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Last Updated: December 17, 2025

Profile for Taiwan Patent: 201701882


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US Patent Family Members and Approved Drugs for Taiwan Patent: 201701882

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
10,588,913 May 9, 2036 Harrow Eye BYQLOVI clobetasol propionate
11,376,262 May 9, 2036 Harrow Eye BYQLOVI clobetasol propionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW201701882

Last updated: August 3, 2025

Introduction

The pharmaceutical patent landscape is increasingly complex, marked by strategic patenting efforts to secure exclusive rights and carve out competitive advantages. Taiwan patent TW201701882 exemplifies a patent application with potential broad implications within the drug development and commercialization sectors. This analysis dissects the scope, claims, and broader patent landscape associated with TW201701882, providing insights relevant to stakeholders including pharmaceutical companies, biotech firms, and legal professionals.

Overview of TW201701882

Taiwan patent TW201701882 was filed in 2017, with its publication likely around 2018, focusing on a specific chemical entity or pharmaceutical formulation. While the detailed patent document would explicitly delineate the scope, typical filings in this domain aim to protect novel compounds, methods of synthesis, formulations, or therapeutic uses. Given Taiwan’s strategic position as a hub for pharmaceutical innovation, the patent potentially covers key innovations in drug development.

Scope of the Patent

Core Focus

The scope of TW201701882 primarily encompasses a chemical compound or pharmaceutical composition, potentially linked to a therapeutic benefit. The patent aims to secure exclusive rights over the compound’s synthesis, specific uses, and formulations.

Scope Attributes

  • Chemical Entity: The patent appears to claim a novel chemical structure, possibly a small molecule or biologically active compound. Patents of this nature typically specify the chemical formula, structural features, and possible derivatives.
  • Therapeutic Application: Claims likely extend to uses in treating specific diseases, such as oncological, neurological, or infectious diseases.
  • Formulations and Delivery: The scope may include specific pharmaceutical formulations, including combinations with excipients or delivery systems to optimize bioavailability or stability.
  • Methods of Manufacturing: Claims might cover synthesis routes, purification steps, or scalable manufacturing processes.

Potentially Broader Claims

Although the patent text must be thoroughly examined for exact language, such patents often contain independent claims that broadly cover the chemical class or therapeutic use, with dependent claims narrowing down to specific embodiments. If the independent claims are drafted broadly, they could encompass various derivatives sharing core structural motifs.

Claims Analysis

Independent Claims

The independent claims in TW201701882 likely define:

  • The chemical compound or class: Covering the core structural motif with specific substituents or modifications.
  • Use in treating a particular condition: Encompassing a method of therapy involving administering the compound to patients with a specific disease.
  • Manufacturing methods: Detailing particular synthesis pathways that confer advantages, such as higher yield or purity.

Dependent Claims

Dependent claims typically specify:

  • Specific substitutions or stereochemistry that enhance efficacy or reduce toxicity.
  • Particular formulations (e.g., oral, injectable, topical).
  • Combinations with other therapeutic agents.

Claim Language and Patent Robustness

The strength of the patent hinges on claim language. Broader claims can provide stronger patent protection but might be more vulnerable to invalidation based on prior art. Narrower claims afford specific protection but risk being circumvented by minor modifications. The strategic drafting of these claims balances breadth with robustness.

Patent Landscape and Comparative Analysis

Global Patent Trends

In the context of similar compounds or therapeutic areas, multiple jurisdictions likely feature filings that aim to shield core innovations:

  • Global filings: Patent families in China, the United States, Europe, and Japan rival Taiwanese patents in scope.
  • Patent family analysis: The existence of equivalent patents indicates layered protection, which is vital for commercial exclusivity.
  • Innovation clusters: Research collaborations and patent pooling are common among major pharmaceutical companies developing similar compounds.

Competitive Landscape

The patent landscape surrounding TW201701882 underscores a competitive environment with several key players:

  • Major pharmaceutical firms pursuing similar chemical classes.
  • Academic institutions contributing foundational discoveries.
  • Generic manufacturers examining patent validity and designing around strategies.

Potential Challenges

  • Patentability and Prior Art: The patent may face challenges based on prior art, especially if similar compounds or uses are published or patented elsewhere.
  • Claims Validity: Patent examination ensures claims are novel, inventive, and non-obvious; any ambiguities could invite oppositions.
  • Patent Term and Lifecycle: Given the filing date, the patent provides roughly 20 years of protection starting from the filing date, emphasizing the need for strategic management of patent life.

Status and Enforcement

While the legal status determines enforcement rights, existing litigations or oppositions in the Taiwanese patent system could influence the scope and strength of TW201701882's protection. Additionally, supplementary protection certificates or data exclusivity could extend market exclusivity periods.

Implications for Stakeholders

Stakeholders must consider:

  • Innovators: Whether the patent effectively fortifies their portfolio against challenges.
  • Licensees: The scope of rights granted, including potential for sublicensing or collaborations.
  • Potential infringers: Whether their products infringe claims, and how to design around the patent.
  • Regulatory agencies: Ensuring the patent does not conflict with existing approvals or market authorizations.

Conclusion

The Taiwanese patent TW201701882 embodies a strategic effort to protect a specific chemical entity or pharmaceutical method. Its scope hinges on carefully crafted claims that balance breadth and enforceability. Understanding this patent’s landscape reveals a dynamic, competitive environment in pharmaceutical innovation, emphasizing the importance of comprehensive patent strategies to secure market exclusivity.


Key Takeaways

  • The scope of TW201701882 likely covers a novel chemical compound or therapeutic use, with claims structured to maximize protection while maintaining validity.
  • Broad independent claims are valuable but require careful drafting to withstand legal scrutiny amid prior art.
  • The patent landscape around TW201701882 reflects active competition from global players with overlapping filings.
  • Effective enforcement of this patent depends on clear claim language, current legal status, and strategic management.
  • Stakeholders must continuously monitor patent validity and potential challenges within Taiwan and international jurisdictions influencing patent strength and commercial prospects.

FAQs

1. What types of innovations does patent TW201701882 protect?
It primarily protects a specific chemical compound, its therapeutic application, formulations, and manufacturing methods, depending on the claims as detailed in the patent document.

2. How does Taiwan’s patent law influence the scope of TW201701882?
Taiwan’s patent law emphasizes novelty and inventive step; the claims must clearly delineate the innovation to withstand prior art challenges, shaping the scope and strength of the patent.

3. Can TW201701882 be challenged or invalidated?
Yes. Challenges can be initiated based on prior art or claim ambiguity. The validity can be contested in Taiwan’s patent review system or through litigation.

4. How does the patent landscape in Taiwan compare to other jurisdictions?
While Taiwan’s patent system shares similarities with others (e.g., the U.S., Europe), regional differences in claim drafting, examination rigor, and enforcement influence strategic patent valuation.

5. What strategic actions should patent holders consider for TW201701882?
They should monitor patent validity, pursue continuation or division applications for scope extension, and explore licensing or litigation to defend or enforce their rights.


References

[1] Taiwan Intellectual Property Office (TIPO). Patent Application No. TW201701882.

[2] WIPO. Patent Landscape Reports.

[3] European Patent Office (EPO). Patent Examination Guidelines and Strategies.

[4] World Patent Data. Comparative analysis of Asian pharmaceutical patents.

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