A Phase 1 Study to Evaluate the Safety and Pharmacokinetics of Entecavir Extended Release (XR) in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

October 20, 2017

Primary Completion Date

May 29, 2018

Study Completion Date

June 20, 2018

Conditions
HBV
Interventions
DRUG

Entecavir

Study drug (entecavir or placebo) will be administered with 240 mL of water following an overnight fast (no food or drink, except water, for at least 10 hours). Subjects will be required to fast (no food or beverages other than water) until after collection of the 4-hour blood draw.

Trial Locations (1)

6009

Linear Clinical Research Ltd, Nedlands

Sponsors
All Listed Sponsors
lead

Aucta Pharmaceuticals, Inc

INDUSTRY

NCT03239353 - A Phase 1 Study to Evaluate the Safety and Pharmacokinetics of Entecavir Extended Release (XR) in Healthy Subjects | Biotech Hunter | Biotech Hunter