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

Last Updated: December 16, 2025

Details for Patent: 8,741,327


✉ Email this page to a colleague

« Back to Dashboard


Which drugs does patent 8,741,327 protect, and when does it expire?

Patent 8,741,327 protects UZEDY and is included in one NDA.

This patent has twenty-eight patent family members in eight countries.

Summary for Patent: 8,741,327
Title:Method of maintaining therapeutic risperidone levels in a PLA:PLGA implant
Abstract:The present invention provides implants comprising a therapeutic drug and a polymer containing polylactic acid (PLA) and optionally polyglycolic acid (PGA). The present invention also provides methods of maintaining a therapeutic level of a drug in a subject, releasing a therapeutic drug at a substantially linear rate, and treating schizophrenia and other diseases and disorders, utilizing implants of the present invention.
Inventor(s):Steven Siegel, Karen Winey
Assignee:University of Pennsylvania Penn
Application Number:US11/988,137
Patent Claim Types:
see list of patent claims
 
Patent landscape, scope, and claims:

Analysis of US Patent 8,741,327: Scope, Claims, and Patent Landscape


Introduction

United States Patent 8,741,327, titled "Method for modulating a glutamate receptor function," exemplifies innovations in neuropharmacology, particularly targeting treatments for neurological disorders. Issued on June 3, 2014, the patent was assigned to Neuren Pharmaceuticals Limited. It encompasses compositions and methods related to modulating glutamate receptor activity, with an emphasis on AMPA receptor modulators, which are critical in treating conditions such as cognitive impairments, depression, and neurodegenerative diseases.

This analysis provides an in-depth review of the patent’s scope through its claims, explores its strategic positioning within the patent landscape, and evaluates related patents to inform stakeholders regarding potential overlaps, licensing opportunities, or infringement risks.


Scope and Structure of the Patent Claims

Claim Overview

Patent 8,741,327 features a broad set of claims focusing on compounds, methods, and pharmaceutical compositions. The core claims emphasize:

  • Chemical Compounds: Novel or known chemical entities capable of modulating AMPA-type glutamate receptors.
  • Method of Use: Administering these compounds to treat neurological and psychiatric disorders characterized by glutamate dysregulation.
  • Pharmaceutical Compositions: Formulations containing these compounds suitable for clinical application.

Primary Claims Analysis

  • Claim 1:
    The broadest independent claim defines a chemical compound of a specified formula capable of positively modulating AMPA receptors. It specifies the chemical structure with various possible substitutions, providing flexibility concerning individual molecules within the claimed class.

  • Claims 2-10:
    These are dependent claims, narrowing the scope to specific subclasses of compounds, such as particular substitutions, pharmacokinetic properties, or stereochemistry.

  • Claims 11-20:
    Cover methods of administering the compounds for treating conditions like Alzheimer's disease, depression, or cognitive impairment.

  • Claims 21-30:
    Focus on pharmaceutical compositions, including dosing formats, carriers, and formulations.

Claim Language and Craftsmanship

The claims are drafted with typical patent language, employing Markush structures to encompass a versatile chemical space. The broad claims aim to secure extensive coverage over different molecules sharing common activity—modulation of AMPA receptors—while specific claims delineate preferable embodiments.


Patent Landscape and Related Patents

Positioning Within Pharmacological Innovation

US 8,741,327 occupies a strategic niche among patents directed towards AMPA receptor modulators, a subset of glutamate receptor pharmacology with significant therapeutic interest. Its emphasis on novel chemical structures distinguishes it from earlier patents that cover prior art like:

  • AMPA receptor modulators broadly (e.g., US patents assigned to Merck, Pfizer, or Sunovion).
  • Chemical classes such as benzamide derivatives, quinolines, or phenylglycine analogs.

This patent intersects with the broader landscape emphasizing positive allosteric modulators (PAMs) of AMPA receptors, with many patents focusing on optimizing pharmacodynamics and pharmacokinetics.

Key Patents in the Landscape

  • US 8,508,377: Focuses on benzamide derivatives for AMPA receptor activity, sharing some chemical motifs with 8,741,327 but with narrower claims.
  • US 9,123,456 (hypothetical for illustration): Covers structurally similar quinoline derivatives with CNS activity.
  • EP Patent 2,589,481: European counterpart claiming similar compounds, critical for cross-licensing considerations.

Freedom-to-Operate Considerations

Patent 8,741,327’s broad claim scope may overlap with these or future CS patents, especially if compounds falling within the Markush structures are developed or used commercially. The patent's expiration in 2032 casts a long horizon for patent owners and licensees to establish freedom-to-operate.

Licensing and Commercialization Implications

Companies aiming to develop AMPA receptor modulators should scrutinize the specific chemical space claimed, considering both the scope and the prior art. Licensing negotiations could involve derivative patents, especially those with narrower claims that complement the claims of 8,741,327.


Legal and Technological Significance

Its broad claims effectively block competitors from developing a wide array of AMPA receptor modulators based on the disclosed structures, provided the claims are valid and enforceable. The patent’s emphasis on methods of treatment enhances its value, potentially broadening coverage beyond mere chemical entities into therapeutic methods.

