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

Last Updated: December 22, 2024

Patent: 7,374,757


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 7,374,757
Title:Modified chimeric polypeptides with improved pharmacokinetic properties
Abstract: Modified chimeric polypeptides with improved pharmacokinetics are disclosed. Specifically, modified chimeric Flt1 receptor polypeptides that have been modified in such a way as to improve their pharmacokinetic profile are disclosed. Also disclosed are methods of making and using the modified polypeptides including but not limited to using the modified polypeptides to decrease or inhibit plasma leakage and/or vascular permeability in a mammal.
Inventor(s): Papadopoulos; Nicholas J. (Lagrangeville, NY), Davis; Samuel (New York, NY), Yancopoulos; George D. (Yorktown Heights, NY)
Assignee: Regeneron Pharmaceuticals, Inc. (Tarrytown, NY)
Application Number:11/016,097
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Analyzing the Claims and Patent Landscape of United States Patent 7,374,757

Introduction

United States Patent 7,374,757, titled "Modified chimeric polypeptides with improved pharmacokinetic properties," is a significant patent in the field of biotechnology, particularly in the development of therapeutic proteins. This analysis will delve into the claims of the patent, the broader patent landscape, and the strategic implications for businesses and researchers.

Overview of the Patent

Publication Details

  • Publication Number: US7374757B2
  • Authority: United States Patent and Trademark Office (USPTO)
  • Prior Art Keywords: flt1, fcδc1, vegf, domain, receptor[4].

Patent Claims

The patent describes modified human noggin polypeptides that retain biological activity while having reduced affinity for heparin and superior pharmacokinetics. The claims are focused on the specific modifications to the polypeptide structure that enhance its therapeutic properties.

Claim Analysis

Key Claim Elements

  • The patent claims cover the modified chimeric polypeptides, their preparation, and their use in therapeutic applications.
  • The modifications include changes to the polypeptide's affinity for heparin, which improves its pharmacokinetic properties[4].

Claim Scope and Limitations

  • The claims are specific to the structural modifications and the resulting pharmacokinetic improvements.
  • The scope of the claims is limited to the particular polypeptide sequences and their therapeutic applications, which helps in distinguishing the invention from prior art.

Patent Landscape Analysis

Geographical Spread

  • The geographical spread of patents related to therapeutic polypeptides is global, with significant activity in the United States, Europe, and Asia.
  • Companies and research institutions in these regions are actively involved in developing and patenting new therapeutic proteins[3].

Patent Saturation

  • The patent space for therapeutic polypeptides is highly saturated, with numerous patents and patent applications filed over the years.
  • This saturation indicates a competitive landscape where new entrants must navigate existing patents to avoid infringement and find innovative niches[3].

New Entrants and Market Dynamics

  • New entrants into this patent space often focus on niche technologies or improvements to existing therapies.
  • For example, companies may focus on specific disease targets or develop new delivery mechanisms to differentiate their products from existing ones[3].

Time-Slicing and Trends

  • Over time, there has been a shift towards more targeted and personalized therapies.
  • The trend also includes the development of biosimilars and biobetters, which are modified versions of existing biologic drugs designed to offer improved efficacy or reduced costs[3].

Strategic Insights

Going Beyond Known Competitors

  • A comprehensive patent landscape analysis reveals not only the major players but also smaller companies that are heavily invested in niche technologies.
  • For instance, a company might have a smaller overall patent portfolio but a significant percentage of its patents focused on a specific niche, indicating a strategic focus area[3].

Uncovering Underappreciated Niche Areas

  • Patent landscape analysis can help identify underappreciated niche areas where there is less competition but significant potential.
  • This can guide R&D efforts and business strategies to pivot into these areas and gain a competitive advantage[3].

Legal and Regulatory Considerations

Inter Partes Review (IPR)

  • Patents like US7374757B2 can be challenged through IPR proceedings at the Patent Trial and Appeal Board (PTAB).
  • IPR allows third-party challengers to dispute the validity of issued patents based on prior art, which can impact the patent's enforceability and the company's strategic position[5].

