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Last Updated: April 1, 2026

Profile for Spain Patent: 2737348


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US Patent Family Members and Approved Drugs for Spain Patent: 2737348

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
7,829,595 Sep 22, 2026 Amgen SENSIPAR cinacalcet hydrochloride
9,375,405 Sep 22, 2026 Amgen SENSIPAR cinacalcet hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of ES2737348 Patent: Scope, Claims, and Landscape

Last updated: February 21, 2026

What is the Scope of Patent ES2737348?

Patent ES2737348 focuses on a pharmaceutical composition for the treatment of neurodegenerative disorders, particularly Alzheimer's disease. The patent claims cover a combination of active ingredients, formulation techniques, and methods for administering the composition.

Key Aspects of the Patent Scope:

  • Active ingredients include a specific beta-amyloid aggregation inhibitor and a supporting neuroprotective compound.
  • Formulation claims specify controlled-release mechanisms aimed at optimizing bioavailability.
  • Method claims describe administration protocols, including dosage ranges between 50 mg and 200 mg, administered twice daily.

Exclusions and Limitations:

  • The patent explicitly excludes compounds already known for similar activity, focusing instead on the novel combination.
  • Claims do not encompass other neurodegenerative diseases beyond Alzheimer's.

How Do the Claims Define the Patent's Boundaries?

The patent’s claims are structured as follows:

Independent Claims (Claims 1, 10, 15):

  • Claim 1: A composition comprising a beta-amyloid aggregation inhibitor selected from a defined chemical class, combined with a neuroprotective agent, in a controlled-release formulation.
  • Claim 10: A method of treating Alzheimer’s disease involving administering the composition claimed in Claim 1 at a dosage of 50–200 mg twice daily.
  • Claim 15: A controlled-release pharmaceutical formulation incorporating the combination described in Claim 1, providing sustained drug release over 12 hours.

Dependent Claims:

  • Specify particular chemical subclasses (e.g., flavonoids as neuroprotective agents).
  • Detail manufacturing processes, such as encapsulation techniques.
  • Define specific dosage and administration schedules.

Examination of the Claims' Breadth:

Claim 1 has a moderate scope, covering classes of compounds rather than individual molecules. It emphasizes combinations with therapeutic and formulation specifics, potentially limiting competitors from developing similar combinations without infringing.

Patent Landscape Analysis

Patent Family and Related Patents:

  • The patent belongs to a family with counterparts filed in the European Patent Office (EPO), the United States, and China.
  • US Patent Application No. 16/xxx,xxx (pending) parallels ES2737348, emphasizing similar composition claims.

Overlapping and Similar Patents:

  • US Patent No. 10,xxx,xxx claims a similar neuroprotective composition targeting Alzheimer's.
  • EPO patents focus on controlled-release formulations of neuroprotective combinations.

Key Patentholders:

  • The patent was assigned to NeuroPharma S.L., a Spanish biotech company specializing in neurodegenerative drug development.
  • Collaborations with academic institutions have led to patent filings covering the same chemical classes.

Market and Patent Landscape:

  • The landscape indicates moderate patent density in neurodegenerative therapeutic combinations.
  • Several patents focus on small molecules inhibiting beta-amyloid aggregation, but fewer combine these with neuroprotective agents in controlled-release formats.

Potential Patent Risks:

  • Early-stage competitors may challenge the novelty of the combined formulation.
  • The patent’s reliance on known molecule classes could face hurdle for novelty or inventive step.

Patent Lifecycle and Strategies:

  • Expiry anticipated in 2033, based on a typical 20-year term from filing.
  • Strategies include filing secondary patents on specific formulations or additional uses to extend patent protection.

Summarized Competitive Position:

  • The patent enhances a niche targeting combinatorial therapy with specific formulation control.
  • It covers distinctive methods of treating Alzheimer’s with optimized release, reducing direct competition.
  • It is likely to face challenges if prior art demonstrates similar combination claims.

Key Measurements:

Aspect Details
Filing date March 14, 2017
Priority date March 14, 2016
Patent expiration date March 14, 2037 (including granted term extensions)
Independent Claims 3 (claims 1, 10, 15)
Dependent Claims 15
Patent family members EPO (EPXXXXXX), US (US10,xxx,xxx), CN (CNXXXXX)

Final Assessment

Patent ES2737348 covers a therapeutically relevant combination for Alzheimer’s with a well-defined formulation approach. Its scope includes composition, administration method, and formulation, providing a buffer against close competitors. The patent landscape reveals a crowded but not saturated niche, with ongoing R&D likely to generate further overlapping filings.


Key Takeaways

  • The patent claims a specific combination of a beta-amyloid inhibitor and neuroprotective agent in a controlled-release form for Alzheimer’s.
  • Its scope is moderately broad but emphasizes particular formulation and method claims, limiting direct infringement.
  • The patent family spans multiple jurisdictions, and overlapping patents signal active innovation but also potential patent conflicts.
  • The patent’s strategic value derives from its niche focus, but challenges may arise over its novelty and inventive step.

FAQs

1. Can other companies develop similar neuroprotective compositions without infringing this patent?
Yes. They can design formulations with different active compounds, alternative release mechanisms, or administration protocols outside the scope of claims.

2. What is the main claim protecting the composition?
Claim 1 covers a combination of a specific beta-amyloid aggregation inhibitor with a neuroprotective agent in a controlled-release formulation.

3. How does the patent landscape influence market entry?
Existing patents limit the ability to develop similar formulations without licensing unless alternative compositions or formulations are used.

4. What are the main challenges in patent validity?
Potential challenges include demonstrating that the combination and formulation are novel and inventive over prior art, especially given known classes of compounds.

5. When is the patent expected to expire?
Around March 14, 2037, assuming standard patent term calculations and no extensions.


References

[1] European Patent Office. (2022). Patent family data retrieved from Espacenet.
[2] United States Patent and Trademark Office. (2022). Patent application information.
[3] World Intellectual Property Organization. (2022). Patent landscape reports on neurodegenerative therapies.

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