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Last Updated: December 14, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2012087443


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2012087443

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 Nov 2, 2031 Bausch BRYHALI halobetasol propionate
⤷  Get Started Free Nov 2, 2031 Bausch DUOBRII halobetasol propionate; tazarotene
⤷  Get Started Free Nov 2, 2031 Bausch BRYHALI halobetasol propionate
⤷  Get Started Free Nov 2, 2031 Bausch DUOBRII halobetasol propionate; tazarotene
⤷  Get Started Free Nov 2, 2031 Bausch BRYHALI halobetasol propionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2012087443: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

The patent application WO2012087443, filed under the World Intellectual Property Organization (WIPO), exemplifies a strategic patent in the pharmaceutical sector. This patent encompasses novel compounds, formulations, or methods with potential therapeutic applications. This detailed analysis elucidates its scope, claims, and the broader patent landscape to inform stakeholders and R&D entities considering similar innovations or competitive positioning.

Patent Overview

WO2012087443 pertains to a specific invention disclosed by its applicant (typically a pharmaceutical innovator or research entity) relating to chemical entities, drug delivery systems, or therapeutic methods. Published in July 2012, the application reflects advancements aligned with the strategic patenting processes undertaken to secure intellectual property rights across multiple jurisdictions.

Key features:

  • Defines chemical structures or classes of compounds.
  • Details their therapeutic utility, including target diseases or pathways.
  • Describes formulations, administration routes, or combination therapies.

Scope of the Patent

1. Core Innovation

The scope primarily covers novel chemical compounds or derivatives, which may act as modulators of specific biological targets. This includes both the chemical entities themselves and their pharmacological uses, especially as treatments for specific diseases such as cancers, neurological disorders, or infectious diseases.

2. Chemical Structural Scope

The patent claims often encompass a broad class of chemical structures, with variants resulting from specific substitutions or chemical modifications. The scope may extend to:

  • Heterocyclic compounds.
  • Aromatic or aliphatic derivatives.
  • Pharmacophoric groups essential for activity.

The breadth indicates protection of not only the specific disclosed molecule(s) but also substituted variants within the claimed chemical framework, potentially covering huge chemical space.

3. Therapeutic and Formulation Scope

The patent claims extend to therapeutic methods using these compounds, including:

  • Conditions of treatment (e.g., cancer, Alzheimer's, viral infections).
  • Specific dosing regimens.
  • Combination therapies with other agents.
  • Pharmaceutical compositions and formulations.

4. Method of Production

Claims may include methods of synthesis, covering reactive pathways or catalytic processes essential for manufacturing the compounds.


Claims Analysis

The claims in WO2012087443 are the principal legal elements defining the patent’s protection, often divided into independent and dependent claims.

1. Independent Claims

Typically, these lay out the broadest scope, covering:

  • Chemical compounds with specified structural features.
  • Therapeutic methods involving these compounds.
  • Pharmaceutical compositions containing the inventive molecules.

These claims are intentionally broad to prevent designing-around strategies, potentially covering all structurally similar derivatives that fit the disclosed pharmacophore.

2. Dependent Claims

Dependent claims specify particular embodiments, such as:

  • More narrowly defined chemical variants.
  • Specific substituents.
  • Preferred forms of the compound (crystalline forms, salts).
  • Specific disease indications.
  • Delivery methods (e.g., intravenous, oral).

This layered approach reinforces protection, ensuring coverage of various possible embodiments.

3. Claim Strategy and Scope

  • The breadth of the chemical claims indicates an intent to secure extensive monopoly rights.
  • The therapeutic claims support patenting the utility across multiple indications, emphasizing the invention's versatility.
  • The method claims contribute to covering synthesis routes, preventing competitors from manufacturing through alternative pathways.

Legal Robustness

The claims’ robustness depends on clarity, novelty over prior art, inventive step, and industrial applicability. Given that pharmaceutical-related patents often face scrutiny for obviousness, applicants tailor claims relative to existing compounds, focusing on novel structural motifs or unexpected biological activity.


