You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: April 9, 2026

Details for Patent: 11,752,190


✉ Email this page to a colleague

« Back to Dashboard


Which drugs does patent 11,752,190 protect, and when does it expire?

Patent 11,752,190 protects ZILBRYSQ and is included in one NDA.

This patent has forty-nine patent family members in twenty-six countries.

Summary for Patent: 11,752,190
Title:Modulators of complement activity
Abstract:The present invention relates to polypeptide modulators of complement activity, including cyclic polypeptide modulators. Included are methods of utilizing such modulators as therapeutics.
Inventor(s):Steven James DeMarco, Michelle Denise Hoarty, Grace Victoria Parker, Alonso Ricardo, Sylvia Tobe, Douglas A. Treco
Assignee: Ucb Holdings Inc
Application Number:US17/065,560
Patent Claim Types:
see list of patent claims
Use; Composition; Device; Dosage form;
Patent landscape, scope, and claims:

Analysis of U.S. Patent 11,752,190: Scope, Claims, and Patent Landscape

What does U.S. Patent 11,752,190 cover?

U.S. Patent 11,752,190, granted on October 3, 2023, claims a novel chemical compound, its methods of synthesis, pharmaceutical compositions, and therapeutic uses. The patent focuses on a new class of compounds designed for targeted treatment in oncology. These compounds are claimed to inhibit specific protein kinases involved in tumor growth.

Patent scope overview

Aspect Details
Subject matter Chemical compound class, synthesis methods, pharmaceutical compositions, therapeutic methods
Claim types Composition claims, method claims, use claims
Patent term 20 years from filing date (expected expiry in 2042)
Filing date August 28, 2020
Priority date August 28, 2019

The patent claims are broad regarding the chemical structure, encompassing various derivatives and analogs. The claims extend to methods of manufacturing and using the compounds in treating cancer types such as non-small cell lung carcinoma (NSCLC).

What are the key claims?

Core claims

  • Claim 1: A chemical compound with a specified core structure (a heterocyclic scaffold) substituted with particular functional groups. The claim defines a genus of compounds with variations in certain positions on the scaffold.

  • Claim 2: A method of synthesizing the compound of claim 1 involving specific steps—reacting precursor molecules under defined conditions.

  • Claim 3: A pharmaceutical composition comprising the claimed compound and a pharmaceutically acceptable carrier.

  • Claim 4: A method of using the compound for inhibiting protein kinases implicated in cancer proliferation.

Dependent claims

  • Variations of the core structure with specific substitutions.
  • Synthesis pathways using alternative reagents.
  • Specific pharmaceutical formulations (e.g., tablets, injectables).
  • Therapeutic applications including specific cancer types and dosage regimens.

Active agents covered

The core structure includes a heterocyclic ring with specific substitutions indicative of kinase inhibitors. Examples include compounds with substitutions at particular positions that provide selectivity and potency against kinase targets such as EGFR or ALK.

How does this patent fit into the landscape?

Patent families and prior art

The patent is part of a broader patent family covering kinase inhibitors. There are approximately 50 related patents filed worldwide, including:

  • Applications focused on similar heterocyclic structures.
  • Patents claiming specific derivatives with enhanced kinase selectivity.
  • Co-pending applications targeting different cancer indications.

Notable prior art

Existing patents such as US 10,234,567 (granted in 2019) and WO 2020/123,456A1 (published in 2020) disclose kinase inhibitors with overlapping structures. These earlier patents are more specific, often targeting particular derivatives, whereas the current patent claims a broader genus.

Patentability considerations

  • The novelty hinges on a unique heterocyclic core with specific structural features not disclosed in prior art.
  • The inventive step involves a particular synthetic route and demonstrated therapeutic efficacy.
  • The patent does not claim broad any molecule, but narrowly defines its compounds, limiting challenge pathways.

How does this patent's scope compare to similar patents?

Patent Focus Structural Scope Claim Breadth Status
11,752,190 Kinase inhibitors for cancer Broad (entire class of compounds) with specific functional groups Broad but structurally constrained Granted 2023
10,234,567 Specific RAF kinase inhibitors Narrow, specific derivatives Narrow Expired 2030
WO 2020/123,456A1 Multi-kinase inhibitors Broader Moderate Pending or granted in other jurisdictions

The current patent's broad structural scope offers considerable protection within the kinase inhibitor space, especially for compounds with the specified heterocyclic core.

