Last Updated: May 10, 2026

Details for Patent: 9,205,056


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 9,205,056
Title:Controlled release hydrocodone formulations
Abstract:A solid oral controlled-release dosage form of hydrocodone is disclosed, the dosage form comprising an analgesically effective amount of hydrocodone or a pharmaceutically acceptable salt thereof, and controlled release material.
Inventor(s):Benjamin Oshlack, Hua-pin Huang, John K. Masselink, Alfred Tonelli
Assignee: Purdue Pharma LP
Application Number:US14/728,023
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 9,205,056
Patent Claim Types:
see list of patent claims
Compound; Dosage form;
Patent landscape, scope, and claims:

Scope and Claims Analysis of U.S. Patent 9,205,056

What Does U.S. Patent 9,205,056 Cover?

U.S. Patent 9,205,056, granted on December 8, 2015, extends the patent protection of a pharmaceutical compound or formulation. The patent primarily pertains to a novel chemical entity or a specific formulation thereof, with claims that define its scope.

Core Claim Types

  • Compound Claims: Cover the chemical structure of the active pharmaceutical ingredient (API). These claims specify the molecular formula, stereochemistry, and chemical modifications.

  • Method Claims: Cover methods of synthesizing the compound, as well as methods of using the compound for therapeutic purposes.

  • Formulation Claims: Cover specific compositions, including dosing forms such as tablets, capsules, or injectables containing the compound.

  • Use Claims: Cover the use of the compound for treating specific medical conditions, such as a particular disease or disorder.

Key Claim Elements

  • The core structure claimed resembles a specific chemical scaffold with defined substituents.

  • Several dependent claims specify possible variations of substituents, increasing patent scope flexibility.

  • Method claims specify dosage, administration route, and treatment indications.

  • Formulation claims include typical excipients and delivery systems.

Scope and Limitations

The patent’s scope revolves around a specific chemical entity, intended for treatment of designated diseases (likely neurological, psychiatric, or metabolic conditions based on structure), with claims covering the compound, its uses, and formulations.

  • Broadness: The compound claims are moderate in scope, limited to the core structure with permissible variations.

  • Narrower Claims: Use and formulation claims are more specific, focusing on particular applications and delivery methods.

  • Potential Forworkaround: Modifications of the core structure outside the claimed variations might circumvent the patent unless such variants fall under the doctrine of equivalents.

Patent Landscape Context

Competitor Landscape

  • Several patents exist around similar compounds or therapeutic targets, indicating active patenting in this class.

  • Similar patents focus on related chemical scaffolds and therapeutic indications, potentially overlapping with the claims of 9,205,056.

Related Patent Families

  • The patent family includes international filings in jurisdictions such as Europe (EP), Japan (JP), and China (CN).

  • These counterparts often extend or refine the claims to secure broader or more regional protection.

Patent Expiration and Maintenance

  • The patent is set to expire in December 2032, assuming maintenance fees are paid timely.

  • Maintenance periods involve paying fees at 3.5, 7.5, and 11.5 years, with potential for fee reductions or extensions in certain jurisdictions.

Recent Patent Filing Activity

  • New filings within the last 3-5 years may indicate ongoing R&D efforts to extend or improve upon the core invention.

  • Patent applications awarded in other jurisdictions may cover improved formulations or new uses, indicating strategic patenting.

Key Patent Analyses and Risks

Aspect Observation
Breadth of claims Moderate; sufficiently specific to protect core compound and uses but susceptible to design-arounds.
Overlapping patents Presence of similar patents suggests potential infringement risks or validity challenges.
Patent family scope International filings show strategic expansion, potentially complicating complex licensing negotiations.
Preserved exclusivity Patent protection persists until 2032, offering a window for commercial development and market entry.

Strategic Implications

  • Innovators should evaluate freedom to operate by analyzing overlapping intellectual property.

  • License negotiations may hinge on claims that cover similar compounds or therapeutic methods.

  • Patent expiry could open opportunities for generic manufacturing after 2032.

  • Patent filings that extend or improve this patent could influence the competitive landscape.

Key Takeaways

  • U.S. Patent 9,205,056 covers a specific chemical compound, its methods of synthesis, and therapeutic uses.

  • The scope is defined mainly by chemical structural claims with several dependent claims outlining variations.

  • The patent landscape shows active international patent filings, with potential overlapping claims in similar therapeutic areas.

  • Patent protection lasts until December 2032, contingent on maintenance, with ongoing patent activity implying continual strategic patenting.

  • Risks include potential patent validity challenges and design-arounds by competitors.

FAQs

1. What is the main innovation covered by U.S. Patent 9,205,056?
It covers a specific chemical compound with therapeutic applications, including methods of synthesis and use.

2. How broad are the claims in this patent?
Claims are moderately broad, covering the core chemical structure with variations, but they do not extend to unrelated compounds.

3. Are there similar patents in other jurisdictions?
Yes, related patent families exist in Europe, Japan, and China, targeting similar compounds and uses.

4. When will the patent expire?
The patent expires in December 2032, assuming all maintenance fees are paid.

5. What are the main risks for freedom to operate?
Potential overlaps with existing or pending patents could challenge the validity or enforceability of this patent.

References

  1. U.S. Patent and Trademark Office. (2015). Patent No. 9,205,056. Retrieved from [USPTO database].

  2. World Intellectual Property Organization. (n.d.). Patent family data. Retrieved from [WIPO PATENTSCOPE].

  3. European Patent Office. (n.d.). Patent status and family information. Retrieved from [EPO Espacenet].

  4. National Patent Office filings. (n.d.). International patent filings related to chemical compounds. Retrieved from [WIPO PATENTSCOPE].

  5. Patent maintenance and expiration guidelines. (2023). [Industry publication].

More… ↓

⤷  Start Trial


Drugs Protected by US Patent 9,205,056

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

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.