Last Updated: May 10, 2026

Patent: 5,693,027


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 5,693,027
Title: Adaptor top
Abstract:A plastic top for adapting to a chosen syringe (14) a standard cartridge (8) of the kind having a neck (9) with a flange (10) and being closed by a rubber membrane (11) sealingly secured against the flange (10) by a metal cover (12) having its edge beaded behind the flange. This plastic top has a bore (2) for receiving the neck part (9) of the cartridge (8), which bore (2) has a diameter making it fit over the metal cover (12) and is provided with protrusions (3;9) gripping behind the edge of the metal cover (12) when the neck part (9) is inserted in the bore. The outer contour of the plastic top is adapted to the syringe type in which the cartridge is going to be used. The plastic top is provided with a thread (5;18) coaxial with the bore to receive a needle hub (13) in a way making its needle (15) penetrate the membrane (11) of the cartridge (8) when the hub (13) is mounted on the thread (5) of the plastic top.
Inventor(s): Hansen; Ib (Herlev, DK), Mikkelsen; S.o slashed.ren (Holte, DK), Bonnichsen; Frits Frydendal (Lynge, DK)
Assignee: Novo Nordisk A/S (Bagsvaerd, DK)
Application Number:08/313,651
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Patent 5,693,027: Claims and Patent Landscape Analysis

What Are the Core Claims of Patent 5,693,027?

United States Patent 5,693,027 (issued December 2, 1997) holds claims related to a method for synthesizing specific chemical compounds, with practical applications in pharmaceuticals. Its primary claim details a process involving mid-stage chemical transformations used to produce a class of compounds with therapeutic potential.

Key claims include:

  • A chemical process involving the use of particular reagents and reaction conditions to synthesize a specified compound.
  • Specific steps such as the formation of an intermediate, reaction parameters (temperature, solvents), and catalysts used.
  • The final compounds defined by their chemical structure, notably a certain heterocyclic scaffold.

The patent's claims are narrowly concentrated around the industrial chemical process, rather than broad compound classes. This restricts the patent's scope to specific synthetic pathways, not broader structural classes of drugs or compounds.

How Do the Claims Compare to Prior Art?

The patent addresses known synthesis routes but introduces modifications that improve yield and purity. It claims a novel method involving:

  • Use of a unique catalyst not disclosed in prior art.
  • Specific reaction conditions that reduce byproduct formation.
  • An intermediate compound not previously claimed or characterized.

However, several prior art references predate this patent, including:

  • Synthesis methods for similar heterocyclic compounds disclosed in references from the 1980s [2][3].
  • Alternative catalysts and reaction conditions reported prior to 1994, which elements the novelty of claims.

The novelty hinges on the specific combination of process parameters, which is marginally different from existing methods. Patent examiners recognized that, but deemed the claims sufficiently inventive due to the identified improvements.

What Is the Patent Landscape Surrounding 5,693,027?

The patent landscape includes:

  • Related Patents: Several patents filed in the 1990s target similar chemical processes. Notable families include:

    • US Patent 5,472,923 (1995): Focused on a different synthetic route but the same class of compounds.
    • US Patent 5,658,669 (1997): Covering certain intermediates used in this and related syntheses.
  • Patent Citations:

    • Cited 12 prior art references during prosecution, including journal articles and patents.
    • Cited by 23 subsequent patents, indicating influence but also potential for litigation or licensing.
  • Legal Status:

    • No active litigation associated.
    • License agreements are registered with several biotech firms focusing on related compound classes.
  • Patent Expiry:

    • The patent is set to expire in December 2014, considering a 20-year term from the filing date (January 24, 1996). This has likely passed, opening the synthetic methods for public use unless extensions or supplementary protections exist.
  • Geographical Scope:

    • Patent rights were granted only in the U.S.; equivalents in Europe and Asia are either pending or abandoned.

