Sustained release formulations of oxymorphone or pharmaceutically acceptable salts thereof; methods for making the sustained release formulations of oxymorphone or pharmaceutically acceptable salts thereof; and methods for using the sustained release formulations of oxymorphone or pharmaceutically acceptable salts thereof to treat patients suffering from pain are provided.
Opioid Formulations Having Reduced Potential For Abuse
Anand Baichwal - Wappingers Falls NY, US Paul Woodcock - Brookfield CT, US Troy McCall - Germantown TN, US
International Classification:
A61K031/485 A61K009/22
US Classification:
424/468000, 514/282000
Abstract:
The invention provides opioid formulations having reduced potential for abuse, and having reduced potential for illegal sale and distribution. The opioid formulations of the invention comprise at least one opioid and a sustained release delivery system.
Methods Of Making Sustained Release Formulations Of Oxymorphone
Anand Baichwal - Wappingers Falls NY, US Troy McCall - Germantown TN, US
Assignee:
Penwest Pharmaceuticals Company - Patterson NY
International Classification:
A61K031/485 A61K009/26
US Classification:
424/470000, 514/282000
Abstract:
Sustained release formulations of oxymorphone or pharmaceutically acceptable salts thereof; methods for making the sustained release formulations of oxymorphone or pharmaceutically acceptable salts thereof; and methods for using the sustained release formulations of oxymorphone or pharmaceutically acceptable salts thereof to treat patients suffering from pain are provided.
Oral Administration Of 6-Hydroxy-Oxymorphone For Use As An Analgesic
Troy McCall - Germantown TN, US David Lee - Wilmington DE, US
Assignee:
Endo Pharmaceuticals, Inc.
International Classification:
A61K031/485
US Classification:
514/282000
Abstract:
In a method of treating pain, a patient is administered a pharmaceutical composition of 6-hydroxy oxymorphone in amount sufficient to induce analgesia. In one embodiment, the pharmaceutical composition is administered orally. Any known or later developed method of oral delivery may be used. To achieve the desired analgesic effect, blood plasma levels of 6-hydroxy oxymorphone are raised to at least approximately 0.2 ng/mL. Most preferably blood plasma levels of 6-hydroxy oxymorphone range at least 0.3 ng/mL during treatment. Administration of compositions containing 6-hydroxy oxymorphone, and one or more carriers, diluents, and excipients in an amount sufficient to induce analgesia is also contemplated.
Anand Baichwal - Wappingers Falls NY, US Troy McCall - Germantown TN, US David Lee - Wilmington DE, US
Assignee:
Endo Pharmaceuticals, Inc.
International Classification:
A61K031/485 A61K009/20 A61K009/22
US Classification:
424/468000, 514/282000
Abstract:
The invention pertains to a method of relieving pain by administering a controlled release pharmaceutical tablet containing oxymorphine which produces a mean minimum blood plasma level 12 to 24 hours after dosing, as well as the tablet producing the sustained pain relief.
Anand Baichwal - Wappingers Fall NY, US Paul Woodcock - Brookfield CT, US Pradeepkumar Sanghvi - New Fairfeild CT, US Dean Dinicola - Prospect CT, US Troy McCall - Germantown TN, US
International Classification:
A61K009/22 A61K031/137
US Classification:
424/468000, 514/651000
Abstract:
The present invention relates to a sustained release oral dosage forms containing a therapeutically effective amount of metoprolol tartrate, methods of preparing such formulations, and to methods of treatment utilizing such formulations.
Sustained Release Matrix Systems For Highly Soluble Drugs
Anand Baichwal - Wappingers Falls NY, US Troy McCall - Germantown TN, US Lirong Liu - Washington Township NJ, US Steve Labudzinski - Poughkeepsie NY, US
Assignee:
Penwest Pharmaceuticals Co. - Patterson NY
International Classification:
A61K009/22
US Classification:
424/468000
Abstract:
Disclosed are sustained release oral solid dosage forms comprising a therapeutically effective amount of a medicament having a solubility of more than about 10 g/l; a pH modifying agent; and a sustained release matrix comprising a gelling agent, said gelling agent comprising a heteropolysaccharide gum and a homopolysaccharide gum capable of cross-linking said heteropolysaccharide gum when exposed to an environmental fluid, said dosage form providing a sustained release of said medicament after oral administration to human patients.
Parenteral Administration Of 6-Hydroxy-Oxymorphone For Use As An Analgesic
Troy McCall - Germantown TN, US David Lee - Wilmington DE, US
International Classification:
A61K031/485
US Classification:
514/282000
Abstract:
In a method of treating pain a patient is administered a pharmaceutical composition of 6-hydroxy oxymorphone in an amount sufficient to induce analgesia. In one embodiment, the pharmaceutical composition is administered parenterally, preferably by injection and intravenous drip. To achieve the desired analgesic effect, blood plasma levels of 6-hydroxy oxymorphone are raised to at least approximately 0.05 ng/mL. Most preferably blood plasma levels of 6-hydroxy oxymorphone range at least 0.075 ng/mL during treatment. Administration of compositions containing 6-hydroxy oxymorphone, and one or more carriers, diluents, and excipients in an amount sufficient to induce analgesia is also contemplated.
Archer Malmo
Acd
Troy Mccall
Freelance and Creative
Archer Malmo Jun 2012 - Jul 2013
Assoc Creative Director
Sullivan Branding Jul 1998 - May 2012
Assoc Creative Director
Rutland Simmons Group Sep 1994 - Jun 1998
Creative Director
Education:
University of Oklahoma
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