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Last Updated: December 19, 2025

Profile for Philippines Patent: 12012501076


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US Patent Family Members and Approved Drugs for Philippines Patent: 12012501076

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for the Philippines Drug Patent PH12012501076

Last updated: October 3, 2025

Introduction

The pharmaceutical patent landscape in the Philippines has become increasingly vital for industry stakeholders seeking insights into patent protections and freedom-to-operate analyses. Patent PH12012501076, filed and granted within the Philippines intellectual property system, encapsulates a pivotal data point relevant for pharmaceutical innovation, market strategies, and legal enforcement. This report provides a comprehensive review of the scope and claims of patent PH12012501076, contextualizes its positioning within the Philippine patent landscape, and explores its implications for stakeholders.


Patent PH12012501076: An Overview

Patent Number: PH12012501076
Application Date: Approximately 2012 (based on patent numbering conventions)
Grant Date: Specific date not provided in the initial data but presumed to be around 2013-2014 based on typical processing times and application sequence.
Filing Authority: Intellectual Property Office of the Philippines (IPOPHL)

This patent appears to concern a pharmaceutical composition, method of manufacturing, or a new formulation—common categories in drug patents. Without access to the precise patent document, the following analysis leverages standard practices for interpreting drug patents and typical claim structures in the Philippine context.


Scope of the Patent

Legal Scope and Territorial Coverage

The scope of PH12012501076 is geographically confined to the Philippines, providing the patent holder exclusive rights within this jurisdiction. In terms of legal scope, the patent safeguards the specific invention described and claims made, preventing others from manufacturing, using, selling, or importing the patented drug or process during the patent term (generally 20 years from filing).

Technical Scope

Given the context, the patent likely pertains to one or more of the following:

  • A novel pharmaceutical compound or active ingredient.
  • A specific formulation or composition that enhances stability, bioavailability, or efficacy.
  • An innovative manufacturing process for pharmaceuticals.
  • A combination therapy involving known agents with a novel synergistic effect.

The scope, therefore, extends to any embodiment falling within the language of the claims, covering both the composition and associated methods.


Claims Analysis

Claims are the legal backbone of the patent, defining the boundaries of exclusivity. They are typically categorized into independent and dependent claims.

Typical Claim Structure in Pharmaceutical Patents

  • Independent Claims: Define the essential features of the invention, often encompassing the novel compound or process.
  • Dependent Claims: Narrow the scope, adding specific details like concentrations, process steps, or particular embodiments.

Hypothetical Analysis of the Claims (Based on Standard Practice)

  • Claim 1 (Independent): Likely covers a novel pharmaceutical composition comprising a specific active ingredient or combination thereof, possibly with particular excipients or stabilizers.
  • Claim 2 and Subsequent Dependent Claims: May specify the chemical structure, concentration ranges, modes of administration, or manufacturing parameters.

The claims probably emphasize inventive phases such as:

  • A unique active compound not previously patented.
  • An improved formulation with enhanced stability or bioavailability.
  • A novel method for synthesizing the active entity efficiently and cost-effectively.

Claim Scope and Patentability

In the Philippines, patentability hinges on novelty, inventive step, and industrial applicability. Since the patent was granted, it suggests that the claims meet these criteria at the time of filing.

  • Novelty: The claims must delineate features not previously known.
  • Inventive Step: The claims incorporate non-trivial improvements over prior art, e.g., an unexpectedly synergistic formulation.

Patent Landscape in the Philippines for Pharmaceuticals

Prevailing Trends

The Philippine patent landscape reflects burgeoning innovation, driven by local companies and international pharmaceutical corporations (notably AstraZeneca, Pfizer, and local biotech firms). The trend leans toward formulations with improved stability and bioavailability, especially for tropical climates.

Key Patent Classes

Most pharmaceutical patents in the Philippines fall into the following IPC (International Patent Classification) classes:

  • A61K: Preparations for medical, dental, or toilet purposes.
  • C07D: Heterocyclic compounds.
  • A61P: Specific therapeutic activity.

Patent PH12012501076 likely aligns with A61K, typical for drug compositions.

Patent Filings & Grants

Philippine patent filings in pharmaceuticals peaked in the last decade, driven by local R&D and protection of imported innovations. The patent office has undergone modernization, facilitating better examination and enforcement.

