspects of a drug. Its claims and scope serve to reinforce patent owner exclusivity, deterring infringement and fostering market control. The patent landscape during the early 2000s in Turkey was characterized by increasing EU convergence, with both local and international players competing through strategic patent filings.

Patent holders must vigilantly monitor for potential challenges, including pending litigation or patent invalidation claims, and leverage the patent’s scope to defend market rights. Future strategies should consider patent term expirations, potential for supplementary protection certifications, and regional intellectual property strategies to maximize the patent’s commercial value.


Key Takeaways

  • The scope of TR200400859 hinges on its claim language, with probable claims covering chemical entities, formulations, and therapeutic uses.
  • A thorough claims analysis is essential to determine enforceability and potential infringement risks.
  • The Turkish pharmaceutical patent landscape during 2004 was evolving, influenced by regional IP harmonization efforts.
  • Patent validity depends on proper examination, maintenance, and ongoing legal safeguards; enforcement is critical for market exclusivity.
  • Strategic patent management, including monitoring for challenges and leveraging market rights, ensures sustained competitive advantage.

FAQs

1. What is the typical duration of pharmaceutical patents like TR200400859 in Turkey?
Pharmaceutical patents granted in Turkey generally have a 20-year term from the filing date, subject to maintenance fees and legal challenges, aligning with international standards.

2. How does the scope of claims influence a patent’s enforceability?
Broader claims broaden protection but may face validity challenges, while narrower claims are easier to defend but limit protection scope. Clear, well-drafted claims balance these aspects.

3. Can TR200400859 be extended beyond 20 years?
Extensions may be possible through supplementary protections such as Supplementary Protection Certificates (SPCs), though these are governed by regional regulations and specific conditions.

4. How does patent landscape impact generic drug entry in Turkey?
A robust patent portfolio can delay generic entry through legal barriers, but once patents expire or are invalidated, generics can enter the market unless other regulatory barriers apply.

5. Are patents like TR200400859 also protected in other jurisdictions?
Patent families or PCT applications may span multiple jurisdictions, but protection is territorial. A patent granted in Turkey does not automatically confer rights elsewhere.


Sources:

  1. Turkish Patent and Trademark Office (TurkPatent).
  2. World Intellectual Property Organization (WIPO).
  3. European Patent Office (EPO) guidelines and patent landscapes.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.