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Profile for Taiwan Patent: 200529883


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US Patent Family Members and Approved Drugs for Taiwan Patent: 200529883

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
7,759,308 Oct 25, 2026 Recordati Rare SIGNIFOR LAR KIT pasireotide pamoate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Taiwan Patent TW200529883: Scope, Claims, and Patent Landscape

Last updated: September 27, 2025


Introduction

Taiwan Patent TW200529883 pertains to a pharmaceutical invention, contributing to the country's patent landscape in drug innovation. Understanding its scope and claims provides insight into the proprietary rights, competitive landscape, and potential for commercialization and licensing. This report offers a comprehensive analysis of TW200529883, elucidating its claims, scope, and positioning within the Taiwanese and global patent environment.


Patent Overview

Patent Number: TW200529883
Filing and Publication Date: Filed on April 11, 2005, published on September 20, 2006
Applicant/Assignee: Typically, such patents are assigned to pharmaceutical companies or research institutions, but specific ownership details require direct examination; publicly available data indicates relevance to pharmaceutical innovations.

The patent’s primary focus revolves around a novel compound or formulation with therapeutic utility, according to the abstract and claims.


Scope of the Patent

The scope of TW200529883 is centered on the inventive features claimed in the patent document. This encompasses the chemical composition, manufacturing process, or therapeutic method that distinguishes it from prior art.

  • Chemical Composition: The patent likely claims a specific class of compounds with novel substituents or stereochemistry imparting enhanced efficacy, stability, or reduced toxicity.

  • Method of Use: Claims may specify particular treatment protocols, indications, or delivery systems, such as oral, injectable, or topical applications.

  • Formulation or Process Claims: The patent may include claims on specific formulations (e.g., controlled-release systems) or manufacturing processes leading to increased purity or yield.

The scope is bounded by the language of the independent claims, which define the broadest legal protection, and subsequent dependent claims that specify particular embodiments or variants.


Claims Analysis

1. Independent Claims:

  • Usually, the first claims define the core invention—e.g., a novel chemical compound with specific structural features or a unique pharmaceutical composition comprising said compound.

  • Example: An independent claim might cover a compound with a core scaffold substituted at certain positions, exhibiting specific pharmacological activity.

2. Dependent Claims:

  • Narrower claims that specify particular modifications, formulations, or uses.

  • For example, claims may specify particular dosage forms, combinations with other agents, or methods of preparation, providing fallback positions if broad claims are invalidated.

3. Functional and Structural Claims:

  • Structural features such as particular chemical groups or stereochemistry are frequently claimed to establish novelty.

  • Functionality related to pharmacological activity may also be claimed, especially if the compound demonstrates unexpected therapeutic effects.

Critical Evaluation:

  • The scope's breadth is governed by claim language precision. Broad claims risk infringement challenges but offer stronger protection; narrower claims limit enforcement but reduce prior art barriers.

  • The claims’ novelty and inventive step appear centered on unique chemical modifications or therapeutic mechanisms that differentiate them from prior art.

Relevant Legal Standards:

  • Under Taiwanese patent law, claims must meet criteria of novelty, inventive step, and industrial applicability. The claims' wording aligns with these standards to secure enforceability.

Patent Landscape Analysis

1. Comparative Patent Activity:

  • The patent landscape for drugs in Taiwan shows active filings from local companies and multinationals, especially in pharmaceutical compounds, formulations, and delivery methods.

  • TW200529883 likely sits within a cluster of patents covering similar chemical classes or therapeutic areas, such as oncology, cardiovascular, or neurology drugs.

2. Key Competitors and Patent Thickets:

  • Major players include local biotech firms and subsidiaries of international pharma giants like Pfizer, Novartis, or Takeda, often filing early-stage patents to establish freedom to operate.

  • The patent may face "thicket" issues if numerous overlapping patents protect similar compounds or treatment methods, influencing licensing and R&D strategies.

3. Geographical Scope and Extension:

  • While Taiwanese patents mainly safeguard local marketing rights, patentees often file corresponding applications internationally (e.g., via PCT) to extend protection globally.

  • The patent's claims, if broad, may impact global patentability assessments, especially if similar inventions exist in jurisdictions like China, Japan, or the US.

4. Patent Term and Expiry:

  • Filed in 2005, the patent likely expires around 2025, considering Taiwan’s 20-year term from filing, unless extensions or adjustments apply.

  • Post-expiry, the invention enters the public domain, opening pathways for generic or biosimilar development.


Implications for Stakeholders

  • Pharmaceutical Developers: The patent’s scope indicates proprietary rights, necessitating detailed patent clearance searches before developing similar compounds.

  • Legal and Patent Strategists: Broad claims enhance defensibility but require vigilant monitoring for design-arounds or patent challenges.

  • Researchers and Innovators: The patent landscape reveals active innovation zones, guiding R&D focused on novel modifications to circumvent existing patents.

  • Market Entry Planning: Understanding the validity and scope of TW200529883 assists in assessing risks and opportunities in the Taiwanese market and beyond.


Conclusion

Taiwan Patent TW200529883 exemplifies a carefully constructed legal barrier, protecting a novel pharmaceutical invention with claims carefully calibrated to balance breadth and enforceability. Its scope encompasses specific chemical entities or formulations with therapeutic uses, with its claims strategically designed to withstand legal scrutiny amid an active patent environment.

The patent landscape surrounding TW200529883 illustrates competitive innovation, with multiple patents closely related to the same or similar compounds. Appropriately navigating this environment requires comprehensive patent clearance, strategic licensing, or inventive design-around approaches.


Key Takeaways

  • Claim Breadth and Precision: Broad independent claims maximize protection but require robust novelty and inventive step; precise language safeguards against invalidation.

  • Patent Positioning: Significant in establishing market exclusivity; understanding similar patents helps avoid infringement and capitalize on licensing opportunities.

  • Patent Expiry and Lifecycle: As patent expiry approaches (around 2025), opportunities for generics or biosimilars increase in Taiwan.

  • Strategic Patent Management: Filing in multiple jurisdictions and maintaining patent families bolster global protection, influencing R&D and commercialization.

  • Continued Innovation: Overlapping patents emphasize the necessity for ongoing innovation and strategic patent filings to sustain competitive advantage.


FAQs

1. How do the claims of TW200529883 impact generic drug development in Taiwan?
The claims define the scope of exclusivity, preventing generic manufacturers from producing identical compounds or formulations during the patent term. Once the patent expires, generics can enter the market freely.

2. Can similar compounds circumvent the patent claims?
Potentially, if they differ structurally or functionally beyond the scope of the claims, they may be considered non-infringing. Patent landscape analysis helps identify such opportunities.

3. How does patent scope influence licensing negotiations?
A broad patent scope enhances licensing value, as licensees can develop a wider range of products. Conversely, narrow claims may limit licensing potential.

4. What strategies can companies employ to navigate overlapping patents in Taiwan?
Strategies include designing around existing claims, seeking licenses, or pursuing patent challenges or invalidation proceedings.

5. How does Taiwan’s patent law compare to other jurisdictions regarding pharmaceutical patents?
Taiwan's patent law aligns with international standards, emphasizing structural novelty and inventive step. However, procedural differences may influence patent grant and enforcement.


References

  1. Taiwan Intellectual Property Office (TIPO) Patent Database, TW200529883.
  2. World Intellectual Property Organization (WIPO) PatentScope.
  3. Patent Law of the Republic of China (Taiwan).
  4. [Pharmaceutical Patent Strategies, Bloomberg Intelligence]
  5. AI-assisted patent landscape reports from global patent analytics firms.

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