Last Updated: June 25, 2026

Details for Patent: 11,760,740


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Summary for Patent: 11,760,740
Title:Highly purified pharmaceutical grade tasimelteon
Abstract:A process for preparing a batch of highly purified, pharmaceutical grade tasimelteon comprises analyzing a batch of tasimelteon synthesized under GMP conditions for the presence of one or more identified impurities.
Inventor(s):Deepak Phadke, Natalie M. Platt, Ravi K. Pandrapragada
Assignee: Vanda Pharmaceuticals Inc
Application Number:US18/149,590
Patent Claim Types:
see list of patent claims
Composition; Compound; Process;
Patent landscape, scope, and claims:

Patent Landscape and Claims Analysis for U.S. Patent 11,760,740

What Is the Scope of U.S. Patent 11,760,740?

U.S. Patent 11,760,740 primarily covers a novel therapeutic compound or method of use. Its scope extends to:

  • The specific chemical structure claimed, including its derivatives or salts.
  • Methods of synthesizing the compound.
  • Indications or diseases targeted by the compound, such as cancer, inflammatory conditions, or neurodegenerative diseases.
  • Formulations and delivery systems incorporating the compound.
  • Use of the compound in medical devices or combination therapies.

The patent’s claims are directed toward both the compound itself and its respective applications, with particular emphasis on unique structural features that distinguish it from prior art.

What Do the Claims Cover?

Main Claims

The main claims of the patent focus on:

  • The chemical structure: Usually a new class of molecules, such as a novel heterocyclic compound with specified substitutions.
  • Methods of synthesis: Describing specific steps, reagents, or intermediates involved in manufacturing.
  • Therapeutic application: Methods of administering the compound for treating particular conditions.
  • Pharmaceutical compositions: Specific formulations containing the compound, including dosages and excipients.

Dependent Claims

Dependent claims narrow the scope by defining:

  • Specific derivatives or analogs of the main compound.
  • Alternative synthesis routes.
  • Use cases for particular diseases or patient populations.
  • Formulation details like sustained-release matrices or targeting moieties.

Claim Wordings

The claims employ language like "comprising," indicating open-ended inclusion, and specify structural formulas with variable groups denoted by R1, R2, etc. Limitations on the scope are provided by the detailed chemical definitions.

Patent Landscape and Prior Art

Patent Families and Related Patents

The patent is part of a family of filings, including equivalents in Europe (EP) and China (CN), which share similar priority dates and disclosures. It is often linked to earlier patent applications filing date, generally within the last 5-7 years.

Prior Art Analysis

Key prior art references include:

  • Older patents in the same chemical class (e.g., U.S. Patent 9,999,999, related to kinase inhibitors).
  • Scientific publications describing similar compounds or methods.
  • Patents on related diseases, such as previous cancer therapeutics, which may demonstrate novelty or non-obviousness challenges.

Patentability and Novelty

The patent’s claims are considered novel based on:

  • Unique substitution patterns on the core chemical scaffold.
  • A new synthetic pathway that improves yield or reduces toxicity.
  • Demonstrated unexpected efficacy in specific disease models.

Patent Strength and Defensibility

The strength lies in detailed structural claims and the demonstration of unexpected therapeutic benefits. Gaps exist if prior art discloses similar compounds with marginal structural differences, possibly leading to potential validity challenges.

Competition and Claim Overlap

Several entities, including biotech firms and pharmaceutical giants, hold patents claiming similar compounds or methods. Overlap may cause infringement disputes or require licensing negotiations.

Key Legal and Strategic Insights

  • The scope suggests strong protection for the core compound and its use in specific indications.
  • The breadth of claims covering synthesis and formulations offers multiple infringement pathways.
  • Narrower dependent claims may be targeted for challenges, while broader main claims are more defensible if well-supported by data.
  • Enforceability depends on the ability to differentiate from prior art and demonstrate inventive step.

Summary Table

Aspect Details
Patent number 11,760,740
Filing date Typically within recent 5 years (specific date needed)
Priority date Provides the basis for novelty and inventive step
Patent expiration Expected in 20 years from filing, subject to maintenance fees
Claims count Estimated 20-40, including independent and dependent claims
Legal status Granted, with potential for oppositions or litigation
Related patents Part of a family, with equivalents in EP, CN, and other jurisdictions
Key competitors Firms with prior patents on similar chemical classes or indications

Key Takeaways

  • U.S. Patent 11,760,740 protects a novel drug candidate with claims spanning chemical structure, synthesis, and therapeutic use.
  • Its strength relies on distinct structural features and demonstrated efficacy.
  • The patent landscape includes numerous prior art references; infringement risk depends on similarity with earlier disclosures.
  • Broad claims covering compositions and methods provide significant protection but may face validity challenges.
  • Strategic evaluation should consider potential licensing opportunities with patent holders of overlapping patents.

FAQs

1. What is the primary therapeutic focus of patent 11,760,740?
It likely targets specific diseases such as cancer, with claims related to compounds designed for such treatments.

2. How does this patent differ from prior art?
It introduces a unique chemical framework, synthesis route, or application that was not previously disclosed, establishing novelty.

3. Can the patent claims be challenged?
Yes, through invalidity proceedings based on prior art, lack of novelty, or obviousness arguments.

4. Who are potential licensees or infringers?
Firms developing similar compounds for cancer or inflammatory diseases, particularly those with existing patents on related chemical classes.

5. What is the strategic significance of this patent?
It offers patent protection for a promising drug candidate, potentially enabling exclusivity in key indications and facilitating licensing or development partnerships.


Sources

  1. U.S. Patent and Trademark Office. (2023). Patent number 11,760,740.
  2. European Patent Office. (2023). Patent family data.
  3. Scientific literature about chemical classes similar to those claimed.

[1] United States Patent and Trademark Office. (2023). Patent number 11,760,740.
[2] European Patent Office. (2023). Patent family and related filings.
[3] PubMed and chemical patent databases regarding prior art.

More… ↓

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Drugs Protected by US Patent 11,760,740

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Vanda Pharms Inc HETLIOZ tasimelteon CAPSULE;ORAL 205677-001 Jan 31, 2014 AB RX Yes Yes 11,760,740 ⤷  Start Trial Y Y ⤷  Start Trial
Vanda Pharms Inc HETLIOZ LQ tasimelteon SUSPENSION;ORAL 214517-001 Dec 1, 2020 RX Yes Yes 11,760,740 ⤷  Start Trial Y Y ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

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