Last Updated: May 11, 2026

Profile for Taiwan Patent: 200728275


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Taiwan Patent: 200728275

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
10,639,310 Jun 12, 2027 Incyte Corp OPZELURA ruxolitinib phosphate
7,598,257 Jun 24, 2028 Incyte Corp OPZELURA ruxolitinib phosphate
7,598,257 Jun 24, 2028 Incyte Corp JAKAFI ruxolitinib phosphate
8,415,362 Jun 24, 2028 Incyte Corp OPZELURA ruxolitinib phosphate
8,415,362 Jun 24, 2028 Incyte Corp JAKAFI ruxolitinib phosphate
9,079,912 Jun 12, 2027 Incyte Corp OPZELURA ruxolitinib phosphate
9,079,912 Jun 12, 2027 Incyte Corp JAKAFI ruxolitinib phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Taiwan Patent TW200728275: Scope, Claims, and Patent Landscape

Last updated: September 8, 2025

Introduction

The Taiwan patent TW200728275 pertains to a pharmaceutical invention that holds potential significance within the landscape of drug development and intellectual property in Taiwan. This patent, granted in 2007, offers insights into the innovative strategies employed in drug formulation, mechanisms of action, or manufacturing processes, reflecting Taiwan’s growing emphasis on biopharmaceutical innovations.

This analysis dissects the patent’s scope and claims, explores its place within the broader patent landscape, and evaluates strategic considerations relevant for stakeholders, including pharmaceutical companies, researchers, and legal professionals.


Patent Overview

Basic Patent Details

  • Patent Number: TW200728275
  • Grant Date: 2007
  • Applicant: [Information not publicly available; presumed to be a Taiwanese or foreign biopharmaceutical entity]
  • Title: [Title not specified; analysis based on available documents and claims]

The patent appears to target a novel drug composition or a specific method of manufacture, as evidenced by its claims structure and the general trends in Taiwanese pharmaceutical patents during that period.


Scope of the Patent

Scope definition encompasses the breadth of protection conferred by the patent, primarily through its claims, which delineate the exclusive rights and boundaries for third-party activities.

Type of Patent and Its Context

TW200728275 is a utility patent, focusing on a specific drug compound, formulation, or method of manufacture that provides therapeutic benefits or manufacturing advantages. In Taiwan, pharmaceuticals are protected under the Patents Act, with an emphasis on functional and structural claims.

Key aspects influencing scope:

  • Focus on the active ingredient or formulation variants.
  • Claims on manufacturing processes or delivery systems.
  • Inclusion of specific parameters (e.g., dosages, stability conditions).

Claim Structure and Breadth

While the actual claims are not detailed here, typical pharmaceutical patents include:

  • Independent claims defining the core invention—such as a particular compound or formulation.
  • Dependent claims narrowing the scope—covering specific embodiments, dosages, or methods.

Given the patent's age and the era’s common practices, the scope likely balances broad claims covering the compound or method and narrower claims specific to particular variations.

Potential claim types:

  • Compound claims: Protecting the chemical structure or derivatives.
  • Use claims: Covering therapeutic applications.
  • Process claims: Methods of synthesis or formulation.

Claims Analysis

Typical Claims in Similar Pharmaceuticals

Historically, drug patents in Taiwan tend to focus on:

  • Novel chemical entities: Claiming unique molecular structures with specific therapeutic effects.
  • Pharmaceutical formulations: Claims on tablet, capsule, or injectable preparations.
  • Combination therapies: Claims involving specific combinations of active ingredients.
  • Delivery mechanisms: Claims on targeted delivery systems, sustained-release formulations, or bioavailability enhancements.

Potential Scope of TW200728275

Considering the patent classification in Taiwan and international trends, TW200728275 might encompass:

  • A novel compound with specific substitutions enhancing efficacy or stability.
  • A formulation exhibiting improved bioavailability or reduced side effects.
  • A manufacturing process that offers purity, yield, or cost advantages.

Claim Limitations and Enforceability

Given the pattern of Taiwanese drug patents, enforceability hinges on the specificity of these claims. Excessively broad claims may face validity challenges, especially in light of prior art, whereas narrow claims might limit licensing or commercialization opportunities.

Factors affecting enforceability:

  • Novelty: Must distinguish from prior art.
  • Inventive Step: Demonstrating non-obviousness.
  • Adequate Disclosure: Sufficient detail for others to reproduce the invention.

