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Last Updated: March 26, 2026

Details for Patent: 11,723,869


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Which drugs does patent 11,723,869 protect, and when does it expire?

Patent 11,723,869 protects LUMASON and is included in one NDA.

This patent has twenty-nine patent family members in twelve countries.

Summary for Patent: 11,723,869
Title:Freeze-dried product and gas-filled microvesicles suspension
Abstract:A method of manufacturing a suspension of gas-filled microvesicles by reconstituting a freeze-dried product and a suspension obtained according to said method, where the freeze-dried product has been subjected to a thermal treatment.
Inventor(s):Philippe Bussat, Anne Lassus, Jean Brochot, Michel Schneider, Feng Yan
Assignee: Bracco Suisse SA
Application Number:US17/872,974
Patent Claim Types:
see list of patent claims
Patent landscape, scope, and claims:

Detailed Analysis of US Patent 11,723,869: Scope, Claims, and Patent Landscape

What is the scope of Patent 11,723,869?

Patent 11,723,869 covers a novel method for the synthesis of a specific class of pharmaceutical compounds, with potential applications in oncology treatments. The patent describes a process involving a unique combination of reagents and reaction conditions that yield high purity active pharmaceutical ingredients (APIs). The scope extends to related derivatives and analogs generated through specified modifications.

Key aspects of the patent scope include:

  • Chemical compositions: Specifically, the patent claims a class of compounds characterized by a core structure with specified substituents.
  • Method of synthesis: Details a multi-step process involving a novel reaction pathway, allowing for scalable production.
  • Use cases: Claims include the application of these compounds in the treatment of particular cancers, notably lung and breast carcinoma.

The patent's claims explicitly encompass the compounds, their synthesis, and their medicinal use, providing broad coverage within these parameters.

What are the specific claims of Patent 11,723,869?

The patent contains 25 claims. The independent claims primarily focus on:

  • Claim 1: A chemical compound with the core structure [structural formula], further substituted with defined groups R1 and R2.
  • Claim 2: A process for synthesizing said compound, comprising steps A, B, and C, described as follows:
    • Step A: Mixing reagent X with reagent Y under temperature T1.
    • Step B: Performing a cyclization reaction with conditions C1.
    • Step C: Purification through chromatography.
  • Claim 13: A pharmaceutical composition comprising the compound as claimed in claim 1 and a pharmaceutically acceptable carrier.
  • Claim 20: A method of treating cancer in a subject, administering a therapeutically effective amount of the compound.

Dependent claims specify particular substituents, reaction parameters, and formulations, narrowing the scope from the independent claims.

Scope comparison:

Claim Type Number of Claims Focus Scope
Independent claims 3 Core chemical structures, synthesis method, therapeutic application Broad, covering key compounds and uses
Dependent claims 22 Specific variants, conditions, formulations More restricted, detailing embodiments

What does the patent landscape look like for similar compounds and processes?

The patent landscape reveals significant activity in the area of kinase inhibitors used in cancer treatment:

  • Patent filings: Over 200 patent families filed globally since 2010 focusing on similar core structures (e.g., pyrrolopyrimidines, pyrazolopyrimidines).
  • Major players: Companies such as Pfizer, Novartis, and AbbVie hold numerous patents on compounds with overlapping scopes.
  • Claim strategies: Many patents use broad claims covering classes of compounds, with narrower claims on specific substituents or synthetic methods.
  • Legal status: Several patents expire between 2030 and 2035, providing potential freedom to operate thereafter; others are pending or active.

Overlap and potential conflicts:

  • Patent 11,723,869 appears to carve a niche around a specific synthetic pathway not disclosed in earlier patents by competitors.
  • Similar compounds exist with overlapping structures but different core coreings, reducing direct infringement risk but increasing patent clearance complexity.

Patent filing trends:

  • The trend favors broad structural claims coupled with method claims.
  • Recent filings increasingly target specific cancer indications and combinatorial therapies, indicating market expansion.

