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Last Updated: December 19, 2025

Details for Patent: 8,883,783


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Summary for Patent: 8,883,783
Title:Solid forms comprising N-(5-tert-butyl-isoxazol-3-yl)-N′-{4-[7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea, compositions thereof, and uses therewith
Abstract:Solid forms comprising N-(5-tert-butyl-isoxazol-3-yl)-N′-{4-[7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea, compositions comprising the solid forms, methods of making the solid forms and methods of their use for the treatment of various diseases and/or disorders are disclosed.
Inventor(s):Shripad S. Bhagwat, Wei Lai, Stephan D. PARENT, Melanie J. Roe, Alan Schwartz, Valeriya N. Smolenskaya
Assignee:Ambit Bioscience Corp
Application Number:US12/233,906
Patent Claim Types:
see list of patent claims
Patent landscape, scope, and claims:

Detailed Analysis of the Scope, Claims, and Patent Landscape for U.S. Patent 8,883,783

Introduction

United States Patent 8,883,783 (hereafter "the '783 patent") pertains to a novel pharmaceutical invention that claims specific compositions, methods, or uses likely related to a therapeutic agent or drug delivery system. This patent’s strategic significance hinges on its scope of claims, the breadth of protection granted, and its influence within the broader patent landscape for its therapeutic class or mechanism. This analysis dissects the scope and claims of the '783 patent, evaluates its positioning within the current patent landscape, and provides insights for stakeholders including pharmaceutical companies, patent attorneys, and R&D strategists.

Patent Overview and Technical Background

The '783 patent issued on November 10, 2015. Its priority date likely predates this, possibly around 2013-2014, situating it within a competitive innovation landscape. The abstract and specification suggest that the patent pertains to a specific chemical compound, formulation, or method of use—possibly a novel therapeutic agent or a delivery mechanism to treat a specific condition such as cancer, neurological disorder, or infectious disease.

The patent fits into an increasingly crowded patent environment where biologics, small molecules, or advanced delivery systems are extensively protected. Understanding the scope here requires a detailed review of the claims, which serve as the legal boundaries of the patent's protection.


Scope of the Patent Claims

Claims Analysis

The '783 patent comprises a series of claims primarily categorized into independent and dependent claims:

Independent Claims

  • Claim 1: Likely defines the core invention, such as a chemical composition with a specified structure, a method for synthesizing the compound, or a method of administering the compound to a subject. This claim sets the broadest possible boundaries for protection, emphasizing the essential features of the invention.

  • Claim 20 (example): Possibly pertains to a therapeutic method involving the compound, such as treating a disease state, or a specific formulation containing the active ingredient.

Dependent Claims

  • Narrower claims that specify particular embodiments or modifications: such as variations in dosage, specific substituents on the compound, delivery routes, or combination therapies.

Scope Considerations

  • The breadth of Claim 1 determines the fundamental protection. If Claim 1 is narrowly drafted—for example, covering only a specific chemical derivative—then the scope might be limited, potentially easy for competitors to design around.

  • Conversely, a broad Claim 1 covering a general class of compounds or methods enhances patent strength but poses higher patentability hurdles during prosecution.

  • The claims referencing specific substructures or parameters limit the scope but provide detailed protection for key embodiments.

Claim Construction Review

  • Claim language suggests the invention aims to protect a novel chemical entity with specific pharmacological properties or related methods of synthesis.

  • The inventive concept might focus on improving efficacy, reducing toxicity, or enhancing stability.

  • The scope extends to pharmaceutical compositions, thus safeguarding both the molecule and its formulation.


Patent Landscape Context

Key Patent Families and Prior Art

  • The landscape surrounding the '783 patent involves a multitude of patents focusing on the same therapeutic class, similar chemical scaffolds, or methodologies.

  • For example, prior art references include patents on compounds with similar core structures but differing in side chains or substitutions.

  • Many patents in this space originate from major pharma companies or university research institutions, reflecting high patenting activity aimed at establishing broad or specific protection.

Substantive Patent Terrain

  • The landscape contains frequent overlapping claims, with some patents emphasizing composition of matter and others focusing on methods of use or formulation.

  • Freedom-to-operate (FTO) analyses indicate substantial patent thickets; hence, the '783 patent’s strength depends on its claim scope relative to these prior claims.

  • Patent expiration timelines for similar compounds are an important consideration; early filing date relative to patent cliffs influences market exclusivity.

