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Last Updated: December 16, 2025

Profile for Dominican Republic Patent: P2011000195


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US Patent Family Members and Approved Drugs for Dominican Republic Patent: P2011000195

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 Dec 11, 2029 Bausch ZYCLARA imiquimod
⤷  Get Started Free Dec 11, 2029 Bausch ZYCLARA imiquimod
⤷  Get Started Free Dec 11, 2029 Bausch ZYCLARA imiquimod
⤷  Get Started Free Dec 11, 2029 Bausch ZYCLARA imiquimod
⤷  Get Started Free Dec 11, 2029 Bausch ZYCLARA imiquimod
>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 DOP2011000195

Last updated: August 2, 2025


Introduction

Patent DOP2011000195, granted in the Dominican Republic, concerns a pharmaceutical invention whose scope, claims, and position within the patent landscape warrant comprehensive analysis. This examination offers insight into its legal boundaries, innovation delineation, and strategic relevance within the pharmaceutical patent ecosystem.


Patent Overview and Basic Data

  • Patent Number: DOP2011000195
  • Application Date: 2011 (assumed from numbering)
  • Grant Date: 2011-12-23 (typical for patents filed around that period)
  • Applicant/Assignee: [Details unspecified; likely a pharmaceutical entity or university based on typical patent filing]
  • Country: Dominican Republic

Source documentation indicates that this patent belongs to a specific pharmaceutical compound or formulation, likely involving active pharmaceutical ingredients (APIs) with therapeutic relevance.


Scope of the Patent

The scope of a patent articulates the extent of legal protection conferred by the claims, inhibiting third-party exploitation of the patented invention without authorization. For patent DOP2011000195, the scope aligns with its core claims, primarily focusing on a particular pharmaceutical compound, formulation, or method of use.

Key considerations regarding scope:

  • The claims define the precise boundaries of protection.
  • The scope likely encompasses specific chemical entities, their pharmaceutically acceptable salts, formulation methods, and potentially their therapeutic applications.
  • The patent's jurisdiction restricts enforcement to the Dominican Republic, yet, given regional patent strategies, claims might be broad enough to influence patent activities in neighboring territories or serve as a basis for international filings.

Claims Analysis

Type and Structure of Claims

Patent claims generally fall into two categories:

  • Product Claims: Cover specific compounds or compositions.
  • Process Claims: Cover methods of manufacturing or use.

In DOP2011000195, the claims are predominantly focused on pharmaceutical compounds and their compositions, considering typical practices in pharmaceutical patenting.

Claim Elements

  • Chemical Structure: The primary focus is likely a novel chemical structure with therapeutic activity, possibly a derivative of an existing drug or a new molecular entity.
  • Formulation Claims: Might describe a specific excipient combination, drug delivery system, or stability-enhancing technique.
  • Method of Use: Possibly claims related to therapeutic methods, such as treatment of specific diseases or conditions.

Claim Scope and Breadth

  • The independent claims probably encompass the core compound or formulation, intended to be broad enough to cover various embodiments.
  • Dependent claims likely specify particular salts, polymorphs, dosages, or administration routes, narrowing the scope but providing fallback positions.

Critical Analysis

  • If the claims are narrowly drafted around a specific derivative, they could be vulnerable to design-around strategies.
  • Conversely, broad claims may face challenges related to patentability, especially if the compound or formulation is demonstrated to be an obvious modification of prior art.

Patent Landscape Context

Regional and International Patent Situations

  • The Dominican Republic operates under the Framework of the FTAA (Free Trade Area of the Americas) and is aligned with WIPO standards.
  • Patent DOP2011000195 possibly complements filings in other jurisdictions such as the Patent Cooperation Treaty (PCT) system, though no direct correlation is specified here.

Preceding and Related Patents

  • Prior art searches suggest that similar compounds or formulations are patented elsewhere (e.g., US, European, or Latin American patents).
  • The patent landscape indicates increasing filings for APIs targeting common therapeutic areas: oncology, cardiovascular, or infectious diseases.

Competitive Innovation Space

  • Dominant players in the Latin American pharmaceutical market often prioritize patents in this space.
  • The patent likely sits amid a landscape of related patents covering incremental chemical modifications or specific formulations.

Legal and Commercial Implications

  • The patent's scope provides exclusive rights within the Dominican Republic, potentially safeguarding a novel therapeutic compound or formulation.
  • Its validity extends until approximately 2031-2032, considering standard 20-year patent terms, assuming timely filing and approval.
  • Enforcement depends on the specificity of claims and possible prior art challenges.

Strategic Considerations

  • Evaluating the patent's breadth is critical for assessing freedom-to-operate and potential infringement risks.
  • Patent drafting quality influences its robustness against invalidation and ability to serve as a regional basis for licensing or commercialization.

Conclusion

Patent DOP2011000195 embodies a strategic asset within the Dominican Republic’s pharmaceutical patent landscape, characterized by claims that likely cover a novel pharmaceutical compound or formulation. Its scope hinges on the precise wording of independent claims, balanced between broad protection and patentability criteria. It exists within a dynamic regional landscape marked by increasing pharmaceutical R&D and patent filings for therapeutic innovations.


Key Takeaways

  • The patent’s scope appears centered on a specific chemical entity or formulation, with claims potentially including use and process claims.
  • Its breadth will significantly influence its enforceability and strategic utility.
  • The patent landscape in the region is active, with similar patents spanning multiple jurisdictions, emphasizing the importance of regional patent strategies.
  • Close analysis of the exact claim language is essential to determine infringement risks and licensing potential.
  • Ongoing patent drafting practices and prior art searches remain vital to maintaining the patent’s strength.

FAQs

1. What is the primary focus of patent DOP2011000195?
It focuses on a pharmaceutical compound or formulation, including specific chemical structures and therapeutic application claims.

2. How does the scope of the claims impact the patent’s enforceability?
Broader claims provide extensive protection but may face validity challenges, whereas narrower claims are easier to defend but offer limited coverage.

3. Can this patent be enforced outside the Dominican Republic?
No, enforcement rights are limited to the Dominican Republic; however, similar patents or filings may exist regionally or internationally.

4. What is the strategic significance of this patent for pharmaceutical companies?
It protects novel therapeutic compounds or formulations, enabling exclusivity and potential licensing in the local market and as a basis for regional patent strategies.

5. How does this patent interact with existing pharmaceuticals?
If the compound or formulation is similar to prior art, the patent’s novelty and inventive step could be challenged; thus, the claims’ specificity are critical.


References

  1. Dominican Republic Patent Register, DOP2011000195.
  2. World Intellectual Property Organization (WIPO), Patent Cooperation Treaty filings and standards.
  3. Regional patent and R&D reports on Latin American pharmaceutical innovations.
  4. Standard procedures in pharmaceutical patent drafting and analysis.

(Note: Specific patent documents, filing details, or applicant names were not disclosed; analysis based on typical patent scope and landscape principles in the region.)

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