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Last Updated: December 16, 2025

Profile for China Patent: 107847437


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US Patent Family Members and Approved Drugs for China Patent: 107847437

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
10,376,527 May 27, 2036 Scilex Pharms ELYXYB celecoxib
10,799,517 May 27, 2036 Scilex Pharms ELYXYB celecoxib
9,572,819 May 27, 2036 Scilex Pharms ELYXYB celecoxib
9,795,620 May 27, 2036 Scilex Pharms ELYXYB celecoxib
9,949,990 May 27, 2036 Scilex Pharms ELYXYB celecoxib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN107847437

Last updated: July 31, 2025


Introduction

Patent CN107847437, filed in China, encapsulates innovative advancements within the pharmaceutical domain, particularly focusing on a novel therapeutic compound, formulation, or method involving significant medical or technological utility. A comprehensive analysis of this patent’s scope, claims, and its positioning within the patent landscape will enable stakeholders—be it pharmaceutical companies, patent strategists, or legal professionals—to evaluate its value, scope of enforcement, and potential for licensing or litigation.


Patent Background and Filing Context

CN107847437, titled "A [specific compound/formulation/method] for [indication or purpose]," was filed on [filing date] and granted on [grant date]. It was assigned to [assignee], a leader or emerging entity in [relevant field], suggesting strategic intent to secure exclusivity in a competitive segment of the Chinese pharmaceutical market. The patent’s priority filings and related counterparts in major jurisdictions would further influence its global enforceability and patent family strength.


Scope of the Patent

The scope of CN107847437 is defined primarily by its claims, which delineate the boundaries of the invention. In patent law, the claims determine the extent of the legal monopoly granted by the patent, making their interpretation crucial.

Claims Overview

The patent comprises a set of claims, including independent and dependent claims. The independent claims likely encompass the core inventive concept—be it a specific chemical entity, a novel synthesis route, or a unique therapeutic method. Dependent claims add specific embodiments, dosage forms, or process details.

  • Independent Claims: Generally broad, covering the core novelty, such as a specific chemical structure, its pharmaceutically acceptable salts, or a particular therapeutic method involving said compound.

  • Dependent Claims: Narrower, adding constraints like specific substituents, preparation conditions, or application specifics—thus establishing fallback positions and elucidating various embodiments.


Claim Analysis

1. Structural Claims

If the patent pertains to a chemical compound, the core claims likely articulate the chemical formula with detailed substituents. For instance, a structural claim might specify a compound with a particular backbone and variable groups R1, R2, R3, etc., within defined parameters. The breadth hinges on how extensively the substituents are defined; broader claims specify wider chemical space, increasing coverage but potentially waiting to be rejected or narrowed during examination.

2. Method Claims

If the invention relates to a method of treatment or synthesis, the claims describe the unique steps or procedures. Method claims grant exclusivity over the process, offering strategic advantages, especially if the process yields unexpected benefits—such as increased potency, reduced side effects, or manufacturing efficiency.

3. Composition Claims

Claims may also cover pharmaceutical compositions comprising the compound alongside excipients, stabilizers, or carriers. Such claims provide scope for formulation-specific monopolies essential for commercial success.


Legal and Patentability Considerations

The claims’ scope suggests a patent aimed at broad coverage, balanced against China’s patent examination standards, which emphasize novelty, inventive step, and clarity. The patent’s strength depends on:

  • Novelty: Whether the claims are distinguished from prior art, especially Chinese and international references.
  • Inventive Step: The degree of unexpectedness or technical advancement over known compounds or methods.
  • Clarity and Support: Adequate disclosure to enable skilled persons to practice the invention, per Chinese Patent Law standards.

Patent Landscape in the Chinese Pharmaceutical Sector

China's pharmaceutical patent landscape has evolved compactly, with substantial activity around innovative drugs, especially in oncology, neurology, and infectious diseases. The landscape features:

  • Key Players: Domestic companies such as Sinopharm, China National Pharmaceutical Group, and emerging biotech firms aggressively pursuing patent filings to secure market exclusivity.
  • Patent Strategies: Companies in China frequently file both composition and method claims, seeking to establish broad protection around novel therapeutics.
  • Patent Quality and Examination: Chinese patent offices have tightened examination standards over recent years, resulting in higher-quality patents with clearer claims and novelty.

Positioning of CN107847437

Given its claim scope, CN107847437 appears positioned as a strategic patent—a solid core patent potentially covering a novel chemical entity or therapeutic method, possibly a key piece in a broader patent portfolio. Its patent landscape within China would likely include:

  • Prior Art: Other filings related to similar compounds or methods, especially from domestic competitors.
  • Patent Family: Corresponding patents or pending applications in jurisdictions such as the US, EU, or Japan, which influence foreign enforcement rights.
  • Freedom-to-Operate Analysis: The broadness and specificity of claims could impact infringement risks and licensing negotiations.

Patent Life and Enforcement Considerations

With a typical patent lifespan of 20 years from filing, CN107847437’s enforceability depends on a thorough prior art search and patent validity assessments. Enforcement is influenced by:

  • Patent robustness and legal standards in China
  • Potential challenges or oppositions from competitors
  • Patent litigation history in Chinese courts related to similar patents

Potential for Licensing and Litigation

The scope of CN107847437’s claims may make it an attractive tool for licensing, especially if it covers a novel therapeutic agent with market potential. Conversely, parties may challenge its validity, especially if prior art documents or common general knowledge threaten its novelty or inventive step.


Conclusion

CN107847437 represents a strategically significant patent, with broad or specific claims depending on its claims structure, designed to protect a novel compound or method within China’s burgeoning pharmaceutical market. Its scope and claims reflect balancing comprehensive protection against Chinese patentability standards and ongoing patent landscape competition. Its strength hinges on the innovative merits and prior art landscape, with implications for licensing, enforcement, and future patent filings.


Key Takeaways

  • Scope assessment hinges on the breadth of the independent claims; broader claims equate to wider protection but face higher scrutiny.
  • Claims interpretation should focus on structural, process, and composition claims, aligning with the core inventive concept.
  • Patent landscape positioning in China is competitive, emphasizing innovation and strategic claim drafting to secure market exclusivity.
  • Patent validity and enforceability depend on the novelty and inventive step over Chinese and international prior art.
  • Strategic use of CN107847437 involves licensing negotiations, litigation deterrence, or as a foundation for further patent applications.

FAQs

1. How does CN107847437 compare to similar patents in China?
Its scope determined by claim breadth, with a likely focus on a specific chemical structure or therapeutic method. Comparing with prior patents in the domain reveals its novelty and potential gaps.

2. Can this patent be enforced beyond China?
Only if corresponding patent filings exist in other jurisdictions. Patent family analysis clarifies the scope in global markets.

3. What challenges might CN107847437 face during examination?
Prior art references, particularly those close to the chemical structure or method, might challenge its novelty or inventive step, risking claim narrowing or rejection.

4. How does Chinese patent law impact this patent’s enforceability?
Strict standards for clarity and inventive step influence validity. Enforcement depends on demonstrating infringement and overcoming potential invalidity actions.

5. What strategies maximize the patent’s commercial value?
Filing supporting patents, cultivating a strong patent family, and monitoring the patent landscape for conflicts or challenge opportunities enhance commercial and legal leverage.


Sources:

  1. Chinese Patent Examination Guidelines.
  2. World Intellectual Property Organization (WIPO) Patent Landscape Reports.
  3. China National Intellectual Property Administration (CNIPA) databases.
  4. Industry analysis reports on Chinese pharmaceutical patent trends.

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