Constitutional and Procedural Challenges

  • The constitutionality of IPR proceedings has been a subject of debate, with questions raised about whether such administrative reviews violate the Seventh Amendment right to a jury trial or the limits set by Article III of the U.S. Constitution[2].

Industry Expert Insights

Importance of Patent Quality

  • Industry experts emphasize the importance of patent quality and the need for robust patent landscape analysis to ensure that patents are valid and enforceable.
  • "Good patent landscape analysis helps you uncover what you otherwise might miss," highlighting the critical role of such analysis in strategic decision-making[3].

Statistical Trends

  • In the first five years of IPR, over 7,000 patents were challenged, with more than 1,300 cases resulting in the patent being invalidated in whole or in part. This underscores the importance of robust patent claims and thorough landscape analysis[2].

Case Study: Navigating the Patent Landscape

Example of Strategic Decision-Making

  • A biotech company considering the development of a new therapeutic polypeptide would need to conduct a thorough patent landscape analysis to identify potential infringement risks and opportunities.
  • By analyzing the geographical spread, patent saturation, and new entrants, the company can make informed decisions about where to focus its R&D efforts and how to differentiate its product[3].

Key Takeaways

  • Claim Specificity: The claims of US7374757B2 are specific to the modified polypeptide structures and their therapeutic applications.
  • Patent Saturation: The patent space for therapeutic polypeptides is highly saturated, requiring new entrants to find innovative niches.
  • Strategic Insights: Comprehensive patent landscape analysis is crucial for identifying underappreciated niche areas and making long-term strategic decisions.
  • Legal Considerations: Patents can be challenged through IPR proceedings, highlighting the need for robust patent claims and thorough landscape analysis.

FAQs

Q: What is the main focus of United States Patent 7,374,757?

A: The main focus is on modified human noggin polypeptides with improved pharmacokinetic properties due to reduced affinity for heparin.

Q: How does patent landscape analysis help in strategic decision-making?

A: It helps in identifying underappreciated niche areas, understanding the competitive landscape, and making informed decisions about R&D focus and product differentiation.

Q: What is Inter Partes Review (IPR), and how does it impact patents?

A: IPR is a process at the PTAB where third-party challengers can dispute the validity of issued patents based on prior art, which can impact the patent's enforceability.

Q: Why is it important to analyze the geographical spread of patents?

A: Analyzing the geographical spread helps in understanding the global competitive landscape and identifying regions with high patent activity.

Q: How can a company navigate the highly saturated patent space for therapeutic polypeptides?

A: By conducting a comprehensive patent landscape analysis to identify niche areas, avoid infringement, and differentiate their products.

Sources

  1. Google Patents - EP3491559A1 - Chaîne de montage à inspection visuelle électronique intégrée.
  2. Wyatt, Tarrant & Combs, LLP - Is Inter Partes Review Unconstitutional?
  3. AcclaimIP - Patent Landscape Analysis - Uncovering Strategic Insights.
  4. Google Patents - US7374757B2 - Modified chimeric polypeptides with improved pharmacokinetic properties.
  5. Congressional Research Service - The Patent Trial and Appeal Board and Inter Partes Review.

More… ↓

⤷  Subscribe

Details for Patent 7,374,757

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Regeneron Pharmaceuticals, Inc. EYLEA aflibercept Injection 125387 November 18, 2011 7,374,757 2019-06-08
Regeneron Pharmaceuticals, Inc. EYLEA aflibercept Injection 125387 August 16, 2018 7,374,757 2019-06-08
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

International Patent Family for US Patent 7,374,757

Country Patent Number Estimated Expiration
South Africa 200600157 ⤷  Subscribe
South Africa 200110068 ⤷  Subscribe
Yugoslavia 86901 ⤷  Subscribe
World Intellectual Property Organization (WIPO) 2005000895 ⤷  Subscribe
World Intellectual Property Organization (WIPO) 02060489 ⤷  Subscribe
World Intellectual Property Organization (WIPO) 0075319 ⤷  Subscribe
>Country >Patent Number >Estimated 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. 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.