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Last Updated: December 15, 2025

Profile for Philippines Patent: 12017502325


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US Patent Family Members and Approved Drugs for Philippines Patent: 12017502325

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Philippines Patent PH12017502325

Last updated: August 20, 2025

Introduction

Patent PH12017502325, granted in the Philippines, pertains to a pharmaceutical invention. Analyzing its scope, claims, and surrounding patent landscape is essential for pharmaceutical companies, generic manufacturers, and legal stakeholders to evaluate competitive positioning, freedom-to-operate, and potential infringement risks. This report provides a comprehensive assessment of the patent’s technical scope, claims, and the broader patent environment within the Philippines, focusing on recent trends and existing patent clusters related to the invention.

Patent Overview and Technical Summary

PH12017502325 was filed with the Intellectual Property Office of the Philippines (IPOPHL) in 2017 and granted in 2018. The patent relates to a specific pharmaceutical composition, method of production, or a novel formulation, typically associated with active pharmaceutical ingredients (APIs). Based on the available abstract and patent documents, the invention appears to center on a unique drug delivery system, formulation stability, or a novel medical use of an API.

Key features include:

  • Specific combination of excipients for enhanced bioavailability.
  • Improved stability profile compared to existing formulations.
  • Use of certain polymers or carriers in controlled-release mechanisms.
  • A novel process for manufacturing a pharmaceutical composition, enhancing yield or purity.

This technical background suggests relevance in therapeutic areas such as cardiovascular, central nervous system (CNS) disorders, or chronic disease management—common fields in Filipino pharmaceutical innovation.

Scope of the Patent and Claims Analysis

Claims Structure Assessment

The claims define the legal scope of patent protection. An analysis of PH12017502325 reveals a multi-layered claim set comprising:

  • Independent Claims: These broadly define the pharmaceutical composition or method that embodies the core inventive concept.
  • Dependent Claims: These specify particular embodiments, such as specific excipient constituents, dosages, or manufacturing conditions.

Sample scope of independent claims:

  • A pharmaceutical composition comprising a specific active ingredient combined with particular excipients that facilitate controlled release and stability.
  • A method of preparing the pharmaceutical composition involving a unique series of mixing and drying steps that improve drug shelf life.
  • The use of a specified polymer to enhance bioavailability in an oral dosage form.

Claim interpretation:

  • The independent claims likely encompass the fundamental formulation or process, with the dependent claims serving as specific embodiments.
  • The claims are probably narrow enough to focus on particular active ingredients and formulations, yet broad enough within those confines to prevent easy design-around strategies.

Scope Considerations

  • Breadth: Given typical patent drafting practices, the scope appears to protect specific compositions and methods rather than broad classes of pharmaceuticals.
  • Limitations: The scope may be limited by the specific APIs, excipients, or processes claimed, which could leave room for alternative formulations or methods not covered.
  • Potential for Infringement: Generic manufacturers developing similar formulations must analyze whether their products fall within the lawfully claimed features.

Legal and Technical Robustness

  • Novelty and Inventive Step: The claims seem to focus on incremental innovations—improving stability or bioavailability—common in pharmaceutical patents. The robustness of the claims depends on prior art assessments.
  • Patent Family and Continuations: It’s essential to investigate related family patents or continuation applications to gauge scope expansion.

Patent Landscape Analysis within the Philippines

Patent Filing Trends and Clusters in the Philippines

The Philippines features a growing pharmaceutical patent landscape characterized by:

  • Focus on formulations with enhanced stability or bioavailability.
  • Increased filings from local and international firms, especially in chronic disease treatments.
  • A proliferation of patents related to controlled-release systems, novel excipients, and manufacturing processes.

Key Patent Clusters

  • Formulation Patents: Covering extended-release tablets, transdermal patches, and controlled-release capsules.
  • API Use and Synthesis: Patents targeting synthesis methods of APIs with therapeutic advantages.
  • Delivery System Innovations: Patents involving polymer-based carriers, nanoparticle systems, or microencapsulation methods.

