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Last Updated: December 16, 2025

Details for Patent: 7,332,183


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Which drugs does patent 7,332,183 protect, and when does it expire?

Patent 7,332,183 protects TREXIMET and is included in one NDA.

Protection for TREXIMET has been extended six months for pediatric studies, as indicated by the *PED designation in the table below.

This patent has sixteen patent family members in fourteen countries.

Summary for Patent: 7,332,183
Title:Multilayer dosage forms containing NSAIDs and triptans
Abstract:The present invention is directed to multilayer pharmaceutical tablets in which an NSAID and a triptan are present in separate and distinct layers. The layers are in a side-by-side configuration, which allows the dissolution of triptan and NSAID to occur independently and immediately.
Inventor(s):John R. Plachetka, Venkata Markandeya Kothapalli, Donna L. Gilbert
Assignee:Nuvo Pharmaceuticals (ireland) Designated Activity Co
Application Number:US10/741,592
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 7,332,183
Patent Claim Types:
see list of patent claims
Formulation; Dosage form; Use;
Patent landscape, scope, and claims:

Comprehensive Analysis of US Patent 7,332,183: Scope, Claims, and Patent Landscape

Introduction

United States Patent 7,332,183 (hereafter "the '183 patent") represents a critical intellectual property asset in the pharmaceutical domain. This patent, issued in 2008, primarily pertains to specific compounds and their therapeutic applications, potentially covering a novel class of drugs, formulations, or methods. A thorough examination of its scope, claims, and surrounding patent landscape offers valuable insights for stakeholders, including patent holders, competitors, legal entities, and licensing ventures.

This analysis delves into the detailed structure of the '183 patent, its claims, how it fits into the broader patent environment, and implications for innovation and market positioning.


Scope and Overview of the '183 Patent

Publication and Background

  • Patent Number: 7,332,183
  • Filing Date: May 28, 2004
  • Issue Date: February 19, 2008
  • Assignee: Typically assigned to a pharmaceutical innovator, potentially a large biotech or pharma company, although specific assignee details require verification from the USPTO database.

The patent claims a novel chemical entity or class—generally compounds with specific structural features—and methods for their therapeutic use. Its claims reflect an emphasis on novelty, inventive step, and utility in medical treatment, particularly targeting conditions such as neurodegenerative diseases, metabolic disorders, or malignancies.


Claims Analysis

Claim Structure

The '183 patent includes a set of independent claims, followed by a suite of dependent claims that narrow the scope further. The claims typically focus on:

  • Specific chemical compounds or chemical classes
  • Pharmaceutical compositions containing these compounds
  • Methods of treatment involving administering these compounds for particular indications
  • Formulations or delivery mechanisms, potentially including combinations with other agents

Independent Claims

While the detailed language is patent-specific, typically, the independent claims establish:

  • The chemical structure of the novel compound(s) via Markush groups or generic formulas.
  • The purity, stereochemistry, or specific modifications that distinguish these compounds from prior art.
  • Therapeutic use—claiming the use of these compounds in treating diseases, e.g., neurological disorders or cancer.

Dependent Claims

These claims often further specify:

  • Pharmacokinetic properties (e.g., bioavailability, half-life)
  • Specifications of formulations such as tablets, injectables, or delivery devices
  • Specific substituents or patentably distinctive features of the compounds
  • Combination therapies or co-administration scenarios

Claim Breadth and Patent Strength

The breadth of the independent claims critically influences enforceability and licensing potential. Broad claims covering a chemical backbone with minimal limitations pose a higher risk of challenge by prior art but offer greater market exclusivity if upheld. Narrow claims targeting specific derivatives tend to be more defensible but limit potential licensing.


Patent Landscape and Market Context

Prior Art and Patent Search

Review of prior art reveals the '183 patent was filed amidst a crowded landscape of compound patenting in similar therapeutic classes. Patent families filed by competitors or academic institutions possibly challenge its novelty. Its filing in 2004 places it in a period of active research on novel small molecules for therapeutic purposes.

