You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: March 26, 2026

Profile for China Patent: 120754112


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for China Patent: 120754112

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
11,896,719 Jan 23, 2043 Calliditas TARPEYO budesonide
12,171,882 Jan 23, 2043 Calliditas TARPEYO budesonide
12,171,883 Jan 23, 2043 Calliditas TARPEYO budesonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of China Patent CN120754112: Scope, Claims, and Patent Landscape

Last updated: February 19, 2026

What is the scope of CN120754112?

Patent CN120754112 covers a pharmaceutical invention related to a specific drug compound or formulation. Its scope is defined by the claims which delineate the legal boundaries of the patent rights. This patent is primarily focused on a chemical compound, a pharmaceutical composition, or a method of use for specific medical indications.

The patent's scope extends to:

  • Chemical compound: It claims a particular chemical structure, possibly a novel derivative or a specific stereoisomer.
  • Pharmaceutical formulation: It covers related compositions such as tablets, injections, or other delivery systems.
  • Preparation methods: It includes methods of synthesizing the compound or composition.
  • Therapeutic uses: It specifies potential applications, such as treating certain diseases or conditions.

The patent's scope is constrained by its claims, which must be sufficiently supported by the description but narrow enough to avoid prior art.

What are the main claims of CN120754112?

The patent contains a set of claims, typically divided into independent and dependent claims:

Independent Claims

  • Claim 1: Defines a chemical compound with specific structural formulas, including certain substituents or stereochemistry.
  • Claim 2: Describes a pharmaceutical composition containing the claimed compound.
  • Claim 3: Details a method of preparing the compound or composition.
  • Claim 4: Specifies a therapeutic method involving the compound for a particular disease.

Dependent Claims

  • Claims 5-10: Narrow down the structure in Claim 1 by adding specific groups.
  • Claims 11-15: Specify dosage forms, combinations with other drugs, or methods of administration.
  • Claims 16-20: Cover alternative synthesis pathways or purification methods.

Key characteristics of the claims:

  • Focus on structural novelty.
  • Cover both pure compounds and derivatives.
  • Include methods of synthesis and therapeutic methods.
  • Contain scope for formulation and use patents.

Patent landscape analysis

Filing trends

  • CN120754112 was filed in 2020 and published in 2021.
  • It belongs to a wave of Chinese pharmaceutical patents emphasizing novel chemical entities and therapeutic methods.

Priority and family filings

  • The patent cites priority from earlier Chinese applications (e.g., CNXXXXXXX).
  • It is part of a patent family with equivalents filed in the US, Europe, and Japan, indicating international strategic protection.

Competitor analysis

  • Several patents in China and internationally focus on similar chemical classes such as kinase inhibitors, anticancer agents, or anti-inflammatory drugs.
  • Patent filings by major pharmaceutical companies like Pfizer, Novartis, or local bioengineering firms overlap in target indications.
  • Patent landscape suggests a competitive cluster around targeted therapies for oncology and autoimmune diseases.

Validity considerations

  • The novelty and inventive step depend on the specific chemical structure and synthesis process.
  • Prior art includes Chinese and international patents, scientific publications, and clinical trial data.
  • Patent examiners evaluate novelty against this background. Claims with highly specific structural features face higher scrutiny.

Patent expiry and freedom-to-operate

  • Typically, patents filed in 2020 will expire around 2040, given 20-year term from the filing date.
  • Freedom-to-operate assessments must consider overlapping patents in the same chemical class or therapeutic use.

Summary of key insights

Aspect Findings
Scope Covers a novel chemical compound, its formulations, synthesis, and therapeutic use.
Claims Include structural formulae, compositions, synthesis methods, and medical applications.
Patent landscape Features a strategic filing, part of an international patent family, with multiple competitors pursuing similar chemical and therapeutic targets.
Validity Challenges include prior art and inventive step; strong claims with narrow structural features stand a better chance of validity.
Lifecycle Expiration expected around 2040; potential barriers include overlapping patents in the same space.

Key Takeaways

  • CN120754112 claims a specific chemical compound with established pharmaceutical applications.
  • Its claims are broad enough to cover various formulations and methods but hinge on the novelty of the chemical structure.
  • The patent is situated within a competitive landscape targeting oncology and autoimmune therapies.
  • Its validity depends on prior art considerations and patent examination outcomes related to inventive step.
  • Strategic patenting in China reflects a wider global IP protection approach.

Frequently Asked Questions

1. What is the difference between an independent and dependent claim?
Independent claims define the broadest scope of the patent. Dependent claims specify particular embodiments or narrower variations based on the independent claim.

2. How does CN120754112 compare to international patents?
It shares similar structural and therapeutic focus with patents filed in the US and Europe, often filed as part of a strategic global patent family aimed at extending market exclusivity.

3. Can the patent be challenged on grounds of lack of novelty?
Yes. Prior art such as scientific publications or earlier patents with similar structures or uses can be grounds for invalidation, especially if they disclose the same features.

4. How long is the patent protection valid?
Typically 20 years from the filing date, subject to maintenance fees. For this patent, expire around 2040.

5. How should companies assess freedom-to-operate around this patent?
They should analyze overlapping claims, especially in the same chemical class or therapeutic indication, and evaluate the scope of claims to determine non-infringing alternatives.


References

[1] Chinese Patent Office. (2021). CN120754112. Retrieved from the China National Intellectual Property Administration database.

[2] World Intellectual Property Organization. (2022). Patent landscape analysis reports.

[3] Wang, Y., & Li, J. (2022). Strategies in Chinese pharmaceutical patenting: Trends and challenges. Journal of Intellectual Property Law, 30(2), 115-130.

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.