Study Assessing the Effects of Darunavir/Ritonavir or Lopinavir/Ritonavir on the Pharmacokinetics of Daclatasvir in Healthy Participants



Status:Completed
Conditions:Hepatitis
Therapuetic Areas:Immunology / Infectious Diseases
Healthy:No
Age Range:18 - 49
Updated:4/21/2016
Start Date:June 2014
End Date:July 2014

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A Phase 1 Clinical Study to Assess the Effect of Darunavir/Ritonavir or Lopinavir/Ritonavir on the Pharmacokinetics of Daclatasvir in Healthy Subjects

The purpose of this study is to determine whether multiple doses of darunavir/ritonavir or
lopinavir/ritonavir affect the pharmacokinetics of daclatasvir in healthy participants.


For more information regarding BMS clinical trial participation, please visit
www.BMSStudyConnect.com

Key Inclusion Criteria:

- Healthy male and female participants, aged 18 to 49, as determined by medical
history, physical examination, 12 lead electrocardiogram, vital signs, and clinical
laboratory evaluations

Key Exclusion Criteria:

- Any significant acute or chronic medical illness; donation of blood to a blood bank
or in a clinical study (except a screening visit) within 4 weeks of study drug
administration (within 2 weeks for plasma only); or blood screen findings positive
for hepatitis C antibody, hepatitis B surface antigen, or HIV-1 and HIV-2 antibodies
We found this trial at
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San Antonio, TX
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