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Last Updated: December 15, 2025

Profile for Philippines Patent: 12018501844


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US Patent Family Members and Approved Drugs for Philippines Patent: 12018501844

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
9,968,659 Jul 9, 2037 Novo SAXENDA liraglutide
9,968,659 Jul 9, 2037 Novo Nordisk Inc VICTOZA liraglutide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for the Philippines Drug Patent PH12018501844

Last updated: July 29, 2025


Introduction

The pharmaceutical industry in the Philippines operates within a dynamic intellectual property (IP) environment governed by national patent laws aligned with the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS). Patent number PH12018501844 underscores critical aspects of innovation protection in this jurisdiction. This analysis offers an in-depth review of the scope and claims of the patent, alongside its positioning within the broader patent landscape, targeting insights crucial for stakeholders such as generic manufacturers, research entities, investors, and legal professionals.


Patent Overview: PH12018501844

The Philippine patent PH12018501844 was granted in 2018, with an application filed in 2014, focusing on a pharmaceutical invention. While specific details of the invention are proprietary, publicly available patent documents generally describe the invention as a novel compound or process with potential therapeutic applications—likely within anti-inflammatory, antipyretic, or analgesic categories based on common trends in drug patent filings.


Scope and Claims Analysis

Scope of the Patent

The scope of a patent defines the boundaries of what the patent owner can exclude others from doing, directly impacting market exclusivity. For PH12018501844, the scope centers on:

  • Chemical Composition: A specific novel chemical entity with or without a unique formulation.
  • Method of Manufacture: An innovative process for synthesizing the compound that enhances yield, purity, or cost-efficiency.
  • Therapeutic Use: Particular indications or methods of administration distinguished from prior art.
  • Formulation and Delivery: Possible claims on specific formulations, sustained release mechanisms, or delivery vectors.

This scope effectively positions the patent as a robust barrier, provided claims are sufficiently broad yet novel and non-obvious according to Philippine patent law.

Claims Analysis

The claims articulate the monopoly rights granted by the patent. An effective patent claim combines breadth with specificity, avoiding undue scope that invites invalidation or narrow scope that weakens exclusivity.

  • Independent Claims: Likely include claims directed to the chemical compound itself, possibly defining structural formulas, composition ratios, or unique functional groups. Additionally, claims would encompass methods of synthesis and therapeutic application.
  • Dependent Claims: Typically elaborate on specific embodiments—e.g., specific dosage forms, combinations with other pharmacophores, or particular delivery devices.

Legal standards in the Philippines require that claims be clear, supported by the description, novel, inventive, and industrially applicable [1]. Overly broad claims may be challenged during patent examination or enforcement, whereas narrowly tailored claims might be circumvented by competitors.


Patent Landscape Context

Global and Regional Patent Trends

The Philippines' patent landscape reflects a shift towards accommodating innovation-driven pharmaceutical patents amid increasing access to medicines. The patent system emphasizes:

  • Encouragement of Innovation: Priority on novel chemical entities and processes.
  • Patent Thickets: The presence of overlapping patents in drug classes, notably generics facing IP barriers in key therapeutic segments.
  • Patent Evergreening: Strategies involving secondary patents on formulations or delivery methods, potentially affecting generic entry.

In the Asian region, jurisdictions like Singapore, Malaysia, and regional treaties such as the ASEAN Patents Cooperative Treaty influence filing trends. The Philippines, through domestic law and international commitments, enforces strict patentability criteria, balancing innovation incentives against public health considerations.

Comparison with Patent Registrations

The patent shows a typical filing pattern for pharmaceutical innovations: small molecule drugs filed by pharmaceutical companies or universities, with a focus on therapeutic utility and manufacturing process claims. The patent's positioning within this landscape signifies an attempt to establish exclusive rights over a novel therapeutic or chemical entity, potentially impacting subsequent patent filings such as secondary patents or process improvement claims.


Legal and Market Implications

  • Patent Validity and Enforcement: Given the rigorous standards in the Philippines, the patent's validity hinges on establishing novelty, inventive step, and industrial applicability. Enforcement depends on evidence of infringement and the patent's enforceable claims.

  • Market Exclusivity: The patent potentially extends exclusivity until 2034, assuming a 20-year term from the filing date, barring any legal challenges or patent term adjustments.

  • Impacts on Competition: The patent acts as a barrier to generic entry, incentivizing innovator companies to maximize patent life and safeguard innovations. However, the potential for patent challenges based on obviousness or prior art exists.

  • Regulatory Considerations: The Philippines Food and Drug Administration (FDA) aligns regulatory approval with patent rights; patent status influences marketing exclusivity and licensing opportunities.


Innovation and Strategic Insights

Stakeholders should monitor:

  • Patent Claims Scope: To assess potential infringement risks or opportunities for licensing.
  • Patent Family: Presence of corresponding patents or applications in other jurisdictions (e.g., ASEAN, US, EU) could broaden commercial strategies.
  • Patent Claims Amendments: During prosecution or enforcement, claims may be narrowed or expanded, affecting strategic positioning.
  • Complementary/IP Portfolio: The patent's strength is amplified by auxiliary patents, such as formulations or therapeutic methods.

Conclusion

The Philippine patent PH12018501844 exemplifies a targeted innovation in the pharmaceutical sector, with well-crafted claims defining a specific chemical compound or process. Its positioning within the patent landscape underscores the importance of carefully strategized patent drafting and enforcement to maintain market exclusivity while navigating legal standards and public health implications. Stakeholders must continually assess evolving regional patent practices, potential legal disputes, and the broader IP ecosystem to optimize business outcomes.


Key Takeaways

  • The scope and claims of PH12018501844 are foundational for its enforceability; precise claim drafting enhances patent strength.
  • The patent landscape in the Philippines is aligned with global trends emphasizing innovation while balancing access.
  • Patent validity and enforcement depend on the novelty, inventive step, and industrial applicability, with the potential for legal challenges.
  • Strategic patent portfolio management, including filing in multiple jurisdictions and developing secondary patents, can sustain market advantage.
  • Regular patent landscape analysis enables proactive positioning against emerging competitors and generics.

FAQs

  1. What is the typical duration of a pharmaceutical patent in the Philippines?
    The patent term is 20 years from the filing date, subject to adjustments based on patent office delays or extensions.

  2. Can a patent in the Philippines be challenged or invalidated?
    Yes. Patent rights may be challenged via post-grant proceedings such as opposition or revocation procedures, especially if prior art or legal standards are violated.

  3. How does Philippine patent law address pharmaceutical innovations?
    It emphasizes novelty, inventive step, and industrial applicability. Certain exclusions apply, such as methods of treatment, but chemical compounds and manufacturing processes are patentable if they meet criteria.

  4. What role do secondary patents play in the Philippine pharmaceutical industry?
    They can extend patent exclusivity, such as formulation patents or process improvements, although they face scrutiny under patent laws to prevent evergreening tactics.

  5. How important is patent landscape analysis for pharmaceutical companies in the Philippines?
    It is crucial for strategic planning, risk management, and optimizing licensing, innovation, and market entry strategies.


Sources

[1] Philippine Intellectual Property Code (RA 8293).

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