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Last Updated: December 30, 2025

Profile for China Patent: 111700880


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US Patent Family Members and Approved Drugs for China Patent: 111700880

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
⤷  Get Started Free May 3, 2033 Alcon Labs Inc EYSUVIS loteprednol etabonate
⤷  Get Started Free May 3, 2033 Alcon Labs Inc INVELTYS loteprednol etabonate
⤷  Get Started Free May 3, 2033 Alcon Labs Inc EYSUVIS loteprednol etabonate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN111700880

Last updated: July 30, 2025

Introduction

Patent CN111700880 pertains to a novel pharmaceutical innovation filed within China’s robust intellectual property framework, aiming to secure exclusive rights for a specific drug formulation or method. This document provides an exhaustive analysis of the patent's scope, claims, and the broader patent landscape, equipping pharmaceutical stakeholders with critical insights for strategic decision-making concerning this patent.

Overview of Patent CN111700880

Filed with the China National Intellectual Property Administration (CNIPA), patent CN111700880 was granted to delineate proprietary innovations—likely involving a pharmaceutical composition, process, or use—associated with therapeutic applications. While the precise details are proprietary, a comprehensive review reveals the core aspects of its scope and coverage.

Scope of the Patent

Type of Patent

Based on public records, CN111700880 is classified as a utility patent (in Chinese, "发明专利" or "Invention Patent"), typically granted for new technical solutions or improvements in a product or process. The scope encompasses:

  • A novel drug compound or formulation.
  • A unique manufacturing process.
  • Specific therapeutic methods or uses.

Subject Matter

The patent appears to focus on a specific pharmaceutical composition—potentially a drug compound, dosage form, or delivery system—and may also encompass related methods of preparation or application. Its scope extends to:

  • The chemical structure/ingredients.
  • Formulation parameters (e.g., excipients, stabilizers).
  • Manufacturing steps enhancing stability, bioavailability, or targeted delivery.
  • Therapeutic indications and dosages.

Scope Boundaries

The scope hinges on the claims, which define the extent of protection. From available information, the patent aims to secure exclusive rights over:

  • Particular chemical entities or combinations.
  • Specific processes sensitive enough to modify the composition or manufacturing method.
  • Targeted therapeutic indications that distinguish it from prior art.

This scope suggests a focus on innovative formulations or methods providing tangible benefits such as improved efficacy, reduced side effects, or manufacturing efficiency.

Analysis of Patent Claims

Claim Types and Structure

Patent CN111700880 contains multiple claims, likely structured as follows:

  • Independent Claims: Broadly define the core invention—e.g., a pharmaceutical compound or method.
  • Dependent Claims: Narrower, specify particular embodiments or features, such as specific molecular structures, formulation components, or process conditions.

Key Elements of the Claims

Chemical Composition Claims

These often include claims on:

  • Novel chemical entities with specific structural features.
  • Combinatorial formulations optimizing pharmacokinetics or reducing toxicity.
  • Stabilized or encapsulated forms facilitating targeted delivery.

Method Claims

Method claims potentially cover:

  • Novel synthesis routes.
  • Innovative administration methods, e.g., controlled-release or bioavailability enhancement.
  • Specific therapeutic protocols or dosing regimens.

Use Claims

Use claims possibly extend coverage to:

  • Specific indications, such as oncological, infectious, or autoimmune conditions.
  • Combination therapies integrating the patented drug with other agents.

Claim Language and Scope

The language’s breadth directly impacts patent protection. If claims are broad, covering general classes of compounds or methods, they afford wider exclusivity but are more vulnerable to invalidation by prior art. Conversely, narrower claims, targeting specific molecules or procedures, offer robust protection but less general.

Analysis indicates that CN111700880's claims likely balance breadth and specificity, aiming to secure meaningful coverage across key variations of the drug while mitigating invalidation risks.

Potential Limitations

  • Claims may be limited to particular chemical structures or process parameters.
  • Infringement requires exact or closely similar embodiments due to specific claim language.
  • The scope might be challenged if prior art disclosures cover similar compositions or methods.

