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Last Updated: December 22, 2024

Details for Patent: 8,173,708


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Which drugs does patent 8,173,708 protect, and when does it expire?

Patent 8,173,708 protects NAMZARIC and is included in one NDA.

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

This patent has fifty-seven patent family members in eighteen countries.

Summary for Patent: 8,173,708
Title:Method and composition for administering an NMDA receptor antagonist to a subject
Abstract: The invention provides methods and compositions for administering an NMDA receptor antagonist (e.g., memantine) to a subject.
Inventor(s): Went; Gregory T. (Mill Valley, CA), Fultz; Timothy J. (Pleasant Hill, CA), Meyerson; Laurence R. (Las Vegas, NV)
Assignee: Adamas Pharmaceuticals, Inc. (Emeryville, CA)
Application Number:12/757,819
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 8,173,708
Patent Claim Types:
see list of patent claims
Use; Dosage form; Formulation;
Patent landscape, scope, and claims:

Understanding the Scope and Claims of United States Patent 8,173,708

Introduction

The United States Patent 8,173,708, titled "Methods and compositions for administering an NMDA receptor antagonist," is a significant patent in the pharmaceutical sector, particularly in the treatment of neurological disorders. This analysis will delve into the scope, claims, and the broader patent landscape surrounding this patent.

Patent Overview

Patent Title and Number

  • Patent Title: Methods and compositions for administering an NMDA receptor antagonist
  • Patent Number: US 8,173,708 B2
  • Grant Date: April 9, 2012[4].

Inventors and Assignees

The patent was granted to inventors associated with Forest Laboratories, Inc., which is now part of Allergan plc. The assignee of the patent is Forest Laboratories, Inc.[4].

Claims

Claim Structure

The patent includes 18 claims, which are divided into independent and dependent claims. Independent claims define the broad scope of the invention, while dependent claims narrow down the invention by adding specific limitations.

Independent Claims

Independent claims in the patent focus on methods and compositions for administering memantine, an NMDA receptor antagonist. For example, Claim 1 describes a method for administering memantine in a specific dosage form to treat conditions such as Alzheimer's disease[4].

Dependent Claims

Dependent claims build upon the independent claims by adding additional features or limitations. These claims often specify particular aspects of the dosage form, such as the concentration of memantine, the type of formulation (e.g., extended-release), and the method of administration[4].

Scope of the Patent

Technological Field

The patent falls under the technological field of pharmaceuticals, specifically in the area of neurology and psychiatry. It involves the development of methods and compositions for administering NMDA receptor antagonists, which are used to treat neurological disorders like Alzheimer's disease[4].

Patent Scope Metrics

Research on patent scope, such as the study by the Hoover Institution, suggests that metrics like independent claim length and independent claim count can be used to measure the breadth of a patent. For US 8,173,708, the claims are relatively detailed, indicating a focused scope rather than overly broad claims[3].

Patent Landscape

Related Patents

The patent is part of a series of patents related to the formulation and administration of memantine. Other patents in this series include US 8,168,209, US 8,283,379, US 8,329,752, US 8,362,085, and US 8,598,233. These patents collectively cover various aspects of memantine formulations and their use in treating neurological conditions[5].

Litigation and Enforcement

The patent has been involved in several legal disputes, particularly in the context of generic drug approvals. For instance, in the case Forest Labs., Inc. v. Teva Pharms. USA, Inc., the court addressed the validity and infringement of several patents, including US 8,173,708, related to the extended-release formulation of memantine hydrochloride[5].

Jurisdiction and Venue

The patent's enforcement and litigation have been subject to U.S. patent laws, specifically under 35 U.S.C. ยง 1 et seq. Cases involving this patent have been heard in federal courts, such as the U.S. District Court for the District of Delaware, and have been appealed to the Federal Circuit[2].

