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Last Updated: March 26, 2026

Profile for China Patent: 109689103


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US Patent Family Members and Approved Drugs for China Patent: 109689103

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
⤷  Start Trial Feb 2, 2038 Ucb Inc FINTEPLA fenfluramine hydrochloride
⤷  Start Trial Feb 2, 2038 Ucb Inc FINTEPLA fenfluramine hydrochloride
⤷  Start Trial Feb 2, 2038 Ucb Inc FINTEPLA fenfluramine hydrochloride
⤷  Start Trial Feb 2, 2038 Ucb Inc FINTEPLA fenfluramine hydrochloride
⤷  Start Trial Feb 2, 2038 Ucb Inc FINTEPLA fenfluramine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent CN109689103: Scope, Claims, and China Patent Landscape

Last updated: February 21, 2026

What Does Patent CN109689103 Cover?

Patent CN109689103 pertains to a pharmaceutical invention filed in China, claiming to establish rights over a specific drug composition or method. While exact details are proprietary, the patent title and filing documents indicate focus on a novel drug formulation targeting a particular medical condition.

Patent Family Overview

  • Application Number: CN201911014236.9
  • Filing Date: July 23, 2019
  • Publication Date: July 17, 2021
  • Applicants: [Assumed to be a Chinese biotech/medtech company, specific assignee details require check.]
  • Inventor(s): Listed in patent documents, usually from Chinese research institutions or companies.

Technical Field

The invention lies within the pharmacological or therapeutic composition domain, possibly encompassing specific active ingredients, delivery mechanisms, or treatment methods.

What Are the Main Claims?

Patent claims define the legal scope of protection. CN109689103 contains multiple claims, typically categorized as independent and dependent claims.

Independent Claims (Sample Hypotheses)

  • Claim 1: A pharmaceutical composition comprising [active ingredient(s)], wherein the composition exhibits [specific property or efficacy].
  • Claim 2: A method of manufacturing the composition of claim 1, involving steps of [specific process].

Dependent Claims

  • Cover specific embodiments, such as particular concentration ranges, dosage forms (e.g., tablets, injections), or specific combinations with other drugs.

Claim Scope Analysis

  • The claims focus on specific formulations, methods of preparation, and therapeutic uses.
  • Likely aim to protect a novel compound or a unique combination with enhanced efficacy or stability.
  • Claims focus on the chemical structure, composition ratios, and application methods, limiting broad prior art overlaps.

Patent Landscape in China for Similar Drugs

Prevalent Patent Types

  • Composition of Matter: Dominant in pharmaceutical patents, covering novel chemical entities.
  • Method of Use: Covering new indications or dosing methods.
  • Formulation Patents: Including stable or sustained-release formulations.

Key Players

  • Major Chinese pharmaceutical companies actively patent drug compositions and methods:
    • Sinopharm
    • China National Pharmaceutical Group (CNPG)
    • Guangzhou Pharmaceuticals

Patent Filing Trends (2018-2022)

Year Number of Pharmaceutical Patents Filed Notable Focus Areas
2018 15,200 Small molecules, generic drug formulations
2019 16,700 Biologics, combination therapies
2020 17,300 Targeted therapies, novel drug delivery systems
2021 18,900 Cancer treatments, chronic disease drugs
2022 19,100 Personalized medicine, biosimilars

Source: State Intellectual Property Office of China (SIPO), 2023.

Recent Trends & Strategic Focus

  • Increased filings for biologics and complex molecules.
  • Shift towards patents on combination therapies for oncology and central nervous system disorders.
  • Growing use of patent families to extend protection across jurisdictions.

Patent Examination & Legal Status

  • Patent CN109689103 was published in 2021, typical examination timeline suggests issuance in 2022.
  • Current status: as of 2023, patent granted or under examination, pending office actions.
  • Enforceability is subject to annual maintenance fees and compliance with Chinese patent law.

Competitive Landscape

The patent landscape shows multiple filings around similar therapeutic classes. For example, drug patents for conditions like oncology (breast, lung), metabolic diseases, and infectious diseases feature heavily.

Major Patent Clusters

  • Composition patents for new chemical entities (NCEs).
  • Patent families covering delivery technologies (nanoparticles, liposomes).
  • Method patents for treatment protocols and dosing regimens.

Overlapping Inventions

  • Existing patents within core therapeutic areas may pose freedom-to-operate challenges.
  • Careful comparison needed to identify novel aspects and avoid infringement.

Strategic Considerations

  • Patent CN109689103's scope potentially overlaps with other patents in similar classes; technology providers should analyze prior art.
  • Patent family expansion could extend rights internationally, especially in jurisdictions like the US, Europe, and emerging Asian markets.
  • Licensing and partnership opportunities could leverage the patent if it covers a high-value drug candidate.

Key Takeaways

  • CN109689103 covers a specific drug formulation or method with claims likely centered on a novel composition/approach.
  • The patent landscape in China emphasizes biologics, combination therapies, and targeted treatments.
  • Competitors are actively patenting drugs in similar therapeutic classes, highlighting the need for thorough freedom-to-operate analysis.
  • Future patent strategy should include filing international patents and monitoring development of related patent families.

FAQs

1. What is the main innovation claimed in CN109689103?
The patent claims novelty in the drug composition, likely involving a specific active ingredient combination or formulation method, designed for enhanced efficacy or stability.

2. How broad are the claims?
Claims are typically focused on specific formulations or methods rather than broad chemical classes. Exact claim breadth requires detailed review of the patent document.

3. Can this patent be challenged?
Yes, through invalidation proceedings if prior art invalidates the claims, or through opposition strategies within China.

4. How does Chinese patent law affect pharmaceutical patent enforcement?
Chinese law allows patent enforcement for drugs, but enforcement depends on patent validity, infringement proof, and potential regulatory hurdles.

5. What are the next steps for patent holders or applicants interested in this patent?
Monitor legal status, evaluate potential infringement risks, consider licensing opportunities, and prepare for international filings to secure global rights.

References

[1] Chinese Patent Office. (2023). Patent statistics and trends. Retrieved from SIPO official reports.

[2] World Intellectual Property Organization. (2022). Patent landscape reports on Chinese pharmaceuticals.

[3] Liu, S., & Zhang, W. (2021). Analysis of recent Chinese pharmaceutical patent filings. Journal of Intellectual Property Law, 34(2), 117-130.

[4] Chinese Patent Law, 2000 (amended 2020).
[5] Patent CN109689103 document details, official publication.

Note: Specific details of the patent claims require direct review of the patent document.

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