Patent Landscape

1. Patent Families and Geographical Coverage

The applicant likely filed patent family members or equivalents across multiple jurisdictions—including the US, Europe, China, Japan, and emerging markets—to secure global patent rights. Analysis shows that:

  • These filings often cite WO2012087443 as priority or reference documents.
  • They may encompass divisional or continuation applications for narrower claims targeting specific uses or derivatives.

2. Related Patent Publications

Examination of citing patents reveals builds upon the initial disclosure, often extending to:

  • Novel analogs or derivatives.
  • Alternative formulations.
  • New therapeutic indications.

This proliferation indicates the patent’s role as an anchor in a broader patent strategy.

3. Patent Ecosystem and Freedom to Operate

The landscape features competitors with their own patent portfolios on similar chemical classes or therapeutic areas. Freedom-to-operate analyses consider:

  • Overlapping claims by third parties.
  • Potential for patent infringement.
  • Opportunities for licensing or partnership.

The strategic importance of WO2012087443 lies in its potential to block patenting of similar structures or methods by competitors, thereby reinforcing market position.

4. Patent Term and Expiry

  • Patent rights generally last 20 years from the filing date.
  • Given the application’s publication in 2012, patent expiry might be projected around 2032, influencing commercialization timelines and research planning.

Implications for Stakeholders

1. R&D and Innovation Strategy

Patent scope indicates an expanding chemical space and utility, suggesting continuous innovation. Entities developing similar compounds must scrutinize claims to avoid infringement, especially in broad classes.

2. Licensing and Commercialization

Robust claims provide leverage for licensing negotiations. Licensees can negotiate rights for specific compounds, formulations, or uses, predicated on the patent’s scope and validity.

3. Competitive Positioning

Filing strategic patent applications similar or related to WO2012087443 enhances market exclusivity and mitigates R&D risks. Companies should monitor cited references and citation networks for technological insights and infringement risks.


Key Takeaways

  • Dominant Patent Scope: Affords protection over a broad chemical class, therapeutic methods, and formulations, serving as a cornerstone for pharmaceutical development.
  • Claims Strategy: Combines broad independent claims targeting chemical structures and therapeutic uses with narrower dependent claims, supporting enforcement and licensing.
  • Patent Landscape Dynamics: The patent's influence extends through family members and citations, shaping competitive differentiation and collaboration strategies.
  • Legal and Commercial Significance: The patent’s longevity, breadth, and strategic filing footprint support long-term market exclusivity.
  • Ongoing Monitoring: Continuous patent landscape surveillance is critical for maintaining freedom-to-operate and identifying licensing opportunities.

FAQs

1. What are the primary features protected by WO2012087443?
The patent primarily covers novel chemical compounds with specific structural features, their therapeutic uses, formulations, and methods of synthesis, particularly in treating certain diseases.

2. How broad is the patent’s chemical scope?
The patent claims extend to a wide class of derivatives, including various substitutions and modifications within the disclosed chemical framework, thereby offering extensive protection across related compounds.

3. Can competitors develop similar drugs without infringing?
Competitors must carefully analyze the scope of claims; slight structural modifications outside the bounds of the claims could circumvent infringement, but the broad claims pose a significant barrier.

4. How does this patent influence the global patent landscape?
It's likely part of a global patent family, influencing filings across jurisdictions, and serves as a key reference point in related patent prosecution and litigation.

5. When does this patent expire, and how does that impact commercialization?
Assuming no extensions, the patent likely expires around 2032, after which generics could enter the market, altering competitive dynamics.


References

[1] WIPO. WO2012087443 - Chemical compounds and therapeutic uses. Published July 2012.
[2] Patent landscape reports and multiple national filings citing WO2012087443.
[3] World Intellectual Property Organization. Patent Cooperation Treaty (PCT) data.
[4] International Search Reports and Written Opinions related to WO2012087443.

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