LivingGLP1
Study S000417

Clinical Study to Evaluate the Pharmacokinetics and Safety of IBI362 Lyophilized Powder and IBI362 Liquid Formulation in Healthy Chinese Male Subjects

Registration

Registration
NCT04773977
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
24
Start
2021-03-03
Primary completion
2021-03-09
Lead sponsor
Innovent Biologics (Suzhou) Co. Ltd.
Conditions
Overweight/Obesity
Interventions
DRUG:IBI362 liquid formulation; DRUG:IBI362 lyophilized powder
Results posted
FALSE

Registered primary outcomes

  • Evaluate the PK parameters of IBI362 in healthy Chinese male subjects [From the first dose of study drug until 8 weeks]

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