Pharmacokinetics and pharmacodynamics following intravenous doses of azimilide dihydrochloride
Azimilide pharmacokinetics and pharmacodynamics were characterized in a safety and tolerance study of intravenously administered azimilide dihydrochloride. This was a parallel-group design (seven treatments), and 68 healthy volunteers received the drug. Single intravenous infusion doses (4.5 to 9 mg/kg) were administered over 60 minutes, and single 4.5 mg/kg intravenous infusion doses were also given over 15 or 30 minutes. Blood and urine specimens were collected and analyzed for azimilide and metabolites. QTc was measured as a marker of class III antiarrhythmic activity. Azimilide pharmacokinetics were dose proportional and did not differ among infusion rates. Azimilide pharmacodynamics did not differ among treatments. Mean Emax ranged from 23 to 28% delta QTc, with mean EC50 of 509 to 566 ng/mL. Peak circadian variation in QTc was equivalent to 14% of Emax. Rapid equilibration occurred between blood and the biophase. Unconfounded pharmacodynamic estimates required inclusion of circadian QTc variation in the pharmacodynamic model.
Medienart: |
Artikel |
---|
Erscheinungsjahr: |
1999 |
---|---|
Erschienen: |
1999 |
Enthalten in: |
Zur Gesamtaufnahme - volume:39 |
---|---|
Enthalten in: |
Journal of clinical pharmacology - 39(1999), 12 vom: 14. Dez., Seite 1263-71 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Corey, A [VerfasserIn] |
---|
Themen: |
74QU6P2934 |
---|
Anmerkungen: |
Date Completed 16.12.1999 Date Revised 26.08.2019 published: Print Citation Status MEDLINE |
---|
Förderinstitution / Projekttitel: |
|
---|
PPN (Katalog-ID): |
NLM105162825 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM105162825 | ||
003 | DE-627 | ||
005 | 20231222134059.0 | ||
007 | tu | ||
008 | 231222s1999 xx ||||| 00| ||eng c | ||
028 | 5 | 2 | |a pubmed24n0351.xml |
035 | |a (DE-627)NLM105162825 | ||
035 | |a (NLM)10586392 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Corey, A |e verfasserin |4 aut | |
245 | 1 | 0 | |a Pharmacokinetics and pharmacodynamics following intravenous doses of azimilide dihydrochloride |
264 | 1 | |c 1999 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ohne Hilfsmittel zu benutzen |b n |2 rdamedia | ||
338 | |a Band |b nc |2 rdacarrier | ||
500 | |a Date Completed 16.12.1999 | ||
500 | |a Date Revised 26.08.2019 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Azimilide pharmacokinetics and pharmacodynamics were characterized in a safety and tolerance study of intravenously administered azimilide dihydrochloride. This was a parallel-group design (seven treatments), and 68 healthy volunteers received the drug. Single intravenous infusion doses (4.5 to 9 mg/kg) were administered over 60 minutes, and single 4.5 mg/kg intravenous infusion doses were also given over 15 or 30 minutes. Blood and urine specimens were collected and analyzed for azimilide and metabolites. QTc was measured as a marker of class III antiarrhythmic activity. Azimilide pharmacokinetics were dose proportional and did not differ among infusion rates. Azimilide pharmacodynamics did not differ among treatments. Mean Emax ranged from 23 to 28% delta QTc, with mean EC50 of 509 to 566 ng/mL. Peak circadian variation in QTc was equivalent to 14% of Emax. Rapid equilibration occurred between blood and the biophase. Unconfounded pharmacodynamic estimates required inclusion of circadian QTc variation in the pharmacodynamic model | ||
650 | 4 | |a Clinical Trial | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Randomized Controlled Trial | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 7 | |a Calcium Channel Blockers |2 NLM | |
650 | 7 | |a Hydantoins |2 NLM | |
650 | 7 | |a Imidazoles |2 NLM | |
650 | 7 | |a Imidazolidines |2 NLM | |
650 | 7 | |a Piperazines |2 NLM | |
650 | 7 | |a azimilide |2 NLM | |
650 | 7 | |a 74QU6P2934 |2 NLM | |
700 | 1 | |a Agnew, J |e verfasserin |4 aut | |
700 | 1 | |a Brum, J |e verfasserin |4 aut | |
700 | 1 | |a Parekh, N |e verfasserin |4 aut | |
700 | 1 | |a Valentine, S |e verfasserin |4 aut | |
700 | 1 | |a Williams, M |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Journal of clinical pharmacology |d 1973 |g 39(1999), 12 vom: 14. Dez., Seite 1263-71 |w (DE-627)NLM000005576 |x 1552-4604 |7 nnns |
773 | 1 | 8 | |g volume:39 |g year:1999 |g number:12 |g day:14 |g month:12 |g pages:1263-71 |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 39 |j 1999 |e 12 |b 14 |c 12 |h 1263-71 |