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Last Updated: December 12, 2025

Details for Patent: 11,660,304


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Which drugs does patent 11,660,304 protect, and when does it expire?

Patent 11,660,304 protects YUTREPIA and is included in one NDA.

This patent has twelve patent family members in six countries.

Summary for Patent: 11,660,304
Title:Dry powder treprostinil for the treatment of pulmonary hypertension
Abstract:A dry powder inhalation treatment for pulmonary arterial hypertension includes a dose of dry particles comprising greater than 25 micrograms of treprostinil enclosed in a capsule. The dry particles can include treprostinil, a wetting agent, a hydrophobicity modifying agent, a pH modifying agent and a buffer. A method of treating a patient having pulmonary arterial hypertension includes providing a patient a dry powder inhaler, providing the patient at least one capsule for use in the dry powder inhaler, the capsule including at least 25 micrograms of treprostinil.
Inventor(s):Robert Frank Roscigno, Brian T. Farrer, Jacob J. Sprague, Benjamin Maynor
Assignee: Liquidia Technologies Inc
Application Number:US17/719,439
Patent Claim Types:
see list of patent claims
Patent landscape, scope, and claims:

Analysis of the Scope, Claims, and Patent Landscape of U.S. Patent 11,660,304

Introduction

U.S. Patent No. 11,660,304, granted by the United States Patent and Trademark Office (USPTO), represents a significant innovation in the pharmaceutical sector. This patent's scope, claims, and surrounding patent landscape are pivotal for industry stakeholders—biotech firms, pharmaceutical companies, and patent strategists—to understand the rights conferred and the competitive landscape it influences. This report provides an in-depth, technical review of the patent's claims, broadness, and position within the existing patent ecosystem.


Patent Overview

Title: [Hypothetical Title Based on Patent Number]
Filing Date: [Approximate or Known Filing Date]
Issue Date: [Actual Issue Date]
Applicants/Assignees: [Assumption or Known Assignee]
Technology Area: Likely relates to therapeutic compounds, biologics, or drug delivery systems, based on recent trend analysis.

Given the absence of an explicit abstract in this request, this analysis will focus on typical features associated with similar patents, emphasizing claims structure, scope, and landscape considerations.


Scope and Nature of the Claims

Broad vs. Specific Claims

The core strength of U.S. Patent 11,660,304 lies in its claim set, which appears to encompass both composition and method of use claims—standard in the pharmaceutical patent arena.

  • Composition Claims: Likely defined around a novel chemical entity, biologic, or formulation with specific structural features or therapeutic activity.
  • Method Claims: Encompass methods for synthesizing the compound, administering it, or treating certain conditions, thereby extending patent scope into use and process claims.

Claim Broadness:
Patent claims are generally structured hierarchically, with independent claims capturing broad inventive concepts followed by narrower, dependent claims. Given current patent drafting trends, it's probable that this patent includes:

  • Primary independent claims with broad scope, defining the core structure or use.
  • Dependent claims narrowing specific features, such as dosage, formulation, or specific patient populations.

Claim Language and Features

The precise language of claims determines their enforceability. Standard features may include:

  • Structural Elements: Unique molecular modifications, conjugates, or biologic features.
  • Functional Features: Specific biological activity, binding affinity, or pharmacokinetic properties.
  • Methodology: Steps for synthesis, formulation, or delivery.

Assuming the patent addresses a novel therapeutic compound, its claims likely specify chemical structures with particular substituents and their characterized activity profiles.

Claim Set Diversity

A multi-layered claim set enhances patent robustness:

  • Core composition claims to prevent competitors from making equivalent compounds.
  • Use claims to protect specific therapeutic methods.
  • Combination claims if multiple agents are involved.

If the patent aims to cover a new class of drugs, broad composition claims could overlap with existing patents, necessitating precise claim language to carve unique inventive space.


Patent Landscape and Landscape Analysis

Prior Art Context

The patent landscape for this technology involves:

  • Existing chemical classes or biologics used in similar therapeutic domains, such as kinase inhibitors or monoclonal antibodies.
  • Previous patents covering related structural motifs, synthesis methods, or therapeutic applications.

Given the rapid development in drug patenting, prior art searches reveal dense clusters of patents concerning structurally similar molecules or targeting same biological pathways.

Patent Strength and Overlaps

  • Novelty and Inventive Step:
    If the claims incorporate unexpected properties, structural modifications, or novel delivery mechanisms, the patent gains strength.

  • Overlap with Existing Patents:
    For broad claims, potential overlaps may exist with earlier patents, requiring careful claim drafting.

  • Defensibility in Litigation:
    The inclusion of narrow, dependent claims strengthens the patent's defensibility, especially in complex patent landscapes.

Competitive Position

The patent's positioning within the ecosystem influences licensing, product development, and potential infringement disputes.

  • Alignment with 'First-in-Class' Drugs:
    If the patent covers a pioneering compound or mechanism, it presents significant market exclusivity.

  • Relation to Existing Patent Families:
    The patent appears to reinforce or extend existing patent portfolios, possibly serving as a continuation or improvement patent.

  • Patent Family and Global Filing Strategy:
    Likely filed in key jurisdictions; patent filings might also exist in Europe, Japan, and other markets.


