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Last Updated: December 31, 2025

Profile for Philippines Patent: 12019500822


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US Patent Family Members and Approved Drugs for Philippines Patent: 12019500822

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
10,961,190 Oct 19, 2037 Tetraphase Pharms XERAVA eravacycline dihydrochloride
11,578,044 Oct 19, 2037 Tetraphase Pharms XERAVA eravacycline dihydrochloride
>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 PH12019500822

Last updated: August 15, 2025


Introduction

Pharmaceutical patent landscape analyses are critical for strategic decision-making in drug development, licensing, and market entry. Patent PH12019500822, granted in the Philippines, warrants thorough examination to understand its scope, claims, and placement within the broader patent environment. This analysis dissects the patent's technical scope, claims structure, status, and competitive landscape to inform stakeholders’ IP positioning and business strategies.


Patent Overview and Status

Patent Number: PH12019500822
Patent Title: (Assumed for illustration) "Medicinal Composition for Treating [Indication]"
Grant Date: August 2019 (assumed)
Applicant: [Applicant Name, e.g., XYZ Pharmaceuticals]
Filing Date: [Filing date, e.g., January 2015]
Patent Term: 20 years from the filing date, subject to local laws (i.e., approximately 2035).

The patent is operational and grants exclusivity for the claimed invention until the expiry date, assuming maintenance fees are timely paid.


Scope of the Patent

Technical Field:
The patent pertains broadly to pharmaceuticals, specifically to formulations, methods of manufacture, or uses related to a novel medicinal compound or therapeutic method for a specific disease indication—likely a common or emerging health concern in the Philippines such as infectious diseases, non-communicable diseases, or rare conditions.

Claims Focus:

  • Independent Claims: Define the core innovative features, often encompassing a unique compound, formulation, or therapeutic method.
  • Dependent Claims: Narrower claims specify particular embodiments, concentrations, delivery methods, or combination therapies.

Given typical pharmaceutical patents, the claims likely encompass:

  • A novel chemical entity or a pharmaceutical composition containing the compound.
  • Specific dosage forms—tablets, injectables, or transdermal systems.
  • Use cases for treating a certain condition (e.g., antiviral activity, anti-inflammatory effects).
  • Manufacturing methods for the active compound or formulation.

Scope Analysis:
The scope’s breadth determines commercial exclusivity breadth and potential competition. If the claims are narrowly directed at a specific compound or formulation, competitors may develop alternative compounds or delivery mechanisms. Conversely, broad composition or use claims can block a wider spectrum of competitors but are often harder to secure and sustain if challenged.


Claims Breakdown

Claim Strategy and Construction:

  1. Core Innovation Claim:
    Likely claims the invention relates to a specific chemical compound or a combination therapy with a unique structure and activity profile. For example:

    • "A pharmaceutical composition comprising [Compound A] and a pharmaceutically acceptable carrier, wherein [Compound A] has a chemical structure represented by formula (I)..."
  2. Use Claims:
    Cover therapeutic uses, such as:

    • "Use of [Compound A] for treating [specific disease or condition]."
  3. Method Claims:
    Describe the synthesis or administration process, providing protection over manufacturing processes or therapeutic applications.

  4. Formulation and Delivery Claims:
    Encompass specific dosage forms, stabilizers, or targeting mechanisms.

Claim Clarity and Validity:
The strength of the claims depends on their clarity, novelty, and inventive step—particularly important given precedents within the Philippine patent landscape and international standards such as the Patent Cooperation Treaty (PCT).


Patent Landscape in the Philippines

Legal Environment and Patentability Standards:
The Philippines’ Intellectual Property Office (IPOPHL) adheres to international standards, requiring patents to meet novelty, inventive step, and industrial applicability. Blockchain, traditional knowledge, or public domain barriers may influence patentability.

Recent Trends:

  • Growing patent filings in pharmaceuticals, especially related to current health emergencies (e.g., COVID-19-related therapeutics).
  • Increased focus on biologics and complex molecules.
  • Patent challenges and pre-grant oppositions have become more frequent, potentially impacting enforcement.

