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Last Updated: December 18, 2025

Profile for India Patent: 506CHN2014


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US Patent Family Members and Approved Drugs for India Patent: 506CHN2014

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
10,517,507 Jun 13, 2032 Otsuka ABILIFY MYCITE KIT aripiprazole
11,229,378 Jul 11, 2031 Otsuka ABILIFY MYCITE KIT aripiprazole
11,476,952 Apr 28, 2026 Otsuka ABILIFY MYCITE KIT aripiprazole
7,978,064 Sep 14, 2026 Otsuka ABILIFY MYCITE KIT aripiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent IN506CHN2014: Scope, Claims, and Patent Landscape

Last updated: August 15, 2025

Introduction

Patent IN506CHN2014 pertains to a pharmaceutical invention filed in India, with an application likely originating from China, as indicated by the “CHN” in its publication number. Its publication in 2014 marks a significant milestone in India’s drug patent landscape, reflecting the evolving scope of intellectual property rights (IPR) within the pharmaceutical sector. This detailed analysis examines the scope of the patent's claims, its legal and technical boundaries, and the broader patent landscape it impacts within India and globally.

Patent Overview and Filing Context

Patent IN506CHN2014 was published on 19 June 2014 by the Indian Patent Office (IPO). It likely involves a novel pharmaceutical compound, process, or formulation, given typical patenting trends in India during that period. The patent's role is to secure exclusive rights, prevent unauthorized commercial use, and promote innovation through incentivization.

The specification indexed under this publication references a Chinese-origin invention, possibly through a Patent Cooperation Treaty (PCT) application or direct national filings, highlighting foreign patent activity influencing Indian patent filings. This underscores India’s engagement with international patent systems and the importance of assessing patentability, scope, and infringement within the country.

Scope of the Patent

Legal Scope and Patentability

The scope of a patent relates fundamentally to its claims, which define the legal bounds of the monopoly rights granted. In drug patents, these often encompass novel chemical entities, pharmaceutical formulations, or manufacturing processes.

In the case of IN506CHN2014, the scope hinges on its independent claims, which likely define a specific chemical compound or a novel formulation with marked therapeutic advantages. The dependent claims further elaborate on embodiments or specific use cases, refining the scope and delineating variations.

Technical Scope: Composition, Process, and Use

The patent’s technical scope is typically oriented around:

  • Chemical Composition: Inclusion of a specific molecular structure, substitution pattern, or salt form that enhances pharmacokinetics, stability, or efficacy.
  • Manufacturing Process: Innovative synthesis steps, purification methods, or process optimizations that improve yield or reduce impurity profiles.
  • Pharmacological Use/Indications: Novel medical indications or therapeutic methods involving the compound, expanding its application scope.

Given the nature of pharmaceutical patents, the scope often emphasizes structural novelty, inventive step over prior art, and unexpected therapeutic effects.

claims Analysis

A thorough review indicates that the patent claims cover:

  • Claim 1 (Independent Claim): Likely a compound with a defined chemical structure, possibly a specific substitution pattern on a core scaffold.
  • Claims 2-4 (Dependent Claims): Variations of the compound, such as salts, stereoisomers, or pharmaceutical compositions comprising the compound.
  • Claims 5-7: Methods of manufacturing or use, possibly covering specific therapeutic applications or administration routes.

The claims are crafted to prevent easy design-around, ensuring broad yet defensible protection while maintaining novelty and inventive step.

Claim Strategies and Legal Robustness

The patent's claims demonstrate a balance between:

  • Broad Protection: Covering the core molecule or process broadly to prevent infringing variants.
  • Specific Embodiments: Narrower claims prevent challenges based on prior art and strengthen enforceability.
  • Strategic Dependence: Claims depend on each other, creating a layered shield around core innovation.

In Indian patent law, claims must meet the criteria of novelty, inventive step, and industrial applicability. The claims appear structured to address these requirements emphatically.

Patent Landscape Analysis

Precedent and Prior Art

The background of the invention reportedly builds on prior art involving chemical modifications or biological activity enhancements. The strategic positioning of claims suggests an anticipation of potential challenges related to obviousness.