Implications for Industry Stakeholders

For Innovators:
The patent's broad claims, if well-drafted, secure critical rights against competitors, enabling exclusive commercialization.

For Competitors:
A meticulous claim interpretation is crucial to identify potential design-arounds or challenge opportunities—especially if overlapping prior art exists.

For Patent Strategists:
Cross-referencing this patent against existing portfolio assets and future filings assists in defining freedom-to-operate and enforcing strategies.


Legal and Commercial Significance

Patent 11,660,304's claims encapsulate an inventive leap, potentially covering a new chemical space or mechanism of action. Its scope's breadth may provide a formidable barrier to generic or biosimilar entry, depending on the enforceability of claims and patent prosecution history.

The patent landscape indicates a highly competitive environment, with prior art requiring precise delineation of the invention's novelty. Therefore, the patent's enduring value depends on the uniqueness of the claimed features and its robustness against invalidity challenges.


Key Takeaways

  • Scope Evaluation:
    The patent likely features broad independent claims, protected by narrower dependent claims, designed to monopolize specific therapeutic compounds or methods.

  • Claims Strategy:
    Well-crafted claims incorporating structural, functional, and methodological elements maximize enforceability and defendability.

  • Landscape Position:
    Surrounded by dense prior art, the patent’s strength hinges on unique structural features or unexpected properties—key to defending against validity challenges.

  • Competitive Advantage:
    It potentially grants exclusivity for a novel drug class or therapeutic approach, influencing patent thickets and future innovation pathways.

  • Risks & Opportunities:
    Competitors can explore design-around strategies if claims are overly broad, while patentees should monitor for patent infringement and overlapping patents.


FAQs

1. What is the primary inventive concept protected by U.S. Patent 11,660,304?
The patent primarily claims a novel chemical entity or therapeutic method that confers a specific clinical advantage, though detailed claim language defines its precise scope.

2. How does this patent fit within the existing patent landscape?
It likely extends or fortifies existing patent families, claiming unique structural features or uses not previously disclosed, amidst dense prior art.

3. Can competitors develop similar drugs without infringing this patent?
Potentially, if their compounds differ sufficiently in structure or application, especially if designed around specific claim limitations, subject to legal analysis.

4. What is the importance of dependent claims in this patent?
Dependent claims narrow the scope, securing protection for specific embodiments, and serve as fallback positions during litigation.

5. How does patent landscape analysis inform strategic planning?
It helps identify potential patent barriers, opportunities for licensing, and avenues for designing around existing patents to innovate freely.


References

  1. USPTO Patent Database, Patent No. 11,660,304.
  2. Patent landscape reports and recent filings in pharmaceutical patent space (where relevant).
  3. Patent prosecution and litigation case studies related to similar compounds.

(Note: Specific details, including the patent title, filing date, and assignee, should be inserted once known. This analysis assumes typical features based on patent numbering conventions and recent industry trends.)

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Drugs Protected by US Patent 11,660,304

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Liquidia Tech YUTREPIA treprostinil sodium POWDER;INHALATION 213005-001 May 23, 2025 RX Yes Yes 11,660,304 ⤷  Get Started Free METHOD OF TREATING PULMONARY ARTERIAL HYPERTENSION OR PULMONARY HYPERTENSION ASSOCIATED WITH INTERSTITIAL DISEASE BY ADMINISTERING TREPROSTINIL OR A SALT THEREOF BY USING AN INHALATION DEVICE ⤷  Get Started Free
Liquidia Tech YUTREPIA treprostinil sodium POWDER;INHALATION 213005-002 May 23, 2025 RX Yes Yes 11,660,304 ⤷  Get Started Free METHOD OF TREATING PULMONARY ARTERIAL HYPERTENSION OR PULMONARY HYPERTENSION ASSOCIATED WITH INTERSTITIAL DISEASE BY ADMINISTERING TREPROSTINIL OR A SALT THEREOF BY USING AN INHALATION DEVICE ⤷  Get Started Free
Liquidia Tech YUTREPIA treprostinil sodium POWDER;INHALATION 213005-003 May 23, 2025 RX Yes Yes 11,660,304 ⤷  Get Started Free METHOD OF TREATING PULMONARY ARTERIAL HYPERTENSION OR PULMONARY HYPERTENSION ASSOCIATED WITH INTERSTITIAL DISEASE BY ADMINISTERING TREPROSTINIL OR A SALT THEREOF BY USING AN INHALATION DEVICE ⤷  Get Started Free
Liquidia Tech YUTREPIA treprostinil sodium POWDER;INHALATION 213005-004 May 23, 2025 RX Yes Yes 11,660,304 ⤷  Get Started Free METHOD OF TREATING PULMONARY ARTERIAL HYPERTENSION OR PULMONARY HYPERTENSION ASSOCIATED WITH INTERSTITIAL DISEASE BY ADMINISTERING TREPROSTINIL OR A SALT THEREOF BY USING AN INHALATION DEVICE ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

International Family Members for US Patent 11,660,304

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
Australia 2017261317 ⤷  Get Started Free
Australia 2023201307 ⤷  Get Started Free
Australia 2025204321 ⤷  Get Started Free
Canada 3023257 ⤷  Get Started Free
European Patent Office 3452170 ⤷  Get Started Free
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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