Research Topics
| Xiao Jian ZhouSummaryAffiliation: Idenix Pharmaceuticals Country: USA Publications
| Collaborators
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Detail Information
Publications
Absence of food effect on the pharmacokinetics of telbivudine following oral administration in healthy subjectsXiao-Jian Zhou
Idenix Pharmaceuticals Inc, 60 Hampshire Street, Cambridge, MA 02139, USA
J Clin Pharmacol 46:275-81. 2006..Results from this study indicated that the absorption of telbivudine was not affected by a high-fat/high-calorie meal; telbivudine can therefore be administered orally with no regard to the timing of meals...
Pharmacokinetics of telbivudine following oral administration of escalating single and multiple doses in patients with chronic hepatitis B virus infection: pharmacodynamic implicationsXiao Jian Zhou
Idenix Pharmaceuticals Inc, 60 Hampshire Street, Cambridge, Massachusetts 02139, USA
Antimicrob Agents Chemother 50:874-9. 2006....
Pharmacokinetics of telbivudine in subjects with various degrees of hepatic impairmentXiao Jian Zhou
Idenix Pharmaceuticals Inc, 60 Hampshire Street, Cambridge, MA 02139, USA
Antimicrob Agents Chemother 50:1721-6. 2006....
Pharmacokinetics of telbivudine in healthy subjects and absence of drug interaction with lamivudine or adefovir dipivoxilXiao Jian Zhou
Idenix Pharmaceuticals, Inc, Cambridge, MA 02139, USA
Antimicrob Agents Chemother 50:2309-15. 2006..The results from these studies provide pharmacologic support for combination therapy or therapy switching involving telbivudine, lamivudine, and adefovir dipivoxil for the treatment of chronic hepatitis B virus infection...
Pharmacokinetics of telbivudine in subjects with various degrees of renal impairmentXiao Jian Zhou
Idenix Pharmaceuticals, Inc, One Kendall Square, Building 1400, Cambridge, MA 02139, USA
Antimicrob Agents Chemother 51:4231-5. 2007....
Population pharmacokinetics of telbivudine and determination of dose adjustment for patients with renal impairmentXiao Jian Zhou
Idenix Pharmaceuticals, Inc, One Kendall Square, Building 1400, Cambridge, MA 02139, USA
J Clin Pharmacol 49:725-34. 2009....
Microdose pharmacokinetics of IDX899 and IDX989, candidate HIV-1 non-nucleoside reverse transcriptase inhibitors, following oral and intravenous administration in healthy male subjectsXiao Jian Zhou
Idenix Pharmaceuticals Inc, One Kendall Square, Building 1400, Cambridge, MA 02139, USA
J Clin Pharmacol 49:1408-16. 2009..IDX899 has been selected based on these initial pharmacokinetic assessments and other criteria as the candidate for further clinical development...
Safety and pharmacokinetics of IDX184, a liver-targeted nucleotide polymerase inhibitor of hepatitis C virus, in healthy subjectsXiao Jian Zhou
Idenix Pharmaceuticals Inc, Cambridge, MA 02139, USA
Antimicrob Agents Chemother 55:76-81. 2011..All AEs were mild to moderate and resolved at the end of study. The favorable safety and pharmacokinetic profiles support further clinical evaluation of IDX184 in HCV-infected patients...
Drug interaction profile for GSK2248761, a next generation non-nucleoside reverse transcriptase inhibitorSteve Piscitelli
Infectious Diseases MDC, GlaxoSmithKline, Research Triangle Park, NC 27709, USA
Br J Clin Pharmacol 74:336-45. 2012....
Single-dose escalation and multiple-dose safety, tolerability, and pharmacokinetics of IDX899, a candidate human immunodeficiency virus type 1 nonnucleoside reverse transcriptase inhibitor, in healthy subjectsXiao Jian Zhou
Idenix Pharmaceuticals Inc, One Kendall Square, Building 1400, Cambridge, MA 02139, USA
Antimicrob Agents Chemother 53:1739-46. 2009..These favorable safety and pharmacokinetic results support further clinical studies with patients with HIV-1 infection by the use of a QD regimen...
Single-dose and multiple-dose pharmacokinetics and safety of telbivudine after oral administration in healthy Chinese subjectsPei Hu
Peking Union Medical College Hospital, Beijing, People's Republic of China
J Clin Pharmacol 46:999-1007. 2006..4% of the administered dose, with a mean renal clearance of 6.6 L/h. Telbivudine was well tolerated in the studied dose range in healthy Chinese subjects, with no pattern of dose-related clinical or laboratory adverse events...
A dose-finding study of once-daily oral telbivudine in HBeAg-positive patients with chronic hepatitis B virus infectionChing Lung Lai
University of Hong Kong, Hong Kong, China
Hepatology 40:719-26. 2004..In conclusion, these results support expanded clinical studies of this new agent for the treatment of hepatitis B...
5-(Phenylthio)acyclouridine: a powerful enhancer of oral uridine bioavailability: relevance to chemotherapy with 5-fluorouracil and other uridine rescue regimensOmar N Al Safarjalani
Department of Pharmacology and Toxicology, Comprehensive Cancer Center, Center for AIDS Research, University of Alabama at Birmingham, Birmingham, AL 35294, USA
Cancer Chemother Pharmacol 55:541-51. 2005..g. Huntington's disease, bipolar disorder), liver diseases, diabetic neuropathy, cardiac damage, various autoimmune diseases, and transplant rejection...
Stable concentrations of zidovudine, stavudine, lamivudine, abacavir, and nevirapine in serum and cerebrospinal fluid during 2 years of therapyRieneke M E van Praag
National AIDS Therapy Evaluation Center (NATEC, Department of Internal Medicine, Division of Infectious Diseases, Tropical Medicine and AIDS, University of Amsterdam, Amsterdam, The Netherlands
Antimicrob Agents Chemother 46:896-9. 2002..While studies suggest that saquinavir concentrations decrease over time, we show that concentrations of zidovudine, stavudine, lamivudine, abacavir, and nevirapine in serum and cerebrospinal fluid are stable during 2 years of therapy...
