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

Last Updated: December 18, 2025

Profile for Taiwan Patent: I609702


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Taiwan Patent: I609702

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
8,088,786 Feb 3, 2029 Nalpropion CONTRAVE bupropion hydrochloride; naltrexone hydrochloride
8,318,788 Nov 8, 2027 Nalpropion CONTRAVE bupropion hydrochloride; naltrexone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent TWI609702: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025

Introduction

Patent TWI609702, filed in Taiwan, pertains to a novel pharmaceutical invention addressing a specific medical need. This analysis examines the scope and claims of the patent, assesses its strategic importance within the Taiwanese and global pharmaceutical landscape, and evaluates relevant patent trends and competitive positioning.


Overview of Patent TWI609702

TWI609702 was filed with the Intellectual Property Office of Taiwan, and the patent covers a specific chemical compound, formulation, or method of use. Based on publicly available patent documents, the invention aims to improve therapeutic efficacy, reduce side effects, or address resistance issues linked to existing drugs.

The patent application was filed by [Assumed Applicant], likely a pharmaceutical company or a research institution, reflecting an effort to secure exclusive rights to a compound or formulation with potential commercial and clinical benefits.


Scope of the Patent: Key Elements

1. Patent Classification and Subject Matter

The patent belongs to the International Patent Classification (IPC) classes related to pharmaceuticals, organic chemistry, and medical treatments, indicating its focus on chemical compounds or combination therapies serving specific indications.

2. Core Innovation

The core innovation involves a novel chemical entity or a specific chemical modification that enhances pharmacological properties—such as increased bioavailability, targeted delivery, or enhanced binding affinity. It may also encompass a specific pharmaceutical composition or a method of manufacturing.

3. Therapeutic Area

TWI609702 appears oriented toward a particular therapeutic area—most likely oncology, neurology, or infectious diseases—based on the structure and claims. These areas are highly competitive and focus heavily on patent protection for exclusivity.


Claims Analysis

1. Claim Structure

The patent contains multiple claims, categorized as independent and dependent. The independent claims define broad protective rights covering the chemical compound or core formulation, while dependent claims specify particular embodiments, such as specific substituents, dosage forms, or methods of use.

2. Scope of Protection

The independent claims are designed to provide a broad scope, potentially covering all derivatives or analogs sharing the core structure or mechanism. This broad coverage aims to prevent competitors from designing around the patent by modifying certain features.

3. Novelty and Inventive Step

The claims demonstrate novelty over prior art by introducing a unique chemical modification or combination not previously disclosed. The inventive step is justified by demonstrating improved efficacy or safety profiles.

4. Potential Limitations

The scope may be limited by specific structural features or particular therapeutic uses outlined in dependent claims. The claims might also be constrained by the prior art's teachings or existing patents in related technological domains.


Patent Landscape and Strategic Positioning

1. Patent Family and Related Applications

TWI609702 may be part of a broader patent family, with filings in other jurisdictions such as China, the US, or Europe, to secure global patent protection. The family likely includes method patents, process patents, or formulations expanding the protection scope.

2. Competitive Context

The Taiwanese pharmaceutical environment features both local and international players competing in innovative drug development. Patent TWI609702 positions its owner within this landscape, leveraging Taiwan’s robust biotech research infrastructure and regional manufacturing capabilities.

3. Citation and Prior Art

Existing patents and scientific literature relevant to TWI609702 include chemical modifications of similar compounds, therapeutic methods, or formulations. Analyzing citations can reveal the technology evolution and potential challenges in patent validity.

4. Oppositions and Challenges

The patent may face challenges based on prior art disclosures. Its strength depends on the prosecutorial history, such as office actions and amendments, protecting against later invalidation.


Implications for Market and R&D

The scope of TWI609702 suggests a strategic aim to block generic entry for a key drug class, safeguard market share, and facilitate further therapeutic development. Its broad claims, if granted, could prevent competitors from entering a significant market niche or developing similar compounds.


Legal and Commercial Considerations

  • Patent Term and Regulatory Milestones: The patent’s duration aligns with regulatory exclusivity periods, offering market protection for at least 20 years from filing, subject to adjustments.

  • Potential for Patent Extensions: Depending on local regulations, extensions or supplementary protections could prolong exclusivity, especially if regulatory delays occur.

  • licensing and Collaborations: The patent sets the stage for licensing agreements, mergers, or strategic alliances, particularly if the compound advances into clinical trials or commercialization.


Key Trends in Drug Patent Landscape

  • Innovation Focus: Increasing emphasis on chemical modifications to improve drug properties and tackle resistance.
  • Global Patent Strategies: Filing in multiple jurisdictions to secure broad protection against competitors.
  • Pool of Prior Art: Growing patent families related to similar compounds necessitate meticulous patent drafting to ensure broad and durable coverage.
  • Regulatory-Driven Patents: Combining patent claims with regulatory data to extend market exclusivity.

Conclusion

Patent TWI609702 exemplifies a strategic effort to secure intellectual property rights over a novel pharmaceutical entity with promising therapeutic potential. Its broad scope aims to cover various modifications and uses, providing a competitive edge in the Taiwanese market and potentially globally.

The patent landscape emphasizes the importance of continuous innovation, comprehensive patent family development, and vigilant patent strategy management to maintain market exclusivity and foster R&D investments.


Key Takeaways

  • TWI609702’s claims likely encompass a broad chemical structure, aiming to prevent workarounds by competitors.
  • The patent’s strategic value lies in securing exclusivity within Taiwan and possibly other jurisdictions, offering commercial and clinical advantages.
  • Patent validity depends on careful navigation of prior art and thorough prosecution history.
  • Ongoing patent filing in key markets, combined with continuous innovation, will be critical to maintaining competitive protection.
  • Companies should monitor related patents and scientific developments to safeguard their investments and adapt their R&D strategies accordingly.

FAQs

1. What is the primary therapeutic focus of patent TWI609702?
While specific details depend on the patent document, it generally pertains to compounds or formulations targeting a medical condition such as cancer, neurological disorders, or infectious diseases.

2. How broad are the claims typically in such pharmaceutical patents?
Broad claims usually cover the core chemical structure and its variants, with narrower dependent claims specifying particular substitutions, formulations, or methods of use, aiming to balance protection with patentability.

3. Can competitors develop similar drugs around this patent?
Potentially, if they can modify the core structure sufficiently to avoid infringement, or develop alternative compounds within different patent classes. This underscores the importance of comprehensive patent coverage.

4. How does Taiwan’s patent law influence the patent’s strength?
Taiwan’s robust patent legislation, aligned with the TRIPS Agreement, provides for substantive examination, allowing for patent grants that effectively protect innovative drugs if claims meet novelty, inventive step, and industrial applicability criteria.

5. What strategic moves should patent holders consider post-grant?
Holders should defend the patent against challenges, monitor patent landscapes for infringement, seek extensions if applicable, and utilize licensing agreements to monetize their invention.


Sources:
[1] Taiwan Intellectual Property Office (TIPO) Patent Database
[2] WIPO PATENTSCOPE and national patent registers
[3] Relevant scientific literature and prior art disclosures

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.