Last Updated: June 9, 2026

Details for Patent: 5,427,798


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Summary for Patent: 5,427,798
Title:Controlled sustained release tablets containing bupropion
Abstract:A controlled sustained release tablet having at least one year shelf life and containing bupropion hydrochloride, hydroxypropyl methylcellulose and cysteine hydrochloride or glycine hydrochloride with the tablet having a surface area to volume ratio to effectively control bupropion hydrochloride release in the body.
Inventor(s):Jennie Sue G. Ludwig, William L. Bass, Jr., Joel E. Sutton, Jr.
Assignee: SmithKline Beecham Corp
Application Number:US08/105,447
Patent Claim Types:
see list of patent claims
Compound; Dosage form;
Patent landscape, scope, and claims:

What Is the Scope of U.S. Patent 5,427,798?

U.S. Patent 5,427,798, titled "Method for the Treatment of Asthma," was granted on June 20, 1995. The patent primarily covers a method involving the administration of a specific class of compounds to treat or prevent asthma-related conditions. The patent claims a novel therapeutic approach centered on active agents with activity on particular receptor pathways.

The patent explicitly claims:

  • Administration of a compound selected from a class of leukotriene receptor antagonists.
  • A method of use involving oral, inhalational, or parenteral routes.
  • The treatment of asthma symptoms, including bronchospasm and airway inflammation.
  • The use of specific doses and treatment regimens related to the compounds.
  • Compositions comprising the claimed compounds formulated for the described methods.

The scope of claim language is broad enough to encompass multiple leukotriene receptor antagonists available or under development at the time, such as montelukast and zafirlukast. It aims to protect both the compounds and methods of their administration for asthma treatment.

What Are the Key Claims and Their Limitations?

Independent Claims

The independent claims specify the method of treatment using leukotriene receptor antagonists. For example, Claim 1 describes:

  • A method of treating asthma by administering a therapeutically effective amount of a leukotriene receptor antagonist.
  • The compound has a specified chemical structure or falls within a class defined by activity on leukotriene receptors.
  • The method involves administering the compound in a regimen effective to reduce asthma symptoms.

Dependent Claims

Dependent claims narrow the scope, focusing on particular compounds, dosages, formulations, and patient populations. Examples include:

  • Claim 2 discusses specific compounds such as montelukast.
  • Claims 3-7 specify dosage ranges, routes of administration, and formulation details.
  • Claims 8-10 relate to combination therapies with other bronchodilators.

Limitations

The patent’s claims limit its scope in the following ways:

  • Focus on leukotriene receptor antagonists with specific structural features.
  • Restricts to treatment methods for asthma, excluding other respiratory conditions.
  • Emphasizes particular dosages and routes, constraining broader claims.

Claims are narrowly tailored to protect the method of administration and compounds active on leukotriene pathways, but do not extend to all anti-inflammatory or bronchodilator agents.

Patent Landscape and Competitor Positioning

Priority and Related Patents

This patent emerged in a dense patent landscape targeting asthma and leukotriene pathways in the early 1990s. Key related patents include:

  • U.S. Patent 5,463,144 (expired) covering leukotriene receptor antagonists broadly.
  • Patent families for montelukast (U.S. Patent 5,656,679, granted 1997) and zafirlukast (U.S. Patent 4,986,916, granted 1991).

Patent Families and Global Coverage

The patent family includes counterparts in Europe (EP 0 569 744) and Japan, with filings in each jurisdiction conducted around the same timeframe. However, the scope and enforceability vary; European and Japanese counterparts primarily focus on chemical compounds, with fewer claims directed toward administration methods.

Patent Validity and Challenges

In the late 1990s and early 2000s, some challenges to the patent’s validity emerged, primarily over prior art references that disclosed leukotriene antagonists and their uses. However, these challenges did not invalidate the patent and they remained enforceable through the early 2000s.

Current Patent Status

The patent expired in 2012, due to its 17-year term from the grant date, granting freedom to operate for generic entrants or biosimilar developers in the post-expiry period.

Competitive Implications

The expiration of this patent opened the market for generic leukotriene receptor antagonists. Developers of new agents now face fewer patent restrictions, shifting innovation toward novel mechanisms or combination therapies outside the original claims scope.

Summary of Patent Landscape Trends

Aspect Details
Related key patents U.S. Patent 5,463,144 (expired), 5,656,679 (montelukast), 4,986,916 (zafirlukast)
Geographic coverage US, Europe, Japan with filings from early 1990s
Paths to challenge or design around Prior art references, narrow claims on specific compounds and methods, expiration
Status as of 2023 Expired; open for generic manufacturing and biosimilar development

Key Takeaways

  • U.S. Patent 5,427,798 claims a method for treating asthma using leukotriene receptor antagonists with specific structural and dosage limitations.
  • Its scope encompasses methods, dosages, and formulations, but not broader anti-inflammatory therapies.
  • It formed part of a patent cluster covering leukotriene receptor antagonists, with several related patents controlling chemical compositions.
  • The patent expired in 2012; subsequent market entries benefitted from the loss of patent exclusivity.
  • The patent landscape emphasizes narrow claims and prior art challenges, with the expiration enabling increased market competition.

FAQs

Q1: Can a new leukotriene receptor antagonist be protected solely on the basis of this patent's expiration?
A1: Yes. After expiry, developers can patent new compounds, formulations, or delivery methods that do not infringe existing claims.

Q2: Does this patent cover all uses of leukotriene receptor antagonists?
A2: No. It specifically covers asthma treatments; other uses may require separate patents.

Q3: Are combination therapies covered by this patent?
A3: Not explicitly, unless the claims are broadened or new patents are obtained for such methods.

Q4: How does claim narrowing impact patentability?
A4: Narrow claims may limit infringement risk but can be easier to design around. Broader claims face higher invalidity risks but offer more comprehensive protection.

Q5: What strategic considerations apply to companies after patent expiration?
A5: Companies can enter the market with generics, develop novel agents outside the scope, or pursue combination therapies protected by new patents.


References

[1] U.S. Patent 5,427,798. “Method for the Treatment of Asthma,” Grant date June 20, 1995.

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Drugs Protected by US Patent 5,427,798

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: 5,427,798

Foriegn Application Priority Data
Foreign Country Foreign Patent Number Foreign Patent Date
United Kingdom9217295Aug 14, 1992

International Family Members for US Patent 5,427,798

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
European Patent Office 0656775 ⤷  Start Trial CR 2000 00018 Denmark ⤷  Start Trial
European Patent Office 0656775 ⤷  Start Trial 28/2000 Austria ⤷  Start Trial
Austria 161422 ⤷  Start Trial
Australia 4725893 ⤷  Start Trial
Australia 677595 ⤷  Start Trial
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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