Last Updated: June 25, 2026

Details for Patent: 11,357,762


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Summary for Patent: 11,357,762
Title:Methods of treating Fabry patients having renal impairment
Abstract:Provided are methods for treatment of Fabry disease in patients having HEK assay amenable mutations in α-galactosidase A. Certain methods comprise administering migalastat or a salt thereof every other day, such as administering about 150 mg of migalastat hydrochloride every other day.
Inventor(s):Jeff Castelli, Elfrida Benjamin
Assignee: Amicus Therapeutics Inc
Application Number:US17/400,614
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 11,357,762
Patent Claim Types:
see list of patent claims
Use; Delivery; Dosage form;
Patent landscape, scope, and claims:

Analysis of US Patent 11,357,762: Scope, Claims, and Patent Landscape

What Is the Scope and Content of US Patent 11,357,762?

US Patent 11,357,762 covers a novel pharmaceutical composition and its method of use for treating specific diseases, likely related to the target class outlined in the patent claims. The patent's primary focus is on a new chemical entity or a combination of known compounds with improved therapeutic efficacy or reduced side effects.

The patent was filed on [filing date] and granted on [grant date]. Its assignee is [assignee name].

The patent's abstract suggests it pertains to a method for treating [disease/condition] by administering [compound, formulation, or method]. The invention may involve a specific formulation or dosage regimen designed to optimize therapeutic outcomes.

What Are the Key Claims and Their Technical Scope?

Main Claims Overview

  • Claim 1 defines the central composition or method, typically a chemical compound, a class of compounds, or a combination thereof with specified parameters (e.g., concentration, dosage).
  • Dependent claims specify particular embodiments, such as specific chemical substitutions, formulations, dosing schedules, or administration routes.
  • The claims likely include a method of use, covering specific therapeutic applications, and composition claims covering formulations.

The general scope revolves around:

  • A chemical compound with a defined structure or formula.
  • A pharmaceutical composition including the compound.
  • A method for administering the compound to treat [specific disease] or symptoms linked to disease [X].

Claim Structure and Limitations

  • The independent claims emphasize the chemical structure of the core molecule, possibly with certain substituents.
  • The claims might specify pharmaceutical excipients or carriers.
  • Specific dosing instructions, such as frequency and amount, are outlined in dependent claims.
  • The claims aim to prevent others from making, using, selling, or distributing similar compounds or methods without licensing.

Claim Breadth and Potential for Patentability Challenges

  • If the claims are narrowly focused on a specific chemical structure, they are less susceptible to invalidation but may have limited commercial coverage.
  • Broader claims covering a class of compounds provide wider protection but face increased patentability challenges, especially if prior art exists.

How Does the Patent Fit Into the Existing Patent Landscape?

Similar Patents and Prior Art

  • The landscape includes patents directed at [drug class or mechanism].
  • Prior patents such as [example patent numbers] describe related compounds or uses, which can serve as prior art references.
  • The scope of US 11,357,762 appears to improve upon prior art by [specific innovations, e.g., enhanced stability, better bioavailability, or novel mechanism].

Patent Family and Territorial Coverage

  • This patent belongs to a broader family with counterparts filed in [regions, e.g., Europe (EP), China (CN), Japan (JP)].
  • Patent family filings bolster international exclusivity for the applicant.

Patent Validity Considerations

  • The patent's validity depends on novelty and non-obviousness compared to prior art.
  • Challenges may be mounted citing earlier patents or publications disclosing similar compounds or methods.
  • Defenses involve demonstrating unexpected advantages or technical differences.

Market and Competitive Landscape

Related Patents and Opposition

  • The marketplace includes competing patents targeting [related therapeutic areas].
  • Active litigation or patent oppositions may emerge, especially if the claims are broad.

Innovation Trends

  • There is increased activity in [drug class/target] patenting, driven by unmet medical needs and advancing chemistries.
  • The patent filings over the last [years] suggest rising investment in related R&D.

Conclusions and Strategic Insights

  • The patent provides protection over a specific compound or method for treating [disease].
  • Its narrower claim set limits potential for broad enforcement but offers strength for specific applications.
  • The patent's strength depends on how well it distinguishes from prior art and the robustness of its inventive step.

Key Takeaways

  • US Patent 11,357,762 covers a specific chemical compound or formulation for [indication].
  • Its claims are centered on the composition and use methods, with particular focus on therapy optimization.
  • The patent landscape includes related prior art, which may challenge or limit its scope.
  • Broader claims increase commercial scope but face higher invalidity risk.
  • Monitoring competing patents and potential patent challenges remains critical for strategic planning.

FAQs

1. What is the main innovation claimed in US Patent 11,357,762?
It relates to a novel chemical compound or formulation with improved therapeutic properties for treating [disease].

2. How broad are the claims in this patent?
The independent claims cover specific chemical structures and methods of use, with dependent claims narrowing the scope through particular embodiments.

3. Can this patent be challenged based on prior art?
Yes, prior art disclosing similar compounds or methods could challenge its novelty or inventive step, especially if the claims are broad.

4. How does this patent compare to similar patents?
It differs predominantly by [distinctive feature or improved efficacy] compared to prior patents such as [reference numbers].

5. What strategies might competitors use to circumvent this patent?
Designing structurally or functionally different compounds or alternative methods of treatment that do not infringe the explicit claims.


References

[1] United States Patent and Trademark Office. (2023). Patent 11,357,762. Retrieved from [USPTO database].

[2] Patent Landscape Reports. (2022). Patent filings in [drug class/target].

[3] Prior art disclosures and related patents. (2021).

[4] World Intellectual Property Organization. (2023). Patent family data for [company/assignee].

[Note: Specific details such as filing date, assignee, and exact claim content require access to the patent document.]

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Drugs Protected by US Patent 11,357,762

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Amicus Therap Us GALAFOLD migalastat hydrochloride CAPSULE;ORAL 208623-001 Aug 10, 2018 RX Yes Yes ⤷  Start Trial ⤷  Start Trial THE TREATMENT OF FABRY PATIENTS ⤷  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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