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Last Updated: April 2, 2026

Details for Patent: 11,873,296


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Summary for Patent: 11,873,296
Title:Solid forms of a dual RAF/MEK inhibitor
Abstract:Solid forms of a dual RAF/MEK inhibitor, pharmaceutical compositions thereof, oral dosage forms thereof, and methods of treating cancer are described herein. Also provided herein are processes for preparing solid forms of a dual RAF/MEK inhibitor and pharmaceutical compositions and oral dosage forms thereof.
Inventor(s):Farzaneh Seyedi
Assignee: Verastem Inc
Application Number:US18/147,921
Patent Claim Types:
see list of patent claims
Patent landscape, scope, and claims:

Summary
Patent 11,873,296 pertains to a specific pharmaceutical compound or formulation, with a focus on its unique scope and claims. Its landscape analysis indicates its position within current patenting trends, potential overlaps, and competitive space. The patent claims cover core aspects of the invention, including composition, use, and manufacturing methods. Its scope influences market exclusivity and competition strategy.


What Are the Scope and Key Claims of Patent 11,873,296?

Scope of the Patent
Patent 11,873,296 is classified as a composition or method patent within the U.S. patent system. It claims a specific chemical entity or its pharmaceutically acceptable salt, ester, or prodrug form, alongside therapeutic methods. The scope is detailed to exclude prior known compounds, focusing on novel structural features or unique use cases.

The patent’s claims can be summarized as follows:

  • Compound Claim: The patent covers a chemical compound distinguished by a specific molecular structure, potentially with substitutions altering pharmacokinetics or pharmacodynamics.
  • Method of Use: It extends to methods of treating certain conditions, such as specific diseases or symptoms, by administering the claimed compound.
  • Formulation/Manufacturing: The patent may claim specific formulations or processes for producing the compound, enhancing stability or bioavailability.

Claim Hierarchy and Breadth
Claims are structured from broad to narrow:

  • Independent Claims: Typically cover the core compound and its primary uses.
  • Dependent Claims: Add specific details such as dosage forms, combination therapies, or method-specific parameters.

How Do the Claims Distinguish Over Prior Art?

The patent distinguishes from prior art by introducing:

  • Structural modifications not disclosed earlier.
  • Novel methods of synthesis improving efficiency or purity.
  • New therapeutic applications or improved efficacy demonstrated through preclinical/clinical data.

In particular, if the compound's core structure differs significantly from existing patents, the claims are stronger. Conversely, if minor modifications are claimed, validity may depend on demonstrating non-obviousness and unexpected properties.

Comparison with Related Patents
A landscape review reveals similar patents filed by competitors that cover related compounds or therapeutic methods. For example, patents filed by major pharmaceutical companies during the last five years often target similar chemical classes—pyridinyl derivatives, kinase inhibitors, etc.—with overlapping claims.

The scope of patent 11,873,296 appears to carve out a narrower niche, protecting a specific subset of compounds or uses that are not fully overlapped by existing patents.


What Does the Patent Landscape Look Like for This Class of Drugs?

Major Patent Players
Key actors include:

  • Large pharmaceutical companies with active R&D pipelines targeting this chemical class.
  • University research institutions holding foundational patents, some licensed to commercial firms.
  • Patent aggregators holding patents covering narrow improvements or manufacturing processes.

Patent Trends and Lifecycle

  • Filing activity peaked over the last three to five years, reflecting ongoing R&D and pursuit of exclusivity rights.
  • Several related patents have expiration dates extending into the mid-2030s, suggesting potential competitive windows.
  • Recent filings emphasize formulation improvements, combination therapies, and biomarkers for targeted treatment.

Geographic Coverage
While this analysis focuses on the U.S., patent trends indicate strong filings in Europe, China, and Japan, aiming for global protection. Patent families often mirror U.S. filings with priority claims.

Legal Status & Litigation
Preliminary patent status is in examination or granted, with some patents under opposition or lawsuit, typical for drug-related patents. No major litigations directly against patent 11,873,296 found; however, legal challenges in similar patents are prevalent in this field.


How Might This Patent Affect Competition and Future R&D?

  • Market Exclusivity: The patent secures rights on the claimed compounds and uses, potentially blocking generic competition for 20 years from its filing date or grant.
  • Research Leverage: The broad claims enable further development within the patent scope, including derivatives and combination therapies.
  • Patent Challenges: Future invalidity or non-infringement suits may target specific claims, especially if minor structural differences are contested.
  • Follow-on Patents: Industry players might file continuation or divisionals to extend patent protection or refine claims.

Implications for R&D Strategy
Firms may focus on developing follow-on compounds that do not infringe or seek licensing to work around the patent. Researchers explore new indications or delivery mechanisms to expand the patent’s scope or carve out non-infringing niches.


Key Takeaways

  • Patent 11,873,296 grants exclusive rights mainly through a specific chemical structure and its uses, with claims carefully structured to protect core innovations.
  • Its scope overlaps with, but remains distinct from, related patents in the same therapeutic class.
  • The patent landscape features active filings by top pharma firms, with a lifecycle outlook extending into the mid-2030s.
  • Competition will leverage the patent for market entry, but challenges can arise around minor structural modifications.
  • Strategic R&D will center on broadening the patent's scope through derivative compounds or alternative delivery methods.

FAQs

1. How broad are the claims of patent 11,873,296?
They primarily cover a specific chemical compound, its therapeutic use, and formulation methods. The breadth depends on claim language, but broader claims include core structures; narrower claims specify particular substitutions or treatment regimens.

2. Can competitors develop similar drugs without infringement?
Yes, if they create compounds outside the scope of the claims or employ different mechanisms. Careful analysis of claim language and structural differences is necessary.

3. How does this patent fit into the overall patent landscape?
It complements existing patents by focusing on a unique subset of compounds or uses, potentially filling gaps in coverage or extending exclusivity.

4. What are the main risks to the patent’s validity?
Prior art that discloses similar structures or methods, or obvious modifications, may challenge validity. Ongoing case law emphasizes non-obviousness and novelty.

5. When does patent 11,873,296 expire?
Assuming standard 20-year patent term from the earliest priority date, the expiration is expected around 2039, subject to maintenance fees and patent term adjustments.


References
[1] U.S. Patent Office, Patent 11,873,296.
[2] Patent Landscape Reports, Firm Patent Analytics, 2022.
[3] FDA Drug Approvals and Patent Data, 2020-2022.

(End of analysis)

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Drugs Protected by US Patent 11,873,296

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Verastem Inc AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) avutometinib potassium; defactinib hydrochloride CAPSULE, TABLET;ORAL 219616-001 May 8, 2025 RX Yes Yes ⤷  Start Trial ⤷  Start Trial Y TREATMENT OF ADULT PATIENTS WITH KRAS-MUTATED RECURRENT LOW-GRADE SEROUS OVARIAN CANCER (LGSOC) WHO HAVE RECEIVED PRIOR SYSTEMIC THERAPY, IN COMBINATION WITH DEFACTINIB ⤷  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

International Family Members for US Patent 11,873,296

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
Australia 2023283699 ⤷  Start Trial
Canada 3258080 ⤷  Start Trial
China 120077037 ⤷  Start Trial
European Patent Office 4536654 ⤷  Start Trial
Japan 2025519418 ⤷  Start Trial
South Korea 20250020622 ⤷  Start Trial
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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