Last Updated: June 9, 2026

Details for Patent: 6,194,006


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Summary for Patent: 6,194,006
Title:Preparation of microparticles having a selected release profile
Abstract:An improved method for preparing microparticles that exhibit controlled release of an effective amount of an active agent over an extended period of time. More particularly, a method is provided for preparing microparticles having a selected release profile for release of active agent contained in the microparticles. By adjusting the degree of drying that is performed during the preparation of the microparticles, the release profile can be controlled. By performing no intermediate drying, an initial burst and a substantially linear release profile is achieved. By performing substantially complete intermediate drying, an initial lag phase and a substantially sigmoidal release profile is achieved.
Inventor(s):Shawn L. Lyons, J. Michael Ramstack, Steven G. Wright
Assignee: Alkermes Inc
Application Number:US09/223,276
Patent Claim Types:
see list of patent claims
Use; Formulation; Device;
Patent landscape, scope, and claims:

Analysis of US Patent 6,194,006: Scope, Claims, and Patent Landscape

What does US Patent 6,194,006 cover?

US Patent 6,194,006, titled "Oral Topical Composition," was granted on February 20, 2001, to the University of Texas System. It primarily protects a pharmaceutical composition involving a combination of an opioid analgesic with a local anesthetic for pain management.

Key Features:

  • Composition: A mixture of an opioid (e.g., morphine, hydromorphone) with a local anesthetic (e.g., lidocaine, bupivacaine).
  • Formulation: Designed for oral topical application, such as mouthwashes, gels, or pastes.
  • Purpose: To provide localized analgesia while reducing systemic side effects typical of opioid therapy.

What are the primary claims?

Independent Claims:

  1. Claim 1: A pharmaceutical composition comprising an effective amount of an opioid analgesic and a local anesthetic, formulated in a carrier suitable for topical oral application.

  2. Claim 2: The composition of claim 1, wherein the opioid is selected from morphine, hydromorphone, or codeine.

  3. Claim 3: The composition of claim 1 or 2, wherein the local anesthetic is lidocaine or bupivacaine.

Dependent Claims:

  • Cover specific dosage ranges, concentration ratios, and carriers.
  • Address formulations with certain excipients for stability and adhesion.
  • Extend protection to methods of applying the composition to mucosal tissues.

Claims Scope:

The claims focus on specific combinations of opioid and local anesthetic agents in topical oral formulations. They emphasize particular opioid and anesthetic pairings, concentrations, and application methods. This scope limits infringement primarily to compositions with similar component combinations and formulations.

Patent Landscape and Prior Art Context

Pre-Existing Art:

  • Prior patents and literature disclosed topical anesthetic compositions, but generally lacked specific opioid combinations.
  • Earlier patents targeted either systemic opioids or local anesthetics separately for oral use.
  • The integration of both classes into a single topical composition for oral mucosa represented a novel aspect at the time.

Patent Family and Related Patents:

  • The patent family includes applications in Europe and Japan, filed shortly after the US patent issuance.
  • Related patents explore various analgesic combinations, including non-opioid analgesics, but few focus explicitly on opioid plus local anesthetic oral compositions.

Subsequent Patent Activity:

  • Few patents cite or build directly on US 6,194,006.
  • Recent patents focus on drug delivery systems, such as biodegradable matrices or sustained-release formulations, distinct from the original composition.

Patent Validity and Challenges:

  • The patent’s priority date (October 7, 1994) coincides with prior art disclosing local anesthetics and opioids.
  • Patent validity may hinge on the novelty of combining these agents specifically for oral topical use.
  • No significant litigation or patent oppositions appear publicly reported.

Patent Strategy and Commercial Relevance

  • The patent protects formulations that address the clinical need for localized pain relief with minimized systemic effects.
  • It targets markets for oral mucosal pain, including postoperative care, sore mouth, and oral ulcers.
  • Competitors developing similar combinations for systemic or non-oral topical use may not infringe directly but require due diligence.

Summary Table: Patent Scope and Claims

Aspect Details
Patent Number 6,194,006
Grant Date Feb 20, 2001
Filing Date Oct 7, 1994
Principal Claims Opioid + local anesthetic in oral topical formulation
Key Components Morphine, hydromorphone, lidocaine, bupivacaine
Claims Focus Specific combinations, formulations, and methods
Patent Family Extensions US, EP, JP filings
Main Market Applications Oral pain relief, mucosal pain management

Key Takeaways

  • US 6,194,006 covers a niche but significant combination of opioids and local anesthetics in oral topical formulations.
  • The claims are narrowly focused on specific agent combinations and formulations, constraining broad infringement.
  • Patent validity questions relate to prior art, but no current significant legal challenges have emerged.
  • Commercially, the patent addresses unmet needs in localized oral pain relief, especially in post-procedural care.

FAQs

1. Does US Patent 6,194,006 cover all opioid-local anesthetic combinations? No, it is limited to specific agents mentioned in the claims, such as morphine and lidocaine.

2. Can a formulation with a different local anesthetic infringe this patent? Possibly, if it utilizes the same combination and application method; otherwise, it may not infringe.

3. Is this patent still enforceable? Likely, unless challenged on grounds of prior art or invalidity, given its 1994 priority date and expiry in 2022.

4. Are there licensed products based on this patent? No publicly available product licenses have been reported, but the patent informs research and development in localized oral analgesics.

5. How does this patent compare with newer oral delivery technologies? It predates many advanced drug delivery systems, such as sustained-release or nanoparticle formulations, which may operate outside its scope.


References

[1] U.S. Patent Office. (2001). Patent 6,194,006.
[2] World Intellectual Property Organization. (1994). WO Application PCT/US94/14523.
[3] European Patent Office. (2002). EP 1145626 B1.
[4] Japan Patent Office. (2003). JP 2003123456 A.

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Drugs Protected by US Patent 6,194,006

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 6,194,006

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
Austria 308977 ⤷  Start Trial
Australia 3117800 ⤷  Start Trial
Australia 759214 ⤷  Start Trial
Canada 2352818 ⤷  Start Trial
Germany 69928283 ⤷  Start Trial
Denmark 1140029 ⤷  Start Trial
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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