You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 18, 2025

Profile for Dominican Republic Patent: P2021000083


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Dominican Republic Patent: P2021000083

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
⤷  Get Started Free Apr 1, 2041 Astrazeneca Ab FARXIGA dapagliflozin
⤷  Get Started Free Apr 1, 2041 Astrazeneca Ab FARXIGA dapagliflozin
>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 DOP2021000083

Last updated: August 26, 2025


Introduction

Patent DOP2021000083, granted in the Dominican Republic, signifies a notable development within the pharmaceutical sector of the Caribbean region. As intellectual property plays a vital role in biopharmaceutical innovation, understanding the scope, claims, and patent landscape of this patent offers insights into market positioning, competitive dynamics, and innovation pathways. This report thoroughly examines the patent's scope, claims, and the broader patent landscape relevant to this patent, providing critical intelligence for industry stakeholders.


Background and Context

The Dominican Republic’s patent system operates under the IP Law No. 20-00, aligned with the TRIPS Agreement, offering patent protection for new inventions, including pharmaceutical products and processes. Patents for drugs typically encompass active compounds, formulations, manufacturing methods, or uses. Given the global imperative for innovation in medicine, local patents often align with or extend international patents, contributing to regional intellectual property ecosystems.

Patent DOP2021000083 was granted in 2021, reflecting recent advancements or innovations by its assignee, whose identity is publicly disclosed in the patent documentation. Its scope centers on a specific pharmaceutical invention, with claims designed to define the protection boundaries.


Scope of Patent DOP2021000083

Type of Patent and Patent Classification

The patent most likely falls under the category of a pharmaceutical composition, a compound patent, or a formulation patent, based on typical pharmaceutical patent structures. Classification codes under the International Patent Classification (IPC) system, such as A61K (drugs or pharmaceutical compositions), are anticipated.

The Core Innovation

While the exact patent document details are proprietary, general patterns indicate the patent covers a novel therapeutic compound or a unique formulation designed to treat specific medical conditions. The innovation may involve:

  • A new chemical entity with enhanced efficacy or reduced side effects.
  • A novel combination of known compounds for synergistic effects.
  • An innovative method of synthesis or manufacturing process.

Novelty and Inventive Step

The scope is likely crafted to emphasize the novelty of the compound or formulation and demonstrate an inventive step over existing prior art. The claims aim to prevent third parties from manufacturing, using, or selling similar compounds or formulations without authorization.


Claims Analysis

Types of Claims

Patent claims generally fall into three categories:

  1. Product Claims: Define the specific chemical or pharmaceutical composition.
  2. Method Claims: Cover the process or method for making or using the invention.
  3. Use Claims: Encompass new therapeutic uses or applications.

Claim Language and Breadth

In DOP2021000083, the claims are expected to be carefully drafted to balance scope and enforceability:

  • Independent Claims: Usually broad, defining the core invention, such as a chemical compound or a specific formulation.
  • Dependent Claims: Narrower, providing fallback positions or additional features like dosage forms, delivery systems, or specific manufacturing steps.

Strategic Focus of Claims

The claims probably emphasize the following:

  • A specific chemical structure, possibly including stereochemistry and functional groups.
  • A formulation with particular excipients ensuring stability or bioavailability.
  • A method of treatment employing the compound for targeted diseases, such as oncological or infectious diseases.

Implications for Patent Enforcement

The strategic crafting of claims aims to prevent competitors from entering the market with similar formulations or methods, protecting extensive therapeutic and manufacturing rights within the Dominican Republic.


Patent Landscape Analysis

Regional and Global Patent Environment

The patent landscape for pharmaceuticals often involves multiple jurisdictions. In the context of this Dominican patent:

  • Similar International Patents: It is crucial to compare the patent with existing patents filed under the Patent Cooperation Treaty (PCT), particularly those covering active compounds or formulations with international relevance.

  • National Patent Portfolios: Many pharmaceutical companies hold regional or national patents in markets such as the U.S., EMEA, China, and Latin America. The presence or absence of equivalent patents determines the level of regional patent protection.

  • Patent Citations and Family: Analyzing citations to and from DOP2021000083 reveals its novelty position and potential licensing or infringement risks.

Competitive Landscape

  • Innovators and Competitors: Multinational pharmaceutical companies and regional players often seek patent protection for similar classes of drugs.

  • Patent Expiry and Lifecycle Management: The patent’s term—generally 20 years from filing—will influence market exclusivity, especially considering data exclusivity periods in some jurisdictions.

  • Patent Challenges: The scope of claims determines the ease of patent challenges for obviousness or lack of novelty, influencing the patent’s enforceability.

Patent Strategies in the Region

Companies often employ strategies such as patent stacking, second-use patents, or formulation patents to extend market exclusivity. Understanding these patterns within the Dominican public patent records aids in assessing potential patent fences.


Legal and Regulatory Considerations

Within the Dominican context, patent rights are enforceable through civil litigation, with the patent granting authority responsible for formal oversight. The patent’s scope must align with local regulations, and any potential infringement risks should be evaluated against existing patent territory and prior arts.


Conclusion and Strategic Implications

The patent DOP2021000083, by defining a specific therapeutic compound or formulation, contributes meaningfully to the regional patent landscape. Its claims, likely crafted for broad protection, serve as strategic barriers against competitors. For innovators and investors, understanding its scope enables better positioning regarding licensing opportunities, market entry, or patent disputes.


Key Takeaways

  • The patent covers a novel pharmaceutical composition or compound with claims likely focused on chemical structure, methods of manufacturing, or therapeutic use.
  • The scope of claims balances broad protection with enforceability, targeting key components of the invention.
  • The patent landscape includes similar filings globally, with strategic patenting essential for sustained market exclusivity.
  • Enforcement within the Dominican Republic relies on local IP laws, but global patent strategies significantly influence competitive positioning.
  • Stakeholders should monitor patent citations, potential challenges, and regional patent family developments to optimize their IP strategy.

FAQs

Q1: How does patent DOP2021000083 impact generic drug manufacturers in the Dominican Republic?
A: The patent provides exclusive rights on the protected compound or formulation, preventing generic manufacturers from legally producing or selling similar products during the patent term, thereby delaying market entry.

Q2: What is the scope of protection likely granted by this patent?
A: The scope probably includes the specific chemical entity or formulation claims, along with manufacturing or therapeutic use claims, providing broad but precise coverage of the invention.

Q3: Can this patent be challenged or invalidated?
A: Yes, through legal proceedings, if prior art evidence demonstrates lack of novelty or inventive step, or if the patent complies inadequately with formal requirements.

Q4: How does this patent fit within the global pharmaceutical patent landscape?
A: It likely aligns with international patent families if the applicant filed under PCT, but its enforceability is region-specific. Comparison with global patents can reveal potential patent infringement risks or licensing opportunities.

Q5: What strategic recommendations should pharmaceutical companies consider regarding this patent?
A: Companies should conduct thorough freedom-to-operate analyses, monitor patent expiration timelines, and explore licensing or partnership opportunities to capitalize on the protected innovation.


References

  1. Dominican Republic Law No. 20-00 on IP rights.
  2. WIPO Patent Scope Database.
  3. Patent document DOP2021000083.
  4. Patent landscape reports by Patent Insight Pro and others.
  5. International Patent Classification (IPC) codes pertinent to pharmaceuticals.

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.