A Phase 1 Study to Evaluate the Safety and Tolerability of CBL-514 Injection on Convexity or Fullness of Abdominal Subcutaneous Fat in Healthy Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

November 27, 2018

Primary Completion Date

August 20, 2019

Study Completion Date

August 20, 2019

Conditions
Subcutaneous Fat
Interventions
DRUG

CBL-514, placebo

"One side of the abdominal region will receive CBL-514, while the other will receive placebo with equal volume.~Which side of the abdominal region to receive CBL-514 or placebo would be randomized.~No PK samples will be collected in this cohort."

DRUG

CBL-514, placebo

"One side of the abdominal region will receive CBL-514, while the other will receive placebo with equal volume.~Which side of the abdominal region to receive CBL-514 or placebo would be randomized."

DRUG

CBL-514

Both sides of the abdominal region will receive CBL-514.

Trial Locations (1)

Unknown

Investigational site, Melbourne

All Listed Sponsors
lead

Caliway Biopharmaceuticals Co., Ltd.

INDUSTRY

NCT04699669 - A Phase 1 Study to Evaluate the Safety and Tolerability of CBL-514 Injection on Convexity or Fullness of Abdominal Subcutaneous Fat in Healthy Volunteers | Biotech Hunter | Biotech Hunter