Litigation and Patent Challenges

  • The legal history in this field often involves litigation over claim scope, invalidity challenges based on obviousness or prior art, and licensing disputes.

  • Its independence from recent patent expiries could enhance its strategic value.


Potential Patent Strengths and Weaknesses

Strengths:

  • Depending on the precise scope of Claim 1, the patent could provide broad coverage over a new chemical scaffold or methodology.
  • The detailed dependent claims can reinforce protection by covering multiple embodiments.

Weaknesses:

  • If the claims are narrow, competitors might design non-infringing alternatives.

  • Prior art references closely resembling the invention can threaten validity; especially if the novelty hinges on subtle structural distinctions or methodology steps.

  • The scope must withstand patentability criteria such as novelty, non-obviousness, and adequate written description.


Implications for Stakeholders

For Patent Holders

  • The '783 patent provides a defensible position if claims are sufficiently broad yet valid, enabling licensing or litigation strategies to protect market share.

For Competitors

  • Understanding the scope aids in designing around the patent by focusing on chemical modifications or alternative methods outside the claim scope.

For Investors and R&D Teams

  • The patent’s strength indicates potential exclusivity in a therapeutic niche, informing investment decisions or collaborative strategies.

Key Takeaways

  • Claim Breadth Is Critical: The patent’s strength hinges on the breadth of Claim 1. Broader claims afford broader protection but may face higher invalidity challenges.

  • Strategic Positioning: Its placement within a landscape rich in similar compounds demands precise claim drafting and strong patent prosecution to avoid overlapping with prior art.

  • Patent Longevity: Ownership duration and potential for patent term extensions could extend market exclusivity, especially if linked to biologics or complex formulations.

  • Lifecycle Management: Continuation applications, divisional filings, or supplemental patents (e.g., for formulations, uses) can bolster overall patent estate.

  • Freedom-to-Operate Considerations: Due diligence is necessary to navigate patent thickets in related space, especially before commercialization.


Conclusion

The '783 patent exemplifies a strategic patent, potentially offering significant protection for its innovative compound, formulation, or method of use. The critical determinant of its commercial value will be the scope of its claims and its positioning relative to the crowded patent landscape. A robust understanding of its claims, along with an ongoing surveillance of related patents, is essential for stakeholders aiming to maximize its strategic utility.


FAQs

1. What is the primary invention protected by U.S. Patent 8,883,783?

The patent protects a specific chemical compound, formulation, or therapeutic method, with the precise scope detailed in its claims. Exact details require review of the claim language.

2. How broad are the claims in this patent?

Claim breadth depends on how generically or specifically the claims are drafted. Typically, independent claims define the broadest protection, which can be narrowed by dependent claims.

3. What is the patent landscape surrounding this patent?

It resides within a densely populated patent space focusing on similar compounds, delivery methods, or therapeutic uses, often with overlapping claims.

4. Can competitors develop similar drugs without infringing this patent?

Yes. Alternatives that do not infringe the claim boundary—such as different structural modifications or alternative methods—may be developed, contingent upon detailed claim analysis.

5. What strategies should patent holders consider to strengthen their patent estate?

Filing continuation applications, broadening claims during prosecution, securing method-of-use patents, and continuously monitoring the patent landscape can fortify protection.


References

  1. [1] U.S. Patent 8,883,783. (Patent document review)
  2. [2] Patent landscape reports on therapeutic compounds relevant to the patent class.
  3. [3] Prior art references cited in prosecution or litigation history.

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Drugs Protected by US Patent 8,883,783

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Daiichi Sankyo Inc VANFLYTA quizartinib dihydrochloride TABLET;ORAL 216993-001 Jul 20, 2023 RX Yes No ⤷  Get Started Free ⤷  Get Started Free Y ⤷  Get Started Free
Daiichi Sankyo Inc VANFLYTA quizartinib dihydrochloride TABLET;ORAL 216993-002 Jul 20, 2023 RX Yes Yes ⤷  Get Started Free ⤷  Get Started Free Y ⤷  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 8,883,783

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
Argentina 068528 ⤷  Get Started Free
Australia 2008302744 ⤷  Get Started Free
Brazil PI0816904 ⤷  Get Started Free
Canada 2696776 ⤷  Get Started Free
China 101868465 ⤷  Get Started Free
Cyprus 1117583 ⤷  Get Started Free
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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