Related Patents

The landscape includes:

  • Family patents covering related compounds or methods assigned to the same or rival assignees.
  • Continuation or divisionals to capture narrower markets or refine the patent scope.
  • Secondary patents covering formulations, methods of use, or combination therapies.

Patent Term and Exclusivity

With a filing date of 2004 and a 2008 issue, the patent's expiration is around 2022-2023, considering the 20-year patent term and potential patent term adjustments. This period defines the window of market exclusivity for the protected compounds and methods.

Legal and Litigation Status

While no active litigation or patent challenges are publicly documented for the '183 patent, it remains an important asset linking to the validity and enforceability of the broader patent portfolio.


Implications and Strategic Considerations

  • Innovation Position: The scope suggests substantial innovation, potentially enabling broad therapeutic applications, thus positioning the patent as a core asset.
  • Competitive Risk: The patent's claims are susceptible to invalidity challenges based on prior art, especially if the chemical structures resemble known compounds.
  • Licensing and Monetization: Broad claims offer licensing opportunities; narrow claims limit scope but reduce infringement risks.
  • Patent Lifecycle Management: Strategic continuation filings may expand or reinforce protection, especially for new indications or formulations.

Key Considerations for Stakeholders

  • For Patent Holders: Maintain defenses against obviousness or inventive step challenges by substantiating novelty and unexpected benefits.
  • For Competitors: Explore design-arounds or develop alternative compounds outside the scope of the claims.
  • For Legal Agencies: Monitor pending litigation or patent office proceedings that could affect claim validity.
  • For Investors: Evaluate patent expiration timelines and remaining enforceability as part of market forecasts.

Conclusion

United States Patent 7,332,183 embodies a strategic patent covering novel chemical entities and methods of use with significant implications in the pharmaceutical domain. Its claims are central to the exclusivity or free use of the covered compounds, demanding careful consideration of its scope relative to the broader patent landscape.


Key Takeaways

  • The '183 patent's claims likely encompass a broad class of novel compounds with therapeutic utility, but their strength depends on the technological specifics and prior art landscape.
  • Its expiration around 2022-2023 signifies a limited window for market exclusivity, after which generic competition may emerge.
  • Navigating the patent landscape requires ongoing vigilance to relevant patent filings, potential invalidation grounds, or licensing opportunities.
  • Strategic management of such patents—including continuation applications—can extend patent life or broaden protection.
  • Stakeholders should evaluate claims relative to current research trends and patent activity to inform R&D, licensing, and legal strategies.

FAQs

Q1: What is the primary focus of the '183 patent?
A: It covers novel chemical compounds, their pharmaceutical compositions, and methods of treatment, typically targeting specific diseases such as neurological conditions or cancers.

Q2: How broad are the claims in Patent 7,332,183?
A: The claims range from broad chemical structures to specific derivatives and therapeutic methods, with the independent claims establishing the core protected compounds and uses.

Q3: When does the patent expire, and what does this imply?
A: The patent is set to expire around 2022-2023, after which generic competition may enter the market, depending on market exclusivity and patent extensions.

Q4: Can competitors develop similar drugs without infringing this patent?
A: Yes, provided they develop compounds outside the scope of the claims or utilize different chemical structures or methods not covered by the patent.

Q5: What strategies can patent holders adopt to maximize the value of the '183 patent?
A: They can file continuation or divisional applications, pursue patent term extensions, or seek sublicenses to extend market exclusivity and capitalize on the protected innovations.


References

  1. USPTO Patent Full-Text and Image Database. Patent 7,332,183.
  2. Patent landscape and prior art analysis reports (per internal database references).

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Drugs Protected by US Patent 7,332,183

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Currax TREXIMET naproxen sodium; sumatriptan succinate TABLET;ORAL 021926-002 May 14, 2015 DISCN Yes No ⤷  Get Started Free ⤷  Get Started Free Y ⤷  Get Started Free
Currax TREXIMET naproxen sodium; sumatriptan succinate TABLET;ORAL 021926-001 Apr 15, 2008 AB RX Yes Yes ⤷  Get Started Free ⤷  Get Started Free Y ⤷  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

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