40
Participants
Start Date
October 2, 2020
Primary Completion Date
January 2, 2021
Study Completion Date
February 1, 2021
HB0017
HB0017 at 100 mg/mL (1 mL/vial) in 2 mL glass vial with a rubber stopper. HB0017 will be administered in the abdominal area by a subcutaneous injection in the mornings. A maximum volume of 1 mL is injected per site.
placebo
A matching injection solution containing a specific volume of normal saline (0.9%, Sodium Chloride Injection USP) and no active substance will be prepared for the subjects who will be assigned to placebo according to the dose schedule.
Auckland Clinical Studies Ltd, Grafton
Lead Sponsor
Huabo Biopharm Co., Ltd.
INDUSTRY