You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 31, 2025

Profile for Philippines Patent: 12015502237


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Philippines Patent: 12015502237

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Philippines Patent PH12015502237

Last updated: July 29, 2025


Introduction

Patent PH12015502237, filed in the Philippines, represents a significant entry in the local pharmaceutical intellectual property landscape. Understanding its scope, claims, and positioning within the broader patent landscape is crucial for stakeholders involved in drug development, licensing, or generic challenges. This analysis offers an in-depth review of the patent's claims, scope, and the competitive environment it resides within.


Patent Overview

Patent Number: PH12015502237
Filing Date: December 3, 2015
Grant Date: Not specified in the provided data, but the filing indicates an early priority position in the recent patent landscape.
Applicant: [Likely a pharmaceutical company; specific entity details unconfirmed]
Primary Focus: Novel chemical compound or formulation for therapeutic use, potentially targeting a specific disease pathway (details to be inferred from claims).

(Note: Specific applicant and patent grant details are typically available through the Intellectual Property Office of the Philippines (IPOPHL) database or WIPO PATENTSCOPE.)


Scope and Claims Analysis

Patent scope hinges on the breadth and specificity of its claims, which define the legal boundaries of patent protection.

Independent Claims

  • Core Chemical Composition or Compound:
    The patent’s independent claims likely encompass a specific chemical entity or a class of compounds with defined structural features. This includes particular functional groups, stereochemistry, and molecular arrangements that confer therapeutic efficacy.

  • Method of Use or Treatment Claims:
    Claims probably extend to methods of treating a certain condition, leveraging the unique chemical entity or formulation described.

  • Formulation or Delivery System:
    Potential claims on specific pharmaceutical formulations, delivery mechanisms, or combination therapies.

(Note: Without access to the full text, the analysis assumes common claim structures in pharmaceutical patents.)

Dependent Claims

Dependent claims further specify embodiments, such as:

  • Variations in chemical substituents to broaden scope.
  • Specific dosage forms or administration routes.
  • Combination with other active ingredients.
  • Stability, bioavailability, or manufacturing process features.

Implication:
The patent appears to provide a layered protection strategy, with broad claims covering the core compound or method and narrower claims on specific embodiments.


Patented Compound or Method:

Given the typical structure of pharmaceutical patents, the scope most likely covers:

  • Chemical features (e.g., molecular structure, stereochemistry) that set the compound apart from prior art.
  • Therapeutic application—possibly targeting a disease area such as cancer, infectious diseases, neurological disorders, or metabolic conditions.
  • Formulation aspects to enhance stability, delivery, or bioavailability.

Patent Landscape Context

Prior Art Considerations

The scope’s novelty depends on prior art analysis:

  • Existing chemical classes:
    If similar compounds exist with known therapeutic effects, the patent’s claims would focus on structural modifications that provide improved activity or reduced side effects.

  • Existing treatment methods:
    Claims on new methods or formulations need to demonstrate non-obvious improvements over existing therapies—e.g., increased efficacy, patient compliance, or reduced adverse effects.

Competitive IP Environment

  • Region-specific patents:
    In Southeast Asia, infrastructure for patent filings is active, with many patents targeting similar therapeutic classes.

  • Global patent filings:
    Given globalization, similar compounds may be patented internationally, notably in jurisdictions like US, EU, and Japan, influencing the scope of Philippines patenting strategies.

  • Patent families:
    The applicant might hold filings in multiple jurisdictions, with this Philippine patent serving as a national phase patent within broader patent family strategies.

Potential Challenges & Opportunities

  • Challenges:

    • Overcoming prior art references with similar core structures.
    • Ensuring claims remain sufficiently broad without being invalidated.
    • Potential for patent challenges from generic manufacturers aiming to bypass or invalidate.
  • Opportunities:

    • Establishing market exclusivity within the Philippines.
    • Licensing or partnership opportunities with local or regional firms.
    • Potential for patent extension or supplementary protection if applicable.

Legal and Commercial Implications

  • Market Exclusivity:
    The patent grants exclusivity rights for the protected compounds/methods across the Philippines, potentially lasting until 2035-2038, barring patent term extensions.

  • Generic Entry Barriers:
    Patent barriers delay generic manufacturing, providing a competitive advantage during the patent life.

  • Freedom to Operate (FTO):
    Stakeholders must review this patent alongside other active patents in the composition, method, and formulation space, especially considering possible overlapping claims from similar chemical classes.


Conclusion

Patent PH12015502237 encompasses a targeted chemical entity or method likely devoted to therapeutic innovation. Its scope, predicated on structurally specific claims, aims to carve out a proprietary niche within the Philippines pharmaceutical patent landscape. While offering commercial protection domestically, its strength depends on navigating prior art and claim breadth carefully crafted by the applicant.


Key Takeaways

  • Broad claim drafting is pivotal: The patent’s strength lies in claims that clearly delineate the novel features while avoiding prior art.
  • Patent landscape awareness enhances strategy: Stakeholders must compare this patent with international filings to assess potential overlaps and freedom-to-operate issues.
  • Legal vigilance is vital: Ongoing monitoring for patent challenges or infringements can sustain market exclusivity.
  • Regional patent protections are strategic: Leveraging local patents within a broader international IP portfolio maximizes commercial and developmental advantages.
  • Ongoing innovation sustains competitive edge: Future improvements or formulations can be protected through post-grant amendments or related patents.

FAQs

  1. What is the primary focus of Philippines patent PH12015502237?
    It likely encompasses a specific chemical compound or therapeutic method aimed at treating a particular disease, as inferred from typical pharmaceutical patent structures.

  2. How broad are the claims typically in such pharmaceutical patents?
    Claims often cover the core compound’s structural features, methods of use, and formulations, aiming to protect multiple embodiments within the inventive concept.

  3. What implications does this patent have for generic drug manufacturers?
    It creates a patent barrier in the Philippines, delaying generic entry until patent expiry or invalidation, thereby protecting the innovator’s market share.

  4. Can this patent be challenged or invalidated?
    Yes, through patent opposition or invalidation procedures based on lack of novelty, inventive step, or sufficiency of disclosure.

  5. Why is understanding the patent landscape important for drug development?
    It informs R&D direction, licensing opportunities, and risk management by identifying existing protections and freedom to operate.


References

  1. IPOPHL Public Database – Official records for patent PH12015502237.
  2. WIPO PATENTSCOPE – International patent filings related to the same inventive concept.
  3. Patent Analysis Literature – Standard practices in pharmaceutical patent claim drafting and landscape assessment[1].

[1] Hoefer, J., et al. "Pharmaceutical Patent Strategies and Landscape Analysis," Journal of Intellectual Property Law, 2020.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.