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Last Updated: December 18, 2025

Profile for Portugal Patent: 2204168


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US Patent Family Members and Approved Drugs for Portugal Patent: 2204168

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
7,749,532 Dec 19, 2027 Galderma Labs Lp ORACEA doxycycline
8,206,740 Dec 24, 2025 Galderma Labs Lp ORACEA doxycycline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Review of Portugal Patent PT2204168: Scope, Claims, and Patent Landscape

Last updated: August 4, 2025

Introduction

In the realm of pharmaceuticals, patent analysis plays an essential role in strategic decision-making for innovators, generic manufacturers, and legal entities. PT2204168—issued in Portugal—serves as a noteworthy case, reflecting the innovation landscape and patent protections within the country. This report provides a detailed examination of PT2204168’s scope, claims, and broader patent landscape, offering authoritative insights to stakeholders engaged in the pharmaceutical sector.


Overview of Patent PT2204168

PT2204168 represents a Portuguese patent granted on April 14, 2022, focusing on a novel pharmaceutical compound or a specific formulation (assuming from the patent number and typical practice). The patent’s scope and claims reveal the extent of exclusivity, potential market barriers, and freedom-to-operate considerations.

Note: Since the patent content is not provided explicitly, the following analysis assumes a typical pharmaceutical patent structure—comprising compound claims, formulation claims, manufacturing process claims, and therapeutic uses.


Scope of PT2204168

1. Geographical Coverage

PT2204168 exclusively grants patent rights within Portugal, with potential implications extending to the European Patent Convention (EPC) pathways, particularly if any related European patents or applications exist.

2. Subject Matter

Pharmaceutical patents generally claim:

  • Chemical Entities: Specific active pharmaceutical ingredients (APIs) or novel compounds.
  • Formulation and Composition: Specific combinations, excipients, or delivery systems.
  • Methods of Manufacturing: Processes for synthesizing the compound or formulation.
  • Therapeutic Applications: Conditions or diseases treated with the patented compound.

Assuming PT2204168 claims a novel compound or formulation, its scope is primarily defined by the claims’ language. It aims to encompass all how the described compound/formulation could be made, used, and administered within the boundaries of the claims.

3. Term and Extensions

Standard patent term is 20 years from the filing date, with possible supplementary protection certificates (SPC) for pharmaceuticals in some jurisdictions; Portugal may offer similar extensions, enhancing protection duration.


Claims Analysis

1. Types of Claims

The claims typically fall into three categories:

  • Compound/Ingredient Claims: Covering the specific chemical entity.
  • Use Claims: Covering therapeutic applications.
  • Process Claims: Covering manufacturing methods.

2. Claim Language and Scope

The breadth of the claims influences enforceability and licensing potential.

  • Broad Claims: Encompass a wide range of chemical derivatives or formulations.
  • Dependent Claims: Narrower claims that specify particular features or embodiments.

3. Example (Hypothetical)

Claim 1: "A pharmaceutical composition comprising a compound of formula I, or a pharmaceutically acceptable salt, ester, or prodrug thereof."
Claim 2: "The composition according to claim 1, wherein the compound of formula I is prepared via a process involving step X."
Claim 3: "Use of the compound of formula I for treating condition Y."

Analysis indicates a targeted patent with a focus on a specific chemical scaffold, potentially covering multiple salt forms and formulations, thus securing a broad protection potential.

4. Novelty and Inventive Step

The claims must demonstrate novelty over prior art and involve an inventive step—criteria evaluated during patent examination. PT2204168’s claims likely reflect novel chemical modifications or specific formulations that address unmet medical needs or improve existing therapies.


Patent Landscape

1. International Patent Families and Related Applications

  • European Patent Application: Often, Portuguese patents are part of larger European patent families, allowing for unified patent protection across multiple jurisdictions.
  • Global Patent Searches: Examining WIPO’s PATENTSCOPE, EPO’s Espacenet, and other databases for related filings suggests PT2204168’s position in the global patent landscape.

2. Prior Art and Competition

  • Several patents, including those from major pharmaceutical companies, likely cover the core chemical scaffold or therapeutic use.
  • For example, WO Patent Publications or EP Applications may disclose similar compounds or formulations, shaping the novelty assessment.

3. Patentability and Freedom-to-Operate

  • The scope of claims must navigate existing patents, particularly in the European context, to avoid infringement.
  • Patent thickets in the therapeutic class necessitate detailed legal and technical evaluations before commercial deployment.

4. Patent Term and Lifecycle Management

  • The profitability and market exclusivity depend on maintaining patent rights, pursuing extensions, or filing follow-up patents for optimized formulations and uses.

Strategic Implications for Stakeholders

1. For Innovators

  • PT2204168’s scope indicates a protective barrier around a potentially valuable compound or formulation.
  • Monitoring overlapping patents is crucial for R&D planning and licensing negotiations.

2. For Generic Manufacturers

  • Given the patent’s claims, market entry efforts may be constrained unless patent expiry or licensing is obtained.
  • Detailed analysis of claim language can reveal possible design-around strategies.

3. For Patent Attorneys and Legal Entities

  • Continuous surveillance of patent landscape and prior art is vital.
  • Consideration of patent invalidity or non-infringement strategies should be aligned with PT2204168’s scope.

Key Takeaways

  • PT2204168 likely claims a specific chemical compound or pharmaceutical formulation, with a scope designed to protect innovative therapeutic applications.
  • Claim language influences the breadth of protection; broad claims enhance exclusivity but may be challenged on grounds of prior art.
  • The patent landscape analysis underscores the importance of positioning within existing patent thickets and regulatory frameworks.
  • Strategic decisions around licensing, patent prosecution, and lifecycle management hinge on the detailed interpretation of claim scope and related patents.
  • Ongoing patent surveillance in Portugal and broader jurisdictions is essential to maintain market advantage and avoid infringement risks.

FAQs

Q1: How does PT2204168 compare to other patents in the same therapeutic class?
A1: Without specific claim language, direct comparison is limited. However, its scope likely overlaps with existing patents, emphasizing the importance of detailed claim analysis to identify differentiation or potential conflicts.

Q2: Can PT2204168’s claims be challenged or invalidated?
A2: Yes. Patent validity can be challenged on grounds of lack of novelty or inventive step, especially if prior art surfaces during examination or post-grant life.

Q3: Does Portugal’s patent law provide memoranda for extensions or supplementary protections?
A3: Yes. Portugal implements mechanisms similar to the European SPC, which may extend patent protection beyond 20 years for pharmaceutical products.

Q4: What are the filing strategies for patents related to PT2204168 in other jurisdictions?
A4: Usually, applicants file under the Patent Cooperation Treaty (PCT) or directly pursue filings in key markets, considering regional patent laws, prosecution costs, and strategic needs.

Q5: How important is patent landscape analysis for lifecycle management?
A5: Extremely important. It informs decisions on licensing, research direction, potential patent expirations, or necessary filings to maintain competitive advantage.


Sources

  1. European Patent Office. Espacenet Patent Database.
  2. WIPO. PATENTSCOPE Database.
  3. Portugal Patent Office (INPI). Patent Publications and Legal Framework.
  4. European Patent Convention (EPC) Regulations.
  5. Intellectual Property Strategy Reports, Healthcare Sector

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