Generated: May 25, 2017
|Title:||Device for transdermal electrotransport delivery of fentanyl and sufentanil|
|Abstract:||The invention provides an improved electrotransport drug delivery system for analgesic drugs, namely fentanyl and sufentanil. The fentanyl/sufentanil is provided as a water soluble salt (e.g., fentanyl hydrochloride), preferably in a hydrogel formulation, for use in an electrotransport device (10). In accordance with the present invention, a transdermal electrotransport delivered dose of fentanyl/sufentanil is provided which is sufficient to induce analgesia in (e.g., adult) human patients suffering from moderate-to-severe pain associated with major surgical procedures.|
|Inventor(s):||Southam; Mary (Menlo Park, CA), Bernstein; Keith J. (Somerville, NJ), Noorduin; Henk (Bergen op Zoom, NL)|
|Assignee:||ALZA Corporation (Mountain View, CA)|
1. A method of obtaining analgesia in a human patient who is suffering from pain, consisting of transdermally delivering solely by electrotransport a dose of about 20
micrograms to about 60 micrograms of fentanyl over a predetermined delivery period of up to about 20 minutes, terminating said delivery at the end of said delivery period and thereafter repeating such transdermal administering up to about 100 additional
of said doses over a period of about 24 hours, wherein the applied electrotransport current density is in the range of about 50 to about 150 microamps per square centimeter.
2. The method of claim 1, wherein about 35 micrograms to about 45 micrograms of fentanyl is delivered over a delivery period of about 5 to 15 minutes.
3. The method of claim 1, wherein about 40 micrograms of fentanyl is delivered over the delivery period.
4. The method of claim 1, wherein the delivery period is about 10 minutes.
5. The method of claim 1, wherein the additional doses are 35 micrograms to 45 micrograms doses of fentanyl.
6. The method of claim 1, wherein the fentanyl comprises a fentanyl salt.
7. The method of claim 6, wherein the fentanyl salt comprises fentanyl hydrochloride.
8. The method of claim 1, wherein the doses are self-administered by the patient suffering from pain.
9. The method of claim 8, wherein the patient is allowed to self-administer no more than six of said doses per hour.
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. thinkBiotech performs no independent verifification 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.