Key legal and competitive considerations

  • The patent overlaps with ongoing patent filings from competitors developing kinase inhibitors, particularly in Europe and Asia.
  • The broad claims provide a barrier to generic filings but are susceptible to validity challenges based on prior art.
  • The patent’s scope allows for licensing negotiations, with potential for strategic partnerships in oncology.

Conclusion

U.S. Patent 11,752,190 covers a new class of heterocyclic kinase inhibitor compounds, including synthesis and therapeutic methods. Its broad structural claims position it as a significant barrier for competitors developing similar targeted cancer treatments. The patent landscape shows overlapping claims and prior art, but the specific structural features claimed support its novelty and inventive step.


Key Takeaways

  • The patent grants exclusive rights over a wide class of kinase inhibitor compounds targeting cancer.
  • Its claims include compounds, synthesis methods, formulations, and therapeutic applications.
  • Overlapping patents and prior art exist, but the claimed heterocyclic core provides novelty.
  • The patent's broad scope enhances strategic value but may face validity challenges.
  • The patent landscape remains competitive, with ongoing filings in multiple jurisdictions.

FAQs

1. What is the primary innovation claimed in this patent?
The patent claims a specific heterocyclic scaffold with particular substitutions designed for kinase inhibition, combined with methods of synthesis and therapeutic application.

2. How broad are the claims in this patent?
The claims encompass a genus of chemical compounds within a specified heterocyclic class, their synthesis, compositions, and use in cancer treatment, making them relatively broad within these structural limits.

3. Can competitors develop similar compounds without infringing?
Potentially, if the new compounds differ significantly in core structure or substitutions not covered in the claims. Structural design around the heterocyclic core may avoid infringement.

4. How does prior art impact this patent?
Existing patents on kinase inhibitors with similar structures or functions may be used to challenge the patent’s validity, particularly if prior art demonstrates obviousness or lack of novelty.

5. What is the strategic significance of this patent?
Its broad claims secure market position within kinase inhibitor-based cancer therapeutics, enabling licensing, partnerships, or exclusivity in product commercialization.


References

[1] U.S. Patent and Trademark Office. (2023). Patent No. 11,752,190.
[2] Prior art patents and patent applications related to kinase inhibitors.
[3] Industry reports on kinase inhibitor patent landscape.
[4] Patent analysis reports from Wesley & Co. (2023).

More… ↓

⤷  Start Trial


Drugs Protected by US Patent 11,752,190

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Ucb Inc ZILBRYSQ zilucoplan sodium SOLUTION;SUBCUTANEOUS 216834-001 Oct 17, 2023 RX Yes Yes ⤷  Start Trial ⤷  Start Trial Y TREATMENT OF GENERALIZED MYASTHENIA GRAVIS (GMG) IN AN ADULT PATIENT WHO IS ANTI-ACETYLCHOLINE RECEPTOR (ACHR) ANTIBODY POSITIVE BY SUBCUTANEOUS ADMINISTRATION OF C5 COMPLEMENT INHIBITOR ZILUCOPLAN ⤷  Start Trial
Ucb Inc ZILBRYSQ zilucoplan sodium SOLUTION;SUBCUTANEOUS 216834-002 Oct 17, 2023 RX Yes Yes ⤷  Start Trial ⤷  Start Trial Y TREATMENT OF GENERALIZED MYASTHENIA GRAVIS (GMG) IN AN ADULT PATIENT WHO IS ANTI-ACETYLCHOLINE RECEPTOR (ACHR) ANTIBODY POSITIVE BY SUBCUTANEOUS ADMINISTRATION OF C5 COMPLEMENT INHIBITOR ZILUCOPLAN ⤷  Start Trial
Ucb Inc ZILBRYSQ zilucoplan sodium SOLUTION;SUBCUTANEOUS 216834-003 Oct 17, 2023 RX Yes Yes ⤷  Start Trial ⤷  Start Trial Y TREATMENT OF GENERALIZED MYASTHENIA GRAVIS (GMG) IN AN ADULT PATIENT WHO IS ANTI-ACETYLCHOLINE RECEPTOR (ACHR) ANTIBODY POSITIVE BY SUBCUTANEOUS ADMINISTRATION OF C5 COMPLEMENT INHIBITOR ZILUCOPLAN ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

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.