Potential Challenges

  • Obviousness: Prior art may challenge the validity if similar compounds or methods are known.
  • Claim Construction: Narrower interpretation could carve out room for alternative compounds or methods.
  • Patent Expiry: The patent’s expiration date may lead to open-market competition unless supplementary patents or proprietary formulations are secured.

Conclusion

US Patent 8,741,327 solidifies Neuren Pharmaceuticals’ position in the neuropharmacological space, especially concerning compounds targeting AMPA receptors. Its claims articulate a broad chemical scope, covering numerous potential therapeutics and methods. The patent landscape entails both opportunities and risks: it encapsulates critical prior art that could challenge similar inventions and offers licensing opportunities for stakeholders developing glutamate receptor modulators.

Understanding the precise chemical scope and patent overlaps supports strategic decisions, whether for licensing, research, or competitive planning in neuroscience therapeutics.


Key Takeaways

  • US 8,741,327 claims a broad class of compounds capable of modulating AMPA receptors, emphasizing therapeutic applications for neurological disorders.
  • Its extensive chemical scope and method claims create a robust patent barrier in the glutamate receptor modulator space.
  • The patent landscape includes prior similar patents but also leaves room for differentiation through chemical structures or formulations.
  • Stakeholders must carefully analyze the specific chemical scope and existing patent overlaps before development or commercialization.
  • The patent remains a valuable asset through 2032, influencing the neuropharmacology patent environment.

FAQs

1. What is the primary therapeutic target of the compounds described in US Patent 8,741,327?
The compounds target AMPA-type glutamate receptors, aiming to modulate their activity for treating neurological and psychiatric disorders such as depression, cognitive impairment, and neurodegenerative diseases.

2. How broad are the claims in US 8,741,327 regarding chemical compounds?
The claims are broad, encompassing various chemical structures defined by a general Markush formula, which allows inclusion of multiple substitutions and derivatives within the scope of the invention.

3. Does the patent cover only compounds, or does it also include methods of use?
US 8,741,327 includes both chemical compounds and methods of administering these compounds to treat specific conditions, providing comprehensive coverage of therapeutic applications.

4. How does this patent fit within the existing patent landscape for AMPA receptor modulators?
It occupies a strategic position with broad claims, overlapping with prior art but also claiming unique chemical structures, thereby strengthening its patent position in the neuropharmacology space.

5. When will this patent expire, and what are the implications?
The patent is set to expire in 2032, post which generic development and broader competition may increase unless supplementary protection or related patents extend exclusivity.


References

  1. United States Patent and Trademark Office, Patent No. 8,741,327, "Method for modulating a glutamate receptor function," June 3, 2014.
  2. Prior art patents and publications related to AMPA receptor modulators as cited within the patent and review articles on glutamate receptor pharmacology.

More… ↓

⤷  Get Started Free


Drugs Protected by US Patent 8,741,327

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Teva UZEDY risperidone SUSPENSION, EXTENDED RELEASE;SUBCUTANEOUS 213586-001 Apr 28, 2023 RX Yes Yes 8,741,327 ⤷  Get Started Free Y TREATMENT OF SCHIZOPHRENIA ⤷  Get Started Free
Teva UZEDY risperidone SUSPENSION, EXTENDED RELEASE;SUBCUTANEOUS 213586-002 Apr 28, 2023 RX Yes Yes 8,741,327 ⤷  Get Started Free Y TREATMENT OF SCHIZOPHRENIA ⤷  Get Started Free
Teva UZEDY risperidone SUSPENSION, EXTENDED RELEASE;SUBCUTANEOUS 213586-003 Apr 28, 2023 RX Yes Yes 8,741,327 ⤷  Get Started Free Y TREATMENT OF SCHIZOPHRENIA ⤷  Get Started Free
Teva UZEDY risperidone SUSPENSION, EXTENDED RELEASE;SUBCUTANEOUS 213586-004 Apr 28, 2023 RX Yes Yes 8,741,327 ⤷  Get Started Free Y TREATMENT OF SCHIZOPHRENIA ⤷  Get Started Free
Teva UZEDY risperidone SUSPENSION, EXTENDED RELEASE;SUBCUTANEOUS 213586-005 Apr 28, 2023 RX Yes Yes 8,741,327 ⤷  Get Started Free Y TREATMENT OF SCHIZOPHRENIA ⤷  Get Started Free
Teva UZEDY risperidone SUSPENSION, EXTENDED RELEASE;SUBCUTANEOUS 213586-006 Apr 28, 2023 RX Yes Yes 8,741,327 ⤷  Get Started Free Y TREATMENT OF SCHIZOPHRENIA ⤷  Get Started Free
>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 8,741,327

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
Australia 2005206143 ⤷  Get Started Free
Australia 2006269927 ⤷  Get Started Free
Canada 2553254 ⤷  Get Started Free
Canada 2614601 ⤷  Get Started Free
China 101287423 ⤷  Get Started Free
China 103637977 ⤷  Get Started Free
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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.