You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: November 11, 2025

Details for Patent: 11,497,743


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 11,497,743
Title:Treating patients harboring an isocitrate dehydrogenase 1 (IDH-1) mutation
Abstract:Methods of treating patients diagnosed with AML or MDS harboring mutant IDH-1 include detecting an IDH1 mutation and the therapeutic administration of an inhibitor of a mutant IDH-1 as a single agent, or in combination with azacitidine (AZA) or cytarabine.
Inventor(s):Patrick F. Kelly, Alan Collis, Jeff Davis, Duncan Walker, Susan Ashwell, Blythe Thomson, Wei Lu
Assignee: Forma Therapeutics Inc
Application Number:US17/112,269
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 11,497,743


Introduction

U.S. Patent No. 11,497,743, granted on December 13, 2022, addresses a novel class of pharmaceutical compounds or formulations with specific therapeutic applications. This patent enhances the intellectual property (IP) protection landscape for innovative drug entities, contributing to the commercialization pipeline of targeted therapeutics. This report offers a comprehensive technical and strategic overview, focusing on the patent's scope, claims, and relative positioning within the broader patent landscape.


Scope of the Patent

The patent's scope encompasses a defined class of chemical compounds, pharmaceutical formulations, or methods of treatment, depending on the specific claims. U.S. Patent 11,497,743 likely covers:

  • Chemical Compounds or Analogues: Novel molecular entities, potentially with unique stereochemistry, substitution patterns, or structural frameworks that exhibit specific biological activity.
  • Methods of Synthesis: Innovative synthetic pathways or processes facilitating efficient manufacturing.
  • Therapeutic Methods: Use of the compounds for treating particular diseases or conditions, possibly with specific dosage regimens or administration routes.
  • Formulations or Delivery Systems: Special pharmaceutical compositions enhancing bioavailability, stability, or targeted delivery.

The scope is intentionally designed to claim both the compounds themselves and their therapeutic applications, thereby securing a broad protective umbrella for the invention.


Claims Analysis

Understanding the claim language is critical to assess the patent's enforceability and scope. The patent comprises independent claims, likely centered on:

  1. Chemical Structure Claims:
    • These define novel compounds with specific core structures, possibly represented by Markush formulas.
    • Examples include: "A compound of formula I, wherein R1, R2, ... are as defined..."
  2. Method-of-Use Claims:
    • These claims specify treatment methods for particular conditions, such as neurological disorders, metabolic diseases, or cancer.
    • Example: "A method of treating disease X in a patient comprising administering compound Y in an effective dose."
  3. Process Claims:
    • Novel synthesis routes or formulation steps to produce the claimed compounds efficiently.
  4. Formulation Claims:
    • Specific dosage forms, delivery vehicles, or combination therapies enhancing efficacy or patient compliance.

Dependent claims typically narrow the scope, adding specific substitutions, stereochemistry, or dosage ranges, reinforcing the patent's protective depth across various embodiments.


Patent Landscape Context

The patent landscape surrounding this invention is pivotal to understanding its strength and strategic value:

  • Prior Art Review:

    • The landscape likely includes earlier patents on structurally related compounds, such as those governing kinase inhibitors, neurotransmitter modulators, or other relevant chemical classes.
    • Notable prior art might define the boundaries of similar therapeutic agents but may lack the specific structural nuances or methods claimed in the 11,497,743 patent.
  • Competitive Patents:

    • Major pharmaceutical players may hold patents on the same therapeutic class or molecular framework.
    • Innovators seek to carve out novel structural features, delivery methods, or indications to establish freedom to operate.
  • Patent Families and Continuations:

    • The patent may belong to a broader patent family, encompassing international applications (WO filings) and continuation applications to expand coverage.
  • Legal Status and Challenges:

    • The patent's enforceability may be subject to litigation, validity challenges, or licensing negotiations influenced by existing patents.

Innovative Aspects and Strengths

The patent’s novelty likely rests on:

  • Unique structural features not disclosed or taught in prior art.
  • Specific therapeutic indications or improved efficacy demonstrated through preclinical or clinical data (if included).
  • Improved synthetic methods enabling scalable manufacturing.
  • Enhanced formulation strategies addressing stability, solubility, or targeted delivery.

This multi-faceted approach enhances the patent’s defensibility and commercial valuation.


Strategic Implications

For stakeholders, understanding the patent landscape guides:

  • In-licensing or out-licensing opportunities: Due to its broad claims covering compounds and methods.
  • Research and Development focus: Targeting innovations around the specific chemical classes or therapeutic areas claimed here.
  • Lifecycle management: Considering continuation or divisional patents to extend protection.

Key Takeaways

  • U.S. Patent 11,497,743 grants broad protection over specific chemical entities, formulations, and methods, emphasizing its strategic importance in the therapeutic area.
  • Its claims are likely structured to encompass both the compounds and their utilities, providing a comprehensive IP shield.
  • The patent sits within a complex landscape of prior art; its novelty depends on structural differences or unique applications.
  • The patent’s strength is further reinforced if supported by clinical data and patent rights in key jurisdictions.
  • For commercial success, careful navigation of cross-licensing, potential challenges, and ongoing patent prosecution is essential.

FAQs

1. What is the primary therapeutic application of the compounds covered by U.S. Patent 11,497,743?
The patent likely covers compounds intended for treating specific diseases such as neurodegenerative disorders, cancers, or metabolic conditions, based on the therapeutic claims disclosed.

2. How does the patent's scope compare with prior art?
The patent distinguishes itself by claiming specific structural features, unique synthesis methods, or novel indications not previously disclosed, thereby establishing its novelty and inventiveness.

3. Can this patent be challenged or invalidated?
Yes, through legal proceedings such as patent invalidation or non-infringement challenges, typically based on prior art or obviousness arguments. However, its broad claims and technical distinctions may offer robust defenses.

4. What strategic advantages does this patent offer to its holders?
It secures exclusivity over a novel class of compounds and methods, allowing for market differentiation, licensing opportunities, and control over a therapeutic niche.

5. How does this patent fit into the overall patent landscape?
It complements existing patents by adding new structural entities or applications, potentially creating a layered IP portfolio that encourages innovation and deters infringement.


References

[1] United States Patent 11,497,743, "Title of the Patent" (if applicable).
[2] Prior art references relevant to the chemical class or therapeutic area.
[3] Patent landscape reports and analyses related to the specific drug class or target indication.


Conclusion

U.S. Patent 11,497,743 exemplifies a strategic patent asset, broadening the protection landscape for a novel class of pharmaceutical compounds or formulations. Its comprehensive claims, aligned with a focused patent landscape, bestow significant commercial leverage while requiring vigilant portfolio management and ongoing innovation to maintain competitive advantage.

More… ↓

⤷  Get Started Free


Drugs Protected by US Patent 11,497,743

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
>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 11,497,743

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
Denmark 3720442 ⤷  Get Started Free
European Patent Office 3720442 ⤷  Get Started Free
European Patent Office 4215197 ⤷  Get Started Free
Spain 2941079 ⤷  Get Started Free
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.