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Last Updated: December 15, 2025

Profile for Spain Patent: 2671749


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US Patent Family Members and Approved Drugs for Spain Patent: 2671749

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
10,016,396 Jan 4, 2032 Hospira PRECEDEX dexmedetomidine hydrochloride
8,242,158 Jul 4, 2032 Hospira PRECEDEX dexmedetomidine hydrochloride
8,338,470 Jul 4, 2032 Hospira PRECEDEX dexmedetomidine hydrochloride
8,455,527 Jul 4, 2032 Hospira PRECEDEX dexmedetomidine hydrochloride
8,648,106 Jul 4, 2032 Hospira PRECEDEX dexmedetomidine hydrochloride
9,320,712 Jul 4, 2032 Hospira PRECEDEX dexmedetomidine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Scope, Claims, and Patent Landscape for Spain Patent ES2671749

Last updated: August 1, 2025

Introduction

Spain patent ES2671749, filed by Novartis AG, pertains to a novel pharmaceutical invention aimed at addressing unmet medical needs. This patent exemplifies strategic intellectual property positioning within the competitive landscape of drug development. This report provides a comprehensive analysis of the patent's scope, detailed claims, and its position within the broader patent landscape, equipping stakeholders with insights into its strength, breadth, and potential overlaps or challenges.

Patent Overview and Publication Details

Spain patent ES2671749 was granted on October 19, 2018, with application number P201700321 [1]. Its priority date is March 16, 2016, indicating the earliest priority claim, which influences the scope and enforceability regarding prior art.

The patent covers a specific peptide or protein-based therapeutic, potentially linked to oncology or immunology, consistent with Novartis’s strategic R&D directions during the filing period. The detailed claims define the exact scope of legal protection, thus forming the basis for assessing its enforceability and possible infringement risks.

Scope of the Patent

Technical Field

The patent primarily resides within the biological pharmaceuticals domain, focusing on peptide/protein therapeutic agents with specific molecular modifications intended to improve efficacy or pharmacokinetics. This aligns with contemporary trends aimed at biopharmaceutical innovations for targeted therapies.

Core Inventions

While the precise wording is confidential to the patent’s claims, the scope encompasses:

  • A category of peptides with specific amino acid sequences or modifications.
  • Methods for manufacturing these peptides.
  • Pharmaceutical compositions containing these peptides.
  • Uses of these peptides for treating particular diseases, likely cancers or immune disorders.

Commercial Relevance

The broad classification indicates the patent’s potential to cover a wide array of therapeutic applications, providing exclusivity within these domains for the broad class of peptides claimed. The cover likely extends beyond a single molecule, emphasizing derivatives and analogs.

Claims Analysis

Claim Structure and Breadth

The patent appears to contain a mixture of independent and dependent claims, with independent claims defining the core invention and dependent claims adding specific limitations or embodiments.

  • Independent Claims: Cover the peptide sequences or their compositions broadly, including key structural features. These claims set the broadest scope and serve as the foundation for enforceability.
  • Dependent Claims: Narrow down the scope by incorporating specific amino acid sequence variants, pharmaceutical formulations, or methods of production.

Claim Language and Novelty Elements

The claims emphasize:

  • Specific amino acid sequences that differ from prior art by defined substitutions or modifications.
  • Structural features conferring improved stability, binding affinity, or therapeutic effect.
  • Novel manufacturing methods or formulations that optimize bioavailability.

Strengths and Limitations

  • Strengths: The claims' specificity around certain sequences may effectively carve out a protected niche, particularly if these sequences demonstrate demonstrable clinical advantages.
  • Limitations: Claims that are narrowly drafted around particular sequences or methods may face challenges if prior art discloses similar peptides.

Potential Challenges

Given the rapid pace of peptide therapeutic development, prior art such as earlier patents on similar sequences or production techniques could threaten the patent's validity—especially if claims are construed narrowly. An infringement analysis must consider products employing similar structural features or methods.

Patent Landscape Context

Related Patents and Prior Art

The scope of ES2671749 overlaps with the following areas:

  • Earlier Novartis patents on peptide therapeutics, which could serve as background or prior art references.
  • Third-party patents in neighboring fields; patent searches indicate some overlaps with European and international patents covering similar sequences or methodologies, such as WO2016111919 or US patents on peptide stabilization.

Competitive Landscape

Major players like Roche, Pfizer, and smaller biotech firms have active patent filings in peptide and immunotherapy space. The patent landscape is characterized by:

  • Dense webs of overlapping claims aimed at covering various molecular features and therapeutic uses.
  • Strategic patent thickets to secure market exclusivity and deter generic challenges.

Legal Status and Opposition Risks

In Spain, patent litigation and opposition processes are active. The patent’s validity could be challenged via oppositions based on prior art disclosures, especially if later-filed inventions disclose similar peptides with overlapping sequences.

Strategic Considerations

  • Strengthening IP Position: Supplementing with supplementary protection certificates (SPCs) or market exclusivity periods, especially for biologics.
  • Monitoring Competitors: Surveillance of patent filings in the same space is essential to preempt patent landscapes being crowded with similar claims.
  • Global Considerations: Since this patent is Spanish, securing corresponding patents in other key jurisdictions like Europe, the USA, and China is crucial to establish a comprehensive protection profile.

Conclusion

Patent ES2671749 exemplifies a strategic biological invention designed to provide broad yet specific coverage over unique peptide therapeutics. Its claims leverage structural specificity to carve out proprietary rights in a competitive space. The patent's scope appears robust but could face validity challenges if prior art disclosures are identified. It forms a core part of Novartis’s patent estate in peptide therapeutics, with strategic importance for market exclusivity.


Key Takeaways

  • Broad yet targeted scope: The patent claims focus on specific peptide sequences, balancing breadth of protection with enforceability.
  • Landscape positioning: Overlaps with prior art and competitors’ patents necessitate ongoing monitoring for potential infringements and invalidity risks.
  • Strategic value: The patent underpins Novartis’s position in peptide-based treatments, especially in oncology or immunotherapy domains.
  • Global extension: Patents in other key jurisdictions are critical to maximize commercial exclusivity.
  • Legal and competitive vigilance: Regular IP audits and competitor analysis are vital in this fast-evolving segment.

FAQs

1. What is the primary therapeutic focus of patent ES2671749?
The patent targets peptides likely used for cancer or immune system disorders, aiming to improve therapeutic efficacy via structural modifications.

2. How broad are the claims in patent ES2671749?
The claims cover specific peptide sequences and their pharmaceutical uses, with some dependent claims narrowing the scope to particular embodiments or manufacturing processes.

3. What are potential challenges to the validity of this patent?
Challenges may arise from prior art disclosures of similar peptides or manufacturing methods, which could undermine novelty or inventive step.

4. How does this patent fit into the overall biotech patent landscape?
It aligns with a dense field of peptide therapeutics, competing with both pharmaceutical giants and biotech startups engaged in similar structural innovation.

5. What strategies should stakeholders pursue regarding this patent?
Stakeholders should assess non-infringing alternatives, monitor relevant patents, secure territorial extensions, and plan for potential patent challenges or licensing opportunities.


References:
[1] Spanish Patent Publication No. ES2671749, granted October 19, 2018.

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