Impact on Innovation

The patent's scope and claims have significant implications for innovation in the pharmaceutical industry. While the patent provides exclusive rights to the inventor, it also sets a precedent for future research and development in similar areas. The debate around patent scope and quality, as highlighted by the Hoover Institution, suggests that narrower claims like those in US 8,173,708 can facilitate innovation by reducing litigation and licensing costs[3].

Conclusion

United States Patent 8,173,708 is a critical patent in the field of neuropharmacology, particularly for the treatment of Alzheimer's disease. Its claims and scope are well-defined, focusing on specific methods and compositions for administering memantine. The patent's involvement in litigation and its place within a broader series of related patents underscore its importance in the pharmaceutical patent landscape.

Key Takeaways

  • Patent Title and Number: Methods and compositions for administering an NMDA receptor antagonist, US 8,173,708 B2.
  • Claims: 18 claims, including independent and dependent claims focusing on methods and compositions for memantine administration.
  • Scope: Focused on pharmaceuticals, specifically neurology and psychiatry.
  • Related Patents: Part of a series including US 8,168,209, US 8,283,379, US 8,329,752, US 8,362,085, and US 8,598,233.
  • Litigation: Involved in cases such as Forest Labs., Inc. v. Teva Pharms. USA, Inc..
  • Impact on Innovation: Narrower claims facilitate innovation by reducing litigation and licensing costs.

FAQs

  1. What is the main subject of United States Patent 8,173,708?

    • The main subject is methods and compositions for administering an NMDA receptor antagonist, specifically memantine, for treating neurological disorders like Alzheimer's disease.
  2. How many claims does the patent include?

    • The patent includes 18 claims, which are divided into independent and dependent claims.
  3. What is the significance of the patent in the pharmaceutical industry?

    • The patent is significant because it provides exclusive rights for the administration of memantine, a crucial drug for treating Alzheimer's disease, and sets a precedent for future research in similar areas.
  4. Has the patent been involved in any legal disputes?

    • Yes, the patent has been involved in several legal disputes, particularly in the context of generic drug approvals, such as in the case Forest Labs., Inc. v. Teva Pharms. USA, Inc.
  5. How does the patent's scope impact innovation?

    • The patent's narrower claims help reduce litigation and licensing costs, which can facilitate innovation by making it easier for other researchers to build upon or work around the existing patent.

Sources

  1. Invention: U.S. and Comparative Global Trends - National Science Foundation.
  2. IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT ... - Insight.rpxcorp.com.
  3. Patent Claims and Patent Scope - Hoover Institution.
  4. United States Patent 8,173,708 B2 - Patentimages.storage.googleapis.com.
  5. Forest Labs., Inc. v. Teva Pharms. USA, Inc. - RobinsKaplan.com.

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Recent additions to Drugs Protected by US Patent 8,173,708

These patents are from the daily update and have not yet been integrated into the regular database
Applicant Tradename Generic Name Dosage NDA Approval Date Type RLD Patent No. Product Substance Delist Req. Patent Expiration Usecode Patented / Exclusive Use
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Type >RLD >Patent No. >Product >Substance >Delist Req. >Patent Expiration >Usecode >Patented / Exclusive Use

Drugs Protected by US Patent 8,173,708

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Abbvie NAMZARIC donepezil hydrochloride; memantine hydrochloride CAPSULE, EXTENDED RELEASE;ORAL 206439-001 Dec 23, 2014 RX Yes No 8,173,708*PED ⤷  Subscribe Y ⤷  Subscribe
Abbvie NAMZARIC donepezil hydrochloride; memantine hydrochloride CAPSULE, EXTENDED RELEASE;ORAL 206439-004 Jul 18, 2016 AB RX Yes No 8,173,708*PED ⤷  Subscribe Y ⤷  Subscribe
Abbvie NAMZARIC donepezil hydrochloride; memantine hydrochloride CAPSULE, EXTENDED RELEASE;ORAL 206439-002 Dec 23, 2014 RX Yes Yes 8,173,708*PED ⤷  Subscribe Y ⤷  Subscribe
>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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