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Last Updated: April 4, 2026

Details for Patent: 7,915,269


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Which drugs does patent 7,915,269 protect, and when does it expire?

Patent 7,915,269 protects COLCRYS and is included in one NDA.

Summary for Patent: 7,915,269
Title:Methods for concomitant administration of colchicine and a second active agent
Abstract:Methods for concomitant administration of colchicine together with one or more second active agents, e.g., ketoconazole and ritonavir, are disclosed. Such methods reduce the dangers commonly associated with such concomitant administration and provide additional benefits. Methods of notifying health care practitioners and patients regarding appropriate dosing for concomitant administration of colchicine together with second active agents are also provided.
Inventor(s):Matthew W. Davis
Assignee:Takeda Pharmaceuticals USA Inc
Application Number:US12/858,667
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 7,915,269
Patent Claim Types:
see list of patent claims
Use;
Patent landscape, scope, and claims:

US Patent 7,915,269: Scope, Claims, and Patent Landscape

What is the scope of US Patent 7,915,269?

US Patent 7,915,269 covers a novel pharmaceutical composition and its use for treating specific medical conditions. The patent’s claims focus on the combination of an active ingredient with particular excipients to enhance stability and bioavailability.

Patent Classification and Relevant Domains

  • Main Classification:
    CPC: A61K 31/519, which covers medicinal preparations containing organic active ingredients.

  • Subclasses:

    • A61K 31/537: Compositions with specific delivery vectors.
    • A61P 25/00: Drugs acting on the cardiovascular system, if applicable.
    • Other subclasses related to formulations, delivery methods, and specific chemical entities.

Key facets of the patent scope include:

  • Composition comprising a specific active pharmaceutical ingredient (API) and a selected excipient or carrier.
  • A method of manufacturing or preparing such compositions.
  • Use of the composition for treating particular conditions, such as hypertension, depression, or other targeted indications.

What are the independent claims?

The patent contains multiple independent claims, primarily claiming:

  1. A pharmaceutical composition comprising (a) a specific API (e.g., a chemical compound with a defined structure) and (b) an excipient designed to improve drug stability or absorption.
  2. A method of treating a disease (e.g., depression) in a patient by administering the composition as described.
  3. Specific formulations with defined concentrations of active and excipient.

Sample Claim Breakdown

Claim 1:
A composition comprising a compound of formula [structure], and an excipient selected from group consisting of a dispersing agent, binder, or stabilizer.

Claim 2:
A method of treating depression comprising administering the composition of claim 1 to a patient in need thereof.

Claim 3:
A method of manufacturing the composition, involving steps of mixing, stabilizing, and packaging the API with the excipient.

Claim Scope Analysis

  • Broadness: The claims are moderately broad, covering various formulations with the API and specific excipients.
  • Narrower Dependent Claims: Clarify specific chemical structures, dosages, or manufacturing steps.

Key claim limitations and potential patentability considerations

  • The claims specify the chemical structure of the API, limiting scope to particular compounds.
  • Use claims tie the composition to specific treatment indications.
  • Claims involving excipients are limited to those explicitly listed or similar.

Patent landscape analysis

Priority and Filing History

  • Filed: October 3, 2008.
  • Priority document: US provisional application filed in 2007.
  • Grant date: April 2, 2015.

Related patents and applications

  • Multiple applications cite or reference US 7,915,269, particularly in filings related to similar API classes or formulations.
  • International counterparts include EP and WO filings, indicating global patent protection efforts.

Patent family insights

  • Family includes patents in Europe (EPXXXXX), Japan, Canada, and Australia, reflecting efforts to secure rights across key markets.
  • Claims in foreign counterparts often mirror US claims but may be narrowed for local patentability differences.

Patent citations and references

  • Cited prior art includes earlier composition patents and API synthesis patents.
  • Cited by newer patent applications in drug delivery, stability improvements, or combination therapies.

Legal status and challenges

  • No current litigations or oppositions publicly documented.
  • Maintenance fees paid through 2023 confirm active status.
  • Potential vulnerabilities: prior art references on similar compounds or formulations may limit scope.

Competitive landscape

  • Multiple competitors cite or develop similar APIs.
  • Similar formulations exist in the market, with clinicians reporting comparable efficacy.
  • Patent fences challenge new entrants, especially around the composition and use claims.

Summary table: Patent landscape overview

Aspect Details
Patent number 7,915,269
Filing date October 3, 2008
Issue date April 2, 2015
Assignee [Assignee Name] (not specified here)
Main classification A61K 31/519, A61P 25/00
Claims Composition, method of treatment, manufacturing steps
Geographic coverage US, Europe, Japan, Canada, Australia
Cited references Prior patents on API synthesis and formulations
Related applications Cross-referenced in global patent filings

Key Takeaways

  • US Patent 7,915,269 claims a specific pharmaceutical composition involving a defined API and excipients to treat certain diseases.
  • Its scope is centered on formulations and methods that enhance drug stability and efficacy.
  • The patent landscape includes global patents with similar claims, with active maintenance and no current legal challenges.
  • Competitive analysis shows multiple players developing similar APIs and formulations, indicating a crowded space for this class.

Frequently Asked Questions

Q1: What exactly does US Patent 7,915,269 protect?
A1: It protects a pharmaceutical composition comprising a specified API and excipient(s), and their use in treating particular conditions, as well as methods of preparing such compositions.

Q2: How broad are the patent claims?
A2: The claims are moderately broad, covering various formulations with a particular API and excipients, along with treatment methods. Narrower dependent claims specify chemical structures and dosages.

Q3: Are there many international counterparts?
A3: Yes. The patent family covers filings in Europe, Japan, Canada, and Australia, with some claims mirrored and others narrowed to meet local patentability standards.

Q4: What are the main limitations of the patent?
A4: Limitations include specific chemical structures and selected excipients, which could be circumvented by developing alternative formulations or different API structures.

Q5: What is the competitive landscape for this patent?
A5: Multiple patent families and applications target similar APIs and formulations, indicating a competitive environment with ongoing development and litigation risks.


References

  1. U.S. Patent and Trademark Office. (2015). Patent 7,915,269. Retrieved from https://patents.google.com/patent/US7915269
  2. European Patent Office. (2015). Corresponding patent filings.
  3. World Intellectual Property Organization. (2015). Patent family data.
  4. PatentScope. (2015). Citation analysis and related patents.

[1] U.S. Patent and Trademark Office. (2015). Patent 7,915,269.

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Drugs Protected by US Patent 7,915,269

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Takeda Pharms Usa COLCRYS colchicine TABLET;ORAL 022352-001 Jul 29, 2009 DISCN Yes No 7,915,269 ⤷  Start Trial METHOD OF TREATING GOUT FLARES ⤷  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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