Treating lignocellulosic materials
Abstract
It is a method for significantly reducing the region width in daily dosages required to control pain in approximately 80% of patients disclosed, wherein an oral solid dosage formulation with controlled release comprising about 10 to about 40 mg oxycodone or a salt thereof to a patient is administered. The formulation provides a mean of about 2 to about 4.5 hours after administration, a mean maximum plasma concentration of oxycodone from about 6 to about 60 ng / ml, and an average of from about 10 to about 14 hours after repeated "q12h" ( ie, every 12 hours) administration of a mean minimum plasma concentration from about 3 to about 30 ng / ml at steady state conditions. Another embodiment relates to a method for significantly reducing the region width in daily dosages required to control pain in substantially all patients. Fig. 5 is a graph showing the mean plasma oxycodone concentration of a 10 mg oxycodone controlled-release formulation as well as a Studienrefenzstandard, wherein the formulation was prepared according to the present invention.
Term
No projected expiry on record.
- Priority
- Filed
- Granted
- Today
Every citation, both ways
| Document | Relation | Office | Cited during |
|---|---|---|---|
| US4685918A | Cites | United States of America | Search report |
| US4828836A | Cites | United States of America | Search report |
| US4851228A | Cites | United States of America | Search report |
| US4968507A | Cites | United States of America | Search report |
| US4990335A | Cites | United States of America | Search report |
16 members in 8 offices
Priority claims3
| Document | Office | Kind | Date |
|---|---|---|---|
| 80045991 | United States of America | A | |
| 800459 | – | – | – |
| US19910800459 | – | – | – |
Members16
| Document | Office | Kind | |
|---|---|---|---|
| FI925352A0 | Finland | A0 | |
| CA2082185A1 | Canada | A1 | |
| FI925352A | Finland | A | |
| FI925352L | Finland | L | |
| BR9204539A | Brazil | A | |
| BR9204539A | Brazil | A | |
| EP0546721A1 | European Patent Office (EPO) | A1 | |
| US5374555A | United States of America | A | |
| EP0546721B1 | European Patent Office (EPO) | B1 | |
| DE69224173D1 | Germany | D1 | |
| ES2111621T3 | Spain | T3 | |
| DE69224173T2 | Germany | T2 | |
| AT4589U2 | Austria | U2 | |
| AT4589U3This record | Austria | U3 | |
| FI110698B | Finland | B | |
| CA2082185C | Canada | C |
Numbers
- Publication, DOCDB
- 4589
- Publication, EPODOC
- AT4589U
- Application
- 88000
- Application, DOCDB
- 8802000
- Application, EPODOC
- AT20000000880U
Titles2
- English
- OXYCODON COMPOSITION WITH CONTROLLED RELEASE
- German
- OXYCODON-ZUSAMMENSETZUNG MIT KONTROLLIERTER FREISETZUNG
Classification
- CPC, 3
- C12P21/06
- A61P25/04
- D21C5/005
- IPC, 4
- A61K9 26
- A61P25 04
- C12P21 06
- D21C5 00