LivingGLP1
Study S003324

A Randomized, Double-blind, Placebo-controlled, Multiple-ascending-dose Phase Ic Study Evaluating the Safety, Tolerability, and Pharmacokinetics of ZT002 Injection in Participants With Overweight or Obesity

Registration

Registration
NCT06371326
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
28
Start
2023-11-21
Primary completion
2024-04-15
Lead sponsor
Beijing QL Biopharmaceutical Co.,Ltd
Conditions
Overweight or Obesity
Interventions
DRUG:ZT002 Injection; DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • Safety and tolerability of a multiple escalation dose of ZT002 through the incidence and severity of treatment emergent adverse events in MAD Cohorts. Number of participants with treatment-emergent adverse events. [up to 270 days]
  • Safety and tolerability of a multiple escalation dose of ZT002 through the incidence severity of serious adverse events in MAD Cohorts. Number of participants with serious adverse events. [up to 270 days]

Linked records (0)

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