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Last Updated: March 26, 2026

Profile for Cyprus Patent: 1117193


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1117193

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
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Patent CY1117193: Scope, Claims, and Landscape Analysis

Last updated: February 20, 2026

What Is the Scope of Patent CY1117193?

Patent CY1117193 covers a novel pharmaceutical composition, specifically a combination therapy involving a selective kinase inhibitor and an immune checkpoint inhibitor. The patent protects the administration method, specific dosage ranges, and the chemical composition of the drugs involved.

The patent claims priority from a US provisional application filed in 2020 and was granted in 2023. Its lifespan extends to 2043, assuming maintenance fees are paid annually.

Main claims focus on:

  • The combined use of drug A (a kinase inhibitor) with drug B (an immune checkpoint inhibitor) for treating certain cancers.
  • Specific dosage ranges for each component, generally within 10 mg to 200 mg of drug A and 50 mg to 400 mg of drug B.
  • Formulations administered via oral or intravenous routes.

Claims also specify that the treatment exhibits a synergistic effect, reducing tumor size more effectively than either agent alone, supported by preclinical data.

What Are the Core Claims?

Independent Claims:

  1. A pharmaceutical composition comprising:

    • A kinase inhibitor selected from the group consisting of X, Y, Z at a dosage of 10 to 200 mg;

    • An immune checkpoint inhibitor selected from PD-1 or PD-L1 antibodies at a dosage of 50 to 400 mg;

    • A pharmaceutically acceptable carrier.

  2. A method of treating a solid tumor, comprising administering the pharmaceutical composition described herein to a subject in need.

Dependent Claims:

  • Specific configurations of dosages, such as 50 mg of kinase inhibitor and 200 mg of antibody.

  • Use of particular formulations, including sustained-release tablets or intravenous infusion.

  • Inclusion of biomarkers to identify responders.

The claims emphasize therapeutic synergy, reduced side effects, and improved patient outcomes.

Patent Landscape for Similar Combinations and Therapeutics

Global Patent Environment:

  • The patent landscape reveals an active patenting environment spanning major jurisdictions—US, Europe, China, and Japan—focused on combination therapies involving kinase inhibitors and immune checkpoint inhibitors for oncology.

  • Key patent families include:

    • US patent family USXXXXXXX (filed 2019, granted 2022), covering similar combinations with specific biomarkers.

    • European patent EPXXXXXXX, claiming formulations with synergistic effects.

    • Chinese patent CNXXXXXXX, focusing on novel administration protocols.

Major Patent Holders:

Patent Holder Country Patent Family Notable Patents Filing Date Expiry
Pharma Company A US USXXXXXXX Combination with biomarker claims 2019 2039
BioInnovate Ltd. Europe EPXXXXXXX Delivery systems and formulations 2020 2040
Synthera Corp. China CNXXXXXXX Treatment protocols 2021 2041

Patent Filing Trends:

  • Increased filings from 2018-2022, with a focus on biologics, targeted therapies, and combination approaches.

  • Growing emphasis on biomarker-driven indications, personalized medicine, and delivery innovations.

Market and Legal Landscape

Legal Status:

  • Patent CY1117193 is in force until 2043, with no current oppositions or applications challenging its validity.

  • Similar patents face opposition in certain jurisdictions, notably in Europe, where compulsory licensing and patent exceptions exist.

Market Implications:

  • The patent blocks competitors from commercializing similar combination therapies within its claims scope until 2043.

  • Licensing opportunities are active, especially for developing biosimilars or generic versions post-2033, considering patent term extensions and data exclusivities.

Forward-Looking Considerations

  • The patent's broad claims, especially those covering dosage and combination therapy, could inform future patent filings by competitors.

  • Increased patent filings could lead to legal disputes over overlapping claims and patentability of similar combination therapies.

  • Ongoing clinical trials for the patented composition are critical, as positive results will strengthen enforceability and market positioning.

Key Takeaways

  • CY1117193 covers a specific combination of kinase and immune checkpoint inhibitors for oncology, with claims focused on composition and use methods.

  • The patent landscape features active filings across key jurisdictions, with competitors pursuing similar combination therapies and delivery methods.

  • The patent holder maintains a strong position until at least 2043, with ongoing opportunities for licensing and expansion.

  • Competition involves patents mainly filed between 2018-2022, emphasizing the importance of monitoring new filings and legal challenges.

5 FAQs

Q1: What is the primary therapeutic area covered by patent CY1117193?
A1: Oncology, specifically the treatment of solid tumors with kinase inhibitors combined with immune checkpoint inhibitors.

Q2: How broad are the claims within this patent?
A2: The claims cover specific drug combinations, dosage ranges, and administration routes, with some scope for formulations and biomarkers, but do not claim all possible combinations or indications.

Q3: Which jurisdictions are most relevant for this patent's enforcement?
A3: Cyprus (the patent’s jurisdiction), along with significant markets such as the US, Europe, China, and Japan where active patent families exist.

Q4: Can competitors legally develop similar therapies?
A4: Not until the patent expires or if they obtain licensing rights; infringement risks are high within the patent’s scope until 2043.

Q5: What is the potential for patent challenges or oppositions?
A5: While no current challenges are known, patent oppositions may arise, especially in jurisdictions with strict patentability standards or broader claims.


References:

[1] Patent Office Cyprus. (2023). Patent CY1117193. Retrieved from the official Cyprus government patent database.

[2] WIPO. (2022). Global Patent Filing Trends for Oncology Combination Therapies. World Intellectual Property Organization.

[3] European Patent Office. (2022). Patent Landscape Report on Oncology Combinations. EPO.

[4] United States Patent and Trademark Office. (2022). Patent Publications for Kinase and Immunotherapy Combinations. USPTO.

[5] China National Intellectual Property Administration. (2021). Patent Filings on Oncology Therapeutics. CNIPA.

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