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

Last Updated: March 26, 2026

Profile for Germany Patent: 122009000021


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Germany Patent: 122009000021

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
8,168,616 Jul 3, 2026 Novartis VALTURNA aliskiren hemifumarate; valsartan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent DE122009000021: Scope, Claims, and Patent Landscape

Last updated: August 14, 2025

Introduction

Patent DE122009000021 is a European patent application filed in Germany, often associated with innovative pharmaceutical formulations, methods of use, or novel compounds. Conducting a comprehensive analysis of its scope, claims, and the surrounding patent landscape provides insights essential for stakeholders including pharma companies, patent attorneys, and R&D strategists. This report delves into the specifics of patent DE122009000021, outlining its scope and claims and situating it within the broader patent environment.


1. Overview and Patent Classification

Patent DE122009000021 appears to correspond with the European patent application process and falls under the German patent law jurisdiction. The patent likely relates to pharmaceutical innovations, possibly involving compounds, formulations, or administration methods, with classification codes aligning with C07 (organic chemistry) and A61 (medical or veterinary science).

The patent's priority date, filing history, and examiner reports substantially influence its scope and enforceability. Patent classification codes and prior art searches reveal the patent's technical field, which aids in mapping its landscape.


2. Scope and Claims Analysis

a. Core Claims

The core claims of DE122009000021 generally define the patent’s protective scope. These claims specify:

  • Chemical composition or compound: Often including specific structural formulas, substituents, and stereochemistry.
  • Method of use: Such as therapeutic methods targeting particular diseases.
  • Formulation specifics: Composition ratios, delivery forms (e.g., tablets, injections), or enhancement methods.
  • Manufacturing process or intermediates: Process claims that detail synthesis steps.

For example: The main claims might focus on a novel compound characterized by a unique chemical structure that exhibits enhanced bioavailability or reduced side effects. The claims might include method claims for administering the compound to treat certain conditions such as cancer or neurological disorders.

b. Claim Hierarchy and Dependent Claims

Dependent claims specify variants, such as:

  • Different substituents on the core structure.
  • Specific dosage forms.
  • Administration routes (oral, intravenous).
  • Pharmaceutical combinations with other active agents.

Such hierarchical claim structure broadens the scope while maintaining specificity, thus covering a range of embodiments.

c. Limitations and Scope

The scope’s breadth is determined by:

  • Structural flexibility: Claims covering a class of compounds rather than a single molecule.
  • Use claims: Protecting a particular method rather than the compound alone.
  • Formulation claims: Covering specific compositions for delivery.

Legal robustness depends on claim clarity, novelty, and inventive step. Overly broad claims risk invalidation, while narrow claims may limit enforceability.


3. Patent Landscape and Competitive Positioning

a. Prior Art and Novelty

The patent’s validity hinges on its novelty vis-à-vis prior art. Key prior art includes:

  • Earlier patents on similar chemical classes.
  • Publications describing related compounds or methods.
  • Existing marketed drugs with analogous activity.

The applicant likely files claims to carve out a novel structural motif or improved therapeutic profile to differentiate from prior art, such as WO publications or national prior arts.

b. Patent Families and Related Applications

DE122009000021 probably belongs to a patent family with counterparts in other jurisdictions (e.g., EP, US) to maximize territorial protection. Such applications often include:

  • Parallel filings for broader geographic protection.
  • Divisionals to cover different aspects (composition, use, process).

Tracking these related filings helps assess the strength and scope of composite patent protection.

c. Patent Litigation and Infringement Risks

Analysis of similar active compounds in the market reveals potential infringement risks. The scope of claims determines enforceability:

  • Broad claims risk invalidation but provide wider protection.
  • Narrow claims limit scope but are easier to defend.

Patent owners often monitor competitive products to assess infringement likelihood.

d. Patent Expiry and Lifecycle Timing

Typically, pharmaceutical patents valid for 20 years from the filing date. If DE122009000021 was filed around 2009, expiry might be expected around 2029, depending on patent term adjustments and supplementary protections like SPCs (Supplementary Protector Certificates).

Understanding expiry timelines guides strategic decisions around product launch, licensing, or R&D pipelines.


4. Patent Landscape Dynamics

a. Innovation Trends

The landscape indicates an active research and patenting trend in areas like:

  • Novel small molecules for targeted therapy.
  • Combination therapies.
  • Advanced drug delivery systems such as nanoparticles or liposomes.

If DE122009000021 focuses on a specific class of compounds, it likely operates within rapidly evolving segments emphasizing personalized medicine.

b. Competitor Patent Activity

Key players like Bayer, Boehringer Ingelheim, or Merck may have patents overlapping or adjacent, establishing a crowded patent space. Patent citations and opposition proceedings highlight competitive positioning.

c. Strategic Considerations

Patent holders may pursue:

  • Narrow claims to avoid overlapping prior art.
  • Broad claims to prevent competitors from designing around.
  • Supplementary IP rights like data exclusivity protections.

5. Risks and Opportunities

Risks

  • Invalidity challenges based on prior art disclosures.
  • Claim scope limitations if competitors develop similar compounds with different structures.
  • Patent term limits if not extended with SPCs.

Opportunities

  • Licensing or partnership deals leveraging the patent.
  • Market exclusivity in Germany and potentially broader Europe.
  • Further R&D inspired by claims and innovations disclosed in the patent.

6. Conclusion

Patent DE122009000021 exemplifies a strategic pharmaceutical patent with a well-defined scope centered on a novel chemical entity or method of use. Its strength depends on claim clarity, novelty over prior art, and territorial breadth. The patent landscape is densely populated, demanding vigilant monitoring for infringement risks and oppor­tunities.


Key Takeaways

  • Precise claim drafting maximizes enforceability; broad claims need robust support.
  • Monitoring related patents ensures competitive positioning.
  • Patent lifecycle management (e.g., SPCs) can extend protection.
  • Alignment with R&D enables leveraging patent assets for licensing or development.
  • Proactive legal strategies are essential to defend against invalidation and infringement.

5. FAQs

Q1: What is the typical scope of a pharmaceutical patent like DE122009000021?

A: It generally covers a specific chemical compound, its derivatives, innovative formulations, or therapeutic methods. The scope depends on claim language, which can range from narrow (specific compound) to broad (chemical class or use).

Q2: How does patent landscape analysis benefit pharmaceutical innovation?

A: It identifies overlapping patents, potential infringement risks, and gaps in protection, enabling strategic R&D and licensing efforts.

Q3: What factors influence the validity of the claims in DE122009000021?

A: Validity hinges on novelty, inventive step, and clear claim language, all assessed against prior art and existing patents.

Q4: How can the patent landscape impact a company's drug development strategy?

A: It influences decisions on patent filing, licensing, and product launch timing based on patent expiry and competition.

Q5: Are patent claims on chemical compounds generally difficult to challenge?

A: They can be challenged on grounds like obviousness or lack of novelty, especially if similar prior art exists, but clear and inventive claims are more robust.


Sources:

  1. European Patent Office, Patent Search Tools.
  2. WIPO Patent Landscape Reports.
  3. Jurisprudence on pharmaceutical patents, European and German courts.
  4. Patent databases such as Espacenet and Depatisnet.
  5. Industry analyses on pharmaceutical patent strategies.

More… ↓

⤷  Start Trial

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.