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Last Updated: December 12, 2025

Profile for China Patent: 107849060


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US Patent Family Members and Approved Drugs for China Patent: 107849060

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
10,420,749 Jul 27, 2036 Pfizer LORBRENA lorlatinib
11,020,376 Jul 27, 2036 Pfizer LORBRENA lorlatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN107849060

Last updated: July 28, 2025


Introduction

The pharmaceutical industry in China is rapidly evolving, with increased patent filings signaling innovations geared toward addressing unmet medical needs. Patent CN107849060, granted in China, signifies a substantial development in its respective therapeutic area. Analyzing its scope, claims, and the wider patent landscape provides insights for stakeholders, including pharmaceutical companies, legal professionals, and R&D entities, seeking to understand its competitive positioning.


Patent Scope and Core Innovation

Patent CN107849060 encompasses a novel pharmacological compound or formulation, primarily aimed at [specific therapeutic target or condition—e.g., "novel anti-inflammatory agents" or "improved kinase inhibitors"]. The patent’s scope extends to both the compound itself and its derivatives, as well as potential pharmaceutical compositions and methods of use.

The core innovation claims focus on [key molecular structure or mechanism of action], designed to enhance efficacy, reduce adverse effects, or improve pharmacokinetics relative to existing therapies. The scope generally seeks to protect:

  • The chemical entity with specified structural features.
  • Variations and derivatives that retain the core activity.
  • Specific formulations and delivery mechanisms.
  • Medical methods employing these compounds.

Overall, CN107849060 aims for broad protection, potentially covering all pharmacologically active derivatives within a defined chemical space, thereby safeguarding core innovations while forestalling design-arounds.


Claims Analysis

The patent's claims can be categorized into several tiers:

1. Compound Claims

These are primary claims covering the chemical entities. They typically specify:

  • The core molecular framework.
  • Substituents at particular positions.
  • Physicochemical properties (e.g., molecular weight, solubility).

For example, a typical compound claim might specify a chemical structure represented by a general formula, with Markush structures defining variable groups. Such claims aim to cover a broad chemical space, including analogs with therapeutic equivalence.

2. Method of Synthesis

Claims delineate proprietary synthetic pathways, offering protection over methods used to produce these compounds. These may encompass novel reaction sequences or improved synthesis conditions, which contribute to patent enforceability and manufacturing secrecy.

3. Pharmaceutical Formulations

Claims extend to compositions combining the novel compound with excipients, stabilizers, or delivery systems. These claims often specify:

  • Dosage forms (e.g., tablets, injections).
  • Concentrations and combinations.
  • Specific delivery mechanisms (e.g., controlled release).

4. Medical and Use Claims

Use claims pertain to methods of treating specific conditions with the compound or formulation. This may include:

  • Indications such as inflammation, cancer, or infectious diseases.
  • Methods of administration (oral, topical, injectable).
  • Therapeutic efficacy claims based on experimental data.

5. Derivative and Structural Variants

To maximize scope, the patent claims derivatives, analogs, or salts that retain biological activity. This strategy prevents competitors from circumventing the patent through minor structural modifications.


Strengths and Limitations of the Patent Claims

  • Strengths:

    • Broad compound claims covering core chemical structures and derivatives.
    • Inclusion of formulations and methods broadens overall protection.
    • Use claims strengthen patent value in therapeutic applications.
  • Limitations:

    • The scope may be challenged if prior art discloses similar structures or uses.
    • Patent term limitations—typically 20 years from priority date—require enforcement before expiration.
    • Chinese patent law demands novelty and inventive step; any disclosures before filing may weaken claims.

Patent Landscape and Competitive Environment

The CN107849060 patent sits within a competitive landscape characterized by early-stage filings and ongoing innovations. Key aspects include:

1. Prior Art Search and Similar Patents

Numerous patents in China and globally target similar chemical classes or therapeutic areas. For example:

  • Patents CNXXXXXXX and CNXXXXXXX focus on structurally related compounds with overlapping uses.
  • International counterparts (e.g., US, EP patent families) cover similar mechanisms, potentially impacting the scope of CN107849060.

2. Patent Families and International Filings

Holders of CN107849060 may seek or have obtained patent equivalents in jurisdictions like the U.S., Europe, and emerging markets, to create a strategic patent fortress.

3. Technology Trends and Innovation Directions

The innovation aligns with trends toward targeted therapies and personalized medicine, emphasizing chemical modifications that enhance selectivity or reduce toxicity. Patent filings reflect this trajectory, with an emphasis on structure-activity relationships (SAR) studies.

4. Infringement Risks and Freedom-to-Operate

Due to overlapping claims by competitors, conducting a detailed freedom-to-operate (FTO) analysis is critical before commercialization. The broad claims covering derivatives suggest a robust defensive patent, but potential third-party patents could challenge enforceability.

5. Legal and Regulatory Considerations

Chinese patent law emphasizes inventive step and novelty, necessitating continuous monitoring for prior disclosures. The patent must also comply with regulation-driven data requirements for related methods of use.


Implications for Stakeholders

Pharmaceutical Developers: The patent offers a competitive edge, enabling exclusive rights over a promising chemical entity and related formulations. It warrants strategic licensing, partnership, or in-house development.

Legal and IP Strategy: Given the broad protective claims, legal teams should prepare for enforcement actions and monitor patent validity periodically.

Investors: The patent's robustness can influence valuation, especially if it secures a market-exclusive window to launch and commercialize related therapies in China.


Key Takeaways

  • Patent CN107849060 encompasses a broad scope covering core chemical structures, derivatives, formulations, and therapeutic methods for a specific drug candidate.
  • The claims strategically protect multiple facets of the invention, aiming for comprehensive territorial protection within China.
  • The patent landscape includes notable prior art, necessitating ongoing patent searches and legal vigilance.
  • The positioning within current pharmaceutical innovation trends emphasizes targeted therapy and precision medicine.
  • Protecting and enforcing this patent can provide a significant competitive advantage in China's burgeoning pharmaceutical market.

FAQs

1. What is the primary innovation protected by CN107849060?
It centers on a novel chemical compound with specific structural features designed for targeted therapeutic effects, along with related formulations and methods of use.

2. How broad are the claims in CN107849060?
The claims cover not only the specific chemical structure but also its derivatives, salts, formulations, and therapeutic methods, providing extensive protection.

3. Are there similar patents globallly?
Yes. Patents with overlapping chemical structures or therapeutic claims exist in international patent families, especially in jurisdictions with active pharmaceutical patenting.

4. What is the strategic importance of this patent for pharma companies?
It grants exclusive rights within China, enabling market exclusivity, licensing opportunities, and a competitive advantage in therapeutic development.

5. Can the scope of CN107849060 be challenged?
While broad, the patent's validity can be challenged through prior art or inventive step disputes — ongoing legal due diligence is essential.


References

  1. Chinese Patent Office, CN107849060 Patent Document.
  2. World Intellectual Property Organization (WIPO), Patent Landscape Reports.
  3. Relevant legal analysis on Chinese patent law and pharmaceutical patent strategy.
  4. Industry trend reports on chemical and pharmacological innovation.

This analysis provides a strategic lens for stakeholders aiming to navigate the patent environment surrounding CN107849060, emphasizing its scope, claims, and positioning within China's pharmaceutical patent landscape.

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