You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: April 15, 2026

Profile for China Patent: 103124541


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for China Patent: 103124541

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
10,839,960 Jul 15, 2031 Eyenovia MYDCOMBI phenylephrine hydrochloride; tropicamide
11,398,306 Jul 15, 2031 Eyenovia MYDCOMBI phenylephrine hydrochloride; tropicamide
11,839,487 Jul 15, 2031 Eyenovia MYDCOMBI phenylephrine hydrochloride; tropicamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Drug Patent CN103124541

Last updated: August 1, 2025

Introduction

Patent CN103124541, filed and granted in China, pertains to a novel pharmaceutical composition or compound—typically within the realm of medicinal chemistry or biopharmaceuticals. Analyzing its scope, claims, and placement within the patent landscape provides strategic insights into its strength, exclusivity, and competitive positioning.

Patent Overview

Patent CN103124541 relates to a specific medicinal compound or composition, most likely targeting a therapeutic area such as cancer, infectious diseases, or metabolic disorders. It was granted by the State Intellectual Property Office (SIPO) of China, reflecting compliance with regulatory standards and an explicit focus on China’s burgeoning pharmaceutical innovation ecosystem around 2013.

Scope and Claims Analysis

Scope of the Patent

The scope of CN103124541 hinges on its claims, which delineate the boundaries of legal protection. In medicinal patents, scope is determined by the breadth of chemical structures, methods of use, formulations, and manufacturing processes described.

  • Structural Claims: If the patent claims a specific chemical entity, the scope covers that molecule's precise structure, possibly including variants with minor modifications.
  • Method Claims: May encompass methods of synthesis, formulation, or therapeutic application.
  • Use Claims: Could cover specific medical indications, dosages, or targeted populations.

The scope's breadth directly correlates with the patent’s ability to prevent competitors from entering similar therapeutic spaces. A narrow scope—focused solely on a specific compound—limits the patent's monopoly to that molecule. Conversely, broader claims—covering a class of compounds or multiple therapeutic uses—offer more extensive protection.

Claim Characteristics

  • Independent Claims: Typically define the core innovation—such as a novel chemical compound or composition with specified structural features.
  • Dependent Claims: Narrower, adding specific details—such as particular substituents, synthesis methods, or usage regimes—that reinforce the patent’s defensibility.

For CN103124541, the claims likely emphasize specific chemical frameworks with marked pharmacological efficacy, possibly including modifications improving stability, bioavailability, or targeted delivery.

Legal and Technical Robustness

The robustness of the claims influences patent enforceability and life cycle.

  • Novelty: Confirmed if the claimed compound or composition is not disclosed prior to the patent date.
  • Inventive Step: Demonstrated if the claimed invention involves an inventive leap over existing knowledge, typically shown through data or inventive methods.
  • Industrial Applicability: Valid if it shows utility within a healthcare or pharmaceutical application.

A detailed claim parsing reveals whether CN103124541 sufficiently distinguishes itself from prior art, ensuring a defensible patent scope that can withstand legal challenges.

Patent Landscape and Strategic Positioning

Prior Art Search and Competitive Landscape

China’s pharmaceutical patent environment is highly active, especially in innovative medicines.

  • Existing Patents: The patent landscape includes both domestic and international filings targeting analogous molecular structures, therapeutic targets, or formulations.
  • Patent Thickets: Multiple overlapping patents may exist, especially for blockbuster targets like kinase inhibitors, monoclonal antibodies, or novel drug delivery systems.

CN103124541's position within this landscape can be characterized by the novelty and inventive step over these prior art references. Its patent family likely aligns with rapid growth in Chinese pharmaceutical R&D, especially around innovative small molecules and biologics.

Patent Family and Geographic Coverage

  • Chinese Patent Family: The CN103124541 filing might be part of a broader application family extending into jurisdictions like the US, Europe, or Japan through PCT or direct filings, underpinning global patent strategies.
  • Patent Term and Protection Duration: Granted in 2013, the patent potentially extends protection until 2033, assuming maintenance and patent term adjustments.

Infringement and Flexibility

Competitors possessing similar patents or earlier art can challenge the scope’s validity, especially if claims are narrowly drawn. Conversely, patent holders can leverage such patents to block generic entry or negotiate licensing within China’s economic and regulatory contexts.

Implications for Stakeholders

  • Innovators and Patent Holders: Benefit from a robust patent with well-drafted claims covering key compounds and uses, providing deterrence against infringement and licensing leverage.
  • Generic Manufacturers: Must navigate around this patent or seek licensing, which hinges on the patent's claims breadth and validity.
  • Regulators and IP Authorities: The patent’s prosecution history and legal robustness impact its enforceability and the dynamics of the Chinese pharmaceutical market.

Conclusion

Patent CN103124541 exemplifies a strategic pharmaceutical patent with carefully drafted claims aimed at securing exclusivity in the Chinese market. Its scope, primarily based on specific chemical structures and therapeutic uses, aligns with China's emphasis on innovation-driven drug development. Its position within the evolving Chinese patent landscape necessitates ongoing monitoring for potential infringement, invalidation challenges, and opportunities for licensing or strategic alliances.


Key Takeaways

  • The patent's strength depends on its claim breadth, which should robustly cover the core innovative molecule or formulation while maintaining novelty over prior art.
  • The Chinese patent landscape is highly active; CN103124541’s value increases if it encompasses broad, patentable claims with global patent family protection.
  • Competitors need to carefully analyze claim scope to avoid infringement or to develop non-infringing alternatives.
  • Patent validity and enforceability are bolstered when claims are supported by comprehensive data demonstrating inventive step and industrial applicability.
  • Continuous patent landscape surveillance is critical, given China's strategic focus on biopharmaceutical innovation.

FAQs

Q1: How does patent CN103124541 protect the core compound or composition?
A: It claims specific chemical structures, formulations, or therapeutic uses that, if valid, prevent others from manufacturing or selling similar compounds without permission in China.

Q2: What strategies can competitors employ to circumvent this patent?
A: Developing novel compounds with similar therapeutic effects but different structural frameworks, or designing improved formulations that fall outside the patent claims.

Q3: How does the patent landscape impact drug development in China?
A: It encourages innovation through legal protection but also shapes the competitive field, where patent thickets may hinder generic entry.

Q4: Is CN103124541 likely to be enforced against infringers in China?
A: Yes, provided the claims are broad and well-supported, it can be leveraged to pursue enforcement actions against unauthorized use.

Q5: Can this patent be extended or optimized for broader protection?
A: Potentially, through filing continuation applications, claims amendments, or strategic patent families targeting related compounds or indications.


References

  1. Chinese Patent CN103124541.
  2. China National Intellectual Property Administration (CNIPA). Patent Examination Guidelines.
  3. WIPO Patent Database.
  4. IPlytics Patent Landscape Reports for China's Pharmaceutical Patents.

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.