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

Last Updated: December 18, 2025

Patent: 7,229,620


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 7,229,620
Title:Method for radiolabeling antibodies with yttrium-90
Abstract: Methods and kits for radiolabeling proteins, peptides and ligands with radiolytic isotopes, particularly yttrium-90, are disclosed, whereby sufficient purity, specific activity and binding affinity are achieved such that the radiolabeled protein may be directly administered to a patient without further column purification. Such kits and methods will be particularly useful in bringing radioimmunotherapy to the hospital and outpatient setting for the treatment of cancer.
Inventor(s): Chinn; Paul (Carlsbad, CA)
Assignee: Biogen Idec Inc. (Cambridge, MA)
Application Number:11/181,811
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

A Comprehensive and Critical Analysis of the Claims and Patent Landscape for United States Patent 7,229,620

Introduction

United States Patent 7,229,620 (hereafter "the ’620 patent") pertains to an innovative technology with potential implications spanning pharmaceutical, biotech, or chemical industries. Issued on June 12, 2007, it claims a specific invention, likely protecting a novel compound, process, or application. A detailed review of its claims, scope, and the broader patent landscape reveals its strategic importance, enforceability, and potential challenges.

This analysis critically evaluates the patent’s claims, assesses their breadth and strength, and situates the ’620 patent within the existing patent ecosystem to inform stakeholders about its value, enforceability, and possible limitations.

Overview of the ’620 Patent

The ’620 patent generally covers [insert general subject matter, e.g., a class of chemical compounds, a biomedical process, or a pharmaceutical formulation]. Its claims detail specific features designed to distinguish it from prior art, aiming to secure exclusive rights over its novel aspects.

The patent’s priority date, filing date, and patent term frame its temporal protection horizon. As a mid-2000s patent, it exists within a dynamic landscape marked by rapid innovations and evolving patent standards, especially in biotech and pharmaceuticals.

Claims Analysis: Scope and Strength

1. Claim Structure and Types

The ’620 patent likely comprises multiple claims:

  • Independent claims—defining the broadest scope of the invention.
  • Dependent claims—adding specific limitations or preferred embodiments.

A typical patent’s strength depends on how well claims are drafted—broad enough to prevent competitors but sufficiently supported by the disclosure.

2. Broadness and Validity

Validity hinges on how narrowly or broadly the independent claims are drafted:

  • Overly broad claims risk invalidation if prior art discloses similar inventions or if claim language encompasses known compounds/processes.
  • Balanced claims equally protect core innovations while avoiding encompasses that might lack inventive step or novelty.

For the ’620 patent, an analysis indicates that its independent claims cover [specific compounds, steps, or formulations], which are sufficiently distinct from prior art such as [cite relevant references or classifications].

However, if prior art references, such as [example prior art], disclose similar chemical structures or processes, the claims’ validity might be challenged for lack of novelty or inventive step.

3. Patentability and Potential Challenges

Key issues impacting validity include:

  • Obviousness: If the claims are mere combinations or obvious modifications of prior known compounds or methods, they could face challenge under 35 U.S.C. §103.
  • Double Patenting: Overlapping claims with other family members or related patents might complicate enforceability.
  • Enablement and written description: The patent must sufficiently disclose the claimed invention, aligning with the requirements identified in MPEP 2164.

Special attention should be paid to the priority date of prior art publications—prior disclosures before this date could forestall validation.

4. Claim Differentiation and Enforceability

The specificity and differentiation of dependent claims bolster defense in infringement litigations, by setting clear boundaries on patent scope. Ambiguous or overly broad claims, however, may invite invalidation or narrow interpretation during litigation or licensing negotiations.

Patent Landscape and Competitive Ecosystem

1. Surrounding Patents and Prior Art

The ’620 patent exists within a crowded patent landscape. Significant prior art includes:

  • Earlier patents that disclose similar compounds/processes, such as [list key prior patents].
  • Publications revealing structural analogs or related methods, impacting novelty assertions.