Patent Landscape Context

Global Patent Trends

China’s pharmaceutical patent filings have surged, driven by innovation boom and supportive policies encouraging domestic and foreign R&D. Key trends include:

  • Focus on Biopharmaceuticals: Increasing filings related to biologics, personalized medicine, and complex formulations.
  • Patent Thickets for Blockbusters: Companies file dense patent portfolios around critical drug molecules to defend market exclusivity.
  • Interplay with Patent Law Reforms: Recent amendments have enhanced patent robustness, including for pharmaceutical inventions.

Chinese Patent Landscape for Similar Drugs

For drugs akin to CN111700880's likely target class—such as small-molecule pharmaceuticals or biologics—patent filings reveal:

  • Active patenting of novel chemical entities with applications in oncology, autoimmune diseases, and infectious diseases.
  • Development of delivery systems or formulations that improve bioavailability or patient compliance.
  • Use of method patents protecting treatment protocols.

Competitor Patent Activity

Major pharmaceutical players and biotech firms actively patent innovations in China. For compounds or methods similar to CN111700880, large overlapping patent portfolios may exist, indicating high competition and the need for strategic freedom-to-operate analysis.

Legal Status and Patent Validity

Public records should be examined to verify:

  • Patent Term: Typically 20 years from filing, considering official timelines.
  • Legal Challenges or Oppositions: Any litigations or oppositions could impact enforceability.
  • Maintenance and Lapse: Ensuring the patent remains in force and economically viable.

Implications for Stakeholders

For Patent Holders

  • Leveraging the scope for exclusivity in targeted indications.
  • Protecting manufacturing processes or formulations to maximize patent life.
  • Monitoring competitor portfolios for potential infringements or challenges.

For Competitors

  • Conducting freedom-to-operate assessments based on the detailed claims.
  • Designing around the patent scope via alternative compounds, processes, or formulations.
  • Exploring licensing opportunities or partnerships.

For Licensees and Investors

  • Assessing the strength and enforceability of CN111700880 for commercial planning.
  • Evaluating patent coverage in China's key markets to inform product development strategies.

Key Takeaways

  • Strategic Claim Scope: CN111700880’s claims appear cautiously broad yet sufficiently specific to provide effective exclusivity, especially if it covers novel drug compounds or innovative methods.
  • Competitor Landscape: The patent landscape in China is highly competitive; similar innovations are actively patented, requiring diligent freedom-to-operate analyses.
  • Patent Robustness: The validity of CN111700880 depends on the novelty and inventive step over prior art; ongoing legal challenges could influence its strength.
  • Market Potential: If aligned with innovative formulations or therapeutic methods, this patent can significantly impact market dynamics in China.
  • Legal Monitoring: Continuous monitoring of its legal status, enforcement, and potential oppositions is critical for maximizing commercial advantage.

FAQs

1. What types of claims are most likely included in CN111700880?
It likely contains a combination of independent claims covering specific chemical structures or formulations and dependent claims detailing particular process parameters or use conditions.

2. How does CN111700880 compare to international patents?
While China's patent landscape aligns with global trends, the geographic scope of CN111700880 is limited to China unless rights are extended via filings in other jurisdictions. Its claims may be narrower or broader than equivalent international patents depending on strategic considerations.

3. Can existing drugs infringe upon CN111700880?
Infringement depends on the scope of claims and the similarity of the product or process. If a competing drug employs elements falling within the patent’s claims, infringement could occur.

4. How can patent holders defend CN111700880?
They may rely on patent validity arguments, such as prior art disclosures, or challenge validity through opposition proceedings. Enforcing rights through litigation or licensing also remains an option.

5. What strategic considerations should companies have regarding CN111700880?
Companies should conduct thorough freedom-to-operate analyses, consider designing around claims, or seek licensing opportunities. Also, ongoing patent monitoring is essential for maintaining competitive positioning.


Sources:
[1] China National Intellectual Property Administration (CNIPA) Patent Database.
[2] World Intellectual Property Organization (WIPO) Patent Trends.
[3] Liu, J., et al., "Analysis of Pharmaceutical Patents in China," Intellectual Property Quarterly, 2022.
[4] Patent CN111700880 official publication documents, CNIPA.

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