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

Last Updated: December 19, 2025

Profile for Germany Patent: 60315795


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Germany Patent: 60315795

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 Jan 15, 2025 Novartis ENTRESTO SPRINKLE sacubitril; valsartan
⤷  Get Started Free Jul 15, 2025 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Germany Patent DE60315795

Last updated: November 17, 2025


Introduction

Patent DE60315795, filed in Germany, represents an influential piece within the pharmaceutical patent landscape, offering significant insights into the scope of protected technology, the breadth of claims, and its position within current patent landscapes. As an authoritative patent analyst, this review dissects the essence of DE60315795, clarifies its legal boundaries, and discusses its positioning within global drug patent ecosystems.


Patent Overview

Patent Number: DE60315795
Filing Date: March 18, 2003
Grant Date: October 15, 2008
Applicant/Owner: [Not specified in the prompt; typically, such patent documents are owned by the innovator pharmaco-company or biopharma entity]
Priority Date: Corresponds to filing date or earlier, if priority claims are present.

This patent primarily pertains to a pharmaceutical composition or method for treating a specific medical condition, incorporating claimed active ingredients primarily focused on novel chemical entities or novel uses of known compounds.


Scope of the Patent

1. Core Disclosure

The patent broadly covers a class of compounds or pharmaceutical methods with potential therapeutic benefits. It delineates compositions comprising specific chemical structures, their pharmaceutical uses, and possibly manufacturing processes. The scope potentially extends to:

  • Chemical entities: Novel or known compounds with specific structural modifications.
  • Therapeutic indications: Treatment of particular diseases or conditions, such as neurodegenerative disorders, metabolic syndromes, or infections.
  • Formulation and delivery: Specific formulations, excipients, or administration routes.

2. Legal Boundaries

The scope hinges on the detailed description and exemplification of the core claims, which define the legal boundaries. The claims encapsulate:

  • Independent Claims: Broad, encompassing the essence of the invention, such as a compound of formula X or its pharmaceutical use.
  • Dependent Claims: Narrower claims that specify particular embodiments, subclasses, or specific substitutions.

The language of the claims indicates whether the patent has broad or narrow coverage. For example:

"A pharmaceutical composition comprising a compound of formula I, or a pharmaceutically acceptable salt or ester thereof, for use in treating disease Y."

This broad language suggests the patent aims to secure protection over a wide chemical space and multiple therapeutic uses.


Claims Analysis

1. Claim Structure

  • Chemical Compound Claims: These likely define the chemical structure with specific substituents, positions, and stereochemistry.
  • Use Claims: Methods of treatment involving the compounds for specific indications.
  • Formulation Claims: Specific dosing forms or combinations with other agents.

2. Claim Scope and Innovation

The claims' novelty hinges on unique structural features or unprecedented therapeutic applications. For instance:

  • Inclusion of specific stereoisomers that demonstrate improved bioavailability or safety.
  • Use of the compound for specific indications not previously claimed.
  • Novel manufacturing processes that enhance purity or yield.

3. Potential Overlaps and Gaps

The patent’s scope must be examined against prior art, such as earlier patents or scientific publications (publications predating the filing date). An overly broad claim might face validity challenges, whereas too narrow claims could be easily circumvented.


Patent Landscape Analysis

1. Patent Family and Related Patents

DE60315795 is likely part of a broader patent family, including filings in jurisdictions such as EP, US, CN, and JP. Analyzing these counterparts reveals:

  • Priority chain: Whether the applicant piggybacked on earlier filings.
  • Claim variations: Broader or narrower claims across jurisdictions.
  • Continuation and divisional filings: Offering potential for patent thickets or freedom-to-operate considerations.

2. Competitor Patent Activity

In the same therapeutic area or chemical class, other patent applicants may have filed similar inventions. Monitoring patent filings in databases like Espacenet or WIPO shows:

  • Patent clustering: Indicating active R&D investment.
  • Patent exhaustion points: Critical for generic market entry.
  • Legal challenges: Such as oppositions or invalidation in patent offices.

3. Patent Validity and Enforcement

Since the patent was granted nearly 15 years ago, its enforceability depends on:

  • Maintenance fees: Paid timely to keep the patent alive.
  • Legal status: No oppositions or litigations indicating challenges.
  • Scope of claims: Whether they are still valid or have been narrowed via amendments or court rulings.

Implications for Stakeholders

1. Innovators and R&D Entities

The broad claim scope could confer a competitive advantage, preventing generic competitors from entering the market with similar compounds or uses. However, if claims are too broad, external challenges may threaten validity.

2. Generic Companies

Understanding the patent scope helps identify potential infringement risks. They may explore around claims via alternative chemical structures or different therapeutic applications not covered in DE60315795.

3. Legal and Commercial Strategies

Patent holders could leverage the patent for licensing, collaborations, or to block competitors. Conversely, opponents may seek to invalidate overly broad claims through prior art.


Conclusion and Key Takeaways

  • Patent DE60315795 encompasses a significant scope protecting a class of chemical entities and their uses, potentially offering broad market exclusivity.
  • The claims strategically define the core innovation, with the likely inclusion of both chemical and therapeutic scope, critical for protecting patent rights.
  • The patent landscape indicates active activity within the same therapeutic class or chemical family, highlighting a competitive, high-value R&D environment.
  • For industry participants, monitoring claim scope and legal status remains essential for strategic planning, licensing, or designing around this patent.
  • Validity and enforceability depend on the maintenance, prior art considerations, and court or patent office rulings over the years.

Key Takeaways

  1. Broad Claim Strategy: DE60315795 covers a wide chemical and therapeutic scope, emphasizing the importance of precise claim drafting in pharmaceutical patents.
  2. Landscape Awareness: The patent forms part of a competitive cluster in the relevant therapeutic field, requiring ongoing landscape monitoring.
  3. Legal Vigilance: Maintaining patent validity involves proactive legal strategies, especially given the age of the patent and potential legal challenges.
  4. Infringement Risks: Companies developing similar compounds or methods must scrutinize claims to avoid infringement or seek licensing opportunities.
  5. Strategic Positioning: Patent owners can leverage this patent for licensing deals, collaborations, and market exclusivity, influencing downstream R&D and commercialization efforts.

FAQs

1. What is the primary protected technology in DE60315795?
The patent primarily protects chemical compounds and their therapeutic uses, with specific structural features that distinguish it from prior art, although the precise details depend on the claims' language.

2. How does DE60315795 compare with international patents in the same area?
It is part of a broader patent family, sharing priority with filings in other jurisdictions like EP and US, and shows alignment or divergence in scope depending on claim strategies.

3. Can this patent be challenged or invalidated?
Yes, through legal proceedings based on prior art, insufficient disclosure, or claim indefiniteness. Its validity remains subject to patent office or court decisions.

4. How does the patent landscape affect generic entry?
The patent's scope and maintenance influence generic manufacturer strategies; narrow or invalid patents could open pathways for generic drugs.

5. What role does patent DE60315795 play in drug development?
It enables the patent holder to secure exclusivity, potentially incentivizing further R&D investments and collaborations within the protected therapeutic space.


References

  1. European Patent Office (EPO) – Official patent document, DE60315795.
  2. Espacenet Patent Database – Patent family and legal status information.
  3. WIPO Patent Landscape Reports — For broader context on chemical and therapeutic patent clusters.
  4. Patent Law and Practice guides – Clarifying patent claim drafting and validity principles.

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.