Competitor Patents and Freedom to Operate (FTO)

India’s patent landscape includes numerous filings in similar classes of drugs, especially in the anti-infective, anticancer, and CNS sectors. Comparing this patent's claims with existing patents reveals:

  • Innovative Differentiation: The patent claims a specific structural configuration or process not disclosed in prior patents.
  • Potential Overlaps: Some overlapping claims with existing patents could pose FTO risks if broader claims encroach on known compounds or methods.

International Patent Implications

Since the patent involves Chinese filings, it reflects transnational patenting strategies. If the patent claims are robust, they could impact global patent strategies, especially in key markets such as the US, Europe, and China, depending on national patent grant outcomes.

Legal and Market Implications

  • Patent Enforcement: The scope determines ease of enforcement against infringers.
  • Generic Entry Barriers: Strong claims hinder generic development, thereby providing market exclusivity.
  • Research and Development (R&D): Patent protection encourages continued innovation but also prompts competitors to develop around strategies.

Regulatory and Commercial Considerations

In India, the patentability of pharmaceuticals is governed by the Patents Act, 1970, amended to comply with the TRIPS Agreement. Patents like IN506CHN2014 must navigate Section 3(d), which restricts patents on new forms of known substances unless they demonstrate enhanced efficacy.

Given this patent’s detailed claims, its enforceability hinges on demonstrating a tangible inventive step beyond existing knowledge, aligning with Indian patent law requirements. The patent's scope influences pricing, licensing strategies, and potential R&D investments.

Key Strategic Insights

  • Scope and Claims: Well-crafted to cover the core inventive concept, providing meaningful market protection.
  • Patent Landscape: Operates within a competitive field sourcing from established prior art, necessitating non-obviousness and inventive step.
  • Legal Risks: Overly broad or vague claims might face invalidation under strict Indian patent standards.
  • FTO and Licensing: The patent’s scope informs licensing negotiations and entry barriers for competitors.

Key Takeaways

  1. Innovative Breadth: The claims likely focus on a specific chemical compound or process with therapeutic advantages, balancing broad coverage with validity.
  2. Patent Strategy: Proper claim drafting facilitates enforcement, deters infringement, and enhances licensing opportunities.
  3. Legal Challenges: Compliance with Indian patent law, particularly Section 3(d), remains crucial for maintaining patent validity.
  4. Market Influence: A robust patent ecosystem promotes R&D investment, but overly narrow claims may limit market exclusivity.
  5. Global Impact: The patent’s strategic relevance extends beyond India, affecting international drug patenting and market entry strategies.

FAQs

1. What is the significance of the ‘CHN’ designation in the patent number IN506CHN2014?
It indicates that the patent application is associated with China, either filed directly there or through international treaties, influencing the patent's territorial scope and strategic importance.

2. How do Indian patent laws impact pharmaceutical patent claims like IN506CHN2014?
Indian patent law emphasizes non-obviousness and efficacy, especially under Section 3(d), which aims to prevent evergreening. Patent claims must clearly demonstrate inventive steps and increased efficacy to be upheld.

3. Can similar patents invalidate or challenge IN506CHN2014?
Yes, prior art references or earlier patents that anticipate the invention or show obvious modifications can challenge the validity of the claims during patent opposition or litigation.

4. What role does patent claims drafting play in this patent’s enforceability?
Precise and comprehensive claims define the scope of protection, influencing enforceability. Overly broad claims risk invalidation, whereas narrowly drafted claims may limit scope but strengthen validity.

5. How does this patent influence the competitive landscape in India’s pharmaceutical sector?
It can serve as a core barrier for generics, shifting market dynamics toward innovator-defined niche markets, R&D investments, and strategic licensing.

References

  1. Indian Patent Act, 1970 (as amended).
  2. Indian Patent Office Guidelines.
  3. WIPO Patent Database.
  4. Patent IN506CHN2014 publication details.
  5. Industry analyses from pharmaceutical patent case law.

[End of Document]

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