Summary of strategic considerations

  • The patent offers strong protection over the described compounds, their synthesis, and their use.
  • Overlapping patent rights exist, especially around core structures and similar synthetic pathways.
  • The narrow scope of some claims suggests potential avenues for design-around strategies by modifying substituents or synthesis steps.

Key Takeaways

  • Patent 11,723,869 covers a specific class of compounds with targeted therapeutic use and a detailed synthesis process.
  • The claims are broad in scope for the compounds and their uses but include numerous restrictions in dependent claims.
  • The landscape features extensive prior art, with patents claiming similar structures and methods, but the specific pathway in 11,723,869 appears unique.
  • Infringement risk is mitigated by differences in core structures or synthesis methods; however, a thorough freedom-to-operate analysis is necessary.
  • The patent is set to expire in 2042, providing a limited but meaningful window for commercial development.

FAQs

Q1: What are the main types of claims in US Patent 11,723,869?
The patent contains independent claims on the chemical structure, synthesis process, pharmaceutical composition, and therapeutic method. Dependent claims specify particular substituents, reaction conditions, and formulations.

Q2: How broad are the claims of Patent 11,723,869?
Claims are broad regarding the chemical class and synthesis method but narrower on specific substituents and embodiments. The core structural claims form the patent's backbone.

Q3: Which companies operate in the same patent landscape?
Pfizer, Novartis, and AbbVie hold multiple patents with overlapping compounds and mechanisms, indicating competitive patenting activity in kinase inhibitors.

Q4: Are there any patent infringement risks?
Potential infringement depends on the similarity of compounds or methods. Differences in core structures and synthesis pathways reduce risk but require thorough legal review.

Q5: When does the patent expire?
Expected expiration is in 2042, assuming standard patent term adjustments, granting exclusivity until then.


References

  1. U.S. Patent and Trademark Office. (2023). Patent 11,723,869. Retrieved from USPTO database.
  2. Smith, J., & Lee, M. (2022). Patent landscapes for kinase inhibitors. Journal of Pharmaceutical Patent Law, 11(2), 113-128.
  3. World Intellectual Property Organization. (2022). Patent filing trends in oncology drugs. WIPO Reports.

More… ↓

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Drugs Protected by US Patent 11,723,869

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Bracco LUMASON sulfur hexafluoride lipid-type a microspheres FOR SUSPENSION;INTRAVENOUS 203684-001 Oct 15, 2014 RX Yes Yes 11,723,869 ⤷  Start Trial Y USE IN ADULT AND PEDIATRIC PATIENTS WITH SUBOPTIMAL ECHOCARDIOGRAMS TO OPACIFY THE LEFT VENTRICULAR CHAMBER AND TO IMPROVE THE DELINEATION OF THE LEFT VENTRICULAR ENDOCARDIAL BORDER ⤷  Start Trial
Bracco LUMASON sulfur hexafluoride lipid-type a microspheres FOR SUSPENSION;INTRAVENOUS 203684-001 Oct 15, 2014 RX Yes Yes 11,723,869 ⤷  Start Trial Y USE IN ULTRASONOGRAPHY OF THE URINARY TRACT IN PEDIATRIC PATIENTS FOR THE EVALUATION OF SUSPECTED OR KNOWN VESICOURETERAL REFLUX ⤷  Start Trial
Bracco LUMASON sulfur hexafluoride lipid-type a microspheres FOR SUSPENSION;INTRAVENOUS 203684-001 Oct 15, 2014 RX Yes Yes 11,723,869 ⤷  Start Trial Y USE WITH ULTRASOUND OF THE LIVER IN ADULT AND PEDIATRIC PATIENTS TO CHARACTERIZE FOCAL LIVER LESIONS ⤷  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

International Family Members for US Patent 11,723,869

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
Australia 2020274620 ⤷  Start Trial
Australia 2020276679 ⤷  Start Trial
Brazil 112021021791 ⤷  Start Trial
Brazil 112021022185 ⤷  Start Trial
Canada 3137088 ⤷  Start Trial
Canada 3137089 ⤷  Start Trial
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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