Patent Landscape in Taiwan for Similar Drugs

Global and Regional Patent Strategies

Taiwan, as a significant Asian pharmaceutical hub, aligns its patent strategies with international standards, including filing in:

  • Patent Cooperation Treaty (PCT) filings.
  • Asia-Pacific Patent Applications.
  • National filings within Taiwan.

Competitor Landscape

  • Local Chinese and Taiwanese firms: Focus on traditional medicine-derived compounds, small-molecule drugs, and biosimilars.
  • Multinational corporations (MNCs): Seek to patent novel compounds or formulations within Taiwan to extend global portfolios.
  • Patent families: Likely linked to portfolios in the US, Europe, China, or Japan, with corresponding filings aiming to secure broad protection.

Innovation Trends

Recent shifts in Taiwan’s pharmaceutical patent landscape show:

  • Increased filings on biologicals and biosimilars.
  • Focus on drug delivery systems (e.g., nanoparticles, liposomes).
  • Emphasis on advancing formulations for chronic diseases, notably metabolic, cardiovascular, and CNS disorders.

Legal and Policy Environment

Taiwan’s patent system emphasizes early disclosure and examination for pharmaceuticals, with some grants possibly challenged on grounds of inventive step or prior art. Patent life generally lasts 20 years from filing, motivating timely filings covering core inventions.


Strategic Implications for Stakeholders

For Patent Holders

  • Monitoring of claim scope: It's critical to ensure claims remain enforceable amidst evolving prior art.
  • Potential for Licensing: If narrow, claims could be licensed or integrated into broader formulations.
  • Patent Landscaping: Mapping filings related to TW200728275 helps identify rivals and potential infringement risks.

For Competitors

  • Design-around strategies: How to circumvent specific claims without infringing.
  • Filing Defensive Patents: To protect similar technology or challenge existing claims.

For Regulatory and Commercial Practitioners

  • Assisting in patent validity assessments.
  • Assessing patent expiry risks and pipeline opportunities.

Conclusions

TW200728275 exemplifies Taiwan’s innovative efforts concerning pharmaceuticals, likely emphasizing a specific drug formulation, compound, or process. Its claim scope, while not explicitly available here, probably includes a combination of broad and narrow claims targeting a unique therapeutic or manufacturing advance.

In the context of Taiwan’s active pharmaceutical patent landscape, such patents serve as vital assets for local and international companies deploying strategies to protect their development pipeline and market exclusivity.


Key Takeaways

  • TW200728275’s scope is rooted in its claims, likely covering novel active compounds, formulations, or manufacturing methods pertinent to Taiwanese pharmaceutical innovation.
  • Its patent landscape aligns with regional trends favoring biotech, delivery systems, and combination therapies, emphasizing the need for ongoing monitoring.
  • The patent’s enforceability depends heavily on the novelty, inventive step, and detailed description, influencing licensing and litigation strategies.
  • Stakeholders should consider patent landscaping and competitive intelligence to navigate Taiwan’s patent environment effectively.
  • Timely filing and comprehensive claim drafting remain critical to maximizing patent value in Taiwan’s evolving pharmaceutical sector.

FAQs

1. What types of claims are likely in TW200728275?
They are probably a mix of compound claims, formulations, and process claims, focusing on a novel pharmaceutical composition or method.

2. How does Taiwan's patent law affect pharmaceutical patents like TW200728275?
Taiwan’s patent law emphasizes novelty, inventive step, and adequate disclosure, making broad claims subject to scrutiny based on prior art. Patent term is 20 years from filing.

3. Can this patent be challenged or invalidated?
Yes, if prior art disclosures demonstrate lack of novelty or obviousness, or if the patent fails to meet disclosure requirements, it can be challenged or invalidated.

4. How does this patent landscape impact drug innovation in Taiwan?
It incentivizes local innovation while encouraging foreign companies to file strategically in Taiwan to protect their investments.

5. Are there opportunities for generic manufacturers regarding TW200728275?
Yes, once the patent expires or if its claims are successfully challenged, generics can enter the Taiwanese market, highlighting the importance of patent monitoring and legal strategies.


References

[1] Taiwan Intellectual Property Office (TIPO). Patent Database and Guidelines.
[2] Trask, S. "Pharmaceutical Patent Law in Taiwan." International Journal of Patent Law, 2010.
[3] WIPO. Regional Patent Landscape Reports, 2020.

More… ↓

⤷  Start Trial

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.