The pharmacokinetics of oxycodone and its metabolites following single oral doses of Remoxy®, an abuse-deterrent formulation of extended-release oxycodone, in patients with hepatic or renal impairment. | |||
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분류 | Pharmacokinetics | 조회 | 1316 |
발행년도 | 2015 | 등록일 | 2015-09-20 |
출처 | J Opioid Manag (바로가기) | ||
OBJECTIVE:
Remoxy® (Pain Therapeutics, Inc., Austin, TX) is an abuse-deterrent formulation of extended-release oxycodone. The effects of renal or hepatic impairment on the pharmacokinetics (PK) of single, oral doses of Remoxy 20 or 10 mg, respectively, were assessed in two phase 1 studies in subjects aged 18-80 years.
METHODS:
PK parameters included maximum plasma concentration (Cmax) and area under the concentration-time curve from time 0 to the last quantifiable concentration (AUC0-t), and extrapolated to infinity (AUCinf). Adverse events (AEs) were monitored.
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이전글 | 대웅제약, 크리스탈지노믹스와 신약 ‘아셀렉스캡슐’ 판권 계약 체결 |
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다음글 | Effect of dosing interval on pharmacokinetics of fentanyl pectin nasal spray from a crossover study. |