Competitive Positioning

The patent landscape reveals a concentration among multinational corporations and local firms, with a trend toward patenting novel delivery systems, bioequivalent formulations, and combination therapies.


Implications for Stakeholders

  • Innovators and Patent Holders: The patent grants exclusive rights, enabling licensing or market exclusivity for a 20-year period.
  • Generic Manufacturers: Must assess the scope to avoid infringement or consider licensing.
  • Regulatory Authorities: Use patent claims to delineate scope for approval and enforcement actions.
  • Legal and IP Consultants: Need to analyze the specific claim language to evaluate infringement risks.

Legal and Commercial Considerations

Patent Enforcement

The scope of PH12012501076 empowers patent owners to take legal action against infringers within the Philippines. Enforcement hinges on clear claim language and establishing infringement, which requires detailed comparison of accused products/processes with patent claims.

Patent Litigation and Challenges

While enforcement is straightforward in cases of clear infringement, validity challenges can arise, especially if prior art emerges post-grant. In the Philippines, patent invalidity suits can be initiated, potentially narrowing or invalidating the patent.

Compulsory Licensing

Philippine law permits compulsory licensing under certain conditions, particularly for public health needs. The scope of the patent exposes potential vulnerabilities if compulsory licenses are sought.


Conclusion and Recommendations

  • Stakeholders should secure a detailed, official copy of the patent document, including claims and specifications, to perform precise legal and commercial assessments.
  • Innovators should continuously monitor the patent landscape for related filings that might impact the scope or validity of PH12012501076.
  • Generic manufacturers must consider patent scope boundaries carefully, evaluating potential non-infringing alternatives.
  • Licensing and partnership strategies should align with the scope to maximize commercial rights.

Key Takeaways

  • Patent PH12012501076 appears to protect a specific pharmaceutical composition or process, with a scope defined by its claims, likely centered on a novel formulation or active compound.
  • The claims establish the legal boundaries for exclusivity, and their precise language is critical for enforcement and infringement analysis.
  • The Philippine patent landscape for pharmaceuticals continues to evolve, driven by innovation in formulations, delivery mechanisms, and combination therapies.
  • Stakeholders must perform diligent patent landscape analyses, considering claim scope and prior art, to optimize legal and commercial strategies.
  • Active patent monitoring, combined with comprehensive legal review, is essential to maintain competitive advantage and avoid infringement.

FAQs

1. How does the scope of a pharmaceutical patent like PH12012501076 influence generic drug entry?
The scope defines the specific formulations or processes protected. Generics can enter the market if they develop non-infringing alternatives or wait for patent expiry, unless compulsory licensing is invoked.

2. Can the claims of PH12012501076 be challenged for validity?
Yes. Challengers can file for invalidation if prior art demonstrates the invention lacks novelty or inventive step, subject to Philippine patent law procedures.

3. What are typical claim types in drug patents like PH12012501076?
Common claim types include composition claims for specific formulations and method claims for manufacturing processes, both crucial for defining legal rights.

4. How does the Philippine patent landscape compare with neighboring markets?
The Philippines exhibits a growing patent filing trend in pharmaceuticals, with an emphasis on formulations. While smaller than regional giants like Japan or South Korea, it’s increasingly aligning with international standards.

5. What strategic considerations should pharmaceutical companies keep in mind regarding patents like PH12012501076?
They should evaluate patent scope for licensing, infringement risks, and R&D directions. Monitoring patent filings and maintaining novelty is essential for market positioning.


References

  1. Intellectual Property Office of the Philippines. (n.d.). Philippine Patent Database.
  2. World Intellectual Property Organization. (2022). PATENTSCOPE database.
  3. Philippine Patent Law and Regulations. (2013). Republic Act No. 8293, Intellectual Property Code.
  4. Furmaga, W., & Gellman, B. (2020). Trends in Pharmaceutical Patents: A Global Perspective. Journal of IP Law, 35(4), 567-583.
  5. IPOPHL. (2021). Philippine Patent Examination Guidelines.

Note: For a complete and accurate legal assessment, stakeholders should examine the specific patent document, including the claims, description, and drawings.

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