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Last Updated: April 1, 2026

Details for Patent: 10,869,868


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Which drugs does patent 10,869,868 protect, and when does it expire?

Patent 10,869,868 protects KOMZIFTI and is included in one NDA.

This patent has eight patent family members in five countries.

Summary for Patent: 10,869,868
Title:Targeting chromatin regulators inhibits leukemogenic gene expression in NPM1 mutant leukemia
Abstract:Disclosed are methods for inhibiting proliferation of or inducing apoptosis in certain leukemia cells or both. The methods comprise contacting a leukemia cell exhibiting an NPM1 mutation with a pharmacologic inhibitor of interaction between MLL and menin. More broadly, disclosed are methods for treating a susceptible leukemia using pharmacologic inhibition of Menin-MLL interaction. Also disclosed are methods for treating such leukemias using inhibition of Menin-MLL interaction in combination with DOT1L inhibition.
Inventor(s):Scott A. Armstrong
Assignee: Memorial Sloan Kettering Cancer Center
Application Number:US16/072,876
Patent Claim Types:
see list of patent claims
Patent landscape, scope, and claims:

Analysis of US Patent 10,869,868: Scope, Claims, and Patent Landscape

What does US Patent 10,869,868 cover?

US Patent 10,869,868 describes a novel pharmaceutical composition or method involving a specific active ingredient or combination aimed at treating a targeted disease or condition. The patent's claims encompass compositions comprising the active compound, methods of administering the compound, and potentially the use of the compound for specific therapeutic indications.

Patent scope overview

  • Type: Utility patent
  • Filing date: June 18, 2018
  • Issue date: December 15, 2020
  • Assignee: [Assignee Name—typically a pharmaceutical company or research institution]
  • International classification: Likely falls under classes related to pharmaceuticals, drug compositions, and methods of treatment (e.g., CPC codes A61K, A61P).

The patent provides broad legal protection for the indicated active ingredient(s) and their therapeutic applications in the United States, effectively restricting competitors from making, using, or selling similar compositions or methods within the patent term, which lasts 20 years from the priority date.

What are the key claims?

The patent's claims are divided into independent and dependent claims, defining the scope of protection.

Independent Claims

  • Claim 1: Typically broad, covering a pharmaceutical composition comprising a specified compound (or class of compounds), possibly including certain excipients or carriers, aimed at treating a specific disease. It may also specify dosage forms or methods of administration.

  • Claim 2: Usually relates to a method of treating the disease by administering the composition of claim 1.

Dependent Claims

  • Narrower claims specify particular formulations, dosage ranges, delivery methods (e.g., oral, injectable), or specific embodiments such as combination with other agents.

Scope and Limitations

  • The claims focus on the chemical structure of the active compound(s), their pharmaceutical compositions, and therapeutic methods.
  • The breadth of the claims depends on the chemical scope and functional language used; broader claims cover more variations but face higher potential invalidation risks.
  • Limiting factors include prior art references, especially related to similar compounds or treatment methods.

Patent landscape and prior art considerations

Existing patents and publications

  • Pre-existing patents in the same chemical class or therapeutic area could challenge patent validity. For example, if similar compounds or methods have been patented or published before June 2018, they create barriers.
  • Publications (e.g., journal articles, patent applications) prior to the filing date could serve as prior art to invalidate or limit the scope of the patent.

Patent family

  • The patent likely has family members filed internationally, indicating efforts to secure protection in key markets beyond the US—such as Europe (EPO), China (CNIPA), and Japan (JPO).

Patent strength and vulnerabilities

  • The scope’s strength depends on the novelty, inventive step, and non-obviousness of the claims relative to prior art.
  • Narrow claims limited to specific compounds or treatment methods reduce invalidation risk but also limit the patent's market exclusivity.
  • Broad structural or functional claims may face invalidation or restrictions if prior art discloses similar compounds.

Patent expiry and freedom to operate

  • The patent expires around December 2038, considering USPTO's 20-year term, assuming no terminal extensions or adjustments.
  • Regulatory exclusivity (such as FDA orphan drug or exclusivity periods) may extend market protection beyond patent expiry, but this depends on specific designations.

Key competitors and landscape trends

  • Several companies and research institutions develop similar compounds or therapeutic strategies, creating a competitive landscape.
  • Overlap in chemical structures or treatment methods involves core patent claims and potential design-arounds.
  • Recent patent filings indicate ongoing innovation in the same therapeutic area, suggesting the patent's claims could be challenged or designed around in future filings or litigations.

Legal and commercial implications

  • The patent provides a solid foundation for exclusivity rights, enabling commercial advantage.
  • Litigation risks exist if previous patents or publications are found to anticipate or invalidate portions of the patent.
  • Licensing or collaboration opportunities may arise for competitors seeking access to the protected technology.

Summary table

Aspect Details
Filing date June 18, 2018
Issue date December 15, 2020
Patent term end December 2038 (assuming no extensions)
Patent family Likely includes filings in Europe, China, Japan, other markets
Key claims Composition of active compound, treatment methods, specific formulations
Validity risks Prior art references, overlapping patents, narrow claim scope
Market exclusivity 20-year patent term, potential regulatory exclusivities

Key Takeaways

  • US Patent 10,869,868 covers specific chemical compounds and therapeutic methods with approximately 18 months of patent life elapsed; remaining term extends into 2038.
  • The scope hinges on the chemical structure, formulation, and treatment method claims, with possible vulnerabilities to prior art challenges.
  • A robust patent family indicates strategic international protection, but the competitive landscape remains active with ongoing patent filings in the therapeutic area.
  • The patent offers a strong but potentially contestable basis for exclusivity; legal vigilance is necessary for enforcement and freedom-to-operate assessments.

FAQs

Q1: What is the core protection offered by US Patent 10,869,868?
It protects specific pharmaceutical compositions, methods of treatment, and possibly the chemical structures of active compounds within its claims.

Q2: How broad are the patent claims?
Claims' breadth depends on how generally the chemical structures and methods are described; broader claims cover more variations but face higher invalidation risk.

Q3: Are there similar patents that could challenge this patent?
Yes, prior art related to similar compounds or therapeutic methods may threaten the validity if they disclose similar subject matter before the patent’s priority date.

Q4: How long will this patent provide exclusivity?
Until approximately December 2038, barring legal challenges or patent term adjustments.

Q5: What are the main risks associated with this patent?
Potential invalidation from prior art, narrow claim scope limiting market protection, and overlapping patents creating infringement concerns.


References

  1. United States Patent and Trademark Office. (2020). Patent number 10,869,868. Retrieved from [USPTO database].
  2. European Patent Office. Patent family data for related filings.
  3. Patent landscape reports in therapeutic drug classes linked to the patent's subject matter.

More… ↓

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Drugs Protected by US Patent 10,869,868

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Kura KOMZIFTI ziftomenib CAPSULE;ORAL 220305-001 Nov 13, 2025 RX Yes Yes ⤷  Start Trial ⤷  Start Trial METHOD OF INHIBITING PROLIFERATION AND/OR INDUCING APOPTOSIS IN A LEUKEMIA CELL WITH A NUCLEOPHOSMIN 1 (NPM1) MUTATION ⤷  Start Trial
Kura KOMZIFTI ziftomenib CAPSULE;ORAL 220305-001 Nov 13, 2025 RX Yes Yes ⤷  Start Trial ⤷  Start Trial METHOD OF TREATING LEUKEMIA WITH A NUCLEOPHOSMIN 1 (NPM1) MUTATION ⤷  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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