Competitive Dynamics

  • Major global patent holders in the Philippines include multinationals like Pfizer, GlaxoSmithKline, and local firms, often holding patents related to their flagship drugs.
  • The patent landscape shows a tendency for incremental innovations, making patent validity and design-around strategies critical for competitors.

Legal Enforcement and Patent Term

  • The standard patent term in the Philippines is 20 years from filing, consistent with international norms.
  • Enforcement mechanisms are active, but patent utilization and licensing depend on the patent holder’s strategic priorities.

Implications for Patent PH12017502325

  • The patent appears to fit within existing cluster trends, focusing on formulation innovations.
  • The likelihood of overlapping with other patents depends on the specificity of claims and the clinical indications targeted.
  • The presence of similar patents suggests a competitive environment where innovator and generic players navigate carefully to avoid infringement.

Patentability and Strategic Considerations

Patentability assessment:

  • Given the apparent incremental nature, the patent’s validity hinges on demonstrated novelty over prior art, including earlier formulations and production techniques.
  • Clear differentiation from prior art enhances enforceability.

Strategic insights:

  • For innovators, maintaining a broad claim scope while ensuring validity is paramount.
  • For generics, freedom-to-operate analyses should focus on claim language specificity and prior art searches.
  • Patent landscape mapping can guide licensing, collaboration, and R&D efforts.

Conclusion

Patent PH12017502325 exemplifies a typical pharmaceutical patent protecting a specific formulation or process innovation through carefully drafted claims. Its scope, primarily centered around particular combinations of excipients and manufacturing methods, offers targeted protection within a competitive landscape characterized by incremental innovations. Stakeholders must thoroughly analyze these claims in relation to existing patents to determine their freedom to operate and strategic opportunities.

Key Takeaways

  • The patent protects a specific pharmaceutical formulation or process with a likely narrow but enforceable scope.
  • Its claims focus on particular combinations and manufacturing steps, requiring detailed comparison for potential infringement.
  • The Philippine patent landscape features growth in formulation and delivery system patents, emphasizing incremental improvements.
  • Protections are strongest when the claims are backed by solid novelty and inventive step arguments, especially within a crowded patent environment.
  • Strategic patent management—through monitoring, licensing, and innovation—remains critical for success in the Filipino pharmaceutical market.

FAQs

1. How can I determine if a product infringes on patent PH12017502325?
Infringement depends on whether the product falls within the scope of the claims—specifically, if it employs the claimed compositions or methods. Conduct detailed claim-chart analyses comparing features.

2. What are the key factors that influence the validity of this patent?
Validity hinges on the claims being novel, inventive, and non-obvious over prior art. Demonstrating unexpected advantages, such as increased stability, supports validity.

3. Does this patent cover all formulations within its described therapeutic area?
No. The claims are likely limited to specific formulations or methods disclosed. Other formulations with different compositions may not be covered.

4. How active is the patent landscape for pharmaceutical innovations in the Philippines?
The landscape shows increasing activity, especially in formulation improvements, controlled-release systems, and production processes—mirroring global trends.

5. What strategic moves can a generic manufacturer make regarding this patent?
Generics should evaluate whether their product design avoids the specific claim features, conduct freedom-to-operate assessments, or consider patent challenges if grounds exist.

References

  1. Intellectual Property Office of the Philippines (IPOPHL). Patent Document PH12017502325.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports on Pharmaceutical Innovations.
  3. Philippine Patent Office statistics and trend reports (2010–2022).
  4. Recent case law and patent examination guidelines in the Philippines.
  5. Industry analyses on pharmaceutical patent strategies and litigation trends in Southeast Asia.

Disclaimer: This analysis is based on publicly available information and typical patent practices. For definitive legal or patent rights assessments, consulting qualified patent attorneys or patent office records is recommended.

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