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

Last Updated: December 12, 2025

Profile for Taiwan Patent: 200938204


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Taiwan Patent: 200938204

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 Feb 3, 2029 Ferring Pharms Inc MILPROSA progesterone
⤷  Get Started Free Feb 3, 2029 Ferring Pharms Inc MILPROSA progesterone
⤷  Get Started Free Jan 21, 2030 Ferring Pharms Inc MILPROSA progesterone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW200938204

Last updated: August 4, 2025

Introduction

Taiwan patent TW200938204 pertains to a pharmaceutical invention filed and granted within Taiwan's patent system, offering exclusivity on specific drug-related innovations. This analysis explores its scope, claims, and position within the patent landscape, equipping industry professionals with a comprehensive understanding of its strategic importance. Such insight is vital for stakeholders involved in drug development, licensing, or patent litigation.


Overview of Taiwan Patent TW200938204

Taiwan patent TW200938204 was granted to secure intellectual property rights pertaining to a specific pharmaceutical composition, method, or compound. The patent application was filed on a certain date (exact dates require patent documentation review), reflecting Taiwan's patent law stipulations, particularly the scope of protection under the Patent Act.

Key Points:

  • Filing date: [Insert, if available]
  • Grant date: [Insert, if available]
  • Patent term: Typically 20 years from filing, adjusted for patent term adjustments in Taiwan
  • Patent classification: Likely categorized within pharmaceutical or chemical patent classifications, based on the invention's nature.

Scope of the Patent

The scope of TW200938204 is primarily defined by its claims, which delineate the legal bounds of patent protection. It potentially encompasses:

  1. Chemical compounds or derivatives
  2. Pharmaceutical compositions
  3. Preparation methods or processes
  4. Uses or methods of treatment

The claimed protection determines whether the patent covers specific formulations, methods, or new chemical entities, or a broad class of compounds.

Claim Structure:

  • Independent Claims: Usually define the core invention, e.g., a novel chemical compound with specified structural features, or a new method of producing a pharmaceutical compound.
  • Dependent Claims: Further specify particular embodiments, such as specific substituents, dosage forms, or application methods, narrowing the scope.

Assessment of Claims:

  • Breadth: Does the patent claim a specific compound, or a broader class or genus?
  • Novelty and Inventive Step: Are the claims differentiating from prior art? Taiwan’s examination standards emphasize novelty, inventive step, and industrial applicability.
  • Language: Precise claim language minimizes patentability challenges.

Claims Analysis

While the exact claims are not provided here, typical types in such patents include:

1. Composition Claims

These focus on the chemical makeup of the drug, such as:

  • A pharmaceutical composition comprising a compound with a specific chemical structure, optionally combined with excipients or stabilizers.
  • Claims might specify the concentration ranges, form (e.g., tablet, injectable), or stabilizing agents.

2. Method Claims

These delineate the specific process steps:

  • Method of synthesizing the compound.
  • Method of administering the drug for particular indications.
  • Claims may specify dosage regimes, administration routes, or treatment protocols.

3. Use Claims

These specify the therapeutic application:

  • Use of the compound in treating specific diseases (e.g., cancer, infectious diseases).
  • Often complemented with structural claims for maximum protection.

4. Formulation Claims

Cover specific formulations such as sustained-release, conjugates, or combination therapies.


Patent Landscape Context

Understanding the patent landscape involves analyzing:

1. Prior Art

The patent's novelty revolves around identifying prior art, including:

  • Earlier patents or applications for similar compounds or methods.
  • Scientific publications disclosing related compounds or therapeutic uses.
  • Existing market drugs that may challenge the patent's novelty.

2. Competitor Patents

  • Other patents in Taiwan or abroad claiming similar drugs, formulations, or therapeutic methods.
  • Interplay with foreign patent rights, particularly in jurisdictions like China, US, and Europe.

3. Patent Families and Strategic Position

  • Whether TW200938204 is part of a larger patent family filed across multiple jurisdictions.
  • Its role in the patent portfolio guiding the drug developer's commercialization and enforcement strategy.

4. Infringement and Freedom-to-Operate (FTO)

  • Potential for infringement if others develop similar compounds.
  • FTO analysis crucial for new entrants planning to develop competing drugs or formulations.

Legal Status and Patent Lifecycle Considerations

  • Check whether the patent remains enforceable—any oppositions or legal challenges?
  • Clarify expiry dates, which influence market exclusivity.
  • Possible patent extensions under Taiwan law if applicable (e.g., for pediatric extensions).

Implications for Industry Professionals

  • Patent Strategy: Ensuring compliance with claim language for robust protection.
  • Research & Development: Navigating around existing claims or leveraging the patent’s scope.
  • Licensing & Commercialization: Assessing patent strength for licensing negotiations.
  • Legal Enforcement: Monitoring for potential infringements or challenges.

Conclusion

Taiwan patent TW200938204 centers on a specific drug-related innovation, defined sharply by its claims. Its scope provides valuable protection within its operational spectrum, but its strength depends on claim breadth, prior art landscape, and legal status. A comprehensive understanding guides strategic decisions in R&D, licensing, or litigation.


Key Takeaways

  • The scope of TW200938204 hinges on its independent claims, which define the novel compound, formulation, or method protected.
  • Broader claims afford wider protection but risk invalidation if challenged by prior art; narrower claims offer specific coverage with potentially reduced enforceability.
  • Its place within the broader patent landscape influences competitive positioning, particularly regarding patent family coverage and potential infringement risks.
  • Continuous legal status monitoring is necessary to maintain patent rights and inform lifecycle management.
  • Effective patent claim drafting and strategic alignment with existing patents are essential for leveraging exclusivity and maximizing commercial value.

FAQs

Q1: How does Taiwan patent TW200938204 compare to international patents on similar drugs?
It may share claims with foreign counterparts via patent family strategies, but the scope and claim language can differ due to jurisdictional legal standards. Reviewing international patent families provides comprehensive protection.

Q2: Can the patent claims be challenged or narrowed?
Yes, third parties can file opposition or invalidation procedures, arguing prior art or lack of inventive step, potentially narrowing or invalidating claims.

Q3: What should companies consider before designing around this patent?
Identify the specific structural features or methods claimed, and develop compounds or processes that avoid infringing these claims while maintaining therapeutic efficacy.

Q4: How long will the patent protection last?
Typically 20 years from the filing date, subject to maintenance fees and any extensions granted under Taiwan law.

Q5: Does the patent cover both the active ingredient and delivery method?
Yes, if claims are drafted to encompass composition and method claims, both aspects can be protected, depending on claim scope and limitations.


References

  1. Taiwan Intellectual Property Office (TIPO). Patent Database.
  2. WIPO PATENTSCOPE. International Patent Documents.
  3. Patent Law of Taiwan.
  4. Industry reports on pharmaceutical 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.