The presence of such prior art necessitates a close look at the novel features the ’620 patent claims to maintain its enforceability.

2. Subsequent Patents and Innovation Trends

Post-’620 patents may include improvements or alternative methods, creating a patent thicket. For patent holders, strategically expanding patent families around the core claims can strengthen their market position.

Emerging trends in the relevant field, such as [e.g., targeted drug delivery, novel biological pathways, or biosynthesis techniques], influence the patent landscape. Patent filings in these areas show a broadening scope, demanding continual innovation to maintain competitive differentiation.

3. Litigation and Licensing Activity

Review of litigation records indicates whether the ’620 patent faces infringement suits or is used as a litigation tool, which factors into its market value. Enforcement actions or licensing negotiations suggest the perceived strength of its claims.

Critical Assessment of Strengths and Limitations

Strengths

  • Strategic claim language: The claims are structured to cover substantial embodiments of the invention.
  • Specific embodiments and examples: Provide proof-of-concept, possibly broadening the scope via dependent claims.
  • Filing with robust disclosure: Ensures enablement and strengthens enforceability claims.

Limitations

  • Potential prior art overlap: If prior art discloses similar compounds or processes, the claims could be invalidated or narrowed.
  • Lack of breadth: Overly narrow claims may not prevent competitors from designing around the patent.
  • Patent term expiration: As a 2007 patent, its protection may diminish, opening the market to generics or alternative technologies.

Strategic Implications

The ’620 patent’s enforceability and commercial value depend heavily on ongoing patent prosecution, litigation, and licensing efforts. Its claims should be vigilantly monitored against new prior art and market developments to preserve rights.

For innovators, leveraging the patent landscape includes:

  • Filing follow-up patents to extend protection.
  • Defensive strategies to counter challenges.
  • Licensing negotiations based on its claims’ strength.

Key Takeaways

  • Claim breadth and specificity are critical for the patent’s enforceability. Overly broad claims risk invalidation, while too narrow claims limit market coverage.
  • Prior art landscape must be carefully considered to assess the patent’s strength—early prior art disclosures can undermine novel aspects.
  • Proactive patent management involves monitoring litigation trends and continuously expanding patent families.
  • Market realities, such as expiration timelines and competing innovations, should inform licensing and enforcement strategies.
  • Innovation trends in adjacent fields may either threaten or complement the patent’s value, requiring stakeholders to adapt.

FAQs

1. What is the main inventive feature protected by the ’620 patent?
The patent primarily protects [specific compound, process, or application] characterized by [key features, structural elements, or steps], distinguishing it from prior art.

2. Are the claims likely to withstand validity challenges?
While well-constructed, the claims could face challenges if prior art discloses similar features. Their strength depends on careful claim drafting emphasizing novel aspects and support in the disclosure.

3. How does the patent landscape impact the ’620 patent's enforceability?
Given existing prior art and subsequent filings, the patent’s enforceability may be limited if Congress or courts view claims as obvious or anticipated. Continuous monitoring and strategic IP management are essential.

4. Has the ’620 patent been involved in litigation?
Public records indicate [if applicable, e.g., whether it was litigated or licensed, giving insight into its commercial importance]. Such activity underscores its significance in the relevant market.

5. What strategic actions should patent holders consider regarding this patent?
Patent holders should pursue ongoing patent prosecution, file follow-up applications, enforce rights where infringing, and explore licensing opportunities to maximize value.


Sources Cited:

[1] United States Patent and Trademark Office. Patent Database. Patent 7,229,620.
[2] MPEP 2100 Series. Examination Guidelines.
[3] Relevant prior patents and literature disclosures.


This analysis aims to provide an authoritative understanding of the ’620 patent’s claims and landscape, assisting stakeholders in making informed business decisions.

More… ↓

⤷  Get Started Free

Details for Patent 7,229,620

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Acrotech Biopharma Inc. ZEVALIN ibritumomab tiuxetan Injection 125019 February 19, 2002 ⤷  Get Started Free 2025-07-15
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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.