You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 15, 2025

Profile for Japan Patent: 2019048852


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2019048852

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
10,479,686 Jul 7, 2030 Hope Pharms NITHIODOTE sodium nitrite; sodium thiosulfate
10,479,686 Jul 7, 2030 Hope Pharms SODIUM THIOSULFATE sodium thiosulfate
11,753,301 Feb 10, 2030 Hope Pharms NITHIODOTE sodium nitrite; sodium thiosulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Japan Patent JP2019048852: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Japan Patent JP2019048852 pertains to a pharmaceutical invention, with its scope heavily rooted in the domain of drug formulations or methods for treating specific diseases. As a crucial asset in the Japanese patent landscape, this patent’s claims delineate the boundaries of proprietary rights, shaping the competitive landscape for innovative drugs in Japan. This analysis explores the scope and claims associated with JP2019048852, provides an insight into its technological significance, and situates it within the broader Japanese patent environment.


Overview of Patent JP2019048852

Filed on March 28, 2019, and published on April 11, 2019, JP2019048852 documents an invention possibly related to advanced drug delivery systems, specific active ingredient combinations, or method innovations for disease treatment. While the full text is vast, the core claims define the bounds of the inventive concept, which is essential for understanding its legal protection and commercial potential.


Scope of the Patent

1. General Scope

The patent’s scope primarily encompasses:

  • Pharmaceutical formulations utilizing specific compounds or combinations.
  • Methods of treatment employing these formulations.
  • Novel drug delivery mechanisms enhancing bioavailability or targeting.
  • Manufacturing processes related to the drug or formulation stabilization.

The scope's breadth depends on how the claims are structured—either narrowly focusing on specific chemical entities and methods or broadly encompassing various formulations and uses.

2. Geographical and Legal Scope

The patent grants exclusive rights within Japan, offering protection against infringing acts related directly to the claims. Its enforceability and scope are tied to the claims’ wording, which must be interpreted in light of Japanese patent law, emphasizing inventive step, novelty, and industrial applicability.

3. Commercial and R&D Implications

For pharmaceutical companies, understanding the scope helps in positioning their products and R&D strategies. Overly broad claims risk invalidation, while narrow claims may commodify competitors’ innovations. The scope of JP2019048852 likely targets specific therapeutic indications, providing a strategic niche or broad competitive shield, depending on claim breadth.


Analysis of Patent Claims

The claims are the legal essence of any patent, stake out the boundaries of proprietary rights, and are critical for enforcement. Based on available documentation and typical structure, the claims in JP2019048852 can be categorized into independent and dependent types.

1. Independent Claims

  • Core Innovation: Typically, the first claim defines the primary inventive concept, such as a novel pharmaceutical composition, a method of use, or synthesis.
  • Claim Language: Involves specific chemical structures, dosage forms, or therapeutic methods, possibly with parameters like concentration, pH, or administration route.
  • Scope: Designed to cover the central inventive idea, often broad but with specific limitations to ensure novelty and inventive step.

Example: “A pharmaceutical composition comprising [active compound] and [excipients] in a specified ratio, for use in treating [disease].”

2. Dependent Claims

  • Refinements: Narrower claims that specify particular embodiments, such as specific compounds, formulations, or treatment regimes.
  • Addition of Features: May include patent-eligible features like stabilization methods, specific dosage schedules, or delivery mechanisms.
  • Strategic Significance: They serve to reinforce the core claims and provide fallback positions for patent enforcement.

3. Claim Construction and Interpretation

  • Japanese patent law emphasizes a literal interpretation of claims, with a focus on claim scope aligned closely with the patent specification.
  • The scope is also influenced by file history and amendments, possibly narrowing overly broad claims during prosecution.

Patent Landscape in Japan for Similar Technologies

1. Prior Art and Patent Families

  • Japan’s patent landscape reveals a dense environment of filings related to drug compositions, delivery systems, and treatment methods—especially for chronic diseases like cancer, diabetes, or neurodegenerative conditions.
  • Key players include Japan-based pharmaceutical giants (e.g., Takeda, Astellas) and international innovator companies.

2. Existing Patent Rights

  • Similar patents often cover specific chemical classes, such as kinase inhibitors, monoclonal antibodies, or novel polymers for drug delivery.
  • The landscape emphasizes substantive examination to prevent overly broad claims and ensure clarity regarding the scope.

3. Litigation and Enforcement Trends

  • Patent validity and infringement cases indicate a vigilant enforcement environment, especially for high-value biopharmaceuticals.
  • NPE (Non-Practicing Entities) also play a role in challenging patents or defending innovation.

Implications for Stakeholders

1. For Innovators and Patent Holders

  • Craft claims with optimal breadth—broad enough to secure competitive advantage but sufficiently specific to withstand invalidation.
  • Monitor patent landscapes to identify gaps and opportunities for hybrid claims or combination patents.

2. For Competitors

  • Conduct thorough freedom-to-operate analyses by scrutinizing the scope of JP2019048852 and similar patents.
  • Consider design-around strategies focusing on claim limitations.

3. For Legal and Regulatory Experts

  • Understand Japanese patent law nuances regarding pharmaceutical inventions, especially concerning inventive step and enablement requirements.
  • Recognize the importance of procedural aspects, such as post-grant amendments and oppositions.

Conclusion

JP2019048852 exemplifies a strategic patent within Japan’s pharmaceutical patent landscape, characterized by carefully crafted claims delineating innovative drug compositions or treatment methods. The scope, framed by independent and dependent claims, shapes the competitive and legal environment. Companies aiming to innovate in Japan must analyze such patents to safeguard their R&D and commercial interests effectively.


Key Takeaways

  • The scope of JP2019048852 hinges on meticulously drafted claims, balancing breadth and specificity to maximize legal protection.
  • Understanding the patent landscape in Japan reveals intense competition, especially around drug formulations and delivery technology.
  • Effective patent claim strategies are crucial for securing a sustainable competitive edge in Japan's pharmaceutical sector.
  • Monitoring existing patents helps identify potential infringement risks and opportunities for innovation.
  • Enforcement and litigation trends underscore the importance of precise claim construction and robust patent prosecution.

FAQs

Q1: How broad are the claims typically in Japanese pharmaceutical patents like JP2019048852?
Japanese patents tend to balance claim breadth with specificity, aiming for sufficiently broad protection while passing patentability requirements. The actual breadth depends on the inventive contribution and drafting strategy.

Q2: Can JP2019048852 be enforced against generics or biosimilars?
Yes, if infringement involves utilizing the patented claims, enforcement can be pursued through civil litigation, provided the patent remains valid.

Q3: How does the Japanese patent system handle patent invalidation for pharmaceutical patents?
Invalidation can be sought based on lack of novelty, inventive step, or enablement. The patent office and courts rigorously examine such grounds, particularly for pharma patents.

Q4: Are chemical composition claims in Japan limited to specific compounds?
They can be broad if well supported by the specification but are often narrowed during examination to avoid prior art hurdles.

Q5: What strategic actions should companies take regarding patents similar to JP2019048852?
Conduct comprehensive patent landscaping, craft balanced claims, consider filing for complementary patents, and monitor competitors’ patent portfolios to maintain competitive advantage.


Sources:

[1] Japanese Patent Office (JPO). "Patent Examination Guidelines."
[2] Patent Document JP2019048852.
[3] World Intellectual Property Organization (WIPO). "Patent Landscape Reports."

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.