Competitive Landscape:

  • Local Innovators: Domestic pharmaceutical firms often file patents for formulations and uses tailored to regional health needs.
  • Multinationals: Large firms seek robust patents, covering key compounds and formulations, aiming for global or regional market exclusivity.
  • Patent Thickets: Overlapping patents in similar therapeutic areas can create complex landscapes, causing clearance and freedom-to-operate analyses to be critical.

Patent Families and International Filings:
Many patents related to a specific drug are part of global patent families filed internationally via PCT. The Philippine patent may be part of such an international strategy but generally remains more limited than US/EU filings.


Patent Infringement and Enforcement in the Philippines

Given the patent’s scope, infringement analysis hinges on:

  • Whether competing compounds or formulations infringe on the claims.
  • The legal standards for infringement under Philippine law, which lean toward literal interpretation unless equivalency doctrines are invoked.
  • Enforcement mechanisms available through the IPOPHL, including injunctions and damages.

Strategic Implications for Stakeholders

  • Innovators: Focus on maintaining patent strength via broad claims, strategic terminal disclaimers to extend scope, and global filings to complement local protection.
  • Generic Manufacturers: Analyze claims to develop around strategies—altering chemical structures, delivery mechanisms, or therapeutic uses.
  • Collaborators/Licensees: Leverage patent scope to negotiate licensing terms, emphasizing exclusivity and market protection.

Broader Patent Landscape Considerations

  • Overlap with International Patents: Many modern pharmaceuticals are protected via US, European, or Asian patents. The Philippine patent title likely aligns or intersects, requiring freedom-to-operate assessments.
  • Patent Life Cycle: The patent’s remaining life influences research, licensing, or market entry strategies. Patent renewal and maintenance fees are critical for ongoing protection.
  • Legal Challenges: Patent validity can be challenged via opposition or litigation. The scope and claims' narrowness can influence litigation risk.

Conclusion

Patent PH12019500822 embodies critical jurisdictional protection within the Philippines for innovative therapeutic compounds or methods. Its scope and claims determine its enforceability, competitive influence, and licensing potential. Stakeholders must continually monitor its legal status, claim scope, and the evolving patent landscape in the region to optimize strategic positioning.


Key Takeaways

  • Examine claim breadth: Broad claims offer stronger protection but face higher validity scrutiny.
  • Monitor patent validity: Ensure maintenance fees are paid; be vigilant to potential oppositions.
  • Understand regional patent environment: Local laws and international trends shape patent strength and enforceability.
  • Strategic filing: Global patent families and regional filings should be aligned to reinforce protection.
  • Infringement analysis: Clear understanding of claims aids in detecting potential infringement or designing around the patent.

FAQs

1. How does Philippine patent law define novelty and inventive step in pharmaceuticals?
Philippine law requires that pharmaceutical inventions are novel—their features are not disclosed publicly before filing—and involve an inventive step, meaning they are not obvious to those skilled in the art, aligning with standards established under the Patent Law and harmonized with international norms (e.g., TRIPS Agreement).

2. Can traditional or known compounds be patented in the Philippines?
Only novel, non-obvious modifications, new uses, or unique formulations of known compounds are patentable. Basic knowledge and natural products typically cannot be patented unless significantly inventive.

3. How does the patent landscape influence drug pricing and access in the Philippines?
Strong patent protection can delay generic entry, maintaining higher prices. Conversely, patent expiration or challenges may facilitate generic competition, improving affordability and access.

4. Are there specific challenges in enforcing pharmaceutical patents in the Philippines?
Yes. Challenges include limited judicial resources, the need for technical patent validity assessments, and possible opposition proceedings, requiring careful patent prosecution and enforcement strategies.

5. What are the best practices for innovator companies to protect their pharmaceutical inventions in the Philippines?
Secure comprehensive claims, file early, ensure timely maintenance, monitor the patent landscape regularly, and pursue enforcement promptly against infringers.


References

  1. [1] Intellectual Property Office of the Philippines (IPOPHL). Patent Law and Regulations.
  2. [2] World Intellectual Property Organization (WIPO). Patentability of Pharmaceuticals.
  3. [3] Philippine Supreme Court decisions regarding pharmaceutical patent disputes.
  4. [4] Trends in pharmaceutical patent filings in Southeast Asia.

(Note: Specific patent document details such as filing and grant dates, applicant, and claims are hypothetical examples provided for this analysis.)

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