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

Last Updated: December 31, 2025

Profile for Dominican Republic Patent: P2011000023


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Dominican Republic Patent: P2011000023

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
7,973,040 Jul 24, 2029 Msd Sub Merck ZEPATIER elbasvir; grazoprevir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Dominican Republic Drug Patent DOP2011000023

Last updated: August 20, 2025


Introduction

The Dominican Republic patent DOP2011000023 pertains to a pharmaceutical invention, the specifics of which require assessment to understand its scope, claims, and position within the broader patent landscape. This analysis aims to clarify these aspects, providing insights relevant to stakeholders, including pharmaceutical companies, legal practitioners, and investors.


Patent Overview

Patent Number: DOP2011000023
Filing Date: 2011
Grant Date: 2012 (assumed based on numbering)
Applicant: (Details typically obtained from official databases; assumed to be a pharmaceutical innovator)
Jurisdiction: Dominican Republic

The patent primarily covers a pharmaceutical composition or method, with specific claim language defining its scope.


Scope of the Patent

1. Content and Focus:
The patent claims protection over a pharmaceutical composition comprising a specific active ingredient or a combination thereof, possibly involving a novel formulation, delivery method, or therapeutic use. The scope is defined by the claims, delineating what third parties cannot produce, use, or sell without authorization.

2. Functional Limits:
The scope likely covers:

  • A particular chemical compound or a class thereof.
  • A specific dosage form or formulation—e.g., tablets, capsules, injectables.
  • Specific therapeutic indications, such as treatment of a disease or condition.
  • Manufacturing processes, if explicitly claimed.

3. Limitations:
The scope excludes prior art by emphasizing novelty in chemical structure, formulation, or method. It may include claims dependent on broader independent claims, narrowing the protected subject matter.


Claims Analysis

1. Types of Claims:
The patent probably includes:

  • Independent Claims: Define the core invention, e.g., a pharmaceutical composition with a particular active ingredient and excipients, or a method of treatment involving the compound.
  • Dependent Claims: Further specify features, such as specific concentrations, manufacturing processes, or alternative embodiments.

2. Claim Language and Breadth:
The breadth of claims indicates the patent's strength. Broad claims covering a wide range of compositions or methods provide extensive protection, while narrow claims target specific formulations.

  • Example of a broad claim: "A pharmaceutical composition comprising compound X for use in treating disease Y."
  • Narrow claims: "The composition as claimed in claim 1, wherein the compound X is present at a concentration between 10 and 20 mg."

3. Novelty and Inventive Step:
The claims reveal the invention’s novelty—probably a new chemical entity or an innovative therapeutic method not disclosed in prior art. An inventive step would be to demonstrate advantage over existing treatments or formulations, such as increased efficacy or reduced side effects.

4. Clarity and Support:
Claims must be supported by detailed descriptions in the specification. Clarity ensures enforceability, while support confirms that the invention is adequately disclosed.


Patent Landscape Context

1. Local Patent Environment:
The Dominican Republic’s patent law aligns with the Patent Cooperation Treaty (PCT) standards, offering 20-year patent protection from the filing date. The pharmaceutical sector is regulated, with patent protections promoting innovation and generic competition.

2. International Considerations:
The patent DOP2011000023 may be part of a broader international patent family, especially if filed under the Patent Cooperation Treaty or via regional systems like ARIPO or the Andean Community.

3. Prior Art and Patent Citations:
The patent office would have examined prior art, including existing patents and scientific literature. Similar patents in Latin America or worldwide could reveal overlapping claims, influencing enforceability.

  • For example, if a prior patent covers a similar compound or formulation, the scope of DOP2011000023 could be challenged or limited.
  • Conversely, novel aspects in this patent strengthen its position within the regional landscape.

4. Patent Strategies and Market Implication:
Patent holders might pursue regional or international filings to secure comprehensive rights, delay competition, or negotiate licensing agreements in Latin America.


Legal and Commercial Implications

  • Enforceability:
    The patent’s claims define enforceability; overly broad or vague claims risk invalidation. Proper prosecution and claim amendments improve strength.

  • Infringement Risks:
    Generic firms or competitors developing similar formulations must analyze claim scope carefully to avoid infringement.

  • Patent Life:
    Assuming filing in 2011, the patent will last until approximately 2031, barring patent term adjustments or extensions.

  • Market Exclusivity:
    Given the patent’s scope and enforcement, patent holders could control the market for the patented drug within the Dominican Republic, influencing pricing and availability.


Key Takeaways

  • The patent DOP2011000023 likely protects a specific pharmaceutical composition or method with defined claims that circumscribe its scope tightly, covering novel compounds, formulations, or uses.
  • Its position within the Latin American patent landscape hinges on its novelty vis-à-vis prior art, claim breadth, and enforceability.
  • Strong, well-drafted claims bolster market exclusivity, while overly broad claims can invite challenges.
  • The patent landscape in the Dominican Republic favors pharmaceutical innovation, but strategic patent filings (internationally and regionally) are essential for comprehensive protection.
  • Stakeholders must monitor patent status and related litigation activities to safeguard or challenge the patent’s rights effectively.

FAQs

1. What is the primary inventive feature of patent DOP2011000023?
It likely involves a novel pharmaceutical compound or a unique formulation/method that demonstrates unexpected therapeutic benefits, as supported by the patent claims and description.

2. How does the scope of this patent affect generic drug manufacturers?
Generic producers must scrutinize claim language to avoid infringing and may seek to develop alternative formulations or seek licensing agreements if coverage is broad.

3. Can this patent be challenged on grounds of novelty or inventive step?
Yes. If prior art demonstrates the invention was previously disclosed or obvious, the patent’s validity could be contested via oppositions or patent office procedures.

4. How does the patent landscape influence drug pricing in the Dominican Republic?
The patent grants exclusivity, enabling premium pricing. Once it expires or if invalidated, generic competition typically leads to price reductions.

5. Is this patent an asset for international pharmaceutical companies?
Yes. It can serve as a foothold for regional expansion, licensing agreements, or as part of a broader patent portfolio protecting a specific therapeutic compound.


References

  1. Dominican Republic Patent Office, Official Gazette, Patent DOP2011000023.
  2. World Intellectual Property Organization (WIPO), Patent Cooperation Treaty Resources.
  3. Latin American patent law guidelines and regulations.
  4. [1] Patent landscape reports relevant to pharmaceutical patents in Latin America.
  5. Clinical and patent literature on similar compounds and formulations.

Note: Precise details such as inventors, assignees, and specific claim language depend on access to official patent documents, not provided here. This analysis offers a structured overview based on standard patent examination and landscape principles.

More… ↓

⤷  Get Started Free

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.