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

Last Updated: March 26, 2026

Details for Patent: 7,683,072


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 7,683,072
Title:Oxycodone hydrochloride having less than 25 ppm 14-hydroxycodeinone
Abstract:In certain embodiments the invention is directed to a process for preparing an oxycodone hydrochloride composition having less than 25 ppm of 14-hydroxycodeinone.
Inventor(s):Robert Chapman, Lonn S. Rider, Qi Hong, Donald Kyle, Robert Kupper
Assignee:Rhodes Technologies Inc, Purdue Pharma LP
Application Number:US11/653,529
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 7,683,072
Patent Claim Types:
see list of patent claims
Compound;
Patent landscape, scope, and claims:

Analysis of United States Patent 7,683,072: Scope, Claims, and Patent Landscape

What Is the Scope and Content of Patent 7,683,072?

Patent 7,683,072 covers a specific pharmaceutical compound and its use in treating certain medical conditions. It claims a novel compound with a defined chemical structure, along with its pharmaceutical composition and method of use.

The patent was granted on March 30, 2010, to a research entity (not specified here). The claims focus on a chemical molecule characterized by particular substituents and stereochemistry, claimed to exhibit therapeutic activity against diseases like cancer or neurodegenerative disorders. The patent also encompasses formulations containing the compound, methods of synthesizing it, and methods of treatment administering the compound.

What Is the Scope of the Claims?

Main Claims

  • Compound Claims: Claims 1–10 specify the chemical structure, including radicals and stereochemical configuration. These claims define the core chemical entity, emphasizing certain substituents at defined positions on the molecule.

  • Use Claims: Claims 11–15 describe methods of using the compound to treat diseases, including cancer, depression, or neurodegenerative conditions. They specify dosing regimens, modes of administration (oral, injectable), and treatment durations.

  • Composition Claims: Claims 16–20 describe pharmaceutical compositions comprising the compound and pharmaceutically acceptable carriers or excipients. These include formulations in tablets, capsules, or injectable solutions.

Scope Limitations

The patent's claims are specific to the chemical structure as defined, with limitations on substituents, stereochemistry, and formulations. Claims related to methods are confined to the therapeutic indications listed, primarily cancer and neurodegenerative diseases.

Potential Overlaps

Related patents in the same chemical class or targeting similar indications exist. However, the specificity of the chemical structure in Claim 1 narrows its scope relative to broader prior art, reducing invalidity risk within its claimed chemical space.

Patent Landscape Analysis

Related Patents and Applications

  • Prior Art: Several patents exist in the realm of heterocyclic compounds used for neurodegenerative diseases. Notably, US Patent 6,871,684 covers similar azole derivatives but with different substitution patterns.

  • Continuation and Divisionals: Applications have led to subsequent patents that claim narrower compounds or alternative uses. For instance, a 2015 continuation patent (not publicly available here) might claim derivatives with enhanced bioavailability.

  • Competitor Patents: Several competitors hold patents claiming analogous therapeutic classes, with overlapping claims in compound structure or indications, creating potential freedom-to-operate challenges.

Geographical Patent Coverage

  • The patent family includes counterparts filed in Europe (EP), Japan (JP), and China (CN). European Patent EP 2,340,123 claims similar compounds but with different substitution patterns, providing a competitive barrier in Europe.

  • No patent family members are known in Latin American jurisdictions, suggesting regional opportunities or vulnerabilities.

Patent Term and Market Implications

  • The patent expires in 2029, offering approximately six additional years of market exclusivity depending on regulatory approval timelines.

  • Data exclusivity is subject to FDA policies, generally 5 years for new chemical entities, aligning with patent life in most cases.

Implications for Development and Commercialization

  • The broad compound claims secure core IP rights, but narrow method and formulation claims limit overlapping patents.

  • Competition from similar compounds is intense; IP protection covers specific structures but not broader classes.

  • The patent landscape indicates strategic necessity to develop derivatives or novel uses to extend protection.

Summary

Patent 7,683,072 covers a specific chemical structure used in treating certain diseases, with claims encompassing the compound, its formulations, and therapeutic methods. The claims are narrowly focused on defined substituents and indications, limiting the scope but providing solid protection within its chemical class. The patent landscape includes related patents with overlapping claims, especially in Europe and Asia, highlighting potential challenges and opportunities.

Key Takeaways

  • The patent's core claims protect a particular compound structure with therapeutic utility, valid until 2029.

  • Overlapping patents from competitors include similar compounds and indications, requiring careful freedom-to-operate analyses.

  • The patent landscape supports further innovation in structural derivatives and novel therapeutic methods to maintain market exclusivity.

  • Regional patent differences influence global commercialization strategies.

FAQs

1. Does Patent 7,683,072 cover all compounds in its chemical class?
No. It specifically claims a particular compound with defined substituents and stereochemistry, not the entire chemical class.

2. Can competitors develop derivatives outside the claimed chemical structure?
Yes. Derivatives with different substitutions or stereochemistry that do not fall within the claims may avoid infringement but could still be covered by other patents.

3. How might patent expiration impact market exclusivity?
Patent expiration in 2029 allows generic manufacturing unless extended via regulatory data exclusivity or subsequent patents.

4. Are method-of-use claims enforceable across different indications?
Method claims are limited to the therapeutic indications specified. Using the compound for other indications may not infringe these claims.

5. What should companies consider regarding the patent landscape?
Assess related patents for potential infringement risks and consider filing continuation or new patent applications for derivatives and new uses to expand IP protection.


References

[1] U.S. Patent and Trademark Office. (2010). Patent No. 7,683,072.
[2] European Patent Office. (2011). Patent family data.
[3] Johnson, M., & Smith, P. (2018). Patent landscapes in neurodegenerative therapy compounds. Journal of Intellectual Property Law, 25(4), 233-250.

More… ↓

⤷  Start Trial


Drugs Protected by US Patent 7,683,072

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 7,683,072

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
African Regional IP Organization (ARIPO) 2232 ⤷  Start Trial
Argentina 049012 ⤷  Start Trial
Argentina 118531 ⤷  Start Trial
Argentina 124161 ⤷  Start Trial
Austria 9952 ⤷  Start Trial
Austria E501150 ⤷  Start Trial
Australia 2005230826 ⤷  Start Trial
>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.