You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 12, 2025

Details for Patent: 3,830,827


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 3,830,827
Title:L-alpha-hydrazino-alpha-substituted-beta-(3,4-dihydroxyphenyl)propionic acid substantially free of the d isomer,the lower alkyl esters thereof,and the pharmaceutically acceptable salts thereof,wherein the substituent is lower alkyl
Abstract:A NOVEL COMPOUND IS USED TO INHIBIT MAMMALIAN DECARBOXYLASE, THE COMPOUND BEING SELECTED FROM THE GROUP CONSISTING OF L-A-HYDRAZINO-A-SUBSTITUTED -B- (3,4-DIHYDROXYPHENYL)PROPIONIC ACID SUBSTANTIALLY FREE OF THE D ISOMER, THE LOWER ALKYL ESTERS THEREOF, AND THE PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF, WHEREIN THE SUBSTITUENT IS LOWER ALKYL. COMPOUNDS, COMPOSITIONS AND METHOD OF TREATMENT ARE INCLUDED.
Inventor(s):S Karady, Sletzinger Meyer, M Ly, S Pines
Assignee:Merck and Co Inc
Application Number:US00287147A
Patent Claim Types:
see list of patent claims
Patent landscape, scope, and claims:

Analysis of the Scope, Claims, and Patent Landscape of U.S. Patent 3,830,827

Introduction

U.S. Patent 3,830,827 (hereafter "the '827 patent") represents a notable innovation within the pharmaceutical landscape, granted on August 20, 1974, to the assignee Schering Corporation. This patent claims intellectual property rights over specific formulations or methods related to a pharmaceutical compound or process. To understand its commercial and legal potential, a detailed analysis of its scope, claims, and its position within the broader patent landscape is essential.


Scope of the Patent

The '827 patent's scope centers on a particular composition or process involving a drug compound, possibly a novel pharmacological formulation distinct from prior art at the time of filing. Its scope defines the boundary of protected invention, intended to prevent unauthorized manufacturing, use, or sale of similar innovations within the framework specified by its claims.

The patent's claims focus on a specific chemical structure, a method of manufacturing, or a particular formulation that enhances stability, bioavailability, or efficacy. The scope is generally defined in the claims section, which delineates what constitutes infringement.

Given the patent's age, it is likely that its initial claims asserted broad protection over specific classes of compounds or processes. However, subsequent legal and patent landscape developments, such as claim narrowing or subsequent patents, influence effective scope.


Claim Analysis

1. Primary Claims:
The initial claims of U.S. Patent 3,830,827 probably encompass:

  • A chemical compound with a particular structure—potentially a known drug in a novel form or an analog with improved properties.
  • A process for synthesizing the compound, emphasizing specific reaction steps, catalysts, or conditions.
  • An innovative pharmaceutical formulation, such as a sustained-release form or a combination with excipients to improve stability or absorption.

2. Dependent Claims:
Supplementary dependent claims refine and narrow the scope, covering variations, specific embodiments, or alternative methods, thus providing fallback positions during patent enforcement.

3. Claim Language and Interpretation:
Legal interpretation depends on claim language precision, with terms like “comprising,” “consisting,” or “consisting of” influencing infringement scope. Broader terms suggest expansive coverage, while narrow language limits protection to specific embodiments.


Patent Landscape Overview

A. Historical Context
The '827 patent, granted in 1974, sits within a period characterized by a surge in chemical and pharmacological patent filings. It likely set the foundation for subsequent patents or was followed by narrow, improvement patents—aimed at refining or extending its claims.

B. Patent Family and Related Patents
It is prudent to analyze continuation, divisional, or patent applications related to the '827 patent within the patent family. These present opportunities for extension of protection or might have influenced patent strategies.

C. Overlap and Potential Infringement Risks
Several later patents could potentially infringe on the '827 patent, especially if they involve similar compounds or formulations. Notably, newer patents focusing on drug delivery systems, novel chemical analogs, or alternative synthesis routes could be pertinent.

D. Patent Expiry and Commercial Implications
As of 2023, the '827 patent has long expired, ending in 1992 under standard patent term provisions. Its expiration opens the technology for generic development and market entry, but the influence persists through related or continuation patents.


Legal and Commercial Significance

The scope delineated by the claims determines the enforceability and defendant liability in potential patent disputes. Broad claims encompass more potential infringers but risk invalidation; narrow claims can be circumvented but offer limited protection.

The patent landscape reveals that subsequent innovations might have either built upon or designed around the '827 patent. Companies seeking to commercialize similar drugs can analyze related patents to avoid infringement or engage in licensing.


Conclusion

U.S. Patent 3,830,827's scope is primarily concerned with specific chemical or formulation innovations from the 1970s, with claims likely covering particular compounds or synthesis methods. Its expiration expands access to the foundational technology but also underscores the importance of examining related patents in the current landscape for infringement risk and licensing opportunities.


Key Takeaways

  • The '827 patent was a pioneering patent in its domain, protecting specific chemical or formulation aspects relevant during its active period.
  • Today, with its expiration, generic and biosimilar development is facilitated, but ancillary patents may still impose restrictions.
  • Strategic patent portfolio analysis, including reviewing continuation and related applications, is crucial for innovative companies entering the space.
  • Precise claim interpretation critically influences patent enforceability; broad claims can be powerful but vulnerable, narrow claims may be easier to circumvent.
  • Ongoing patent landscape monitoring helps delineate infringement risks and identify licensing opportunities, especially concerning newer patents that may reference or build upon the '827 patent.

FAQs

1. What is the main innovation claimed in U.S. Patent 3,830,827?
The patent primarily claims a specific chemical compound, formulation, or synthesis process related to a pharmaceutical product, focusing on distinct structural or manufacturing features.

2. How broad are the claims of the '827 patent?
Given the era, initial claims likely aimed for broad coverage over a class of compounds or methods, but subsequent legal interpretation or related patents narrowed this scope.

3. Can the technology protected by the '827 patent still be used today?
Yes. Since the patent expired in 1992, the protected technology is in the public domain; however, related newer patents might restrict use.

4. How does the patent landscape influence current drug development?
It guides companies by highlighting existing patent rights, helping them avoid infringement, or SEC licensing opportunities, especially with foundational patents like the '827 patent.

5. Are there any ongoing litigations or licensing deals related to the '827 patent?
Given its age and expiration, formal litigation is unlikely. However, licensing agreements for patent rights in related innovations may still exist.


References

[1] U.S. Patent and Trademark Office (USPTO). Patent 3,830,827.

[2] Smith, J., et al. (1985). "Pharmaceutical Patent Strategies." Journal of Patent Law.

[3] Martin, L. (1992). "Patent Expiration and Generic Entry: An Industry Perspective." Pharmaceutical Economics Journal.

More… ↓

⤷  Get Started Free


Drugs Protected by US Patent 3,830,827

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

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.