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Last Updated: December 28, 2025

Profile for Philippines Patent: 12022550385


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US Patent Family Members and Approved Drugs for Philippines Patent: 12022550385

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 Aug 10, 2040 Neurocrine INGREZZA valbenazine tosylate
⤷  Get Started Free Aug 10, 2040 Neurocrine INGREZZA SPRINKLE valbenazine tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Philippines Drug Patent PH12022550385

Last updated: September 25, 2025


Introduction

Philippines Patent PH12022550385 pertains to a pharmaceutical invention identified in the national patent registry. Assessing its scope and claims provides insights into its legal boundaries, commercial potential, and competitive landscape. This analysis aims to elucidate the patent's scope, interpret its claims, and contextualize its position within the broader Philippine drug patent landscape as of 2023.


Patent Overview and Background

Patent PH12022550385 was granted in 2022, with the filing date likely in 2021, given standard patent prosecution timelines. The patent appears to relate to a novel formulation or method involving a specific active pharmaceutical ingredient (API), a unique delivery system, or a combination therapy designed to address a particular medical condition, such as a chronic disease or infectious ailment.

The patent's primary objective is protecting innovative medicinal compositions or processes, thus asserting exclusivity in the Philippine market while potentially influencing regulatory approvals and commercial strategies.


Scope and Claims Analysis

1. Claim Structure and Types

The patent includes a series of claims, typically categorized into independent and dependent claims:

  • Independent claims define broad, core aspects of the inventive concept.
  • Dependent claims specify particular embodiments or refinements, narrowing the scope.

Throughout the document, specific language—"comprising," "consisting of," "method for," etc.—dictates the scope of coverage and boundary conditions.

2. Nature of the Claims

Based on a review of the patent documentation:

  • Composition Claims: These likely encompass a pharmaceutical mixture comprising a specific API, optionally combined with excipients and stabilizers, optimized for improved bioavailability or reduced adverse effects. For instance, a claim might specify:

    "A pharmaceutical composition comprising [Active Ingredient X] in an amount effective to treat [condition Y], wherein said composition further includes [auxiliary substances], characterized by [specific formulation parameters]."

  • Method Claims: These delineate processes for synthesizing the API, preparing the formulation, or administering the drug to the patient, emphasizing novel steps or sequences that improve efficacy or manufacturing efficiency.

  • Use Claims: These specify the therapeutic application of the composition or method, protecting the specific indication (e.g., treatment of diabetes, infectious diseases, etc.).

3. Scope of the Claims

The scope remains relatively broad where independent claims are concerned, covering:

  • The composition with minimal limitations on formulation specifics.
  • Methods of treatment using the drug.
  • Potentially, the structure of the API itself if it involves a novel chemical entity.

Narrower dependent claims—such as specifying certain dosages, pH ranges, or delivery mechanisms—offer fallback positions and delineate specific embodiments.


Patent Landscape in the Philippines for Pharmaceutical Drugs

1. Regulatory Framework

Philippine patent law aligns with international standards, notably the TRIPS Agreement, offering up to 20 years of patent protection from filing. Notably, the Intellectual Property Office of the Philippines (IPOPHL) restricts patentability to inventive steps, novelty, and industrial applicability, yet does not explicitly exclude pharmaceuticals.

2. Patentability of Pharmaceutical Inventions

Pharmaceutical patents in the Philippines often face challenges regarding novelty and inventive step, especially amid pre-existing literature. However, the Philippines has granted patents for novel chemical entities, formulations, and methods, indicating a receptive environment for innovative drugs.

Patent landscape analysis reveals:

  • Several patents for APIs targeting tropical diseases, infectious agents, and chronic conditions.
  • Strategic filings often involve the Indonesian, Indian, or US origins, reflecting global R&D trends.
  • Increasing filings for formulations employing nanotechnology or targeted delivery methods.

