A Study of Injection HB0017 in Adult Healthy Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

October 2, 2020

Primary Completion Date

January 2, 2021

Study Completion Date

February 1, 2021

Conditions
Healthy Subjects
Interventions
DRUG

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.

DRUG

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.

Trial Locations (1)

8963

Auckland Clinical Studies Ltd, Grafton

Sponsors
All Listed Sponsors
lead

Huabo Biopharm Co., Ltd.

INDUSTRY