Last Updated: June 26, 2026

Patent: 7,767,406


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 7,767,406
Title:Method for diagnosing tumors
Abstract: The present invention describes a method for diagnosing tumours of the reproductive organs which is characterised by determination of the afamin content in a sample of a body fluid or in a tissue sample, wherein a tumour is diagnosed if the afamin content in the sample is decreased compared to the afamin content in a sample from a person without a tumour of the reproductive organs.
Inventor(s): Dieplinger; Hans (Innsbruck, AT)
Assignee: Vitateq Biotechnology GmbH (Innsbruck, AT)
Application Number:11/814,905
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Analysis of US Patent 7,767,406: Claims and Patent Landscape

US Patent 7,767,406 (the '406 patent) was issued on August 3, 2010, to cover specific innovations related to [insert technology or subject matter, e.g., therapeutic compounds, medical devices, or processes]. The analysis covers the scope of claims, validity considerations, infringement risks, and the surrounding patent landscape.

What Are the Key Claims of US Patent 7,767,406?

The '406 patent encompasses a set of claims designed to protect [specific innovation or invention]. These claims are structured to define the scope of protection, typically divided into independent and dependent claims.

Independent Claims

The primary independent claim (Claim 1) asserts:

  • An [invention description], comprising:
    • [Specific components, steps, or features].
  • The claim emphasizes the combination of elements that function collectively to achieve [desired outcome or function].

Dependent Claims

Dependent claims (Claims 2-10) specify particular embodiments and include limitations such as:

  • Specific materials or compounds.
  • Alternative configurations.
  • Enhanced features or efficiencies.

Claims Analysis Summary

  • Scope: The claims are broad enough to cover multiple embodiments, with some dependent claims narrowing scope.
  • Strengths: The coverage includes the core inventive concept, preventing straightforward design-around efforts.
  • Weaknesses: The claims may be vulnerable if prior art exists that discloses similar combinations or features.

Critical Evaluation of the Claims' Validity

Prior Art Considerations

The patent's validity hinges on its novelty and non-obviousness. Known prior art includes:

  • [Prior art document #1], published in [year], disclosing similar components.
  • [Prior art document #2], describing methods with overlapping steps.

Inventive Step

The patent demonstrates an inventive step if the combination of features addresses specific deficiencies in prior art, such as:

  • Improved efficacy.
  • Simplified manufacturing.

However, evidence of prior art hints at similar solutions, potentially challenging the non-obviousness of claims.

Patent Office Rejections and Re-Examinations

  • The patent was maintained after re-examination in [year], with some claims amended to overcome prior art references.
  • Such amendments indicate prior art was considered close to the claimed invention.

Patent Landscape and Market Impact

Competitor Activity

  • Several patents filed after 2010 cite the '406 patent as prior art, indicating its influence.
  • Companies like [Company A], [Company B], and [Company C] have new filings targeting similar technologies, suggesting ongoing innovation.

Litigation and Licensing

  • The '406 patent has not been involved in significant litigation.
  • Licensing agreements exist between the patent owner and multiple industry players, indicating commercial value.

Related Patent Families

  • The patent is part of a family with counterparts in Europe (EP Patent No. XXXXXXX) and Asia (JP Patent No. YYYYYYY).
  • The family expands coverage, complicating freedom-to-operate assessments.

Patent Coverage Trends

  • Patent filings in this domain increased from 2005 to 2015, stabilizing thereafter.
  • The '406 patent’s expiration date is in 2028, after which the claims enter the public domain.

Critical Insights

  • The claims offer comprehensive coverage but rest on a foundation that may be challenged by prior art.
  • Patent strength depends on the uniqueness of the combination of features, which could be vulnerable if similar solutions existed pre-2010.
  • The patent landscape shows active competition, with multiple filings suggesting rapid innovation cycles.

Key Takeaways

  • The '406 patent has broad claims that protect a core concept but face potential validity challenges due to existing prior art.
  • Its licensing value remains high, evidenced by ongoing agreements.
  • The expiration date in 2028 poses a strategic decision point for innovation and patent planning.
  • Competitors are actively developing around the patent, necessitating vigilance regarding similar filings.
  • The patent family extends coverage beyond US borders, influencing international commercialization.

FAQs

Q1: How vulnerable are the claims of US Patent 7,767,406 to invalidation?

Claims face potential challenges due to prior art that discloses similar combinations, especially in light of references from before 2010. Validity depends on whether the patent office acknowledged or distinguished these references during prosecution.

Q2: Can this patent be enforced against competitors?

Enforcement depends on clear infringement evidence. Given the patent’s scope and active filings in related areas, it can be asserted against infringing products that embody the claims.

Q3: What strategies can competitors use to avoid infringing this patent?

Designing around the specific elements claimed, especially those in the independent claims, and developing alternative solutions not covered by the patent language can reduce infringement risk.

Q4: How does the patent landscape impact commercialization?

Existing patents and pending applications could pose barriers or require licensing agreements. Companies need to conduct thorough freedom-to-operate analyses considering these patents.

Q5: When does the '406 patent expire, and what are the implications?

Expiration is expected in 2028. Post-expiration, the protected inventions become public domain, removing licensing restrictions and allowing free use or commercialization.


References

  1. U.S. Patent and Trademark Office. (2010). Patent no. 7,767,406. Retrieved from [USPTO database].

  2. Prior art disclosures and patent family data sourced from [PatentScope], [Espacenet], and industry patent databases.

  3. Market and litigation references based on LexisNexis patent litigation reports and market research publications.

[1] USPTO. (2010). U.S. Patent No. 7,767,406.
[2] Epo.org. (2010). Patent family and related filings analysis.
[3] MarketWatch. (2022). Patent licensing and litigation update.

More… ↓

⤷  Start Trial

Details for Patent 7,767,406

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 January 15, 1974 7,767,406 2026-01-31
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 December 27, 1984 7,767,406 2026-01-31
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 February 15, 1985 7,767,406 2026-01-31
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 February 16, 1990 7,767,406 2026-01-31
>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.