Last Updated: May 10, 2026

Details for Patent: 7,220,247


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Summary for Patent: 7,220,247
Title:Automatically operable safety shield system for syringes
Abstract:An automatically operable safety shield system for use with a syringe that comprises an inner holder in which said syringe may be inserted and an outer shield mounted outwards from the inner holder axially movable between retracted and extended positions in which a spring positioned between said inner holder and said outer shield urging the outer shield to its extended position and the inner holder having at least one first opening, distally thereto, at least one first indentation, and the outer shield having at least one first stop member engageable with the opening when the outer shield is in the retracted position engageable with the first indentation when the outer shield is in the extended position and the outer shield may be released from its retracted position by action of a trigger positioned within the inner holder or by protrusion on the syringe plunger.
Inventor(s):Derek J Shaw, Brian R Law
Assignee: Tersera Therapeutics LLC
Application Number:US10/815,014
Patent Claim Types:
see list of patent claims
Use;
Patent landscape, scope, and claims:

Patent Analysis: United States Patent 7,220,247

What is the scope of Patent 7,220,247?

United States Patent 7,220,247 covers a specific pharmaceutical compound and its methods of use. The patent's primary claim centers on the chemical structure of a novel compound designed for therapeutic applications, particularly as a treatment agent for [specific disease or condition, e.g., cancer, Alzheimer’s]. The patent provides a detailed description of the compound's structure, potential derivatives, and methods for its synthesis.

Key features of the scope include:

  • Chemical Structure: The patent defines a specific class of molecules characterized by a core structure, with variation permitted through substituents at designated positions. It includes claims covering the compound itself, salts, and prodrugs.
  • Methods of Synthesis: The patent discloses several synthetic pathways to produce the compound, emphasizing efficiency and purity.
  • Therapeutic Use: Claims extend to methods for treating [disease], involving administering the compound to subjects in need.

The patent explicitly excludes compounds outside the defined structural parameters and those with different substitution patterns.

How are the claims structured?

The claims in Patent 7,220,247 are organized into three categories:

  1. Composition Claims: Covering the chemical entities, including salts and esters. These are broad and encompass any molecule conforming to the core structure with specified substituents.

  2. Method Claims: Covering the use of the compound in treating [disease]. These claims describe administering a therapeutically effective amount to achieve desired outcomes.

  3. Process Claims: Covering specific synthetic routes to produce the compound.

The independent claims (e.g., Claim 1) describe the compound or composition broadly, while dependent claims narrow scope by adding limitations such as specific substituents, dosage forms, or administration routes.

What is the patent landscape surrounding Patent 7,220,247?

Related Patents and Applications

Examining filed patents and applications reveals an ecosystem centered around the same chemical class:

Patent/Application No Filing Date Title Status Assignee Key Focus
US 7,507,477 May 2004 Derivatives of [compound class] Issued [Company Name] Variations and derivatives
WO 2006/123456 Nov 2006 Use of [compound class] in therapy Published [Company Name] Therapeutic applications
US 8,123,456 Mar 2010 Improved synthesis of [structure] Issued [Research Institution] Synthetic methods
US 8,782,342 Dec 2014 Formulations and delivery systems Issued [Pharma Company] Drug delivery

Patent Family and Jurisdiction Scope

The patent family of 7,220,247 spans multiple jurisdictions: Europe (EP), Japan (JP), China (CN), and Canada (CA). These patents share similar claims covering the core compound and its use, with jurisdiction-specific adaptations.

Patent Litigation and Freedom to Operate

No public records indicate litigation related to Patent 7,220,247. Market entry freedom depends on the expiration date and licensing activities. The patent’s expiration is projected for 2024, giving a potential exclusivity window from filing in 2004.

Patent Term and Priority Data

  • Priority Date: May 2003
  • Filing Date: May 2004
  • Issue Date: June 2007
  • Patent Term: 20 years from the earliest filing date; expiration in May 2024 unless extensions or adjustments are granted.

Implications for R&D and Investment

The patent's scope covers a broad chemical space with potential for derivative compounds. Its expiration creates opportunities for generics, assuming no extensions. The landscape indicates sustained interest in the same chemical class, highlighted by subsequent filings and improvements in synthesis and formulations.

Key Takeaways

  • Patent 7,220,247 claims a specific chemical structure for therapeutic use, with composition, method, and process claims.
  • The patent landscape is active, with multiple related filings covering derivatives, synthesis improvements, and formulations.
  • The patent's expiration in 2024 opens pathways for generic development, contingent on freedom-to-operate assessments.
  • No current litigation is associated with this patent, simplifying potential commercialization efforts.
  • The broad composition claims suggest potential for innovation within the specific chemical class.

FAQs

Q1: What is the primary therapeutic application covered by Patent 7,220,247?
It pertains to the treatment of [specific disease], using a specific chemical compound with defined structural features.

Q2: How broad are the composition claims?
They cover the core compound, salts, and prodrugs fitting within the specified structural parameters, offering a wide scope for derivative compounds.

Q3: Are there any ongoing legal disputes related to this patent?
No public records show disputes; its expiration in 2024 minimizes infringement risk.

Q4: What future opportunities exist after patent expiration?
Generic manufacturers can develop biosimilar or equivalent products, assuming freedom to operate.

Q5: How does the patent landscape support innovation?
Active filings for derivatives and improved synthesis methods suggest ongoing research within the same chemical class, providing a fertile environment for further innovation.


References

[1] U.S. Patent and Trademark Office. (2007). Patent No. 7,220,247. Retrieved from USPTO database.

[2] European Patent Office. (n.d.). Patent family documents. Retrieved from EPO database.

[3] World Intellectual Property Organization. (2006). WO 2006/123456. Retrieved from WIPO PATENTSCOPE.

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Drugs Protected by US Patent 7,220,247

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

Foreign Priority and PCT Information for Patent: 7,220,247

Foriegn Application Priority Data
Foreign Country Foreign Patent Number Foreign Patent Date
United Kingdom0003790.3Feb 18, 2000

International Family Members for US Patent 7,220,247

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
Argentina 027445 ⤷  Start Trial
Austria 344075 ⤷  Start Trial
Australia 3209901 ⤷  Start Trial
Australia 770373 ⤷  Start Trial
Bulgaria 106938 ⤷  Start Trial
Bulgaria 65506 ⤷  Start Trial
Brazil 0108460 ⤷  Start Trial
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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