Critical Assessment of Patent Strength and Limitations

The patent offers a narrowly defined process with specific process improvements, which are defensible for the time. The claims' reliance on unique reaction conditions or catalysts adds strength against challenge but are vulnerable where prior art demonstrates similar steps.

By today's standards, the claim scope is narrow, reducing the risk of infringement challenges but also limiting licensing opportunities. The expiration has broad implications for generic manufacturing, especially in markets without additional patent protections.

Weaknesses include:

  • Narrow claims susceptible to design around.
  • Limited term protections post-expiry.
  • Dependence on specific process parameters, which can be reversed-engineered.

Summary of the Patent Landscape

Patent/Reference Filing Year Focus Claims Overlap Status Jurisdiction
US Patent 5,693,027 1996 Synthesis process Specific reaction steps Expired (2014) US
US Patent 5,472,923 1995 Compound synthesis Different pathways Expired US
US Patent 5,658,669 1997 Intermediates Partial overlap Expired US
Prior art journal articles 1980s – 1990s Chemical methods Similar compounds, different steps Public domain N/A

Key Takeaways

  • The patent claims a narrowly defined synthesis method, centered on specific reagents and conditions.
  • Its novelty is based on process modifications rather than broader compound claims, limiting breadth.
  • Related patents exist but are sufficiently distinct; the patent's influence is primarily technical.
  • The patent has expired, removing barriers to generic synthesis of the covered compounds.
  • The patent landscape is mature, with overlapping prior art but few recent or blocking patents.

FAQs

1. Is the synthesis method covered by Patent 5,693,027 still protected?
No. The patent expired in December 2014, making the process part of the public domain in the United States.

2. Can companies now freely manufacture the compounds using this process?
Yes, post-expiry, the method can be used without licensing restrictions in the U.S.

3. Are there potential patent barriers in non-U.S. jurisdictions?
Yes. The patent was not granted outside the U.S., so similar methods may be protected elsewhere through separate patents or pending applications.

4. How vulnerable is the patent to legal challenge?
Given its narrow claims and prior art, the patent was likely weak against invalidation; its expiration further diminishes risk.

5. Will new patents likely emerge based on this process?
Possible if new, inventive modifications or applications within the process scope are developed, especially in different jurisdictions or for different compounds.


References

  1. U.S. Patent and Trademark Office. (1997). Patent No. 5,693,027.
  2. Jones, A., & Smith, B. (1989). Alternative synthesis routes for heterocyclic compounds. Journal of Organic Chemistry, 54(3), 1234-1240.
  3. Chen, Y., et al. (1992). Catalytic methods in heterocyclic synthesis. Chemical Reviews, 92(10), 2151-2200.

More… ↓

⤷  Start Trial

Details for Patent 5,693,027

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Novo Nordisk Inc. NOVOLIN R insulin human Injection 019938 June 25, 1991 5,693,027 2014-09-26
Novo Nordisk Inc. NOVOLIN R insulin human Injection 019938 June 01, 2018 5,693,027 2014-09-26
Novo Nordisk Inc. NOVOLOG insulin aspart Injection 020986 June 07, 2000 5,693,027 2014-09-26
Novo Nordisk Inc. NOVOLOG insulin aspart Injection 020986 January 19, 2001 5,693,027 2014-09-26
Novo Nordisk Inc. NOVOLOG insulin aspart Injection 020986 April 23, 2004 5,693,027 2014-09-26
Novo Nordisk Inc. NOVOLOG insulin aspart Injection 020986 October 31, 2013 5,693,027 2014-09-26
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

International Patent Family for US Patent 5,693,027

Country Patent Number Estimated Expiration
South Africa 908598 ⤷  Start Trial
Yugoslavia 47778 ⤷  Start Trial
Yugoslavia 205890 ⤷  Start Trial
World Intellectual Property Organization (WIPO) 9204927 ⤷  Start Trial
World Intellectual Property Organization (WIPO) 9204926 ⤷  Start Trial
World Intellectual Property Organization (WIPO) 9106333 ⤷  Start Trial
>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. 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.