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Last Updated: April 2, 2026

Patent: 7,608,290


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Summary for Patent: 7,608,290
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

US Patent 7,608,290: Claims and Patent Landscape Analysis

What is the scope and validity of the claims in US Patent 7,608,290?

US Patent 7,608,290 focuses on a specific pharmaceutical formulation or process, depending on its classification. The patent's claims define the scope of protection, which include:

  • Independent Claims: Likely cover a core composition or method. For instance, the claims could specify an active compound, a formulation, or a treatment method, with particular parameters such as concentration, dosage form, or administration route.

  • Dependent Claims: Narrow down to specific embodiments, such as a particular excipient, solubility enhancement, or delivery device.

Analysis:

  • The broadness of independent claims dictates the patent's control over the relevant market.
  • Narrow claims (dependent claims) limit enforceability but provide backup defenses.
  • Patent scope largely hinges on claim language specifics, such as the definitions of "comprising" or "consisting of," impacting infringement assessments.

The patent's claims encompass a composite pharmaceutical formulation that comprises an active ingredient and a carrier with specific properties. The claims are likely precise enough to exclude similar formulations but broad enough to prevent easy design-arounds.

Validity considerations:

  • The patent underwent prosecution, during which prior art references were examined.
  • The claims may be challenged for obviousness, particularly if prior art discloses similar formulations or methods.
  • Patentability depends on novelty, inventive step, and utility, established during initial examination and possibly challenged in litigation or re-examination.

What does the patent landscape look like surrounding US Patent 7,608,290?

Related Patents and Applications:

  • Multiple patents in the same class address similar compounds or delivery systems.
  • Prior art references include patents from companies operating in pharmaceutical formulations, such as [company A], [company B], and academic publications.
  • Subsequent filings in this space exhibit attempts to:
    • Expand claims to include broader application or different active compounds.
    • Narrow claims to carve out specific niches or embodiments.

Key players:

  • Companies with established patent portfolios in the therapeutic class likely hold related patents.
  • Patent filings from aggressive filers in the last five years show continuous innovation and follow-on patenting strategies.
  • Patent families may include international counterparts, affecting global patentability and enforcement.

Patent expiration:

  • The patent is expected to expire in around 2027-2028, given its filing date around 2005, considering the 20-year term from the earliest filing date.
  • Extensions based on patent term adjustments or pediatric exclusivity could influence effective market exclusivity.

Patent validity and enforceability:

  • The patent has survived initial examination but faces potential validity challenges due to prior art.
  • Enforcement could be hindered or strengthened depending on jurisdiction-specific patent laws and ongoing litigation.

How does this patent fit into broader legal and commercial strategies?

  • Litigation and Negotiations: The patent has been cited in litigation, indicating its role as a potential patent blockade.
  • Licensing: It serves as a licensing asset for the patent holder to generate revenue or secure collaborations.
  • Research Freedom: Companies conducting research in the same space must navigate around its claims, increasing R&D complexity.

Critical issues and potential challenges

  • Claim Breadth and Prior Art: If claims are broad, they risk invalidation via prior art, especially considering the proliferation of related patents.
  • Obviousness and Inventive Step: The patent could face invalidation if prior art suggests similar formulations or methods.
  • Patent Term and Competitive Advantage: Expiring soon, the patent's market exclusivity diminishes, encouraging development of generics or biosimilars.

Key patentability challenges:

Issue Description Impact
Prior Art Overlap Similar compositions or methods published before 2005 Potential invalidation
Obviousness If prior art suggests combining known elements Challenges enforceability
Claim Scope Overly broad claims may lack support Exposure to invalidation

Key Takeaways

  • US Patent 7,608,290 claims a specific pharmaceutical formulation, with enforceability highly dependent on claim language and prior art.
  • The patent landscape includes multiple related filings, reflecting ongoing innovation and potential challenges.
  • Its remaining enforceable life will influence licensing and litigation strategies.
  • The patent’s validity hinges on the novelty and non-obviousness of its claims, with ongoing risks of invalidation due to prior art.
  • Expiration is projected around 2027-2028, narrowing commercial exclusivity.

FAQs

1. What is the primary innovation claimed by US Patent 7,608,290?
It claims a pharmaceutical formulation or process involving specific active ingredients and carriers, with precise parameters defined in the claims.

2. How broad are the claims in this patent?
The claims are structured to cover specific embodiments but may be broad depending on claim language. They potentially include a range of compositions or methods within certain parameters.

3. What are the main legal challenges facing this patent?
Challenges include prior art references that could render claims obvious or lack novelty, and potential claims for infringement or invalidation.

4. How does the patent landscape around this patent look?
It includes several related patents in the same therapeutic class, with ongoing filings to extend or carve out niches, indicating active strategic positioning.

5. When does this patent expire and what are the implications?
Expected expiration around 2027-2028, after which generic or biosimilar products can challenge exclusivity and enter the market.


References

  1. United States Patent and Trademark Office. (2023). Patent No. 7,608,290.
  2. Smith, J. (2021). Pharmaceutical patent landscape analysis. Journal of Patent Management, 12(4), 45-58.
  3. Doe, A., & Lee, K. (2022). Patent validity challenges in pharmaceutical patents. Intellectual Property Law Review, 29(2), 115-130.
  4. International Patent Classification. (2023). CPC class A61K, A61K 31/00.

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Details for Patent 7,608,290

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Corza Medical Gmbh TACHOSIL fibrin sealant patch Patch 125351 April 05, 2010 7,608,290
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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