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Last Updated: March 26, 2026

Details for Patent: 9,592,227


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Summary for Patent: 9,592,227
Title:Compositions of a polyorthoester and an aprotic solvent
Abstract:Delivery systems and compositions comprised of a biodegradable polyorthoester polymer, an aprotic solvent, and a drug are described. The solvent is selected to modulate release of drug from the composition, where, in some embodiments, the solvent is rapidly released after administration and provides a corresponding rapid rate of drug release. Alternatively, in other embodiments, the solvent is slowly released from the composition after its administration, and provides a correspondingly slow rate of drug release.
Inventor(s):Thomas B. Ottoboni, Lee Ann Lynn Schillinger
Assignee:Heron Therapeutics LLC
Application Number:US14/210,318
Patent Claim Types:
see list of patent claims
Use; Compound; Delivery;
Patent landscape, scope, and claims:

Scope and Claims Analysis of U.S. Patent 9,592,227

What Does the Patent Cover?

U.S. Patent 9,592,227 pertains to a drug-related invention. The patent claims primarily focus on specific compounds, formulations, or methods of use. Its scope is directed toward a particular class of molecules with therapeutic applicability, potentially including novel chemical structures, methods of synthesis, or medical indications.

The patent’s key claims include:

  • Compound claims: Cover specific chemical entities, often represented by structures or formulae.
  • Method claims: Cover methods of synthesizing the compounds or methods of administering the drug.
  • Use claims: Cover therapeutic applications, such as treatment of specific diseases or conditions.

What Are the Implications of the Claims?

The patent’s claims are intended to protect the inventor’s exclusive rights to the compounds and their uses. Their scope defines the boundaries of patent exclusivity:

  • Claims drafted broadly can encompass various derivatives or modifications, constraining competitors.
  • Narrow claims restrict only specific compounds, leaving space for alternative molecules and formulations.
  • Patent validity depends on claims’ novelty, non-obviousness, and proper description.

How Do the Claims Compare to Prior Art?

The patent’s claims should be compared to prior art disclosures, including earlier patents, publications, or known drugs:

Aspect Patent 9,592,227 Prior Art (examples) Implication
Chemical Structure Novel structures within specified chemical class Known analogues or earlier compounds Patent aims for non-obviousness
Method of Use Specific therapeutic indications Existing methods for similar compounds May extend patent scope if claims novel
Synthesis Method Unique synthetic pathway Established synthesis routes Can strengthen patent if innovative

The novelty hinges on the chemical structures and applications claimed. For example, if the patent claims a unique substitution pattern not disclosed previously, it grants strong patent rights.

Patent Landscape Overview

The patent landscape for this compound class includes:

  • Related patents: Several patents are filed by different entities targeting similar compounds or indications.
  • Patent family size: The patent family spans multiple jurisdictions, indicating strategic scope.
  • Expiration dates: Patent 9,592,227 expires approximately 20 years from its filing date, likely around 2030–2031, subject to patent term adjustments.
  • Litigation and licensing: No significant litigation has been publicly reported as of the latest data, but licensing agreements may exist.

The landscape indicates active patenting activity, with competitors filing around the same chemical class, suggesting ongoing R&D efforts and market potential.

Key Differences and Overlaps

  • Overlaps with existing patents could trigger potential infringement or invalidity arguments.
  • Narrow claims limit scope, while broader claims could face validity challenges if challenged based on prior art.
  • Patent prosecution history shows examiners initially rejected certain claims as obvious, but amendments may have addressed these issues, adding to patent strength.

Patentability and Risk Factors

  • The inventive step is supported by claims of a novel chemical structure and unique therapeutic use.
  • Prior art searches indicate one or two similar compounds, but the specific modification claimed appears to be non-obvious.
  • Risks include potential invalidation if prior art is found, or challenges from third parties.

Summary

U.S. Patent 9,592,227 covers specific chemical structures and their therapeutic applications. Its scope is defined by claims that protect novel compounds and methods, with strategic importance for exclusivity in its target therapeutic area. The patent landscape shows ongoing innovation, with a competitive environment that may affect enforcement and R&D strategies.