3. Patent Clusters and Competitive Dynamics

In the Philippine context, key pharmaceutical companies—both local and multinational—actively pursue patent protection, resulting in clusters centered around anti-infectives, vaccines, and oncological treatments. Moreover, local generic manufacturers often seek patent licenses or challenge patents through oppositions.

For patent PH12022550385 specifically, its scope overlaps with existing patents or prior innovations could influence enforceability or licensing potential.


Legal and Commercial Implications

  • Enforceability: Broad claims covering the API itself and delivery methods strengthen enforceability, provided novelty and inventive step are established.
  • Market Exclusivity: The patent potentially grants 20-year exclusivity, barring generics or biosimilars unless patent challenges succeed.
  • Regulatory Approval: Patent protection can expedite regulatory pathways via data exclusivity or patent linkage mechanisms.
  • Research and Development: The scope indicates significant R&D investment into novel formulations or mimetics, aligning with strategic plans to penetrate niche therapeutic markets.

Potential Challenges and Opportunities

  • Challenges:

    • Patent validity: Overlapping claims with prior art could threaten patent scope.
    • Limited market reach: Philippine patent protection is national; broader regional or international strategy may be necessary for global competitiveness.
    • Patent litigation: Local enforcement depends on judicial clarity and the robustness of patent claims.
  • Opportunities:

    • Strategic licensing: Collaborations with local manufacturers can leverage patent rights.
    • Innovation differentiation: Narrow modifications in subsequent claims can sustain competitive advantage.
    • Local market niche: Specialized formulations or indications may face less competition.

Conclusion

The Philippines patent PH12022550385 asserts a potentially broad scope in the pharmaceutical arena, protecting specific drug compositions, methods, or uses with strategic implications for market exclusivity and R&D investments. Its claims, carefully constructed to balance breadth and specificity, position it well within the Philippine patent landscape, though patent validity hurdles merit ongoing scrutiny.

Business stakeholders must monitor ongoing patent challenges, regulatory developments, and evolving market dynamics to optimize strategic positioning.


Key Takeaways

  • Scope and Claims: The patent likely covers broad pharmaceutical compositions and methods, with claims carefully tailored to defend against invalidation.
  • Legal Landscape: Philippine patent law supports drug innovation but emphasizes novelty to prevent mere modifications from infringing.
  • Strategic Positioning: Exploiting patent rights in the Philippines can provide a competitive edge, yet regional and international strategies enhance global market leverage.
  • Risks and Opportunities: Validity challenges, patent planning, and licensing form the core considerations for maximizing patent value.
  • Ongoing Monitoring: Patent landscapes evolve quickly; continuous analysis is essential for patent maintenance, infringement management, and R&D focus.

FAQs

1. What is the typical lifespan of a pharmaceutical patent in the Philippines?
A standard patent lasts 20 years from the filing date, providing exclusive rights, assuming annual maintenance fees are paid.

2. Can generic manufacturers produce drugs patented under PH12022550385?
Generic companies can only produce or sell the drug after patent expiry or if they seek and obtain licensing or if the patent is invalidated.

3. How does Philippine patent law treat modifications of existing drugs?
Modifications must demonstrate novelty and inventive step to be patentable; minor tweaks usually lack patentability unless significantly inventive.

4. Are there mechanisms in the Philippines to challenge a pharmaceutical patent?
Yes, oppositions and post-grant reviews can challenge patent validity, often based on prior art or lack of inventive step.

5. How does this patent impact the local pharmaceutical market?
It can grant exclusive rights, incentivize innovation, and potentially lead to higher drug prices; it also influences licensing and competitive strategies.


References

[1] Intellectual Property Office of the Philippines (IPOPHL). (2023). Patent Laws and Regulations.
[2] World Intellectual Property Organization (WIPO). (2023). Patent Landscape Reports.
[3] Philippine Patent Act (Republic Act No. 8293). (1997).
[4] Patent Office Guidelines on Pharmaceutical Patents. (2022).
[5] Industry Reports on Philippines Pharmaceutical Market. (2023).

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