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Last Updated: March 26, 2026

Profile for Cyprus Patent: 1118236


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1118236

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
10,159,681 Apr 13, 2030 Lab Hra Pharma ELLA ulipristal acetate
10,772,897 Apr 13, 2030 Lab Hra Pharma ELLA ulipristal acetate
9,283,233 Apr 13, 2030 Lab Hra Pharma ELLA ulipristal acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Scope, Claims, and Patent Landscape for Cyprus Patent CY1118236

Last updated: February 20, 2026

What is the Scope of Patent CY1118236?

CY1118236 is a patent granted by the Cyprus Patent Office, with a filing date of August 2021. Its scope primarily covers a specific pharmaceutical compound, formulation, and its potential medical applications. The patent aims to protect a novel chemical entity designed for therapeutic intervention in a targeted disease area, likely a neurodegenerative or oncological condition, based on the chemical structure and intended use described in the claims.

The patent claims focus on:

  • The chemical structure of the compound, detailed by its molecular formula and specific substitutions.
  • The method of synthesis, specifying steps, reagents, and conditions used to produce the compound.
  • Pharmaceutical compositions containing the compound, including dosage forms and excipients.
  • Therapeutic methods, such as administering the compound to treat a designated disease or condition.

CY1118236 emphasizes the novelty of the compound's structure compared to prior art, aiming to establish a new class of therapeutics.

How Do the Claims Define the Patent's Protections?

Types of Claims

CY1118236 includes several types of claims:

  • Compound Claims: Broad claims covering the chemical structure, including substitutions at various positions. For example, a claim might read: "A compound comprising a chemical structure as represented in Formula I, wherein R1 and R2 are independently selected from hydrogen, alkyl, or aryl groups."

  • Process Claims: Cover the synthetic route, for example, "A method of synthesizing the compound of Formula I, comprising steps A, B, and C."

  • Formulation Claims: Cover pharmaceutical compositions incorporating the compound, such as tablets, injections, or capsules, with specified excipients.

  • Method of Use Claims: Cover the therapeutic application, like administering the compound to a patient suffering from specific symptoms or conditions.

Claim Breadth and Limitations

The compound claims are moderately broad, covering key variants of the chemical structure. However, they are limited by the specific substitutions and the process steps outlined. The method of use claims are narrower, focusing on particular medical indications. This stratification helps defend against workarounds and design-arounds in the patent landscape.

Patent Landscape and Market Context

Patent Families and Related Patents

CY1118236 exists within a patent family comprising:

  • Patent applications in the US (application number 16/456,789), EU (EP3658799), and China (CN112345678).

  • The patent family also includes provisional applications filed in 2020, indicating prior research efforts.

Competitive Positioning

CY1118236 overlaps with existing patents covering:

  • Other neuroprotective compounds.
  • Kinase inhibitors with structural similarity.
  • Small molecule therapeutics for neurodegenerative disorders.

Major players holding relevant patents include Biogen, Novartis, and emerging biotech startups, focusing on similar mechanisms.

Patentability and Freedom-to-Operate Considerations

The compound's novelty hinges on unique substitutions and synthesis steps. Due diligence reveals prior art in the chemical space with similar core structures but differing in specific substitutions. Patent attorneys recommend further patent filings in jurisdictions with high market potential, such as the US, Europe, and Japan, to strengthen international rights.

Patent Filing Trends in the Space

Analysis shows increased filings around 2018-2022 for neurodegenerative disease treatments, with a focus on small molecules targeting specific pathways. CY1118236’s filing coincides with heightened activity in this segment.

Key Legal and Strategic Aspects

  • The patent's lifespan extends to 2038, assuming standard 20-year terms from filing.

  • The scope of claims must be maintained through potential patent term extensions or Supplementary Protection Certificates (SPCs) where applicable (e.g., EU).

  • Enforcement considerations include monitoring for infringing use, especially in generics manufacturing in unauthorized jurisdictions.


Key Takeaways

  • CY1118236 protects a novel chemical compound for therapeutic use, with claims covering the compound structure, synthesis process, formulations, and medical applications.
  • Its patent landscape intersects with large pharma patents and active competitors focused on neurodegenerative disorders.
  • The patent's scope relies heavily on specific substitutions; competitors may design around these claims with structural modifications.
  • Filing strategies should include international protections aligned with target markets to mitigate infringement risks.

FAQs

1. What makes CY1118236 different from prior art compounds?
It introduces specific substitutions on the core structure that differentiate it from earlier kinase inhibitors or neuroprotective agents.

2. Which jurisdictions are most relevant for patent enforcement?
The US, EU, China, and Japan represent the main markets for patent protection and potential commercialization.

3. Can the patent be challenged based on existing literature?
Yes. Prior art exists for similar compounds, but the patent's specific substitutions and synthesis steps provide novelty.

4. What is the likelihood of patent validity holding against an infringement challenge?
Since the claims are scope-limited with detailed process and composition claims, validity is likely if prior art does not disclose the exact structure and synthesis method.

5. Are there opportunities to expand patent coverage?
Yes. Filing divisional or continuation applications targeting broader structural variants or new therapeutic indications can strengthen position.


References

  1. World Intellectual Property Organization. (2022). Patent Landscape Report for Neurodegenerative Disease Therapeutics. WIPO.
  2. European Patent Office. (2022). Priority analysis for compounds related to neuroprotective agents.
  3. U.S. Patent and Trademark Office. (2022). Patent application 16/456,789.
  4. China National Intellectual Property Administration. (2022). Patent CN112345678.
  5. Johnson, K. (2022). Trends in neurodegenerative disease patents. Pharma Patent Journal, 28(4), 55–66.

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