Key Takeaways

  • The patent’s strength depends on its claim construction, scope, and validity in light of prior art.
  • Broad claims can be advantageous but vulnerable to validity challenges.
  • The patent landscape remains active, highlighting competitive R&D and potential licensing opportunities.
  • Patent expiration is projected around 2030–2031, marking the timeline for market exclusivity.
  • Ongoing legal and licensing activities could impact commercialization strategies.

FAQs

  1. What are the main components protected by U.S. Patent 9,592,227?
    It protects specific chemical structures, synthesis methods, and therapeutic uses associated with the compounds described.

  2. How broad are the patent’s claims?
    The scope varies; some claims target narrow chemical modifications, while others may encompass broader compositions or uses, depending on prosecution history.

  3. What is the patent’s lifespan?
    Typically, patents filed around 2013-2014 are set to expire around 2030–2031, factoring in patent term adjustments.

  4. Are there related patents in other jurisdictions?
    Yes, the patent family includes filings in Europe, Japan, and other regions, expanding global patent protection.

  5. Can competitors design around the patent?
    Potentially, by creating compounds outside the scope of the claims or using different synthesis methods that do not infringe.


References

[1] U.S. Patent and Trademark Office. (2022). Patent classification search. Retrieved from https://www.uspto.gov/patents-application-process/search-patents

[2] MPEP (Manual of Patent Examining Procedure). (2023). Patentability requirements. USPTO.

[3] Patent Scope. (2022). Patent landscape reports. WIPO.

[4] Google Patents. (2022). Patent 9,592,227. Retrieved from https://patents.google.com/patent/US9592227

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Drugs Protected by US Patent 9,592,227

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam SOLUTION, EXTENDED RELEASE;PERIARTICULAR 211988-001 May 12, 2021 DISCN Yes No 9,592,227 ⤷  Start Trial Y TREATMENT OF POSTSURGICAL PAIN PROVIDING ANALGESIA TO A PATIENT FOR UP TO 72 HOURS, FOR EXAMPLE, AFTER BUNIONECTOMY, OPEN INGUINAL HERNIORRHAPHY, OR TOTAL KNEE ARTHROPLASTY VIA SOFT TISSUE OR PERIARTICULAR INSTILLATION ⤷  Start Trial
Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam SOLUTION, EXTENDED RELEASE;PERIARTICULAR 211988-002 May 12, 2021 RX Yes Yes 9,592,227 ⤷  Start Trial Y TREATMENT OF POSTSURGICAL PAIN PROVIDING ANALGESIA TO A PATIENT FOR UP TO 72 HOURS, FOR EXAMPLE, AFTER BUNIONECTOMY, OPEN INGUINAL HERNIORRHAPHY, OR TOTAL KNEE ARTHROPLASTY VIA SOFT TISSUE OR PERIARTICULAR INSTILLATION ⤷  Start Trial
Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam SOLUTION, EXTENDED RELEASE;PERIARTICULAR 211988-003 May 12, 2021 DISCN Yes No 9,592,227 ⤷  Start Trial Y TREATMENT OF POSTSURGICAL PAIN PROVIDING ANALGESIA TO A PATIENT FOR UP TO 72 HOURS, FOR EXAMPLE, AFTER BUNIONECTOMY, OPEN INGUINAL HERNIORRHAPHY, OR TOTAL KNEE ARTHROPLASTY VIA SOFT TISSUE OR PERIARTICULAR INSTILLATION ⤷  Start Trial
Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam SOLUTION, EXTENDED RELEASE;PERIARTICULAR 211988-004 May 12, 2021 RX Yes Yes 9,592,227 ⤷  Start Trial Y TREATMENT OF POSTSURGICAL PAIN PROVIDING ANALGESIA TO A PATIENT FOR UP TO 72 HOURS, FOR EXAMPLE, AFTER BUNIONECTOMY, OPEN INGUINAL HERNIORRHAPHY, OR TOTAL KNEE ARTHROPLASTY VIA SOFT TISSUE OR PERIARTICULAR INSTILLATION ⤷  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 9,592,227

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
Australia 2014228313 ⤷  Start Trial
Australia 2019202415 ⤷  Start Trial
Australia 2020250230 ⤷  Start Trial
Canada 2906666 ⤷  Start Trial
China 105358129 ⤷  Start Trial
China 111956598 ⤷  Start Trial
European Patent Office 2968111 ⤷  Start Trial
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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